Appointment dossier — Lung Adenocarcinoma
Bring this to your appointment. It summarizes what published studies report — it is not medical advice and does not say anything works. Decisions are yours and your care team’s.
Compounds studied in Lung Adenocarcinoma
- Etoposide — Human evidence · 1 positive · PMID 35147672
- Doxorubicin — Animal evidence · 1 positive · PMID 38445013
- Fuzuloparib — Review evidence · 1 positive · PMID 34118019
- Genistein — Review evidence · 1 positive · PMID 42133114
- Indole-3-Acetic Acid — Animal evidence · 1 positive · PMID 40802513
- Nivolumab †Rx — Review evidence · 1 positive · PMID 27197542
- Pembrolizumab — Review evidence · 1 positive · PMID 27197542
- Cisplatin — Review evidence · 0 positive / 1 negative-mixed · PMID 38520879
- Crizotinib — Review evidence · 0 positive · PMID 29488330
- Curcumin / Theracurmin — Review evidence · 0 positive / 1 negative-mixed · PMID 36358986
“Positive” means a study reported a positive result — most are early lab/animal work that may not translate to people.
Guideline-backed standard of care
Anatomic resection (lobectomy/segmentectomy) with systematic nodal dissection when operable, Sublobar resection considered for small peripheral lesions or limited reserve, VATS/robotic approaches common, For oligometastatic disease responding to systemic therapy, consider metastasectomy case-by-case, SBRT for medically inoperable early-stage disease (curative intent), Post-op or definitive chemoradiation for positive margins/unresectable disease, SRS for brain metastases, Palliative RT for symptomatic bone, chest wall, airway, or CNS lesions, Driver-positive: matched TKI first-line (EGFR, ALK, ROS1, RET, METex14, BRAF V600E, NTRK, HER2), Driver-negative: PD-L1 ≥50% → single-agent PD-1/PD-L1, Pemetrexed-based regimens favored in non-squamous NSCLC, Later lines guided by resistance profile (e, Platinum + Pemetrexed (± Pembrolizumab) (first-line driver-negative non-squamous), Platinum + Taxane (± Pembrolizumab/Bevacizumab) (first-line non-squamous alternative), Single-agent Pemetrexed Maintenance (post-induction), Docetaxel (± Ramucirumab) (subsequent line), Gemcitabine/Vinorelbine/Other Doublets (selected cases), EGFR, ALK, ROS1, RET, METex14, BRAF V600E, NTRK, HER2: prioritize matched TKIs with CNS-active options where possible, KRAS G12C: G12C inhibitors active, PD-L1 high driver-negative disease: consider IO monotherapy, Avoid initiating IO just before TKIs with high pneumonitis/hepatitis overlap, Re-biopsy/ctDNA at progression to reveal on-target mutations (e, Combinations to overcome resistance (TKI + MET/MEK/other) best pursued on trials.
The established options for Lung Adenocarcinoma — ask which apply to your case. Investigational options appear in the compounds list above.
Open recruiting trials (18)
- NCT07405086 · Phase 4 — Morning Versus Afternoon Administration of Immunotherapy for the Treatment of Advanced or Metastatic Solid Tumors, The Knight SHIFT Study (United States)
- NCT03755739 · Phase 2 / Phase 3 — Trans-Artery/Intra-Tumor Infusion of Checkpoint Inhibitors Plus Chemodrug for Immunotherapy of Advanced Solid Tumors (China)
- NCT06851663 · Phase 2 / Phase 3 — Trop2-targeted immunoPET Imaging of Solid Tumors (China)
- NCT07058428 · Phase 3 — FSRT Combines With Bevacizumab for Multiple Brain Metastases in Lung Adenocarcinoma (China)
- NCT07481786 · Phase 3 — Bevacizumab Plus FSRT Versus Hippocampus-Avoidant WBRT in Lung Adenocarcinoma With Extensive Brain Metastases (China)
- NCT05055908 · Phase 3 — Efficacy and Biomarker Development for Lung Cancer Treated With Immune Checkpoint Inhibitors (China)
- NCT06417008 · Phase 2 / Phase 3 — A Study of HS-20117 Combined With Aumolertinib in Participants With Advanced Non-Squamous Non-Small Cell Lung Cancer (China)
- NCT05668650 · Phase 3 — Double-blind Study to Evaluate the PK, Efficacy, Safety and Immunogenicity of MB12 Versus Keytruda® in Stage IV NSCLC (Argentina)
- NCT07223047 · Phase 1 / Phase 2 — A Study to Evaluate the Safety, Tolerability, and Efficacy of BMS-986523 Alone and in Combination With Anti-Cancer Agents in Participants With Advanced Solid Malignancies (United States)
- NCT06283719 · Phase 1 / Phase 2 — Dose Escalation Study of ZG006 in Participants With Advanced Small Cell Lung Cancer or Neuroendocrine Carcinoma, Followed by Dose Expansion Study in Participants With Advanced Small Cell Lung Cancer (China)
- NCT05937906 · Phase 1 / Phase 2 — Clinical Trial Evaluating the Safety and Efficacy of Chemoimmunotherapy Plus Short Course of Mek Inhibitor in First Line of Treatment of Metastatic Non Squamous Non Small Cell Lung Adenocarcinoma With PDL1 < 50 %. (France)
- NCT05266846 · Phase 2 — Pembrolizumab Plus Bevacizumab and Chemotherapy for ALK-rearranged NSCLC With Persistent 5'ALK (China)
- NCT04895709 · Phase 1 / Phase 2 — A Study of BMS-986340 as Monotherapy and as Combination Therapy in Participants With Advanced Solid Tumors (United States)
- NCT04969315 · Phase 1 / Phase 2 — TT-10 (PORT-6) and TT-4 (PORT-7) as Single Agents and in Combination in Subjects With Advanced Selected Solid Tumors (United States)
- NCT06440057 · Phase 1 / Phase 2 — Dose Escalation Study of ZG006 in Participants With Advanced Small Cell Lung Cancer or Neuroendocrine Carcinoma, Followed by Dose Expansion Study in Participants With Neuroendocrine Carcinoma. (China)
- NCT05579366 · Phase 1 / Phase 2 — Rinatabart Sesutecan (Rina-S, PRO1184, GEN1184) for Advanced Solid Tumors (GCT1184-01/ PRO1184-001) (United States)
- NCT05377658 · Phase 2 — AK104 With Chemotherapy as Neoadjuvant and Adjuvant Therapy for Resectable Non-small Cell Lung Cancer (China)
- NCT06769971 · Phase 2 — Phase II Study of Ivonescimab and Cadonilimab in Combination with Chemotherapy in Patients with ES-SCLC (China)
Most-relevant first: trials that name Lung Adenocarcinoma, then broader trials you may still qualify for. 288 recruiting trials name this cancer on ClinicalTrials.gov. Eligibility is decided by each trial's team — bring these NCT numbers to your appointment.
Interactions & safety to discuss
Not a complete check — a drug not listed here is not therefore safe. Show your pharmacist your full list.
- Curcumin / Theracurmin × CYP3A4/P-gp substrates (e.g., TKIs, chemo) (high-stakes) — Monitor (moderate)
- Curcumin / Theracurmin × Anticoagulants (high-stakes) — Monitor (minor)
- Curcumin / Theracurmin × Platinum chemotherapy (high-stakes) — Consider (beneficial)
- Nivolumab †Rx × immunosuppressants (high-stakes) — Avoid (high)
- Nivolumab †Rx × Ipilimumab — Synergize (moderate)
- Nivolumab †Rx × corticosteroids — Use For IrAE (low)
Financial help to look into
- PAN Foundation — Copay assistance funds by diagnosis (funds open and close as money allows). https://www.panfoundation.org/
- HealthWell Foundation — Copay and premium assistance funds by disease. https://www.healthwellfoundation.org/
- CancerCare — financial assistance — Limited grants plus free financial counseling. https://www.cancercare.org/financial
- Family Reach — Help with everyday living costs (rent, transport, food) during treatment. https://familyreach.org/
- NeedyMeds — Searchable directory of drug patient-assistance and discount programs. https://www.needymeds.org/
For each medicine above, search manufacturer and nonprofit programs at medicineassistancetool.org.
Questions to ask your oncologist
- Has my tumor been tested for EGFR activating mutations (ex19 del, L858R; uncommon: G719X, L861Q, S768I), and would the result open up targeted treatments or trials?
- Has my tumor been tested for ALK fusions (e.g., EML4-ALK), and would the result open up targeted treatments or trials?
- Has my tumor been tested for ROS1 fusions, and would the result open up targeted treatments or trials?
- I've read that Etoposide has been studied in people for Lung Adenocarcinoma — what's the evidence, and is it an option or available in a trial for me?
- Of the open trials I found (for example NCT07405086), am I eligible for any — here or at a larger cancer center?
- Do I have a targetable driver (EGFR, ALK, ROS1, RET, METex14, BRAF V600E, NTRK, HER2, KRAS G12C)?
- If no driver, what is my PD-L1 and best IO±chemo plan?
- Is surgery or SBRT an option for my stage? Could oligomet sites be consolidated after response?
- What is our plan if first-line therapy stops working—when and how will we test for resistance?
- Do my co-mutations (STK11/KEAP1/TP53) affect treatment choice?
- How will we monitor and manage IO irAEs and TKI toxicities?
- Would I benefit from pulmonary rehab, nutrition support, or prehab before treatment?
- Am I eligible for clinical trials now or at progression?
- What is the plan for brain surveillance and treatment if needed?
- How will we coordinate supplements/OTC meds to avoid interactions?
- What is my exact diagnosis — the type, subtype, stage, and grade?
- Has my tumor had molecular or genomic testing (e.g. next-generation sequencing), and what did it find?
- Should I have inherited (germline) genetic testing, and could it affect my treatment or my family?
- What is the goal of treatment for me — cure, long-term control, or comfort?
- What are all of my standard treatment options, and what does each one involve?
- What is the realistic benefit of each option, in actual numbers?
- What are the most common and the most serious side effects, and how are they managed?