First salvage treatment in patients with advanced germ cell cancer after cisplatin-based chemotherapy: analysis of a registry of the German Testicular Cancer Study Group (GTCSG)

Journal of Cancer Research and Clinical Oncology - Tập 140 - Trang 1211-1220 - 2014
Lars Arne Berger1, Carsten Bokemeyer1, Anja Lorch2,3, Marcus Hentrich4, Hans-Georg Kopp5, Thomas Christoph Gauler6, Jörg Beyer7, Maike de Wit8, Frank Mayer5,9, Ina Boehlke1, Christoph Oing1, Friedemann Honecker1, Karin Oechsle1
1Department of Oncology, Hematology, BMT with Section of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
2Department of Internal Medicine, Hematology and Oncology, University Hospital Giessen and Marburg, Marburg, Germany
3Division of Conservative Urologic Oncology, Department of Urology, University Hospital Düsseldorf, Düsseldorf, Germany
4Department of Hematology, Oncology and Palliative Care, Harlaching Hospital, Munich, Germany
5Department of Oncology and Hematology, University Hospital Tübingen, Tübingen, Germany
6Department of Medicine (Cancer Research), University Hospital Essen, Essen, Germany
7Department of Internal Medicine, Hematology and Oncology, Vivantes Klinikum am Urban, Berlin, Germany
8Department of Internal Medicine, Hematology and Oncology, Vivantes Klinikum Neukoelln, Berlin, Germany
9Praxis und Tagesklinik PD Dr. Helmut Oettle/Prof. Dr. Dr. Frank Mayer, Friedrichshafen, Germany

Tóm tắt

We analyzed prognostic categories at first relapse according to the International Prognostic Factors Study Group (IPFSG) criteria as well as the efficacy of salvage treatment. 143 patients with relapsed or refractory germ cell cancer undergoing first salvage treatment with conventional-dose (CD-CX, n = 48) or high-dose chemotherapy with autologous stem cell support (HD-CX, n = 95) contributed by nine centers were retrospectively analyzed. Prognostic subgroups according to IPFSG criteria were: very low risk 13/143, low risk 36/143, intermediate risk 66/143, high risk 22/143, and very high risk 6/143 patients. The IPFSG categories significantly correlated with overall survival (OS) (p = 0.025) after 1st salvage treatment. After a median follow-up of 19 months, 55 % of all patients had relapsed and 33 % had died. For the entire cohort, progression-free survival (PFS) rate after 2 years was 43 %, and OS rate after 5 years was 52 %. Compared to the HD-CX group, vital carcinoma was found more often in secondarily resected lesions following CD-CX (22/29 vs. 22/45; p = 0.021). Second relapse rate was higher with 75 versus 44 %, resulting in a shorter median PFS with 8 versus 42 months (p < 0.001), but this did not translate into different OS (p = 0.931). At subsequent relapses, 26/36 patients received HD-CX as ≥2nd-salvage treatment. This analysis confirms the prognostic value of the IPFSG prognostic score. HD-CX seemed superior to CD-CX as first salvage treatment with respect to PFS in this retrospective analysis.

Tài liệu tham khảo

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