Research Radartracking 1,138 published studies · 277 human · 6 safety signals · 42 clinical trials · 44 cancer pages · updated Jul 2026Open the Research Map →

Squamous Cervical Carcinoma

Auto-discovered from research; not yet curated.

Auto-added · review pending
Educational only: This page is not medical advice. Coordinate decisions with your oncology team.

OncoForge editorial · How we review →

AI extractedhuman reviewedsources checkedretractions suppressed

Evidence at a glanceHuman trial / meta-analysisMixed results⚠ Studies disagree
19 published studies that name Squamous Cervical Carcinoma15 human studies approved & graded (trial, observational, or meta-analysis)9 human clinical studies in the Squamous Cervical Carcinoma corpus124 source documents in the Squamous Cervical Carcinoma corpus
Why this grade?

Human trial / meta-analysisIncludes human trial or meta-analysis evidence.

Computed deterministically from the studies’ types and reported outcomes — not written by AI, and not a claim that anything works.

What the guidelines say

NCI PDQESMONCCNASCO

We link the authoritative guidelines rather than reproduce them. Below, the treatments on this page are split into standard care, guideline or regulatory options, supportive care, and studied but not standard so established care is not mixed with experimental or supportive items.

Guideline / FDA options - context-specific
  • Pembrolizumab
Studied, not standard - investigational
  • Cisplatin
  • Topotecan
  • Trastuzumab Deruxtecan
  • Trastuzumab-Deruxtecan (T-Dxd)

Read the guidelines

Cancer-specific deep links aren’t curated yet — these search the authoritative sources for Squamous Cervical Carcinoma.

Treatment map: Squamous Cervical Carcinoma

Open as a full page →

Standard care plus every compound studied in the literature (each cited) and graded by evidence, organized by clinical readiness. A category, not a verdict that anything works — confirm anything here with your oncology team.

5
Interventions
0
Standard of care
4
Tested in people
0
Lab / animal
0
Named in lit.
4
Classes
Standard of care (0) Guideline option (1) Tested in people (4) Lab / animal only (0) Named in the literature (0)

Tested in people, by trial phase: Phase II ×2 · phase not reported ×2

Clinical evidence
Preclinical evidence
Standard of care
Guideline option
Tested in people
Lab / animal only
Named in the literature
Chemotherapy
1
Targeted therapy
2
Immunotherapy
1
Other
1

Columns group into clinical evidence (used in, or tested on, people) and preclinical evidence (lab/animal, or only named in the literature). Cell = number of interventions; a dashed cell means none recorded there.

Established care — detail (1)
Immunotherapy
Pembrolizumab
FDA-approved for this cancer.
Guideline option
Investigational & adjunct compounds — detail (4)

"Tested in people" rows show the highest trial phase found in that compound's cited human studies (Phase I–IV; "phase not reported" = a human study with no phase tag). "Studied" = named in the cited literature for this cancer. "FDA ✓" = FDA-approved for this cancer; "off-label" = an FDA-approved drug used outside its approved indications (per openFDA). Not a claim that anything works.

Reported figures

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What supports this page

The kinds of sources behind this page, strongest at the top. Faint rungs show what is not here yet.

Guideline
1
Meta-analysis
1
Systematic review
1
Randomized trial
1
Clinical trial
9
Observational
0
Case report
14
Review
83
Preclinical
0
Other
14

Living document — last change June 12, 2026: New cancer type added.

Overview

Squamous Cervical Carcinoma is tracked here from the published studies that mention it. This page shows the research evidence collected so far — it is not a curated clinical overview.

Pooled evidence across studies

PubMed
  • Sample_size: 2852 patients (113–5591 across studies) · (regimen unspecified)
    2 studies · 0% agree · heterogeneous361810499470836
  • Follow-up duration: 70.55 months (59.1–82 across studies) · (regimen unspecified)
    2 studies · 0% agree · heterogeneous354800949470836
  • Recurrence site distribution: 50% (38.8–61.2 across studies) · (regimen unspecified)
    2 studies · 0% agree · heterogeneous35480094
  • Recurrence rate after radical trachelectomy: 4% (0–8 across studies) · (regimen unspecified)
    2 studies · 0% agree · heterogeneous15099964

Compounds compared by evidence

PubMed

How to read this: Ranked by the strength and volume of the evidence — NOT by how well a treatment works. A higher rank means a compound has been studied more, or in stronger study designs (e.g. randomized trials over lab studies), not that it produces better outcomes. The effect column shows the largest pooled figure reported, not a head-to-head comparison.

#CompoundEvidence strengthStudiesLargest pooled effect
1Cisplatin ChemotherapyHuman trial / meta-analysis1
2Topotecan OtherHuman trial / meta-analysis1
3Trastuzumab Deruxtecan Targeted therapyHuman · observational1
4Trastuzumab-Deruxtecan (T-Dxd) Targeted therapyHuman · observational1
5Pembrolizumab ImmunotherapyAnimal only1

Medicines & supplements studied for Squamous Cervical Carcinoma

PubMedFDAClinicalTrials.gov

Every drug, supplement, and other agent the published studies cover for Squamous Cervical Carcinoma, ranked by how strong the evidence is — what studies report, not a recommendation. Tap any to see its full profile.

Medicines · 5

CisplatinHuman trial / meta-analysisReported positive1 human

Includes human trial or meta-analysis evidence.

Largest credible effect: treatment_completion 96%, n=92 PMID 23151423 · response rates 13–77 across 9 studies

Most authoritative study: Weekly topotecan and cisplatin (TOPOCIS) as neo-adjuvant chemotherapy for locally-advanced squamous cervical carcinoma: Results of a phase II multicentric study

Based on a single study.
ChemotherapyFDA off-labelPhase 21 studyFull profile →
TopotecanHuman trial / meta-analysisReported positive1 human

Includes human trial or meta-analysis evidence.

Largest credible effect: treatment_completion 96%, n=92 PMID 23151423 · response rates 13–77 across 9 studies

Most authoritative study: Weekly topotecan and cisplatin (TOPOCIS) as neo-adjuvant chemotherapy for locally-advanced squamous cervical carcinoma: Results of a phase II multicentric study

Based on a single study.
OtherFDA off-labelPhase 21 studyFull profile →
Trastuzumab DeruxtecanHuman · observationalReported positive1 human

Human observational evidence only — no trials.

Largest credible effect: median PFS 5.4 mo [0.8–9.8], n=10 PMID 39639215 · effect sizes 1–5 across 3 studies

Most authoritative study: Real-world evidence of Trastuzumab Deruxtecan (T-DXd) Efficacy in HER2-expressing gynecological malignancies

Based on a single study.
Targeted therapyFDA off-label1 studyFull profile →
Trastuzumab-Deruxtecan (T-Dxd)Human · observationalReported positive1 human

Human observational evidence only — no trials.

Largest credible effect: median PFS 5.4 mo [0.8–9.8], n=10 PMID 39639215 · effect sizes 1–5 across 3 studies

Most authoritative study: Real-world evidence of Trastuzumab Deruxtecan (T-DXd) Efficacy in HER2-expressing gynecological malignancies

Based on a single study.
Targeted therapy1 studyFull profile →
PembrolizumabAnimal onlyReported positive1 animal

Animal studies only — no human data.

Most authoritative study: Targeting PI3Kα increases the efficacy of anti-PD-1 antibody in cervical cancer

No human studies yet · No numeric effect sizes reported · Based on a single study.
ImmunotherapyFDA approved1 studyFull profile →

What recent studies report in Squamous Cervical Carcinoma

These are reviewed studies whose abstracts concern Squamous Cervical Carcinoma. Each describes only what that study reported. This is not a claim by OncoForge that any compound helps or harms Squamous Cervical Carcinoma. Most are early lab, animal, or small human studies, and findings often conflict.

19 studies15 human1 animal⚠ Conflicting evidenceMechanism (12)Trial (1)Supportive care (1)

Tracking 19 published studies of Squamous Cervical Carcinoma: 15 in humans, 1 in animals, 3 reviews/other.

Reported direction across studies: 9 positive, 3 mixed, 4 negative, 3 inconclusive.

Findings conflict — both supportive and negative/mixed results exist (see below). Human evidence is limited.

These counts summarize what the studies reported; they are not a measure of whether anything works for Squamous Cervical Carcinoma.

Compounds with studies mentioning Squamous Cervical Carcinoma

Trastuzumab deruxtecan t dxd (1)Trastuzumab deruxtecan (1)Pembrolizumab (1)Topotecan (1)Cisplatin (1)
Human · observationalReported positiveLimited evidenceTier 3 · early humann = 10

Real-world evidence of Trastuzumab Deruxtecan (T-DXd) Efficacy in HER2-expressing gynecological malignancies

BMC cancer · Dec 2024 · retrospective cohort

Trastuzumab-deruxtecan-t-dxdTrastuzumab-deruxtecanendometrial neoplasmsovarian neoplasmscervical neoplasmsuterine carcinosarcomauterine leiomyosarcomauterine serous carcinomaovarian carcinosarcomahigh-grade serous ovarian carcinomamucinous ovarian carcinomasquamous cervical carcinoma

This retrospective single-center study identified 10 patients with HER2-expressing (IHC 2+/3+) recurrent or metastatic gynecological cancers who received trastuzumab deruxtecan (5.4 mg/kg IV every 3 weeks). The cohort had a median progression-free survival of 5.4 months (95% CI 0.8-9.8). Five patients had a partial response, one had stable disease at 12 weeks, and four had disease progression at initial assessment. Clinical benefit was observed mainly in tumors with HER2 IHC 3+.

Reported effects: median PFS 5.4 mo [0.8–9.8], n=10 · partial responses 5, n=10 · +2 more

Key findings
  • 10 patients with recurrent/metastatic HER2-expressing gynecological malignancies were treated with T-DXd.
  • Histologies included uterine neoplasms (n=5), cervical squamous carcinoma (n=1) and ovarian cancers (n=4).
  • Median age was 65.4 years (25th-75th percentile, 58.1-75.2 years).
  • HER2 by IHC: 5 patients were 3+ and 5 patients were 2+.
  • Median number of prior therapy lines was 4 (range 2-6); 2 uterine serous carcinoma patients were pretreated with trastuzumab and 4 patients had prior immunotherapy.
  • Dose: T-DXd 5.4 mg/kg IV every 3 weeks until progression/toxicity.
  • Median progression-free survival (PFS) in the cohort was 5.4 months (95% CI 0.8-9.8 months).
  • Responses: 5 patients had partial response (including 2 previously treated with trastuzumab), 1 patient had stable disease at 12 weeks, 4 patients had disease progression at initial assessment.
  • Most patients who derived clinical benefit had HER2 IHC 3+ expression.
Limitations: Retrospective, single-center design; Very small sample size (n=10); No control or comparator arm; Heterogeneous mix of gynecologic histologies; Heavily pre-treated population limits generalizability; Limited/absent reporting of safety or adverse event data in the abstract; Potential selection and reporting bias inherent to retrospective series.

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed · Full text

Human · observationalMechanismReported positiveLimited evidenceTier 3 · early humann = 169

Progesterone receptor isoform B in the stroma of squamous cervical carcinoma: An independent favorable prognostic marker correlating with hematogenous metastasis

Taiwanese journal of obstetrics & gynecology · Nov 2024 · retrospective cohort study

squamous cervical carcinoma

This retrospective cohort study examined ERα, PR (A+B) and PRB expression in tumor and stromal compartments of 169 cervical carcinoma samples. Stromal PRB expression was associated with lower 5-year cancer mortality and with lower rates of hematogenous metastasis, and remained an independent predictor of lower 5-year mortality in multivariable analysis. Adding stromal PR or PRB to FIGO stage improved survival prediction accuracy.

Reported effects: stromal PRB association with 5-year mortality, p=0.011, n=169 · stromal ERα association with hematogenous distant metastasis rates, p=0.013, n=169 · +2 more

Key findings
  • ERα and PRs were predominantly expressed in the stromal compartment rather than within cervical cancer cells.
  • Stromal PRB expression significantly correlated with a lower 5-year mortality because of cervical cancer (p = 0.011).
  • Stromal ERα and PRB expressions correlated with lower hematogenous distant metastasis rates (p = 0.013 and p = 0.011, respectively).
  • In multivariable logistic regression analyses, stromal PRB independently conferred a lower risk of 5-year mortality (p = 0.022) regardless of age, histology, FIGO stage, tumor differentiation, lymphovascular space invasion, and lymphatic and hematogenous metastases.
  • Incorporation of stromal PR (A + B) and PRB expression into FIGO stage significantly enhanced the accuracy of survival prediction.
Limitations: Retrospective, observational single-center design; Correlative biomarker study that cannot establish causation; Potential subjectivity in immunohistochemical scoring by pathologists; No external validation cohort reported in the abstract; Abstract does not report effect sizes (HRs/ORs) or confidence intervals for the associations.

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed

ReviewInconclusiveLimited evidenceTier 3 · early human

Locally advanced squamous cervical carcinoma (M0): management and emerging therapeutic options in the precision radiotherapy era

Japanese journal of radiology · Apr 2024 · narrative review

squamous cervical carcinoma (locally advanced, M0)

This narrative review discusses diagnostic and clinical management advances for locally advanced squamous cervical carcinoma (M0), including PET-MRI to improve staging, new radiation technologies to deliver higher doses while lowering toxicities, evolving surgical concepts, and the growing potential role of targeted therapies and immunotherapy. It summarizes emerging options in the precision radiotherapy era but does not present new experimental data.

Key findings
  • PET-MRI can improve clinical staging accuracy for squamous cervical carcinoma.
  • New radiation therapy technologies permit delivery of higher doses while lowering toxicities.
  • New surgical concepts could contribute to overall management in this setting.
  • Targeted therapies and immunotherapy are anticipated to have an increasing role in the management of locally advanced SCC.
Limitations: Narrative review (not a systematic review) with potential for subjective selection and interpretation of literature.; No original experimental or quantitative data reported in the abstract.; Abstract does not specify particular targeted agents, immunotherapies, or clinical trial results..

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed

Animal studyReported positivePreclinical onlyTier 2 · animal

Targeting PI3Kα increases the efficacy of anti-PD-1 antibody in cervical cancer

Immunology · Nov 2023

Pembrolizumabcervical cancersquamous cervical carcinoma

The study examined how activation of the PI3K pathway and PIK3CA-E545K mutation affect PD-L1 expression and CD8+ T cells in cervical cancer tissues and cell models. The authors report that PIK3CA-E545K increases PD-L1 via upregulation of IRF1 and represses CD8+ T cell differentiation. A PI3Kα-specific inhibitor activated the tumour immune microenvironment and promoted CD8+ T cell differentiation in PIK3CA-mutant xenografts, and combining the inhibitor with anti-PD-1 increased anti-tumour efficacy in cell-derived and patient-derived xenograft models. A single clinical case of complete remission with pembrolizumab in a PIK3CA-E545K patient is also described.

Studied with: anti-PD-1 antibody (pembrolizumab).

Key findings
  • PD-L1 overexpression was more frequent in older women with squamous cervical carcinoma and associated with longer progression-free and overall survival (no numeric values reported in abstract).
  • PIK3CA mutation (E545K) increased PD-L1 mRNA and protein levels and repressed CD8+ T cell differentiation in cervical cancer.
  • PIK3CA-E545K promotes PD-L1 expression by upregulating the transcription factor IRF1 (shown by luciferase and ChIP assays).
  • A PI3Kα-specific inhibitor activated the immune microenvironment, regulated PD-1/PD-L1-related pathways, and promoted CD8+ T cell differentiation and proliferation in Caski CDX models with PIK3CA-E545K mutation.
  • PI3Kα inhibitor significantly enhanced the anti-tumour efficacy of PD-1 blockade in both CDX and PDX models.
  • A single reported case: continuous pembrolizumab monotherapy induced complete remission in a recurrent metastatic cervical cancer patient with PIK3CA-E545K mutation (single case observation).
Limitations: Predominantly preclinical evidence: in vitro assays and mouse xenograft (CDX/PDX) models; no controlled clinical trial data presented.; Human evidence limited to correlative tissue analyses and a single patient case report; results from one patient cannot establish efficacy.; Abstract does not report sample sizes, dosing, or statistical effect sizes for findings.; Safety, toxicity, and tolerability of PI3Kα inhibitor ± anti-PD-1 not reported in abstract.; Potential selection bias and lack of randomized comparison in described experiments (not specified in abstract)..

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed

Human · observationalMechanismMixed resultsLimited evidenceTier 3 · early humann = 5591

Prognostic factors for squamous cervical carcinoma identified by competing-risks analysis: A study based on the SEER database

Medicine · Sep 2022 · retrospective cohort analysis of SEER database (2004-2013)

squamous cervical carcinomauterine cervical neoplasms

Researchers analyzed SEER registry data from 2004–2013 including 5,591 patients with squamous cervical carcinoma and compared Cox regression with competing-risks methods (cause-specific and sub-distribution models). Several factors (age, metastasis, AJCC stage, surgery, chemotherapy, radiation sequence with surgery, lymph node dissection, tumor size, and tumor grade) were identified as prognostic across the three methods, while results for race, radiation status, and marital status differed between models. The authors conclude that competing-risks (especially the sub-distribution model) may more accurately identify prognostic factors than conventional Cox regression.

Reported effect: sample_size 5591, n=5591

Key findings
  • A total of 5591 SCC patients met the inclusion criteria.
  • Univariate analysis with the cumulative incidence function was performed and significant covariates (P < .05) were included in multivariable models.
  • Three methods were compared: Cox regression, cause-specific (CS) hazard model, and sub-distribution (SD) hazard model.
  • Age, metastasis, American Joint Committee on Cancer stage, surgery, chemotherapy, radiation sequence with surgery, lymph node dissection, tumor size, and tumor grade were prognostic factors affecting survival in all three methods.
  • Race and radiation status were prognostic in Cox regression and CS analysis but differed in the SD analysis.
  • Being separated, divorced, or widowed was an independent prognostic factor in Cox regression, but results differed in CS and SD analyses.
  • The authors suggest the SD competing-risks model may be better suited to estimate clinical prognosis and that SD results were close to CS analysis.
Limitations: Retrospective registry-based analysis (SEER) subject to limitations of observational data.; Potential for unmeasured confounding and coding/misclassification in registry data.; Prognostic associations cannot establish causality..

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed · Full text

Human · observationalMechanismReported positiveLimited evidenceTier 3 · early humann = 472

Prognostic Effect of Primary Recurrence Patterns in Squamous Cervical Carcinoma After Radical Surgery

Frontiers in oncology · Apr 2022

squamous cervical carcinoma

This observational study analyzed 472 stage IB-IIA squamous cervical cancer patients after initial treatment to examine how primary recurrence patterns relate to prognosis. Median follow-up was 59.1 months; 5-year overall survival was 33.7% and median overall survival was 24.0 months. Nodal recurrence had higher overall survival than organ recurrence (38.3% vs 30.7%, P = 0.001). Several clinicopathological features (recurrence subtype, therapy for relapse, FIGO stage, adjuvant radiotherapy, preoperative SCC-Ag, and risk subgroup) were independently associated with overall survival and a prognostic nomogram was generated.

Reported effects: median follow-up 59.1 mo, n=472 · 5-year overall survival (OS) 33.7%, n=472 · +9 more

Key findings
  • A total of 472 patients were included; median follow-up 59.1 months, 5-year OS 33.7%, median OS 24.0 months.
  • Overall, 38.8% of patients had locoregional recurrence and 61.2% had distant metastasis; survival rates were comparable between these groups.
  • Patients with nodal recurrence had better OS than those with organ recurrence (38.3% vs 30.7%; P = 0.001).
  • Patients not receiving adjuvant radiotherapy were reported to have increased risk of pelvic recurrence (OR = 0.148; 95% CI: 0.075-0.291; P = 0.000).
  • Positive lymph-vascular space invasion was associated with increased risk of distant metastasis (OR = 1.928; 95% CI: 1.151-3.229; P = 0.013).
  • No chemotherapy was associated with risk of distant metastasis (OR = 0.521; 95% CI: 0.317-0.733; P = 0.040).
  • Positive lymph node status after initial treatment was associated with nodal recurrence (OR = 3.729; 95% CI: 1.838-7.563; P = 0.000).
  • Elevated preoperative SCC-Ag levels were associated with organ recurrence (OR = 1.642; 95% CI: 1.325-2.265; P = 0.002).
  • Recurrence subtype, therapy for relapse, FIGO stage, adjuvant radiotherapy, preoperative SCC-Ag levels, and risk subgroup were independently associated with overall survival; a prognostic nomogram was generated.
Limitations: Observational human cohort (causality cannot be inferred).; Study design (prospective vs retrospective, single- vs multi-center) is not specified in the abstract.; Potential for unmeasured confounding and selection bias inherent to observational analyses.; Nomogram generation is reported but external validation is not described in the abstract..

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed · Full text

Human · observationalMechanismReported positiveLimited evidenceTier 3 · early human

PI3KCA Mutations in Uterine Cervix Carcinoma

Journal of clinical medicine · Jan 2021 · bioinformatic analysis of TCGA genomic data comparing squamous cervical carcinomas with and without PIK3CA mutations

squamous cervical carcinoma

The authors analyzed publicly available TCGA data to characterize PIK3CA mutations in squamous cervical carcinomas. They found PIK3CA mutations in 27.1% of cases and that PIK3CA-mutated tumors have higher tumor mutation burden and more frequent co-mutations in RTK/K-RAS/BRAF/MAPK and Wnt/β-catenin pathway genes. The authors suggest these findings could point to opportunities for PI3K-directed and immunotherapy approaches, but no clinical testing was reported.

Reported effect: PIK3CA mutation frequency 27.1%

Key findings
  • PIK3CA mutations were observed in 27.1% of squamous cervical cancers.
  • PIK3CA was the most frequently mutated gene in these cancers.
  • PIK3CA-mutated cervical cancers showed higher rates of mutations in other cancer-associated pathways, including tyrosine kinase receptors/K-RAS/BRAF/MAPK and Wnt/β-catenin pathways.
  • PIK3CA-mutated cervical cancers displayed a higher tumor mutation burden (TMB) than non-mutated cancers.
  • Authors propose that frequent PIK3CA mutations may represent opportunities for development of PI3K inhibitors and that increased TMB may confer immunotherapy sensitivity (hypothesis only).
Limitations: Analysis uses retrospective, publicly available TCGA data (observational genomic analysis).; Sample size is not reported in the abstract.; No functional validation or experimental/clinical testing of targeted therapies or immunotherapy sensitivity was reported.; No clinical outcome or treatment-response data are provided in the abstract to link mutations with prognosis or therapeutic benefit.; Possible selection biases and limitations inherent to TCGA cohort (not detailed in abstract)..

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed · Full text

Case reportInconclusiveLimited evidenceTier 3 · early humann = 1

Gynecological tumor triplicity

Ceska gynekologie · Jan 2018 · case report

squamous cervical carcinoma (stage IB1)endometrioid adenocarcinoma of the uterusserous borderline tumor of the left ovary (with non-invasive implants)borderline ovarian tumor

This single-patient case report describes a 64-year-old woman planned for laparoscopic radical hysterectomy for confirmed stage IB1 squamous cervical carcinoma. Surgery was converted to laparotomy after unexpected findings of a left ovarian borderline tumor and tiny peritoneal implants; the patient underwent radical abdominal hysterectomy, bilateral salpingo-oophorectomy, omentectomy, appendectomy, pelvic lymphadenectomy and peritonectomy. Final histology showed three distinct neoplasms: endometrioid adenocarcinoma of the uterus, a serous borderline tumor of the left ovary with non-invasive implants, and no residual cervical carcinoma.

Key findings
  • Patient: 64-year-old female with confirmed squamous cervical carcinoma stage IB1 who was scheduled for total laparoscopic radical hysterectomy.
  • Intraoperative finding prompted conversion to laparotomy because of an unexpected left ovarian malignancy and tiny implants on the uterus and pelvic walls.
  • Performed procedures: radical abdominal hysterectomy, bilateral salpingo-oophorectomy, omentectomy, appendectomy, pelvic lymphadenectomy and peritonectomy.
  • Definitive postoperative histology: endometrioid adenocarcinoma of the uterus, serous left ovary borderline tumor with non-invasive implants, and no residual tumor of the cervical carcinoma.
  • Authors state this is the first reported case of three simultaneous gynecologic tumors ('tumor triplicity') at one time.
Limitations: Single-case report (n=1) — results are not generalizable.; No long-term follow-up or outcomes reported (oncologic outcomes, recurrence, survival absent).; No molecular, genetic, or pathological detail beyond histologic diagnoses provided.; No comparison group or systematic data — descriptive only..

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed

Human · observationalMechanismMixed resultsLimited evidenceTier 3 · early humann = 380

Correlation Between Platelet and Hemoglobin Levels and Pathological Characteristics and Prognosis of Early-Stage Squamous Cervical Carcinoma

Medical science monitor : international medical journal of experimental and clinical research · Dec 2015 · retrospective analysis

early-stage squamous cervical carcinoma

This retrospective study analyzed 380 patients with early-stage squamous cervical carcinoma to assess associations between preoperative hemoglobin and platelet levels and pathological features and survival. Low hemoglobin (<120 g/L) was associated with worse overall survival and was an independent risk factor on Cox regression. High platelet count (>300×10^9/L) was associated with adverse pathological features (higher stage, larger tumor diameter, lymphatic metastasis) but was not significantly associated with overall survival alone; the subgroup with both high platelets and low hemoglobin had significantly worse survival.

Reported effects: total_sample_size 380, n=380 · Number of patients by PLT group 69, p P<0.05, n=380 · +5 more

Key findings
  • Of 380 patients, 69 had PLT levels >300×10^9/L and 311 had PLT levels ≤300×10^9/L; these PLT groups differed significantly in tumor staging, tumor diameter, and lymphatic metastasis (P<0.05).
  • 134 patients had HGB levels <120 g/L and 246 had HGB levels ≥120 g/L; these HGB groups differed significantly in tumor staging, extent of differentiation, and lymphatic metastasis (P<0.05).
  • Overall survival was lower in the PLT >300×10^9/L group than in the PLT ≤300×10^9/L group, but this difference was not statistically significant.
  • Overall survival was significantly lower in the HGB <120 g/L group than in the HGB ≥120 g/L group (P<0.05).
  • The group with PLT >300×10^9/L and HGB <120 g/L had significantly lower overall survival than the group with PLT ≤300×10^9/L and HGB ≤120 g/L (P<0.05).
  • Cox regression identified pre-operative HGB <120 g/L as an independent risk factor for prognosis.
Limitations: Retrospective observational design with potential for selection bias and unmeasured confounding.; No hazard ratios, confidence intervals, or absolute survival rates were reported in the abstract.; Details of covariates included in the Cox regression are not specified in the abstract.; Findings are from a single retrospective cohort and may lack external validation..

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed · Full text

Human trialTrialReported positiveLimited evidenceTier 4 · clinicaln = 92

Weekly topotecan and cisplatin (TOPOCIS) as neo-adjuvant chemotherapy for locally-advanced squamous cervical carcinoma: Results of a phase II multicentric study

European journal of cancer (Oxford, England : 1990) · Mar 2013 · Phase II multicenter, single-arm neoadjuvant chemotherapy trial

TopotecanCisplatinsquamous cervical carcinomaadenosquamous cervical carcinomalocally-advanced cervical cancer (FIGO IB2, IIA, IIB)

This phase II multicenter study enrolled 92 patients with locally advanced squamous or adenosquamous cervical cancer who received six weekly courses of topotecan (2 mg/m2) plus cisplatin (40 mg/m2) as neoadjuvant chemotherapy. The regimen was deliverable (96% completed six courses; 95% of courses given at full dose) and produced a clinical response rate of 77% and an overall pathologic response in 67% (optimal response 32%, downstaging 57%). Grade 3-4 hematologic toxicity occurred in 28% of patients, supportive therapies were given to 24%, and with median follow-up 18 months, 76% were alive and recurrence-free while 24% relapsed and 13% died.

Reported effects: treatment_completion 96%, n=92 · full_dose_course_percentage 95%, n=92 · +13 more

Studied with: cisplatin.

Key findings
  • 96% of patients completed the six planned courses of chemotherapy.
  • 95% of courses were administered at a full dose and without interruption or delay.
  • Grade 3-4 haematological toxicity was observed in 28% of patients (5% out of cycles).
  • Support therapies were given to 24% of patients.
  • Clinical response rate was 77%.
  • Overall pathologic response observed in 67% of patients.
  • Optimal pathologic response rate was 32%.
  • Disease downstage occurred in 57% of patients.
  • Nodal metastases occurred in 36% of patients.
  • Adjuvant radiotherapy and/or chemotherapy was prescribed in 55% of patients.
  • Median follow-up was 18 months; 76% alive and free from recurrence, 24% relapsed, 13% died.
Limitations: Single-arm Phase II design with no randomized or concurrent control group; Relatively short median follow-up (18 months) for survival outcomes; Adjuvant therapy was given to 55% of patients, which may confound interpretation of longer-term outcomes; Sample size (n=92) limits precision of survival and subgroup estimates; Endpoints are primarily response and short-term outcomes rather than long-term randomized efficacy.

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed

Human · observationalMechanismReported positiveLimited evidenceTier 3 · early humann = 39

Levels of Circulating TIMP-2 and MMP2-TIMP2 Complex Are Decreased in Squamous Cervical Carcinoma

Obstetrics and gynecology international · Jan 2010 · case-control

squamous cervical carcinoma

The authors measured serum MMP-9, MMP-2-TIMP-2 complex, TIMP-1, and TIMP-2 by ELISA in 12 patients with squamous cervical carcinoma and 27 healthy volunteers. They found that median serum TIMP-2 and MMP-2-TIMP-2 complex levels were lower in patients than in healthy controls, with the TIMP-2 difference reported as statistically significant. The paper reports an association between lower circulating TIMP-2 / MMP-2-TIMP-2 complex levels and squamous cervical carcinoma in this sample.

Reported effects: serum TIMP-2 (median) 136, p < .000, n=39 · serum proMMP2-TIMP2 complex, p < .006, n=39

Key findings
  • Serum TIMP-2 values decreased significantly from healthy controls (median 323 mug/l, range 305-342 mug/l) to malignant (median 136 mug/l, range 120-151 mug/l) squamous cervical carcinoma patients (P < .000).
  • Serum proMMP2-TIMP2 complex values decreased from control patients to squamous cervical carcinoma patients (P < .006).
  • MMP-9 and TIMP-1 were analyzed by ELISA, but the abstract reports the primary between-group differences for TIMP-2 and MMP-2-TIMP-2 complex.
Limitations: Small sample size (12 patients, 27 controls).; Cross-sectional / case-control design with single timepoint serum measurements.; Abstract gives limited clinical detail (no tumor stage, treatment status, or potential confounder adjustment reported).; No longitudinal data or assessment of clinical outcomes (prognosis, metastasis) provided in the abstract..

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed · Full text

Human · observationalMechanismReported positiveLimited evidenceTier 3 · early humann = 129

The risk of residual neoplasia in women with microinvasive squamous cervical carcinoma and positive cone margins

International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · Mar 2006 · retrospective histopathology review

squamous cervical carcinomacervical microinvasive carcinoma

This retrospective review examined hysterectomy specimens from 129 women with microinvasive squamous cervical carcinoma who had high-grade lesions or invasive carcinoma at cone margins. 59.7% had residual disease, 44.2% had residual high-grade lesions, and 15.5% had residual invasive carcinoma. Positive postconization endocervical curettage, positive cone margins for invasive carcinoma, and stromal invasion depth >1 mm were significantly associated with residual disease; positive cone margins predicted residual invasive disease in Cox analysis (HR 3.22, 95% CI 1.21-8.60, P=0.019). The authors recommend repeat cone biopsy to determine lesion severity before planning treatment.

Reported effects: residual disease prevalence 59.7%, n=129 · residual high-grade lesions prevalence 44.2%, n=129 · +5 more

Key findings
  • Of the 129 patients, 77 (59.7%) had residual disease in the hysterectomy specimens.
  • 57 (44.2%) had residual high-grade lesions.
  • Twenty patients (15.5%) had residual invasive carcinoma: 18 were microinvasive and 2 were invasive.
  • Factors significantly affecting the risk of residual disease included positive postconization endocervical curettage (P= 0.001), positive cone margins for invasive carcinoma (P= 0.003), and depth of stromal invasion >1 mm (P= 0.014).
  • Cox proportional hazards analysis revealed positive cone margins for invasive carcinoma as significant predictor of residual invasive disease (hazard ratio, 3.22; 95% CI 1.21-8.60, P= 0.019).
  • Authors recommend repeat cone biopsy to determine lesion severity before planning treatment.
Limitations: Retrospective study design.; Study includes only patients who proceeded to hysterectomy after cone biopsy, creating selection bias.; Moderate sample size (n=129).; Abstract does not report adjustment for potential confounders beyond the Cox model or long-term clinical outcomes..

AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed

Browse all studies mentioning Squamous Cervical Carcinoma

Where the evidence is

What has been studied, and how strong it is, by topic. A dashed cell means no studies were found for that combination — a gap, not evidence of no effect. Open a row to see its studies.

CompoundHuman evidenceMechanismSafetyTrial
Cisplatin11
Topotecan11
Trastuzumab Deruxtecan1
Trastuzumab-Deruxtecan (T-Dxd)1
Pembrolizumab1

Study mix

19 published studies by what they were done in. Lab and animal findings often do not carry over to people.

15 Human1 Animal3 Review/other
Reported directionReported positive9Mixed results3Reported negative4Inconclusive3

Compounds with reported-positive results in Squamous Cervical Carcinoma

Where at least one study reported a positive result, shown with the full picture, not just the wins. Positive results are more likely to be published, and most of these are early lab or animal studies that may not translate to people. This reports what studies found, not what works.

Human evidence

Limitations: Retrospective, single-center design; Very small sample size (n=10); No control or comparator arm; Heterogeneous mix of gynecologic histologies; Heavily pre-treated population limits generalizability; Limited/absent reporting of safety or adverse event data in the abstract.
Cited positive studies (1)
Trastuzumab Deruxtecan1 positive1 human
Limitations: Retrospective, single-center design; Very small sample size (n=10); No control or comparator arm; Heterogeneous mix of gynecologic histologies; Heavily pre-treated population limits generalizability; Limited/absent reporting of safety or adverse event data in the abstract.
Cited positive studies (1)
Topotecan1 positive1 human
Limitations: Single-arm Phase II design with no randomized or concurrent control group; Relatively short median follow-up (18 months) for survival outcomes; Adjuvant therapy was given to 55% of patients, which may confound interpretation of longer-term outcomes; Sample size (n=92) limits precision of survival and subgroup estimates; Endpoints are primarily response and short-term outcomes rather than long-term randomized efficacy.
Cited positive studies (1)
Cisplatin1 positive1 human
Limitations: Single-arm Phase II design with no randomized or concurrent control group; Relatively short median follow-up (18 months) for survival outcomes; Adjuvant therapy was given to 55% of patients, which may confound interpretation of longer-term outcomes; Sample size (n=92) limits precision of survival and subgroup estimates; Endpoints are primarily response and short-term outcomes rather than long-term randomized efficacy.
Cited positive studies (1)
Preclinical only: lab / animal (1)
Pembrolizumab1 positive1 animal
Limitations: Predominantly preclinical evidence: in vitro assays and mouse xenograft (CDX/PDX) models; no controlled clinical trial data presented.; Human evidence limited to correlative tissue analyses and a single patient case report; results from one patient cannot establish efficacy.; Abstract does not report sample sizes, dosing, or statistical effect sizes for findings.; Safety, toxicity, and tolerability of PI3Kα inhibitor ± anti-PD-1 not reported in abstract.; Potential selection bias and lack of randomized comparison in described experiments (not specified in abstract)..
Cited positive studies (1)

Evidence at a glance: compounds studied in Squamous Cervical Carcinoma

A deterministic grade of what published studies report for each: strength of evidence, the reported direction, and the largest credible effect, strongest-evidence first. This summarizes findings; it is not a claim that anything works.

CisplatinHuman trial / meta-analysisReported positive1 human

Includes human trial or meta-analysis evidence.

Largest credible effect: treatment_completion 96%, n=92 PMID 23151423 · response rates 13–77 across 9 studies

Most authoritative study: Weekly topotecan and cisplatin (TOPOCIS) as neo-adjuvant chemotherapy for locally-advanced squamous cervical carcinoma: Results of a phase II multicentric study

Based on a single study.
TopotecanHuman trial / meta-analysisReported positive1 human

Includes human trial or meta-analysis evidence.

Largest credible effect: treatment_completion 96%, n=92 PMID 23151423 · response rates 13–77 across 9 studies

Most authoritative study: Weekly topotecan and cisplatin (TOPOCIS) as neo-adjuvant chemotherapy for locally-advanced squamous cervical carcinoma: Results of a phase II multicentric study

Based on a single study.
Trastuzumab DeruxtecanHuman · observationalReported positive1 human

Human observational evidence only — no trials.

Largest credible effect: median PFS 5.4 mo [0.8–9.8], n=10 PMID 39639215 · effect sizes 1–5 across 3 studies

Most authoritative study: Real-world evidence of Trastuzumab Deruxtecan (T-DXd) Efficacy in HER2-expressing gynecological malignancies

Based on a single study.
Trastuzumab-Deruxtecan (T-Dxd)Human · observationalReported positive1 human

Human observational evidence only — no trials.

Largest credible effect: median PFS 5.4 mo [0.8–9.8], n=10 PMID 39639215 · effect sizes 1–5 across 3 studies

Most authoritative study: Real-world evidence of Trastuzumab Deruxtecan (T-DXd) Efficacy in HER2-expressing gynecological malignancies

Based on a single study.
PembrolizumabAnimal onlyReported positive1 animal

Animal studies only — no human data.

Most authoritative study: Targeting PI3Kα increases the efficacy of anti-PD-1 antibody in cervical cancer

No human studies yet · No numeric effect sizes reported · Based on a single study.

What the research shows for Squamous Cervical Carcinoma

A plain-language summary of the reviewed studies OncoForge tracks for Squamous Cervical Carcinoma. It reports what those studies described, not a claim that any compound or therapy helps or harms Squamous Cervical Carcinoma. Most of this evidence is early, and findings often conflict.

  • A meta-analysis of published data on conservative surgical approaches (including radical trachelectomy) for FIGO IA2 squamous cervical cancer reported recurrence rates after radical trachelectomy of about 0%–8% and noted over 35 live births among roughly 210 women, based on heterogeneous published series.
  • A narrative review of locally advanced (M0) squamous cervical carcinoma described evolving diagnostic and management approaches—such as PET-MRI for staging, newer radiation technologies to escalate dose while aiming to reduce toxicity, and changing surgical concepts—but drew no definitive conclusions about superior strategies.
  • A retrospective single-center study identified 10 patients with HER2-expressing (IHC 2+/3+) recurrent or metastatic gynecologic cancers who received trastuzumab deruxtecan (5.4 mg/kg IV every 3 weeks) and reported a median progression-free survival of 5.4 months for the cohort; the sample was small, retrospective, and included mixed gynecologic tumor types.
  • Overall, the available reports are limited in size and design (surgical case series, narrative reviews, and small retrospective cohorts) and provide early, sometimes mixed, information rather than consistent, high-quality evidence specific to squamous cervical carcinoma.

Compounds studied in Squamous Cervical Carcinoma

Trastuzumab Deruxtecan1 study
In a retrospective single-center series that included HER2-expressing recurrent or metastatic gynecologic cancers (including cervical cases), trastuzumab deruxtecan (5.4 mg/kg IV every 3 weeks) was reported with a cohort median progression-free survival of 5.4 months, but the analysis was small (10 patients), retrospective, and included mixed gynecologic tumor types.

Supportive & alternative options discussed

  • Hyperthermia (heat): Also discussed as a supportive option to increase local tumor control when combined with radiotherapy in locally advanced cervical cancer, though not evaluated in the studies summarized above.
  • Acupuncture: Also discussed as a supportive option for managing treatment-related symptoms (for example pain or nausea) in cervical cancer care, but not addressed by the studies summarized above.
  • Exercise / prehabilitation: Also discussed as a supportive strategy to improve quality of life and functional status for people with cervical cancer, though not evaluated in the studies summarized above.
  • Mind–body (MBSR / CBT): Also discussed as a supportive approach for coping and symptom management in cervical cancer, but not studied in the reports summarized here.
  • Mistletoe (VAE): Also discussed in some contexts as an adjunctive or supportive therapy for cancer patients, but it was not evaluated in the studies summarized above.

What we don’t know yet

  • Do HER2-targeted antibody–drug conjugates like trastuzumab deruxtecan improve clinically meaningful outcomes specifically for squamous cervical carcinoma in prospective randomized trials?
  • What is the prevalence and prognostic significance of HER2 expression specifically in squamous cervical carcinoma, and which patients (if any) might derive benefit from HER2-directed therapies?
  • What are the long-term oncologic and fertility outcomes after radical trachelectomy for FIGO IA2 squamous cervical cancer in larger, prospective cohorts?
  • What are the optimal dosing, schedule, and safety profile of trastuzumab deruxtecan in cervical cancer patients, including those with prior therapies and comorbidities?
  • How do newer imaging modalities (for example PET-MRI) and advanced radiotherapy techniques affect staging accuracy, treatment selection, toxicity, and long-term outcomes in locally advanced squamous cervical carcinoma?
  • Are there randomized, controlled data comparing conservative surgical approaches versus standard surgery or (chemo)radiation for early-stage squamous cervical carcinoma that establish comparative benefits and harms?
The evidence summarized here is preliminary and limited—mostly narrative reviews, small retrospective series, and pooled surgical case data—so it does not establish benefits, risks, or standard-of-care recommendations for these interventions in squamous cervical carcinoma.

Clinical trials in Squamous Cervical Carcinoma

37 ongoing · 38 completed · tracked from ClinicalTrials.gov. Recruiting is not the same as proven, and completed is not the same as positive — read the results. Not a recommendation.

Completed
13 stopped (terminated / withdrawn / suspended)

Search all trials on ClinicalTrials.gov →

Getting care & support

Nonprofit / Gov

Practical, vetted help for Squamous Cervical Carcinoma — advocacy, paying for treatment, second opinions, and caregivers.

If you’re struggling emotionally, you don’t have to wait.

Advocacy & community

No dedicated organization for this specific cancer is curated yet — these general organizations can help in the meantime.

Financial help

  • PAN FoundationCopay assistance funds by diagnosis (funds open and close as money allows). · status changes often — check the fund’s site
  • HealthWell FoundationCopay and premium assistance funds by disease. · status changes often — check the fund’s site
  • CancerCare — financial assistanceLimited grants plus free financial counseling. · status changes often — check the fund’s site
  • Family ReachHelp with everyday living costs (rent, transport, food) during treatment. · status changes often — check the fund’s site
  • NeedyMedsSearchable directory of drug patient-assistance and discount programs. · status changes often — check the fund’s site
What you’ll typically need to apply
  • Your diagnosis and, if you have it, the specific drug/treatment name (from your care team).
  • Insurance details — your member ID card, or a note that you're uninsured (some funds require active insurance, some don't).
  • Proof of income and household size (recent pay stubs, a tax return, or a benefits letter) — most funds are income-based.
  • Your prescriber's contact information; some programs need the clinic to submit part of the application.
  • Apply early and re-check: funds open and close as money is available, so a closed fund may reopen.

General guidance — each program sets its own eligibility. Confirm requirements on the program’s site.

Help paying for the medicines on this page

Second opinions

Caregiver support

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