Germ cell tumours (GCT) comprise exquisitely chemosensitive neoplasms, and cure is possible in patients presenting with a high metastatic tumour burden. For the few patients with high-risk disease or who relapse after first-line chemotherapy, the administration of a tandem or a triple course of high-dose chemotherapy (HDCT) with carboplatin and etoposide with stem cell support may represent a valuable therapeutic option. From November 1981 to December 2015, 1179 patients aged ⩾40 years were identified from a total of 5295 registered patients (22%) from 226 EBMT centres.the present data may aid physicians who are treating advanced GCT to improve their knowledge of the mortality-rate after HDCT administration in older patients. HDCT can be safely administered in these high-risk patients and still represents their first therapeutic option in the salvage setting, pending prospective validation through clinical trials.

Administration of high-dose chemotherapy with stem cell support in patients 40 years of age or older with advanced germ cell tumours: A retrospective study from the European Society for Blood and Marrow Transplantation database

Lanza F.
Penultimo
Data Curation
;
2017

Abstract

Germ cell tumours (GCT) comprise exquisitely chemosensitive neoplasms, and cure is possible in patients presenting with a high metastatic tumour burden. For the few patients with high-risk disease or who relapse after first-line chemotherapy, the administration of a tandem or a triple course of high-dose chemotherapy (HDCT) with carboplatin and etoposide with stem cell support may represent a valuable therapeutic option. From November 1981 to December 2015, 1179 patients aged ⩾40 years were identified from a total of 5295 registered patients (22%) from 226 EBMT centres.the present data may aid physicians who are treating advanced GCT to improve their knowledge of the mortality-rate after HDCT administration in older patients. HDCT can be safely administered in these high-risk patients and still represents their first therapeutic option in the salvage setting, pending prospective validation through clinical trials.
2017
Necchi, A.; Lo Vullo, S.; Rosti, G.; Badoglio, M.; Giannatempo, P.; Raggi, D.; Secondino, S.; Mariani, L.; Lanza, F.; Pedrazzoli, P.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/2416106
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