๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-26

Testing the Addition of a New Immunotherapy Drug, Atezolizumab (MPDL3280A), to the Usual Chemoradiation (CRT) Therapy Treatment for Limited Stage Small Cell Lung Cancer (LS-SCLC) (NCT03811002)

๐Ÿ”ต Active, Not Recruiting Phase3 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: National Cancer Institute (NCI)

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This phase III trial studies how well chemotherapy and radiation therapy (chemoradiation) with or without atezolizumab works in treating patients with limited stage small cell lung cancer. Drugs used in chemotherapy, such as etoposide, cisplatin, and carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Radiation therapy uses high energy x-rays to kill tumor cells and shrink tumors. Immunotherapy with monoclonal antibodies, such as atezolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving chemoradiation with or without atezolizumab may work better in treating patients with limited stage small cell lung cancer.

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (22 items) and avoid the listed exclusions (26 items).

Location: University of Alabama at Birmingham Cancer Center โ€” Birmingham, Alabama

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Usually NOT eligible if any of the following apply:

  • Exclusion Criteria:
  • Definitive clinical or radiologic evidence of metastatic disease
  • Definitive surgical resection of small cell lung cancer
  • Prior invasive malignancy (except non-melanomatous skin cancer, localized prostate cancer, or any early stage cancer treated with curative intent resection) unless disease free for a minimum of 2 years (carcinoma in situ of the breast, oral cavity, or cervix are all permissible)
  • More than 1 cycle of prior platinum-based chemotherapy for SCLC prior to enrollment; note that prior chemotherapy for a different cancer is allowable
  • Any prior atezolizumab or other immunotherapy agent
  • Prior radiotherapy to the lungs or mediastinum that would result in clinically significant overlap of radiation therapy fields; prior tangent fields for breast cancer with minimal overlap with target volumes are allowed per approval of study principal investigators (PIs)
  • Patients with cytologically positive pleural or pericardial fluid are not eligible
  • An active, known or suspected autoimmune disease. Patients are permitted to enroll if they have vitiligo, type I diabetes mellitus, residual hypothyroidism due to autoimmune condition only requiring hormone replacement, psoriasis not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger
  • Active or prior documented inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis)
  • History of allogeneic organ transplant
  • History of primary immunodeficiency

๐Ÿ” Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

๐Ÿ“ All Participating Trial Locations (542 Sites)

  • University of Alabama at Birmingham Cancer Center โ€” Birmingham, Alabama
  • Fairbanks Memorial Hospital โ€” Fairbanks, Alaska
  • Banner MD Anderson Cancer Center โ€” Gilbert, Arizona
  • CTCA at Western Regional Medical Center โ€” Goodyear, Arizona
  • Banner University Medical Center - Tucson โ€” Tucson, Arizona
  • University of Arizona Cancer Center-North Campus โ€” Tucson, Arizona
  • NEA Baptist Memorial Hospital and Fowler Family Cancer Center - Jonesboro โ€” Jonesboro, Arkansas
  • University of Arkansas for Medical Sciences โ€” Little Rock, Arkansas
  • Sutter Auburn Faith Hospital โ€” Auburn, California
  • Alta Bates Summit Medical Center-Herrick Campus โ€” Berkeley, California
  • City of Hope Comprehensive Cancer Center โ€” Duarte, California
  • Los Angeles General Medical Center โ€” Los Angeles, California
  • USC / Norris Comprehensive Cancer Center โ€” Los Angeles, California
  • Memorial Medical Center โ€” Modesto, California
  • UC Irvine Health/Chao Family Comprehensive Cancer Center โ€” Orange, California
  • Sutter Roseville Medical Center โ€” Roseville, California
  • Sutter Medical Center Sacramento โ€” Sacramento, California
  • University of California Davis Comprehensive Cancer Center โ€” Sacramento, California
  • California Pacific Medical Center-Pacific Campus โ€” San Francisco, California
  • Gene Upshaw Memorial Tahoe Forest Cancer Center โ€” Truckee, California
  • UCHealth University of Colorado Hospital โ€” Aurora, Colorado
  • Penrose-Saint Francis Healthcare โ€” Colorado Springs, Colorado
  • UCHealth Memorial Hospital Central โ€” Colorado Springs, Colorado
  • Memorial Hospital North โ€” Colorado Springs, Colorado
  • AdventHealth Porter โ€” Denver, Colorado

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
๐Ÿ›๏ธ View Official NIH Record โ†—