A Phase 3 Trial of Whole Brain Radiation Therapy and Stereotactic Radiosurgery Alone Versus WBRT and SRS With Temozolomide or Erlotinib for Non-Small Cell Lung Cancer and 1 to 3 Brain Metastases: Radiation Therapy Oncology Group 0320
Journal Article
·
· International Journal of Radiation Oncology, Biology and Physics
- RTOG Statistical Center, Philadelphia, Pennsylvania (United States)
- University of Wisconsin Medical School Cancer Center, Madison, Wisconsin (United States)
- Wilmot Cancer Center, University of Rochester, Rochester, New York (United States)
- Thomas Jefferson University, Philadelphia, Pennsylvania (United States)
- University of Texas MD Anderson Cancer Center, Houston, Texas (United States)
- McGill University, Montreal, Quebec (Canada)
- Fox Chase Cancer Center, Philadelphia, Pennsylvania (United States)
- University of Wisconsin Hospital, Madison, Wisconsin (United States)
- Akron City Hospital, Akron, Ohio (United States)
- Christiana Care Health Services, Inc, CCOP, Newark, Delaware (United States)
- University of Texas Southwestern Medical School, Dallas, Texas (United States)
- The Ottawa Hospital Cancer Centre, Ottawa, Ontario (Canada)
- Cleveland Clinic Foundation, Cleveland, Ohio (United States)
- Northwestern Memorial Hospital, Chicago, Illinois (United States)
Background: A phase 3 Radiation Therapy Oncology Group (RTOG) study subset analysis demonstrated improved overall survival (OS) with the addition of stereotactic radiosurgery (SRS) to whole brain radiation therapy (WBRT) in non-small cell lung cancer (NSCLC) patients with 1 to 3 brain metastases. Because temozolomide (TMZ) and erlotinib (ETN) cross the blood-brain barrier and have documented activity in NSCLC, a phase 3 study was designed to test whether these drugs would improve the OS associated with WBRT + SRS. Methods and Materials: NSCLC patients with 1 to 3 brain metastases were randomized to receive WBRT (2.5 Gy × 15 to 37.5 Gy) and SRS alone, versus WBRT + SRS + TMZ (75 mg/m{sup 2}/day × 21 days) or ETN (150 mg/day). ETN (150 mg/day) or TMZ (150-200 mg/m{sup 2}/day × 5 days/month) could be continued for as long as 6 months after WBRT + SRS. The primary endpoint was OS. Results: After 126 patients were enrolled, the study closed because of accrual limitations. The median survival times (MST) for WBRT + SRS, WBRT + SRS + TMZ, and WBRT + SRS + ETN were qualitatively different (13.4, 6.3, and 6.1 months, respectively), although the differences were not statistically significant. Time to central nervous system progression and performance status at 6 months were better in the WBRT + SRS arm. Grade 3 to 5 toxicity was 11%, 41%, and 49% in arms 1, 2, and 3, respectively (P<.001). Conclusion: The addition of TMZ or ETN to WBRT + SRS in NSCLC patients with 1 to 3 brain metastases did not improve survival and possibly had a deleterious effect. Because the analysis is underpowered, these data suggest but do not prove that increased toxicity was the cause of inferior survival in the drug arms.
- OSTI ID:
- 22224423
- Journal Information:
- International Journal of Radiation Oncology, Biology and Physics, Journal Name: International Journal of Radiation Oncology, Biology and Physics Journal Issue: 5 Vol. 85; ISSN IOBPD3; ISSN 0360-3016
- Country of Publication:
- United States
- Language:
- English
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