Survival and neurologic outcomes in a randomized trial of motexafin gadolinium and whole-brain radiation therapy in brain metastases

被引:335
作者
Mehta, MP
Rodrigus, P
Terhaard, CHJ
Rao, A
Suh, J
Roa, W
Soukami, L
Bezjak, A
Leibenhaut, M
Komaki, R
Schultz, C
Timmerman, R
Curran, W
Smith, J
Phan, SC
Miller, RA
Renschler, MF
机构
[1] Univ Wisconsin, Sch Med, Dept Human Oncol Radiat Oncol, Madison, WI 53792 USA
[2] Med Coll Wisconsin, Froedtert Mem Lutheran Hosp, Milwaukee, WI 53226 USA
[3] Kaiser Permanente, Los Angeles, CA USA
[4] Radiol Assoc Sacramento, Sutter Hosp, Sacramento, CA USA
[5] Pharmacyclics Inc, Sunnyvale, CA USA
[6] Cleveland Clin, Cleveland, OH 44106 USA
[7] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[8] Indiana Univ, Med Ctr, Indianapolis, IN USA
[9] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
[10] Dr Bernard Verbeeten Inst, Tilburg, Netherlands
[11] Acad Ziekenhuis, Utrecht, Netherlands
[12] Cross Canc Inst, Edmonton, AB, Canada
[13] Montreal Gen Hosp, Montreal, PQ, Canada
[14] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
关键词
D O I
10.1200/JCO.2003.12.122
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This phase III randomized trial evaluated survival as well as neurologic and neurocognitive function in patients with brain metastases from solid tumors receiving whole-brain radiation therapy (WBRT) with or without motexafin gadolinium (MGd). Patients and Methods: Patients were randomly assigned to 30 Gy of WBRT +/- 5 mg/kg/d MGd. Survival and time to neurologic progression determined by a blinded events review committee (ERC) were coprimary end points. Standardized investigator neurologic assessment and neurocognitive testing were evaluated. Results: Four hundred one (251 non-small-cell lung cancer) patients were enrolled. There was no significant difference by treatment arm in survival (median, 5.2 months for MGd v 4.9 months for WBRT, P = .48) or time to neurologic progression (median, 9.5 months for MGd v 8.3 months for WBRT, P = .95). Treatment with MGd improved time to neurologic progression in patients with lung cancer (median, not reached for MGd v 7.4 months for WBRT, P = .048, unadjusted). By investigator, MGd improved time to neurologic progression in all patients (median, 4.3 months for MGd v 3.8 months for WBRT, P = .018) and in lung cancer patients (median, 5.5 months for MGd v 3.7 months for WBRT, P = .025). MGd improved neurocognitive function in lung cancer patients. Conclusion: The overall results did not demonstrate significant differences by treatment arm for survival and ERC time to neurologic progression. Investigator neurologic assessments demonstrated an MGd treatment benefit in all patients. In lung cancer patients, ERC- and investigator-determined time to neurologic progression demonstrated an MGd treatment benefit. MGd may improve time to neurologic and neurocognitive progression in lung cancer. (C) 2003 by American Society of Clinical Oncology.
引用
收藏
页码:2529 / 2536
页数:8
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