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Identifying the Optimal Number of Neoadjuvant Chemotherapy Cycles in Patients with Muscle Invasive Bladder Cancer.
D'Andrea, David; Black, Peter C; Zargar, Homayoun; Dinney, Colin P; Soria, Francesco; Cookson, Michael S; Montgomery, Jeffrey S; Kassouf, Wassim; Dall'Era, Marc A; Sridhar, Srikala S; McGrath, John S; Wright, Jonathan L; Thorpe, Andrew C; Holzbeierlein, Jeff M; Carrión, Diego M; Di Trapani, Ettore; Bivalacqua, Trinity J; North, Scott; Barocas, Daniel A; Lotan, Yair; Grivas, Petros; Stephenson, Andrew J; van Rhijn, Bas W; Daneshmand, Siamak; Spiess, Philippe E; Shariat, Shahrokh F.
Afiliación
  • D'Andrea D; Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
  • Black PC; Department of Urologic Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
  • Zargar H; Department of Urologic Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
  • Dinney CP; Department of Urology, Western Health, Melbourne, Australia.
  • Soria F; Department of Urology, MD Anderson Cancer Center, Houston, Texas.
  • Cookson MS; Department of Urology, Molinette Hospital, University of Turin, Turin, Italy.
  • Montgomery JS; Department of Urology, University of Oklahoma College of Medicine, Oklahoma City, Oklahoma.
  • Kassouf W; Department of Urology, University of Michigan Health System, Ann Arbor, Michigan.
  • Dall'Era MA; Department of Surgery (Division of Urology), McGill University Health Center, Montreal, Canada.
  • Sridhar SS; Department of Urology, University of California at Davis, Davis Medical Center, Sacramento, California.
  • McGrath JS; Princess Margaret Hospital, Toronto, Ontario, Canada.
  • Wright JL; Department of Surgery, Exeter Surgical Health Services Research Unit, Royal Devon and Exeter NHS Trust, Exeter, UK.
  • Thorpe AC; Department of Urology, University of Washington, Seattle, Washington.
  • Holzbeierlein JM; Department of Urology, Freeman Hospital, Newcastle Upon Tyne, UK.
  • Carrión DM; Department of Urology, University of Kansas Medical Center, Kansas City, Kansas.
  • Di Trapani E; Department of Urology, Louisiana Paz University Hospital, Madrid, Spain.
  • Bivalacqua TJ; Department of Urology, European Institute of Oncology, IRCCS, Milan, Italy.
  • North S; Department of Urology, The James Buchanan Brady Urological Institute, The Johns Hopkins School of Medicine, Baltimore, Maryland.
  • Barocas DA; Cross Cancer Institute, Edmonton, Alberta, Canada.
  • Lotan Y; Department of Oncology, University of Alberta, Edmonton, Alberta, Canada.
  • Grivas P; Department of Urologic Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Stephenson AJ; Department of Urology, University of Texas Southwestern Medical Center, Dallas, Texas.
  • van Rhijn BW; Department of Medicine, Division of Medical Oncology, University of Washington School of Medicine and Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Daneshmand S; Department of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.
  • Spiess PE; Department of Urology, MD Anderson Cancer Center, Houston, Texas.
  • Shariat SF; Department of Urology, The Netherlands Cancer Institute - Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
J Urol ; 207(1): 70-76, 2022 01.
Article en En | MEDLINE | ID: mdl-34445891
ABSTRACT

PURPOSE:

We investigated the pathological response rates and survival associated with 3 vs 4 cycles of cisplatin-based neoadjuvant chemotherapy (NAC) in patients with cT2-4N0M0 muscle invasive bladder cancer. MATERIALS AND

METHODS:

In this cohort study we analyzed clinical data of 828 patients treated with NAC and radical cystectomy between 2000 and 2020. A total of 384 and 444 patients were treated with 3 and 4 cycles of NAC, respectively. Pathological objective response (pOR; ypT0-Ta-Tis-T1 N0), pathological complete response (pCR; ypT0 N0), cancer-specific survival and overall survival were investigated.

RESULTS:

pOR and pCR were achieved in 378 (45%; 95% CI 42, 49) and 207 (25%; 95% CI 22, 28) patients, respectively. Patients treated with 4 cycles of NAC had higher pOR (49% vs 42%, p=0.03) and pCR (28% vs 21%, p=0.02) rates compared to those treated with 3 cycles. This effect was confirmed on multivariable logistic regression analysis (pOR OR 1.46 p=0.008, pCR OR 1.57, p=0.007). On multivariable Cox regression analysis, 4 cycles of NAC were significantly associated with overall survival (HR 0.68; 95% CI 0.49, 0.94; p=0.02) but not with cancer-specific survival (HR 0.72; 95% CI 0.50, 1.04; p=0.08).

CONCLUSIONS:

Four cycles of NAC achieved better pathological response and survival compared to 3 cycles. These findings may aid clinicians in counseling patients and serve as a benchmark for prospective trials. Prospective validation of these findings and assessment of cumulative toxicity derived from an increased number of cycles are needed.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Vejiga Urinaria / Terapia Neoadyuvante Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Urol Año: 2022 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Vejiga Urinaria / Terapia Neoadyuvante Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Urol Año: 2022 Tipo del documento: Article País de afiliación: Austria