Phase II Clinical Trial of Oxaliplatin and Bevacizumab in Refractory Germ Cell Tumors
被引:20
作者:
Jain, Amit
论文数: 0引用数: 0
h-index: 0
机构:
Indiana Univ Sch Med, Indianapolis, IN 46202 USA
Melvin & Bren Simon Canc Ctr, Indianapolis, IN USAIndiana Univ Sch Med, Indianapolis, IN 46202 USA
Jain, Amit
[1
,2
]
Brames, Mary J.
论文数: 0引用数: 0
h-index: 0
机构:
Indiana Univ Sch Med, Indianapolis, IN 46202 USA
Melvin & Bren Simon Canc Ctr, Indianapolis, IN USAIndiana Univ Sch Med, Indianapolis, IN 46202 USA
Brames, Mary J.
[1
,2
]
Vaughn, David J.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Penn, Abramson Canc Ctr, Philadelphia, PA 19104 USAIndiana Univ Sch Med, Indianapolis, IN 46202 USA
Vaughn, David J.
[3
]
Einhorn, Lawrence H.
论文数: 0引用数: 0
h-index: 0
机构:
Indiana Univ Sch Med, Indianapolis, IN 46202 USA
Melvin & Bren Simon Canc Ctr, Indianapolis, IN USAIndiana Univ Sch Med, Indianapolis, IN 46202 USA
Einhorn, Lawrence H.
[1
,2
]
机构:
[1] Indiana Univ Sch Med, Indianapolis, IN 46202 USA
[2] Melvin & Bren Simon Canc Ctr, Indianapolis, IN USA
[3] Univ Penn, Abramson Canc Ctr, Philadelphia, PA 19104 USA
来源:
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS
|
2014年
/
37卷
/
05期
Background: Salvage chemotherapy has curative potential in germ cell tumors (GCTs). However, novel therapies are still needed for patients failing to be cured with standard salvage chemotherapy. Bevacizumab in combination with chemotherapy has clinical activity in many solid tumors. This is the first study of bevacizumab with oxaliplatin in refractory GCT patients. Patients and Methods: Patients with metastatic GCT with progressive disease after second-line or later salvage chemotherapy were eligible. Prior high-dose chemotherapy and paclitaxel and/or gemcitabine were required unless primary mediastinal nonseminomatous GCT or late relapse. Patients received oxaliplatin-85 mg/m(2) and bevacizumab-10 mg/kg every 2 weeks for a maximum of 14 cycles. Results: Twenty-nine patients were enrolled and evaluated. Nine patients were late relapses and 5 had primary mediastinal nonseminomatous GCT. Median number of prior chemotherapy regimens was 4. There was no grade 4 and only 1 grade 3 toxicity. Although the primary endpoint of 12 months disease-free survival was not achieved, 8 patients (27.6%) had objective response including 1 complete remission. Median duration of remission was 5 months (range, 4 to 22 mo). Conclusions: Oxaliplatin plus bevacizumab was well tolerated in heavily pretreated GCTs with manageable adverse events. There was modest clinical activity but only 1 patient achieved complete remission.