Primary retroperitoneal lymph node dissection for metastatic non-seminomatous germ cell tumours: outcomes and adjuvant chemotherapy.

adjuvant chemotherapy non‐seminoma primary retroperitoneal lymph node dissection surveillance testicular cancer

Journal

BJU international
ISSN: 1464-410X
Titre abrégé: BJU Int
Pays: England
ID NLM: 100886721

Informations de publication

Date de publication:
05 Jul 2024
Historique:
medline: 5 7 2024
pubmed: 5 7 2024
entrez: 5 7 2024
Statut: aheadofprint

Résumé

To compare the outcomes and treatment burden of primary retroperitoneal lymph node dissection (pRPLND) alone versus pRPLND + adjuvant chemotherapy (AC) in patients with pathological stage II (PSII) non-seminomatous germ cell tumours (NSGCT). Retrospective review of the Princess Margaret Cancer Center eTestes cancer database identified patients with PSII NSGCT after pRPLND between 1995 and 2020. The primary outcome was relapse-free survival (RFS). Secondary outcomes included disease-specific survival (DSS), burden of relapse treatment, and factors associated with relapse. A total of 109 PSII patients were included in the study. There were 96 patients treated with pRPLND alone and 13 treated with pRPLND + AC. The median follow-up was 61 months. The 5-year RFS was 72% for the pRPLND-only group vs 92% for the pRPLND + AC group (hazard ratio [HR] 4.372, 95% confidence interval [CI] 0.59-32.36; P = 0.11). Within the pRPLND-only group the 5-year RFS differed by pN stage (pN1 = 94% vs pN2/N3 = 67%, P = 0.03). Despite a higher relapse rate within the pRPLND-only group, the DSS was similar at 5 years (98% pRPLND only vs 100% pRPLND + AC, P = 0.48). Only 24 (25%) of the patients in the pRPLND-only group required any subsequent chemotherapy. Despite achieving similar survival, the cumulative post-RPLND treatment burden was less for the pRPLND-only group than the pRPLND+AC group overall (average 1.23 vs 2.46 cycles of chemotherapy per patient in group). The majority of patients with PSII NSGCT treated with pRPLND alone do not experience a recurrence or require chemotherapy. Despite a lower relapse risk when AC is given, no difference in survival was seen but higher chemotherapy burden was entertained. AC may constitute overtreatment for most patients with PSII NSGCT treated with pRPLND.

Identifiants

pubmed: 38967557
doi: 10.1111/bju.16448
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Dell'Elce Family Testis Cancer Research Fund

Informations de copyright

© 2024 The Author(s). BJU International published by John Wiley & Sons Ltd on behalf of BJU International.

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Auteurs

Ahmad Mousa (A)

Division of Urology, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
Division of Urology, Department of Surgery, Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.

Lynn Anson-Cartwright (L)

Division of Urology, Department of Surgery, Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.

Eshetu G Atenafu (EG)

Biostatistics Core, University Health Network, University of Toronto, Toronto, Ontario, Canada.

Michael A S Jewett (MAS)

Division of Urology, Department of Surgery, Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.

Philippe Bedard (P)

Division of Medical Oncology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.

Di Maria Jiang (DM)

Division of Medical Oncology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.

Rachel Glicksman (R)

Department of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.

Peter Chung (P)

Department of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.

Padraig Warde (P)

Department of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.

Martin O'Malley (M)

Department of Medical Imaging, University of Toronto, Toronto, Ontario, Canada.

Susan Prendeville (S)

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.

Robert J Hamilton (RJ)

Division of Urology, Department of Surgery, Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.

Classifications MeSH