Carboplatin Induction Chemotherapy in Clinically Lymph Node-positive Bladder Cancer.

Carboplatin Induction chemotherapy Oligometastatic Survival Urinary bladder neoplasms

Journal

European urology open science
ISSN: 2666-1683
Titre abrégé: Eur Urol Open Sci
Pays: Netherlands
ID NLM: 101771568

Informations de publication

Date de publication:
May 2023
Historique:
accepted: 23 02 2023
medline: 16 5 2023
pubmed: 16 5 2023
entrez: 15 5 2023
Statut: epublish

Résumé

There are currently no guideline recommendations regarding the treatment of cisplatin-ineligible, clinically lymph node-positive (cN+) bladder cancer (BCa). To investigate the oncological efficacy of gemcitabine/carboplatin induction chemotherapy (IC) in comparison to cisplatin-based regimens in cN+ BCa. This was an observational study of 369 patients with cT2-4 N1-3 M0 BCa. IC followed by consolidative radical cystectomy (RC). The primary endpoints were the pathological objective response (pOR; ypT0/Ta/Tis/T1 N0) rate and the pathological complete response (pCR; ypT0N0) rate. We applied 3:1 propensity score matching (PSM) to reduce selection bias. Overall survival (OS) and cancer-specific survival (CSS) were compared across groups using the Kaplan-Meier method. Associations between the treatment regimen and survival endpoints were tested in multivariable Cox regression analyses. After PSM, a cohort of 216 patients was available for analysis, of whom 162 received cisplatin-based IC and 54 gemcitabine/carboplatin IC. At RC, 54 patients (25%) had a pOR and 36 (17%) had a pCR. The 2-yr CSS was 59.8% (95% confidence interval [CI] 51.9-69%) for patients who received cisplatin-based IC versus 38.8% (95% CI 26-57.9%) for those who received gemcitabine/carboplatin. For the pOR ( Cisplatin-based IC seems to be superior to gemcitabine/carboplatin and should be the standard for cisplatin-eligible patients with cN+ BCa. Gemcitabine/carboplatin may be an alternative treatment for selected cisplatin-ineligible patients with cN+ BCa. In particular, selected cisplatin-ineligible patients with cN1 disease may benefit from gemcitabine/carboplatin IC. In this multicenter study, we found that selected patients with bladder cancer and clinical evidence of lymph node metastasis who cannot receive standard cisplatin-based chemotherapy before surgery to remove their bladder may benefit from chemotherapy with gemcitabine/carboplatin. Patients with a single lymph node metastasis may benefit the most.

Sections du résumé

Background UNASSIGNED
There are currently no guideline recommendations regarding the treatment of cisplatin-ineligible, clinically lymph node-positive (cN+) bladder cancer (BCa).
Objective UNASSIGNED
To investigate the oncological efficacy of gemcitabine/carboplatin induction chemotherapy (IC) in comparison to cisplatin-based regimens in cN+ BCa.
Design setting and participants UNASSIGNED
This was an observational study of 369 patients with cT2-4 N1-3 M0 BCa.
Intervention UNASSIGNED
IC followed by consolidative radical cystectomy (RC).
Outcome measurements and statistical analysis UNASSIGNED
The primary endpoints were the pathological objective response (pOR; ypT0/Ta/Tis/T1 N0) rate and the pathological complete response (pCR; ypT0N0) rate. We applied 3:1 propensity score matching (PSM) to reduce selection bias. Overall survival (OS) and cancer-specific survival (CSS) were compared across groups using the Kaplan-Meier method. Associations between the treatment regimen and survival endpoints were tested in multivariable Cox regression analyses.
Results and limitations UNASSIGNED
After PSM, a cohort of 216 patients was available for analysis, of whom 162 received cisplatin-based IC and 54 gemcitabine/carboplatin IC. At RC, 54 patients (25%) had a pOR and 36 (17%) had a pCR. The 2-yr CSS was 59.8% (95% confidence interval [CI] 51.9-69%) for patients who received cisplatin-based IC versus 38.8% (95% CI 26-57.9%) for those who received gemcitabine/carboplatin. For the pOR (
Conclusions UNASSIGNED
Cisplatin-based IC seems to be superior to gemcitabine/carboplatin and should be the standard for cisplatin-eligible patients with cN+ BCa. Gemcitabine/carboplatin may be an alternative treatment for selected cisplatin-ineligible patients with cN+ BCa. In particular, selected cisplatin-ineligible patients with cN1 disease may benefit from gemcitabine/carboplatin IC.
Patient summary UNASSIGNED
In this multicenter study, we found that selected patients with bladder cancer and clinical evidence of lymph node metastasis who cannot receive standard cisplatin-based chemotherapy before surgery to remove their bladder may benefit from chemotherapy with gemcitabine/carboplatin. Patients with a single lymph node metastasis may benefit the most.

Identifiants

pubmed: 37187719
doi: 10.1016/j.euros.2023.02.014
pii: S2666-1683(23)00122-2
pmc: PMC10175724
doi:

Types de publication

Journal Article

Langues

eng

Pagination

39-46

Informations de copyright

© 2023 The Author(s).

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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.

Bas W G van Rhijn (BWG)

Department of Urology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Department of Urology, Caritas St. Josef Medical Centre, University of Regensburg, Regensburg, Germany.

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.

Siamak Daneshmand (S)

USC/Norris Comprehensive Cancer Center, Institute of Urology, University of Southern California, Los Angeles, CA, USA.

Peter C Black (PC)

Vancouver Prostate Centre, Department of Urologic Sciences, University of British Columbia, Vancouver, Canada.

Maximilian Pallauf (M)

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

David D'Andrea (D)

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

Marco Moschini (M)

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

Francesco Soria (F)

Division of Urology, Department of Surgical Sciences, San Giovanni Battista Hospital, University of Studies of Torino, Turin, Italy.

Francesco Del Giudice (F)

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

Luca Afferi (L)

Department of Urology, Luzerner Kantonsspital, Luzern, Switzerland.

Ekaterina Laukhtina (E)

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Institute for Urology and Reproductive Health, Sechenov University, Moscow, Russia.

Takafumi Yanagisawa (T)

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Department of Urology, Jikei University School of Medicine, Tokyo, Japan.

Tatsushi Kawada (T)

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Jeremy Y-C Teoh (JY)

S.H. Ho Urology Centre, Department of Surgery, The Chinese University of Hong Kong, Hong Kong, China.

Mohammad Abufaraj (M)

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Division of Urology, Department of Special Surgery, The University of Jordan, Amman, Jordan.

Guillaume Ploussard (G)

Department of Urology, La Croix Du Sud Hospital, Quint-Fonsegrives, France.

Mathieu Roumiguié (M)

Department of Urology, CHU Toulouse-IUCT Oncopole, Toulouse, France.

Pierre I Karakiewicz (PI)

Cancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montreal Health Center, Montreal, Canada.

Marko Babjuk (M)

Department of Urology, Hospital Motol, Second Faculty of Medicine, Charles University, Prague, Czechia.

Paolo Gontero (P)

Division of Urology, Molinette Hospital, University of Studies of Torino, Torino, Italy.

Evanguelos Xylinas (E)

Department of Urology, Bichat-Claude Bernard Hospital, AP-HP, Paris University, Paris, France.

Michael Rink (M)

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

Shahrokh F Shariat (SF)

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

Benjamin Pradere (B)

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

Classifications MeSH