High-dose chemotherapy (HDCT) as second-salvage treatment in patients with multiple relapsed or refractory germ-cell tumors

被引:54
作者
Lorch, A. [3 ,4 ]
Neubauer, A. [3 ,4 ]
Hackenthal, M. [1 ,2 ]
Dieing, A. [5 ,6 ]
Hartmann, J. T. [7 ,8 ]
Rick, O. [9 ,10 ]
Bokemeyer, C. [11 ,12 ,13 ]
Beyer, J. [1 ,2 ]
机构
[1] Vivantes Klinikum Urban, Dept Hematol, D-10967 Berlin, Germany
[2] Vivantes Klinikum Urban, Dept Oncol, D-10967 Berlin, Germany
[3] Univ Klinikum Giessen & Marburg GmbH, Dept Hematol, Marburg, Germany
[4] Univ Klinikum Giessen & Marburg GmbH, Dept Oncol, Marburg, Germany
[5] Charite Campus Mitte, Dept Hematol, Berlin, Germany
[6] Charite Campus Mitte, Dept Oncol, Berlin, Germany
[7] SW German Comprehens Canc Ctr, Dept Hematol, Tubingen, Germany
[8] SW German Comprehens Canc Ctr, Dept Oncol, Tubingen, Germany
[9] Klin Reinhardshohe, Dept Hematol, Bad Wildungen, Germany
[10] Klin Reinhardshohe, Dept Oncol, Bad Wildungen, Germany
[11] UCCH Univ Med Ctr Hamburg Eppendorf, Hubertus Wald Tumorzentrum, Sect Pneumol, Dept Oncol, Hamburg, Germany
[12] UCCH Univ Med Ctr Hamburg Eppendorf, Hubertus Wald Tumorzentrum, Sect Pneumol, Dept Hematol, Hamburg, Germany
[13] UCCH Univ Med Ctr Hamburg Eppendorf, Hubertus Wald Tumorzentrum, Sect Pneumol, Dept BMT, Hamburg, Germany
关键词
autologous transplantation; chemotherapy; germ-cell tumor; retrospective study; salvage therapy; testicular cancer; SALVAGE CHEMOTHERAPY; TESTICULAR-CANCER; PHASE-I/II; IFOSFAMIDE; PACLITAXEL; CISPLATIN; ETOPOSIDE; CARBOPLATIN; RESCUE; TRIAL;
D O I
10.1093/annonc/mdp366
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Survival after high-dose chemotherapy (HDCT) as second-salvage treatment (SST) in multiple relapsed germ-cell tumors (GCTs). Patients and methods: Existing databases in Berlin and Marburg of HDCT trials from 1989 to 2008 were retrospectively screened. Among 534 patients, 71 of 534 (13%) patients were scheduled for HDCT having failed previous conventional-dose first-line and first-salvage chemotherapy regimens; those 49 patients who had received at least cisplatin plus etoposide first-line as well as conventional-dose cisplatin-based first-salvage regimens and were diagnosed after 1 January 1990 were further analyzed. Results: Median age at SST was 32 years (range 19-52 years). Median follow-up for surviving patients was 4 years (range 1.7-8.5 years). Three of 49 (6%) patients either progressed or died before scheduled HDCT; the remaining 46 of 49 (94%) received either single or sequential HDCT. The rate of favorable responses to HDCT was 27 of 49 (55%). Nine patients remain alive and free of progression. One additional patient was lost to follow without progression at 4 years. The projected overall survival rate at 5 years was 17% (95% confidence intervals 7% to 30%). Conclusion: HDCT can induce remissions in patients with multiple relapsed GCTs with a long-term survival rate of similar to 17%.
引用
收藏
页码:820 / 825
页数:6
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