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Breast Invasive Ductal Carcinoma (IDC)

Breast Invasive Ductal Carcinoma (IDC): treatment map

Standard care plus compounds studied in the literature, organized by clinical readiness.

Educational only. This is not medical advice and not a recommendation. Confirm anything here with your oncology team.

Treatment map: Breast Invasive Ductal Carcinoma (IDC)

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.

128
Interventions
50
Standard of care
29
Tested in people
2
Lab / animal
45
Named in lit.
9
Classes
Standard of care (50) Guideline option (2) Tested in people (29) Lab / animal only (2) Named in the literature (45)

Tested in people, by trial phase: phase not reported ×29

Clinical evidence
Preclinical evidence
Standard of care
Guideline option
Tested in people
Lab / animal only
Named in the literature
Surgery & procedures
7
11
11
Radiotherapy
9
6
14
Chemotherapy
6
Targeted therapy
15
1
6
Immunotherapy
4
1
Hormonal therapy
9
2
5
6
Repurposed drugs
1
2
Supplements & natural agents
4
Other
1
2
5

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 (52)
Surgery & procedures
Breast-conserving surgery (lumpectomy) + SLNB when feasible
Breast-conserving surgery (lumpectomy) + SLNB when feasible; oncoplastic techniques expand eligibility and cosmesis.
CurativeStandardCurated
Mastectomy when disease extent, multicentricity, prior RT, or patient preference dictates; nipple-sparing
Mastectomy when disease extent, multicentricity, prior RT, or patient preference dictates; nipple-sparing is feasible in selected cases with careful margin assessment.
CurativeStandardCurated
Immediate reconstruction planning (implant or autologous)
Immediate reconstruction planning (implant or autologous) should be coordinated with anticipated radiation to minimize complications and optimize outcomes.
CurativeStandardCurated
Z0011 approach: omit ALND with 1–2 positive SLNs if lumpectomy + whole-breast RT
Z0011 approach: omit ALND with 1–2 positive SLNs if lumpectomy + whole-breast RT is planned and no gross extranodal extension.
CurativeStandardCurated
Targeted axillary dissection post-NAT for initially node-positive patients (retrieve clipped node + SLNs) to accurately restage and potentially de-escalate ALND
Targeted axillary dissection post-NAT for initially node-positive patients (retrieve clipped node + SLNs) to accurately restage and potentially de-escalate ALND.
CurativeStandardCurated
Re-excision for positive margins; for invasive cancer, ‘no ink on tumor’
Re-excision for positive margins; for invasive cancer, ‘no ink on tumor’ is adequate. For pure DCIS, aim ≥2 mm.
CurativeStandardCurated
Place surgical clips in the tumor bed to guide boost RT and future imaging
Place surgical clips in the tumor bed to guide boost RT and future imaging.
CurativeStandardCurated
Radiotherapy
Whole-breast irradiation (WBI) after lumpectomy
Whole-breast irradiation (WBI) after lumpectomy is standard; hypofractionation preferred for most (e.g., ~3 weeks). Five-fraction regimens are reasonable in selected patients.
StandardCurated
Tumor-bed boost for higher local-recurrence risk (younger age, close margins, high grade, extensive intraductal component)
Tumor-bed boost for higher local-recurrence risk (younger age, close margins, high grade, extensive intraductal component).
StandardCurated
Post-mastectomy radiation (PMRT) for ≥4 positive nodes
Post-mastectomy radiation (PMRT) for ≥4 positive nodes; consider for 1–3 positive nodes with additional risk factors (large tumor, LVI, close margins).
StandardCurated
Regional nodal irradiation (RNI) to axillary/supraclavicular ± internal mammary nodes based on nodal burden, biology, and response to NAT
Regional nodal irradiation (RNI) to axillary/supraclavicular ± internal mammary nodes based on nodal burden, biology, and response to NAT.
StandardCurated
Deep-inspiration breath hold (DIBH) for left-sided WBI/PMRT to reduce heart dose
Deep-inspiration breath hold (DIBH) for left-sided WBI/PMRT to reduce heart dose; consider proton therapy in select complex IMN cases.
StandardCurated
Stereotactic radiosurgery (SRS) for limited brain metastases
Stereotactic radiosurgery (SRS) for limited brain metastases; SBRT for oligometastatic bone/liver/lung lesions case-by-case.
Advanced / metastaticStandardCurated
Partial-breast irradiation (PBI)
Partial-breast irradiation (PBI) can be considered for carefully selected low-risk early cases as a shorter alternative to WBI.
StandardCurated
Oligometastatic disease: discuss consolidative local therapy (SBRT, surgery) after systemic response in a multidisciplinary tumor board
Oligometastatic disease: discuss consolidative local therapy (SBRT, surgery) after systemic response in a multidisciplinary tumor board.
Advanced / metastaticStandardCurated
Oligometastatic scenarios (all subtypes): consider SBRT or surgery after systemic response in tumor board
Oligometastatic scenarios (all subtypes): consider SBRT or surgery after systemic response in tumor board.
Advanced / metastaticStandardCurated
Chemotherapy
Ovarian protection: consider GnRH agonist during chemotherapy for premenopausal patients to reduce ovarian failure risk and preserve fertility
Ovarian protection: consider GnRH agonist during chemotherapy for premenopausal patients to reduce ovarian failure risk and preserve fertility.
StandardCurated
AC-T (doxorubicin/cyclophosphamide → paclitaxel) (early/high-risk)
Common adjuvant/neoadjuvant backbone; monitor cardiotoxicity and neuropathy.
StandardCurated
TC (docetaxel/cyclophosphamide) (early)
Non-anthracycline option; consider in lower cardiac reserve.
StandardCurated
THP / TCHP (taxane ± carboplatin + trastuzumab/pertuzumab) (HER2+ neoadjuvant)
Preferred for stage II–III HER2+; adapt adjuvant based on pCR/residual disease.
NeoadjuvantStandardCurated
Capecitabine (post-neoadjuvant TNBC residual)
Improves outcomes in residual TNBC after neoadjuvant chemo.
NeoadjuvantStandardCurated
Platinum agents
Platinum agents remain valuable in TNBC (particularly HRD contexts).
StandardCurated
Targeted therapy
Use genomic assays to decide on adjuvant chemotherapy in HR+/HER2– node-negative and select 1–3 node-positive patients undergoing upfront surgery
Use genomic assays to decide on adjuvant chemotherapy in HR+/HER2– node-negative and select 1–3 node-positive patients undergoing upfront surgery.
AdjuvantStandardCurated
Postmenopausal HR+/HER2–: consider adjuvant bisphosphonates to reduce bone recurrence and fractures
Postmenopausal HR+/HER2–: consider adjuvant bisphosphonates to reduce bone recurrence and fractures.
AdjuvantStandardCurated
HER2+ stage II–III: neoadjuvant taxane-based ± anthracycline + trastuzumab/pertuzumab
HER2+ stage II–III: neoadjuvant taxane-based ± anthracycline + trastuzumab/pertuzumab; if residual disease, switch to adjuvant T-DM1 to complete ~1 year of anti-HER2 therapy.
NeoadjuvantStandardCurated
Small node-negative HER2+ (e
Small node-negative HER2+ (e.g., T1a/b): consider paclitaxel + trastuzumab (TH) adjuvant de-escalation for appropriate candidates.
AdjuvantStandardCurated
Metastatic HER2+: first line taxane + trastuzumab + pertuzumab; second line trastuzumab deruxtecan (T-DXd) preferred; later lines
Metastatic HER2+: first line taxane + trastuzumab + pertuzumab; second line trastuzumab deruxtecan (T-DXd) preferred; later lines include tucatinib + trastuzumab + capecitabine (especially with brain mets), neratinib- or lapatinib-based regimens as appropriate.
Advanced / metastaticStandardCurated
gBRCA-mutated, high-risk HER2– (HR+ or TNBC): consider 1 year of adjuvant olaparib per criteria
gBRCA-mutated, high-risk HER2– (HR+ or TNBC): consider 1 year of adjuvant olaparib per criteria.
AdjuvantStandardCurated
Alpelisib for PIK3CA-mutant HR+/HER2– after AI
Alpelisib for PIK3CA-mutant HR+/HER2– after AI; start glucose monitoring and rash prophylaxis (non-sedating antihistamine).
StandardCurated
PARP inhibitors (olaparib/talazoparib) for gBRCA/PALB2: adjuvant (select high-risk HER2–) and metastatic
PARP inhibitors (olaparib/talazoparib) for gBRCA/PALB2: adjuvant (select high-risk HER2–) and metastatic; plan for anemia monitoring and contraception.
AdjuvantStandardCurated
HER2 sequence (metastatic): taxane + trastuzumab/pertuzumab → trastuzumab deruxtecan (T-DXd) → tucatinib + trastuzumab + capecitabine (brain-active) → other TKIs (neratinib/lapatinib) case-by-case
HER2 sequence (metastatic): taxane + trastuzumab/pertuzumab → trastuzumab deruxtecan (T-DXd) → tucatinib + trastuzumab + capecitabine (brain-active) → other TKIs (neratinib/lapatinib) case-by-case.
Advanced / metastaticStandardCurated
Residual disease after neoadjuvant HER2 therapy: switch to adjuvant T-DM1 to reduce recurrence risk
Residual disease after neoadjuvant HER2 therapy: switch to adjuvant T-DM1 to reduce recurrence risk.
NeoadjuvantStandardCurated
Extended adjuvant neratinib for high-risk HR+/HER2+ after trastuzumab (diarrhea prophylaxis mandatory) — center-specific use
Extended adjuvant neratinib for high-risk HR+/HER2+ after trastuzumab (diarrhea prophylaxis mandatory) — center-specific use.
AdjuvantStandardCurated
T-DXd active in HER2-low (IHC 1+ or 2+/ISH–) metastatic after prior lines — emphasize ILD vigilance and early drug holds if symptomatic
T-DXd active in HER2-low (IHC 1+ or 2+/ISH–) metastatic after prior lines — emphasize ILD vigilance and early drug holds if symptomatic.
Advanced / metastaticStandardCurated
Sacituzumab govitecan
Sacituzumab govitecan is a preferred later-line option in metastatic TNBC; early use of growth-factor support and loperamide reduces dose-limiting toxicity.
Advanced / metastaticStandardCurated
gBRCA TNBC benefits from PARP inhibitors (metastatic) and adjuvant olaparib (select early)
gBRCA TNBC benefits from PARP inhibitors (metastatic) and adjuvant olaparib (select early).
AdjuvantStandardCurated
HER2+ CNS disease: tucatinib-based regimens
HER2+ CNS disease: tucatinib-based regimens provide intracranial responses; integrate SRS/surgery with neuro-oncology.
StandardCurated
Immunotherapy
High-risk early TNBC: neoadjuvant anthracycline/taxane ± platinum with pembrolizumab
High-risk early TNBC: neoadjuvant anthracycline/taxane ± platinum with pembrolizumab; continue adjuvant pembrolizumab. If residual disease, add adjuvant capecitabine.
NeoadjuvantStandardCurated
Metastatic TNBC: PD-L1–positive → pembrolizumab + chemotherapy; later lines
Metastatic TNBC: PD-L1–positive → pembrolizumab + chemotherapy; later lines include sacituzumab govitecan; gBRCA mutation → PARP inhibitor considered.
Advanced / metastaticStandardCurated
Pembrolizumab for high-risk early TNBC (neoadjuvant + adjuvant) improves pCR/EFS
Pembrolizumab for high-risk early TNBC (neoadjuvant + adjuvant) improves pCR/EFS; in metastatic TNBC, add to chemo for PD-L1–positive disease.
NeoadjuvantStandardCurated
Rare MSI-H/TMB-H/NTRK fusion
Rare MSI-H/TMB-H/NTRK fusion can unlock tumor-agnostic immunotherapy/TRK inhibitors; screen with broad NGS when feasible.
StandardCurated
Hormonal therapy
HR+/HER2– early: endocrine therapy (tamoxifen or aromatase inhibitor) ± ovarian function suppression (OFS) based on menopausal status and risk
HR+/HER2– early: endocrine therapy (tamoxifen or aromatase inhibitor) ± ovarian function suppression (OFS) based on menopausal status and risk; duration typically 5 years, extend to 7–10 years for selected higher-risk cases.
StandardCurated
High-risk, node-positive HR+/HER2–: consider adjuvant abemaciclib + endocrine therapy per eligibility criteria
High-risk, node-positive HR+/HER2–: consider adjuvant abemaciclib + endocrine therapy per eligibility criteria.
AdjuvantStandardCurated
Metastatic HR+/HER2–: endocrine therapy + CDK4/6 inhibitor
Metastatic HR+/HER2–: endocrine therapy + CDK4/6 inhibitor is standard first line. On progression, personalize by biomarkers (ESR1 → SERD; PIK3CA → alpelisib + fulvestrant; AKT1/PTEN/PIK3CA → capivasertib + fulvestrant; consider everolimus combinations). Later-line ADCs (e.g., sacituzumab govitecan) are options.
Advanced / metastaticStandardCurated
CDK4/6 + endocrine therapy (AI or fulvestrant)
CDK4/6 + endocrine therapy (AI or fulvestrant) is first-line standard for metastatic HR+/HER2–; choose agent by comorbidity (e.g., ribociclib OS data; abemaciclib diarrhea but less neutropenia).
Advanced / metastaticStandardCurated
Post-CDK4/6 progression: re-profile (tumor or ctDNA)
Post-CDK4/6 progression: re-profile (tumor or ctDNA). ESR1 mutation → SERD strategy (e.g., fulvestrant; oral SERDs where available).
StandardCurated
Capivasertib + fulvestrant improves outcomes in tumors with PI3K/AKT/PTEN alterations
Capivasertib + fulvestrant improves outcomes in tumors with PI3K/AKT/PTEN alterations; counsel on diarrhea, rash, and hyperglycemia.
StandardCurated
Everolimus + exemestane restores endocrine sensitivity in some AI-resistant HR+
Everolimus + exemestane restores endocrine sensitivity in some AI-resistant HR+; prevent stomatitis with dexamethasone mouthwash.
StandardCurated
Adjuvant abemaciclib for high-risk node-positive HR+/HER2– improves IDFS when added to endocrine therapy (strict eligibility)
Adjuvant abemaciclib for high-risk node-positive HR+/HER2– improves IDFS when added to endocrine therapy (strict eligibility).
AdjuvantStandardCurated
Later-line ADCs in HR+/HER2–: sacituzumab govitecan after endocrine + targeted therapies
Later-line ADCs in HR+/HER2–: sacituzumab govitecan after endocrine + targeted therapies; manage neutropenia/diarrhea proactively.
StandardCurated
anastrozole
FDA-approved for this cancer.
Guideline option
tamoxifen
FDA-approved for this cancer.
Guideline option

Established care shown from OncoForge editorial curation · reviewed September 15, 2025 — authoritative citations (NCI PDQ / FDA) are being added.

Supportive care (18)
  • Lymphedema program: prehab education, early PT/OT, compression fitting, and progressive weight training; prompt eval for arm swelling/tightness or axillary web syndrome.
  • Shoulder mobility & scar management: early ROM, myofascial techniques, and desensitization to prevent frozen shoulder and chronic pain.
  • Menopause symptom toolkit on endocrine therapy: non-hormonal options (SSRIs/SNRIs, gabapentin, clonidine), vaginal moisturizers/lubricants, and pelvic floor therapy; consider low-dose vaginal estrogen only after oncology review.
  • Sexual health: address dyspareunia, libido, and body image; consider specialized pelvic PT and counseling.
  • AI bone program: weight-bearing/resistance exercise, vitamin D/calcium, baseline and periodic DEXA; consider adjuvant bisphosphonates (postmenopausal) or denosumab with dental clearance.
  • Cardio-oncology: manage BP, lipids, diabetes; baseline CV risk assessment before anthracyclines/HER2 therapy; lifestyle coaching for activity, weight, and sleep.
  • Return-to-work & cognitive rehab: graded return plan, fatigue pacing, occupational therapy, and ‘chemo-brain’ strategies (sleep hygiene, cognitive exercises).
  • Alopecia and neuropathy mitigation: scalp cooling during sensitive chemo; frozen gloves/booties during taxanes to reduce CIPN and nail toxicity.
  • Stomatitis prevention: steroid mouthwash with everolimus; salt/bicarbonate rinses broadly; early dental issues triage to avoid ONJ when on bone agents.
  • GI playbooks: diarrhea (abemaciclib/capecitabine/sacituzumab) start loperamide early; nausea bundles with evidence-based antiemetics; constipation prevention with opioids/antiemetics.
  • Pulmonary vigilance: new cough/dyspnea/fever on T-DXd or everolimus → urgent ILD/pneumonitis evaluation and drug hold.
  • Dermatologic care: alpelisib/capivasertib rash prophylaxis (non-sedating antihistamines), urea-based emollients; HFS care on capecitabine.
  • Metabolic monitoring: proactive glucose/A1c and dietitian input with alpelisib/capivasertib; avoid unsupervised fasting in underweight/sarcopenic patients.
  • Multimodal analgesia: NSAIDs/acetaminophen, neuropathic agents (duloxetine for CIPN), interventional options when needed; early palliative/supportive care improves QoL.
  • Sleep, anxiety, and mood: CBT-I, mindfulness, exercise; screen for depression/PTSD and treat promptly.
  • Vaccination plan: inactivated vaccines per guidelines; avoid live vaccines during cytotoxic therapy/biologics; consider HBV screening in at-risk patients.
  • Port care: educate on infection/DVT signs; coordinate holds around procedures (anticoagulants, bone agents).
  • Navigation and financial counseling: transportation, work leave, medication access, and clinical trial matching to reduce care gaps.
Investigational & adjunct compounds — detail (76)
Meta-analysis (29)
Acetyl-L-carnitineacupressureacupuncturealoe veraAromatase inhibitorsAromatase inhibitors· Adjuvant (after surgery)axillary lymph node dissection (ALND)bone-modifying agentsbreast-conserving surgery (BCS)endocrine therapyendocrine therapy· First-line (advanced disease)gingerginsengGonadotrophin-releasing hormone agonists (GnRHa)Hippocampal avoidanceimmediate breast reconstruction (lumpectomy reconstruction)mastectomyMemantineoff-labelradiation therapy (RT)· Adjuvant (after surgery)re-excisionregional nodal irradiation (RNI)sentinel lymph node biopsy (SLNB)· Neoadjuvant (before surgery) · hormone receptor-positive, human epidermal growth factor receptor 2-negativesentinel lymph node biopsy (SLNB)sperm, oocyte, and embryo cryopreservationStereotactic radiosurgerySurgerytargeted systemic therapyWhole-brain radiotherapywhole-breast radiation therapy (whole-breast RT)
Named in the literature
estrogen therapy / hormone therapy (ET/HT)Primary endocrine therapyAdjuvant systemic therapy· Adjuvant (after surgery)Bone-modifying drugsNeoadjuvant systemic treatment options· Neoadjuvant (before surgery)Supportive carebreast MRI (diagnostic)breast MRI (screening)breast ultrasound (diagnostic)Breath-hold techniques (e.g., deep-inspiration breath hold)diagnostic mammography and tomosynthesismammography and digital breast tomosynthesismammography (male screening)Oncoplastic Breast Surgerysurgical resectionAccelerated partial breast irradiation (APBI)Hypofractionated whole-breast irradiationintraoperative radiation therapyIntraoperative radiotherapypostmastectomy radiation therapy (PMRT)· First-line (advanced disease)postmastectomy radiation therapy (PMRT)· Neoadjuvant (before surgery)postmastectomy radiation therapy (PMRT)Postmastectomy radiotherapy (PMRT) to chest wall and supraclavicular nodesRadiotherapyRegional nodal irradiation (supraclavicular)Single-fraction radiotherapy (8 Gy) for bone metastasesstereotactic ablative body radiotherapy (SBRT)Boost dose over the tumour bedcapivasertibCDK4/6 inhibitorsPIK3CA inhibitorsTargeted therapiesAxillary irradiation?anti-HER2 therapy· Maintenance · biomarker-selectedbilateral risk-reducing mastectomy (BRRM)· CDH1 pathogenic variant carriersOvarian suppressionImmunotherapeutic agentRisk-reducing bilateral salpingo-oophorectomy· pathogenic germline variant in the BRCA1, BRCA2, and other ovarian cancer-associated genesexemestaneraloxifeneAromatase inhibitors· First-line (advanced disease) · estrogen receptor-positivebisphosphonateszoledronic aciddenosumab· Adjuvant (after surgery)
Lab / animal only

"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.