Adjuvant Chemotherapy and Immunotherapy for Completely Resected Small Cell Lung Cancer
Trial Status: active
This is a phase II trial of adjuvant chemotherapy and immunotherapy for completely resected small cell lung cancer (SCLC).
Inclusion Criteria
- Age ≥ 18 years.
- Body weight >30 kg.
- Must have a life expectancy of at least 12 weeks.
- Must have histologically or cytologically confirmed diagnosis of pathologic T1-T2 N0-1 M0 small-cell lung cancer per the American Joint Committee on Cancer staging system, 8th edition.
- Have completely resected (wedge resection, segmentectomy, lobectomy, sleeve lobectomy, bilobectomy, or pneumonectomy) small-cell lung cancer within 78 days of enrollment.
- Complete mediastinal lymph node dissection (MLND) or systematic mediastinal lymph node sampling is required.
- No prior systemic therapies, for small cell lung cancer.
- Post-operative radiation for the resected small cell lung cancer is acceptable per treating physician in the setting of N1 disease, but no other prior radiation for small cell lung cancer.
- ECOG performance status 0-1.
Exclusion Criteria
- Patients who are receiving any other investigational agents.
- Concurrent enrollment in another clinical study involving investigational treatment directed to treatment of patients with small cell lung cancer.
- Prior treatment with durvalumab.
- History of another primary malignancy except for:
- Malignancy treated with curative intent and with no known active disease ≥2 years before the first dose of IP and of low potential risk for recurrence.
- Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease.
- Superficial bladder cancer without active disease after treatment.
- Low grade prostate cancer without indication for active treatment.
- Adequately treated carcinoma in situ without evidence of disease.
- Patients with a history of cerebrovascular accident including transient ischemic attack (TIA), pulmonary embolism or insufficiently treated deep venous thrombosis (DVT) within the past 3 months.
- Patients with hemoptysis in excess of 2.5 mL within 2 weeks prior to the first dose of study medication.
- Patients requiring concomitant therapy with phenytoin, phenobarbital, or carbamazepine.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT07149363.
Locations matching your search criteria
United States
Massachusetts
Boston
Brigham and Women's Hospital
Status: Approved
Name Not AvailableDana-Farber Cancer Institute
Status: Approved
Name Not AvailableMassachusetts General Hospital Cancer Center
Status: Approved
Name Not AvailableVirginia
Charlottesville
University of Virginia Cancer Center
Status: Active
Name Not AvailableThis is a phase II open-label, single-arm, multi-center study to evaluate the efficacy
and safety of adjuvant immunotherapy with chemotherapy for completely resected pathologic
T1-T2, N0-N1, M0 small cell lung cancer (SCLC). The statistical design includes a
predefined range of alpha and power to detect an improvement in 2-year disease free
survival (DFS).
Trial PhasePhase II
Trial Typetreatment
Lead OrganizationAlliance Foundation Trials LLC
Principal InvestigatorEvanthia Galanis
- Primary IDAFT-61
- Secondary IDsNCI-2026-02683
- ClinicalTrials.gov IDNCT07149363