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High-dose chemotherapy (HDCT) as second-salvage treatment in patients with multiple relapsed or refractory germ-cell tumors.
Lorch, A; Neubauer, A; Hackenthal, M; Dieing, A; Hartmann, J T; Rick, O; Bokemeyer, C; Beyer, J.
Afiliação
  • Lorch A; Departments of Hematology and Oncology, Universitätsklinikum Giessen und Marburg GmbH, Marburg.
  • Neubauer A; Departments of Hematology and Oncology, Universitätsklinikum Giessen und Marburg GmbH, Marburg.
  • Hackenthal M; Departments of Hematology and Oncology, Vivantes Klinikum Am Urban, Berlin.
  • Dieing A; Departments of Hematology and Oncology, Charite Campus Mitte, Berlin.
  • Hartmann JT; Departments of Hematology and Oncology, South West German Comprehensive Cancer Center, Tübingen.
  • Rick O; Departments of Hematology and Oncology, Klinik Reinhardshöhe, Bad Wildungen.
  • Bokemeyer C; Departments of Oncology, Hematology and BMT with section Pneumology, Hubertus Wald Tumorzentrum - UCCH University Medical Center Hamburg Eppendorf, Hamburg, Germany.
  • Beyer J; Departments of Hematology and Oncology, Vivantes Klinikum Am Urban, Berlin. Electronic address: joerg.beyer@vivantes.de.
Ann Oncol ; 21(4): 820-825, 2010 Apr.
Article em En | MEDLINE | ID: mdl-19822531
ABSTRACT

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 approximately 17%.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Testiculares / Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Embrionárias de Células Germinativas Tipo de estudo: Evaluation_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Humans / Male / Middle aged Idioma: En Ano de publicação: 2010 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Testiculares / Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Embrionárias de Células Germinativas Tipo de estudo: Evaluation_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Humans / Male / Middle aged Idioma: En Ano de publicação: 2010 Tipo de documento: Article