MedPath

Adjuvant Chemotherapy and Immunotherapy for Completely Resected Small Cell Lung Cancer

Not Applicable
Not yet recruiting
Conditions
Small Cell Lung Cancer (SCLC)
Interventions
Registration Number
NCT07149363
Lead Sponsor
Alliance Foundation Trials, LLC.
Brief Summary

This is a phase II trial of adjuvant chemotherapy and immunotherapy for completely resected small cell lung cancer (SCLC).

Detailed Description

This 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).

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
65
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 & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Durvalumab and one of the two chemotherapy combinations: cisplatin or carboplatin, and etoposideDurvalumab 50 MG/ML65 participants will be enrolled.
Primary Outcome Measures
NameTimeMethod
Disease free survival (DFS)2 years

To determine whether the addition of durvalumab to adjuvant chemotherapy after surgery for limited-stage SCLC leads to improved disease free survival (DFS) when compared to historical data of participants who received adjuvant chemotherapy without immunotherapy after surgery for SCLC. DFS is measured in months from the time of surgery.

Secondary Outcome Measures
NameTimeMethod
Overall survival (OS)3 years

To determine whether the addition of durvalumab to adjuvant chemotherapy after surgery for limited-stage SCLC leads to improved overall survival (OS) when compared to historical data of participants who received adjuvant chemotherapy without immunotherapy after surgery for SCLC. OS is measured in months from the time of surgery.

Safety of the regimen5 years

The frequency of grade 3+ all-cause adverse events will be reported.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.