Pembrolizumab and Concurrent Chemoradiotherapy or Radiation Therapy in Treating Patients With Small Cell Lung Cancer
Part of paid clinical trials in Houston, Texas.
- Sponsor
- M.D. Anderson Cancer Center
- Study ID
- NCT02402920
- Phase
- PHASE1
- Status
- Completed
Conditions
- Extensive Stage Small Cell Lung Carcinoma
- Limited Stage Small Cell Lung Carcinoma
- Neuroendocrine Neoplasm
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Carboplatin — DRUGGiven IV
- Cisplatin — DRUGGiven IV
- Etoposide — DRUGGiven IV
- Laboratory Biomarker Analysis — OTHERCorrelative studies
- Pembrolizumab — BIOLOGICALGiven IV
- Radiation Therapy — PROCEDUREUndergo radiation therapy
Study Details
This phase I trial studies the side effects and best dose of pembrolizumab when given together with chemoradiotherapy or radiation therapy in treating patients with small cell lung cancer. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Radiation therapy uses high energy x-rays to kill cancer cells and shrink tumors. Giving chemotherapy with radiation therapy may kill more cancer cells. Giving pembrolizumab with chemoradiotherapy or radiation therapy may be a better treatment for small cell lung cancer.
Key Dates
- Start date
- Jul 22, 2015
- Status verified
- Feb 2026
- Primary completion
- Dec 23, 2025
- Completion
- Feb 9, 2026
Study Design
- Enrollment
- 83 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Part A (LS-SCLC, pembrolizumab, chemoradiotherapy)Patients receive pembrolizumab IV over 30 minutes on day 1 and undergo radiation therapy BID 5 days a week for 3 weeks. Patients also receive cisplatin IV over 2 hours or carboplatin IV over 30 minutes and etoposide IV over 4 hours on days 1, 2, and 3. Treatment repeats every 3 weeks for 16 courses (1 course for radiation therapy, 4 courses for chemotherapy) in the absence of disease progression or unacceptable toxicity. Patients who achieve systemic disease control and do not exhibit severe (grade \> 3) pembrolizumab related toxicity during/after completion of 16 courses may receive 16 additional courses of pembrolizumab in the absence of disease progression or unacceptable toxicity.
- Experimental: Part B (ES-SCLC, pembrolizumab, radiation therapy)Beginning after the completion of chemotherapy, patients receive pembrolizumab IV over 30 minutes on day 1 and undergo radiation therapy BID 5 days a week for 3 weeks. Treatment repeats every 3 weeks for 16 courses (1 course for radiation therapy) in the absence of disease progression or unacceptable toxicity.
Primary Outcome Measure
Dose Limiting Toxicity (DLT) [ Time Frame: Median of 7.3 months (range: 1 to 13 months) following initation of treatment ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| M D Anderson Cancer Center | Houston | Texas | 77030 | - |
Related coverage on Hipa.ai
- Keytruda with Chemoradiotherapy for SCLC: Median OS 39.5 Months in LS-SCLCPembrolizumab · Mar 10, 2026 · ClinicalTrials.gov
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