Whole-Brain Radiation Therapy Plus Concomitant Temozolomide for the Treatment of Brain Metastases From Non-Small-Cell Lung Cancer: A Randomized, Open-Label Phase II Study

被引:63
|
作者
Chua, Daniel [1 ]
Krzakowski, Maciej [2 ]
Chouaid, Christos [3 ]
Pallotta, Maria G. [4 ]
Martinez, Jose I. [5 ]
Gottfried, Maya [6 ]
Curran, Walter [7 ]
Throuvalas, Nikolaos [8 ]
机构
[1] Univ Hong Kong, Dept Clin Oncol, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
[2] Maria Sklodowska Curie Mem Inst Oncol, Klin Leczenia Nowotworow Kltatki Piersiowej & Plu, Centrum Onkol Inst Oncol, Warsaw, Poland
[3] Hop St Antoine, AP HP, Serv Pneumol, F-75571 Paris, France
[4] Hosp Italiano Buenos Aires, Oncol Clin, Lab Cent, Buenos Aires, DF, Argentina
[5] Cansercoop Unidad Med Oncol, Bogota, Colombia
[6] Meir Med Ctr, Inst Oncol, Kefar Sava, Israel
[7] Thomas Jefferson Univ Hosp, Philadelphia, PA 19107 USA
[8] Athens Med Ctr, Dept Radiotherapy, Athens, Greece
关键词
Brain metastasis; Central nervous system progression; TMZ; GLIOBLASTOMA-MULTIFORME; RADIOTHERAPY; MANAGEMENT; TRIAL; SURVIVAL;
D O I
10.3816/CLC.2010.n.022
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A previously published study of temozolomide concurrent with whole-brain radiation therapy (WBRT) reported significant improvement in response rates and a nonsignificant trend toward improved overall survival compared with WBRT alone in patients with brain metastases primarily from lung cancer. This study sought to confirm the benefit of adding temozolomide to WBRT in patients with non-small-cell lung cancer (NSCLC) with brain metastases. Patients and Methods: This planned phase III study (target = 380 events) was converted to a phase II study (target = 70 events) because of poor enrollment. Patients with NSCLC and >= 1 newly diagnosed brain lesion were randomized to WBRT (30 Gy in 10 fractions) alone or combined with temozolomide (75 mg/m(2)/day) for 21 or 28 days. Endpoints included overall survival and time to central nervous system (CNS) progression. Results: Median overall survival and median time to CNS progression was 4.4 and 3.1 months in the WBRT + temozolomide arm (n = 47) versus 5.7 and 3.8 months in the WBRT arm (n = 48). However, there were imbalances in the percentages of patients receiving previous chemotherapy and with synchronous brain metastases. Adding temozolomide to WBRT increased the frequency of nausea, vomiting, alopecia, fatigue, anorexia, and constipation. Most adverse events were mild to moderate. Conclusion: The benefit of adding temozolomide to WBRT was not confirmed; however, the accrual goal for the planned phase III trial was not reached, and the study regimen differed from regimens used previously. Therefore, the role of temozolomide in treating brain metastases remains unresolved.
引用
收藏
页码:176 / 181
页数:6
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