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Outcome of Men With Relapses After Adjuvant Bleomycin, Etoposide, and Cisplatin for Clinical Stage I Nonseminoma

Authors :
Konstantinos Koutsoukos
Carl W. Langberg
Jonathan Shamash
Matthew Wheater
Jeff White
Olof Ståhl
Torgrim Tandstad
Constance Thibault
Anis A. Hamid
Jorge Aparicio
Christian D. Fankhauser
Costantine Albany
Marcus Hentrich
Carsten Bokemeyer
Bruno Vincenzi
Jörg Beyer
Angelika Terbuch
Axel Heidenreich
Gabriella Cohn-Cedermark
Stefanie Fischer
Anja Lorch
Andrea Necchi
Dirk Klingbiel
Silke Gillessen
Fischer, S.
Tandstad, T.
Cohn-Cedermark, G.
Thibault, C.
Vincenzi, B.
Klingbiel, D.
Albany, C.
Necchi, A.
Terbuch, A.
Lorch, A.
Aparicio, J.
Heidenreich, A.
Hentrich, M.
Wheater, M.
Langberg, C. W.
Stahl, O.
Fankhauser, C. D.
Hamid, A. A.
Koutsoukos, K.
Shamash, J.
White, J.
Bokemeyer, C.
Beyer, J.
Gillessen, S.
University of Zurich
Gillessen, Silke
Source :
J Clin Oncol
Publication Year :
2020
Publisher :
American Society of Clinical Oncology, 2020.

Abstract

PURPOSE Clinical stage I (CSI) nonseminoma (NS) is a disease limited to the testis without metastases. One treatment strategy after orchiectomy is adjuvant chemotherapy. Little is known about the outcome of patients who experience relapse after such treatment. PATIENTS AND METHODS Data from 51 patients with CSI NS who experienced a relapse after adjuvant bleomycin, etoposide, and cisplatin (BEP) from 18 centers/11 countries were collected and retrospectively analyzed. Primary outcomes were overall and progression-free survivals calculated from day 1 of treatment at first relapse. Secondary outcomes were time to, stage at, and treatment of relapse and rate of subsequent relapses. RESULTS Median time to relapse was 13 months, with the earliest relapse 2 months after start of adjuvant treatment and the latest after 25 years. With a median follow-up of 96 months, the 5-year PFS was 67% (95% CI, 54% to 82%) and the 5-year OS was 81% (95% CI, 70% to 94%). Overall, 19 (37%) of 51 relapses occurred later than 2 years. Late relapses were associated with a significantly higher risk of death from NS (hazard ratio, 1.10 per year; P = .01). Treatment upon relapse was diverse: the majority of patients received a combination of chemotherapy and surgery. Twenty-nine percent of patients experienced a subsequent relapse. At last follow-up, 41 patients (80%) were alive and disease-free, eight (16%) had died of progressive disease, and one patient (2%) each had died from therapy-related or other causes. CONCLUSION Outcomes of patients with relapse after adjuvant BEP seem better compared with patients who experience relapse after treatment of metastatic disease but worse compared with those who have de-novo metastatic disease. We found a substantial rate of late and subsequent relapses. There seem to be three patterns of relapse with different outcomes: pure teratoma, early viable NS relapse (< 2 years), and late viable NS relapse (> 2 years).

Details

Language :
English
Database :
OpenAIRE
Journal :
J Clin Oncol
Accession number :
edsair.doi.dedup.....7c667edd1dd731f532fcdb98c9dc4d9c
Full Text :
https://doi.org/10.7892/boris.139302