The role of high-dose chemotherapy in the management of germ cell tumors

被引:1
作者
Bastos, Diogo A. [1 ]
Feldman, Darren R. [2 ,3 ]
机构
[1] Hosp Sirio Libanes, Ctr Oncol, Sao Paulo, Brazil
[2] Mem Sloan Kettering Canc Ctr, Genitourinary Oncol Serv, Dept Med, New York, NY 10065 USA
[3] Cornell Univ, Dept Med, Weill Med Coll, New York, NY 10021 USA
关键词
autologous stem cell transplantation; germ cell tumors; high-dose chemotherapy; testicular cancer; BONE-MARROW-TRANSPLANTATION; PHASE-II TRIAL; SALVAGE TREATMENT; 1ST-LINE THERAPY; PLUS IFOSFAMIDE; INTENSIVE CHEMOTHERAPY; RANDOMIZED-TRIAL; ETOPOSIDE; CARBOPLATIN; CANCER;
D O I
10.1097/CCO.0000000000000070
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of reviewTo discuss the current role and future perspectives of high-dose chemotherapy (HDCT) in the management of advanced germ cell tumors (GCTs).Recent findingsMultiple studies have demonstrated the safety and efficacy of HDCT, consisting of carboplatin and etoposide followed by stem cell reinfusion, for the salvage treatment of GCTs. However, three randomized trials showed no benefit for HDCT over conventional dose chemotherapy in the first-line setting. Similarly, adding a third drug to etoposide with carboplatin does not seem to substantially improve treatment efficacy and may increase toxicity and mortality. Recent retrospective data from single centers and a large international collaboration demonstrated better outcomes with use of HDCT in the initial (rather than later) salvage setting as well as with sequential rather than single cycle regimens. However, randomized data are lacking. Prognostic factors for outcome to salvage HDCT were recently established and enhanced supportive measures such as growth factors and antibiotic prophylaxis have resulted in a dramatic decrease in morbidity and mortality.SummaryHDCT plays an integral role in the salvage treatment of patients with advanced GCTs. However, optimal timing (initial vs. later salvage), dosing, number of high-dose cycles, and patient selection remain to be defined.
引用
收藏
页码:284 / 293
页数:10
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