A Phase 1/2 Study of Rapamycin and Cisplatin/Gemcitabine for Treatment of Patients With Muscle-Invasive Bladder Cancer.


Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
04 2023
Historique:
received: 12 09 2022
revised: 02 11 2022
accepted: 06 12 2022
medline: 28 3 2023
pubmed: 30 1 2023
entrez: 29 1 2023
Statut: ppublish

Résumé

Cisplatin-based neoadjuvant chemotherapy (NAC) followed by cystectomy is the standard for muscle-invasive bladder cancer (MIBC), however, NAC confers only a small survival benefit and new strategies are needed to increase its efficacy. Pre-clinical data suggest that in response to DNA damage the tumor microenvironment (TME) adopts a paracrine secretory phenotype dependent on mTOR signaling which may provide an escape mechanism for tumor resistance, thus offering an opportunity to increase NAC effectiveness with mTOR blockade. We conducted a phase I/II clinical trial to assess the safety and efficacy of gemcitabine-cisplatin-rapamycin combination. Grapefruit juice was administered to enhance rapamycin pharmacokinetics by inhibiting intestinal enzymatic degradation. Phase I was a dose determination/safety study followed by a single arm Phase II study of NAC prior to radical cystectomy evaluating pathologic response with a 26% pCR rate target. In phase I, 6 patients enrolled, and the phase 2 dose of 35 mg rapamycin established. Fifteen patients enrolled in phase II; 13 were evaluable. Rapamycin was tolerated without serious adverse events. At the preplanned analysis, the complete response rate (23%) did not meet the prespecified level for continuing and the study was stopped due to futility. With immunohistochemistry, successful suppression of the mTOR signaling pathway in the tumor was achieved while limited mTOR activity was seen in the TME. Adding rapamycin to gemcitabine-cisplatin therapy for patients with MIBC was well tolerated but failed to improve therapeutic efficacy despite evidence of mTOR blockade in tumor cells. Further efforts to understand the role of the tumor microenvironment in chemotherapy resistance is needed.

Identifiants

pubmed: 36710146
pii: S1558-7673(22)00261-0
doi: 10.1016/j.clgc.2022.12.003
pii:
doi:

Substances chimiques

Cisplatin Q20Q21Q62J
Gemcitabine 0
Sirolimus W36ZG6FT64
Deoxycytidine 0W860991D6
TOR Serine-Threonine Kinases EC 2.7.11.1

Types de publication

Clinical Trial, Phase II Clinical Trial, Phase I Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

265-272

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Disclosure The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper

Auteurs

Dimitrios Makrakis (D)

Department of Medicine, Division of Medical Oncology, University of Washington, Seattle, WA. Electronic address: dmakrak@uw.edu.

Jonathan L Wright (JL)

Department of Urology, University of Washington, Seattle, WA; VA Puget Sound Health Care System, Seattle, WA; Fred Hutchinson Cancer Research Center, Seattle, WA.

Martine P Roudier (MP)

Department of Urology, University of Washington, Seattle, WA.

Jose Garcia (J)

Department of Urology, University of Washington, Seattle, WA.

Funda Vakar-Lopez (F)

Department of Pathology, University of Washington, Seattle, WA.

Michael P Porter (MP)

Department of Urology, University of Washington, Seattle, WA; VA Puget Sound Health Care System, Seattle, WA.

Yan Wang (Y)

Department of Urology, University of Washington, Seattle, WA.

Atreya Dash (A)

Department of Urology, University of Washington, Seattle, WA.

Daniel Lin (D)

Department of Urology, University of Washington, Seattle, WA; Fred Hutchinson Cancer Research Center, Seattle, WA.

George Schade (G)

Department of Urology, University of Washington, Seattle, WA.

Brian Winters (B)

Kaiser Permanente Washington, WA.

Xiotun Zhang (X)

CellNetix Pathology and Laboratories LLC, Seattle, WA.

Peter Nelson (P)

Department of Medicine, Division of Medical Oncology, University of Washington, Seattle, WA; Fred Hutchinson Cancer Research Center, Seattle, WA.

Elahe Mostaghel (E)

VA Puget Sound Health Care System, Seattle, WA.

Heather H Cheng (HH)

Department of Medicine, Division of Medical Oncology, University of Washington, Seattle, WA; Fred Hutchinson Cancer Research Center, Seattle, WA.

Michael Schweizer (M)

Department of Medicine, Division of Medical Oncology, University of Washington, Seattle, WA.

Sarah K Holt (SK)

Department of Urology, University of Washington, Seattle, WA.

John L Gore (JL)

Department of Urology, University of Washington, Seattle, WA; Fred Hutchinson Cancer Research Center, Seattle, WA.

Evan Y Yu (EY)

Department of Medicine, Division of Medical Oncology, University of Washington, Seattle, WA.

Hung Ming Lam (HM)

Department of Urology, University of Washington, Seattle, WA.

Bruce Montgomery (B)

Department of Medicine, Division of Medical Oncology, University of Washington, Seattle, WA; VA Puget Sound Health Care System, Seattle, WA.

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Classifications MeSH