A Phase 1/2 Study of Rapamycin and Cisplatin/Gemcitabine for Treatment of Patients With Muscle-Invasive Bladder Cancer.
Humans
Cisplatin
/ therapeutic use
Gemcitabine
Sirolimus
/ adverse effects
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Urinary Bladder Neoplasms
/ pathology
Deoxycytidine
Neoadjuvant Therapy
/ adverse effects
Cystectomy
Muscles
/ pathology
TOR Serine-Threonine Kinases
Neoplasm Invasiveness
Tumor Microenvironment
Cystectomy
Damage response
MIBC
Neoadjuvant chemotherapy
Rapamycin
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
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
265-272Informations 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