Phase III study of efaproxiral as an adjunct to whole-brain radiation therapy for brain metastases

被引:136
|
作者
Suh, JH
Stea, B
Nabid, A
Kresl, JJ
Fortin, K
Mercier, JP
Senzer, N
Chang, EL
Boyd, AP
Cagnoni, PJ
Shaw, P
机构
[1] Cleveland Clin Fdn, Brain Tumor Inst, Dept Radiat Oncol, Cleveland, OH 44195 USA
[2] Univ Arizona, Hlth Sci Ctr, Tucson, AZ USA
[3] Arizona Oncol Serv, Barrow Neurol Inst, Phoenix, AZ USA
[4] US Oncol Res Inc, Dallas, TX USA
[5] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[6] Allos Therapeut Inc, Westminster, CO USA
[7] Wake Forest Univ, Sch Med, Winston Salem, NC 27109 USA
[8] Univ Sherbrooke, Ctr Hosp, Sherbrooke, PQ J1K 2R1, Canada
[9] Hop Hotel Dieu, Ctr Hosp Quebec, Quebec City, PQ, Canada
[10] Hosp Maisonneuve Rosemont, Montreal, PQ, Canada
关键词
D O I
10.1200/JCO.2004.00.1768
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To determine whether efaproxiral, an allosteric modifier of hemoglobin, improves survival in patients with brain metastases when used as an adjunct to whole-brain radiation therapy (WBRT). Patients and Methods Patients with brain metastases from solid tumors and a Karnofsky performance score of >= 70 were randomly assigned to receive WBRT with supplemental oxygen and either efaproxiral at 75 or 100 mg/kg efaproxiral arm) or no efaproxiral (control arm). The primary end point was survival. Results The study consisted of 515 eligible patients (efaproxiral arm, n = 265; control arm, n = 250), The median survival time (MST) was 5.4 months for the efaproxiral arm versus 4.4 months for the control arm (hazard ratio [HR] = 0.87; P = 16), For the subgroup of patients with non-small-cell lung cancer (NSCLC) or breast cancer, the MST was 6.0 and 4.4 months, respectively (HR = 0.82; P =.07). Cox multiple regression analysis demonstrated a significant reduction in the risk of death for the efaproxiral arm in both primary populations, Further analysis indicated that the benefit may be restricted to the subgroup of patients with breast cancer, Response rates (radiographic complete response plus partial response) improved by 7% (P = 10) and 13% (P = 01) for all patients and for NSCLC and breast cancer patients in the efaproxiral arm, respectively, The most common severe adverse event in patients treated with efaproxiral was hypoxemia, which was reversible and effectively managed with supplemental oxygen in most patients. Conclusion The addition of efaproxiral, a noncytotoxic radiation sensitizer, to WBRT may improve response rates and survival in patients with brain metastases, particularly metastases from breast cancer, A confirmatory trial for breast cancer patients has been initiated.
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收藏
页码:106 / 114
页数:9
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