The optimal number of induction chemotherapy cycles in clinically lymph node-positive bladder cancer.

cN+ induction chemotherapy pathology survival urinary bladder neoplasms

Journal

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

Informations de publication

Date de publication:
12 Mar 2024
Historique:
medline: 12 3 2024
pubmed: 12 3 2024
entrez: 12 3 2024
Statut: aheadofprint

Résumé

To investigate the optimal number of induction chemotherapy cycles needed to achieve a pathological response in patients with clinically lymph node-positive (cN+) bladder cancer (BCa) who received three or four cycles of induction chemotherapy followed by consolidative radical cystectomy (RC) with pelvic lymph node dissection. We included 388 patients who received three or four cycles of cisplatin/gemcitabine or (dose-dense) methotrexate, vinblastine, doxorubicin, and cisplatin (MVAC), followed by consolidative RC for cTanyN1-3M0 BCa. We compared pathological complete (pCR = ypT0N0) and objective response (pOR = yp ≤T1N0) between treatment groups. Predictors of pCR and/or pOR were assessed using uni- and multivariable logistic regression analysis. The secondary endpoints were overall (OS) and cancer-specific survival (CSS). We evaluated the association between the number of induction chemotherapy cycles administered and survival outcomes on multivariable Cox regression. Overall, 101 and 287 patients received three or four cycles of induction chemotherapy, respectively. Of these, 72 (19%) and 128 (33%) achieved pCR and pOR response, respectively. The pCR (20%, 18%) and pOR (40%, 31%) rates did not differ significantly between patients receiving three or four cycles (P > 0.05). The number of cycles was not associated with pCR or pOR on multivariable logistic regression analyses. The 2-year OS estimates were 63% (95% confidence interval [CI] 0.53-0.74) and 63% (95% CI 0.58-0.7) for patients receiving three or four cycles, respectively. Receiving three vs four cycles was not associated with OS and CSS on uni- or multivariable Cox regression analyses. Pathological response and survival outcomes did not differ between administering three or four induction chemotherapy cycles in patients with cN+ BCa. A fewer cycles (minimum three) may be oncologically sufficient in patients with cN+ BCa, while decreasing the wait for definitive local therapy in those patients who end up without a response to chemotherapy. This warrants further validation.

Identifiants

pubmed: 38470089
doi: 10.1111/bju.16319
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Investigateurs

Luca Afferi (L)
Alessandro Antonelli (A)
Luca Antonelli (L)
Mara Bacchiani (M)
Alberto Bianchi (A)
Ronan Flippot (R)
Mattia Longoni (M)
Elisabeth Maier (E)
Nicolas Penel (N)
Julien Sarkis (J)
Francesco Soria (F)
Solomon Woldu (S)

Informations de copyright

© 2024 The Authors. BJU International published by John Wiley & Sons Ltd on behalf of BJU International.

Références

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Auteurs

Markus von Deimling (M)

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Department of Urology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Laura S Mertens (LS)

Department of Urology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Marc Furrer (M)

Department of Urology, University Hospital of Bern, University of Bern, Bern, Switzerland.
Department of Urology, Solothurner Spitäler AG, Kantonsspital Olten and Bürgerspital Solothurn, Switzerland.

Roger Li (R)

Department of Genitourinary Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.

Guus A H Tendijck (GAH)

Department of Urology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Jacob Taylor (J)

Department of Urology, University of Texas Southwestern, Dallas, TX, USA.

Felice Crocetto (F)

Department of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples "Federico II", Naples, Italy.

Moritz Maas (M)

Department of Urology, Eberhard Karls University Tübingen, Tübingen, Germany.
Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada.

Andrea Mari (A)

Unit of Oncologic Minimally-Invasive Urology and Andrology, Department of Experimental and Clinical Medicine, Careggi Hospital, University of Florence, Florence, Italy.

Renate Pichler (R)

Department of Urology, Comprehensive Cancer Center Innsbruck, Medical University of Innsbruck, Innsbruck, Austria.

Marco Moschini (M)

Department of Urology, Urological Research Institute, Vita-Salute San Raffaele, Milan, Italy.

Karl H Tully (KH)

Department of Urology and Neurourology, Marien Hospital Herne, Ruhr-University Bochum, Herne, Germany.

David D'Andrea (D)

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.

Ekaterina Laukhtina (E)

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.

Francesco Del Giudice (F)

Department of Maternal Infant and Urologic Sciences, Policlinico Umberto I Hospital, "Sapienza" University of Rome, Rome, Italy.

Gautier Marcq (G)

Department of Urology, CHU Lille, Claude Huriez Hospital, Lille, France.
CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, UMR9020-U1277 - CANTHER - Cancer Heterogeneity Plasticity and Resistance to Therapies, University of Lille, Lille, France.

Maud Velev (M)

Department of Cancer Medicine, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Andrea Gallioli (A)

Department of Urology, Fundació Puigvert, Autonomous University of Barcelona, Barcelona, Spain.

Simone Albisinni (S)

Urology Unit, Department of Surgical Sciences, Tor Vergata University Hospital, University of Rome Tor Vergata, Rome, Italy.
Service d'Urologie, Hôpital Erasme, Université Libre de Bruxelles, Bruxelles, Belgium.

Keiichiro Mori (K)

Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.

Abhinav Khanna (A)

Department of Urology, Mayo Clinic, Rochester, MN, USA.

Michael Rink (M)

Department of Urology, Marienkrankenhaus, Hamburg, Germany.

Margit Fisch (M)

Department of Urology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Andrea Minervini (A)

Unit of Oncologic Minimally-Invasive Urology and Andrology, Department of Experimental and Clinical Medicine, Careggi Hospital, University of Florence, Florence, Italy.

Peter C Black (PC)

Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada.

Yair Lotan (Y)

Department of Urology, University of Texas Southwestern, Dallas, TX, USA.

Philippe E Spiess (PE)

Department of Genitourinary Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.

Bernhard Kiss (B)

Department of Urology, University Hospital of Bern, University of Bern, Bern, Switzerland.

Shahrokh F Shariat (SF)

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Karl Landsteiner Institute of Urology and Andrology, Vienna, Austria.
Department of Urology, University of Texas Southwestern, Dallas, TX, USA.
Department of Urology, Weill Cornell Medical College, New York, NY, USA.
Hourani Center for Applied Scientific Research, Al-Ahliyya Amman University, Amman, Jordan.
Department of Urology, Second Faculty of Medicine, Charles University, Prague, Czech Republic.

Benjamin Pradere (B)

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Department of Urology, Urosud, La Croix Du Sud Hospital, Quint-Fonsegrives, France.

Classifications MeSH