Abstract
Background: Immune checkpoint inhibitors (ICI) improve overall survival (OS) in patients with locally advanced, unresectable, or metastatic urothelial carcinoma (aUC), but response rates can be modest. We compared outcomes between patients with and without prior intravesical Bacillus Calmette-Guerin (BCG), who received ICI for aUC, hypothesizing that prior intravesical BCG would be associated with worse outcomes. Patients and Methods: We performed a retrospective cohort study across 25 institutions in US and Europe. We compared observed response rate (ORR) using logistic regression; progression-free survival (PFS) and OS using Kaplan-Meier and Cox proportional hazards. Analyses were stratified by treatment line (first line/salvage) and included multivariable models adjusting for known prognostic factors. Results: A total of 1026 patients with aUC were identified; 614, 617, and 638 were included in ORR, OS, PFS analyses, respectively. Overall, 150 pts had history of prior intravesical BCG treatment. ORR to ICI was similar between those with and without prior intravesical BCG exposure in both first line and salvage settings (adjusted odds radios 0.55 [P= .08] and 1.65 [P= .12]). OS (adjusted hazard ratios 1.05 [P= .79] and 1.13 [P= .49]) and PFS (adjusted hazard ratios 1.12 [P= .55] and 0.87 [P= .39]) were similar between those with and without intravesical BCG exposure in first line and salvage settings. Conclusion: Prior intravesical BCG was not associated with differences in response and survival in patients with aUC treated with ICI. Limitations include retrospective nature, lack of randomization, presence of selection and confounding biases. This study provides important preliminary data that prior intravesical BCG exposure may not impact ICI efficacy in aUC.
Original language | English (US) |
---|---|
Pages (from-to) | 165-175 |
Number of pages | 11 |
Journal | Clinical Genitourinary Cancer |
Volume | 20 |
Issue number | 2 |
DOIs | |
State | Published - Apr 2022 |
Keywords
- BCG
- Bladder cancer
- Immunotherapy
- Outcomes
- Urinary tract neoplasms
ASJC Scopus subject areas
- Oncology
- Urology
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Response and Outcomes to Immune Checkpoint Inhibitors in Advanced Urothelial Cancer Based on Prior Intravesical Bacillus Calmette-Guerin. / Talukder, Rafee; Makrakis, Dimitrios; Diamantopoulos, Leonidas N. et al.
In: Clinical Genitourinary Cancer, Vol. 20, No. 2, 04.2022, p. 165-175.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Response and Outcomes to Immune Checkpoint Inhibitors in Advanced Urothelial Cancer Based on Prior Intravesical Bacillus Calmette-Guerin
AU - Talukder, Rafee
AU - Makrakis, Dimitrios
AU - Diamantopoulos, Leonidas N.
AU - Carril-Ajuria, Lucia
AU - Castellano, Daniel
AU - De Kouchkovsky, Ivan
AU - Koshkin, Vadim S.
AU - Park, Joseph J.
AU - Alva, Ajjai
AU - Bilen, Mehmet A.
AU - Stewart, Tyler F.
AU - McKay, Rana R.
AU - Santos, Victor S.
AU - Agarwal, Neeraj
AU - Jain, Jayanshu
AU - Zakharia, Yousef
AU - Morales-Barrera, Rafael
AU - Devitt, Michael E.
AU - Grant, Michael
AU - Lythgoe, Mark P.
AU - Pinato, David J.
AU - Nelson, Ariel
AU - Hoimes, Christopher J.
AU - Shreck, Evan
AU - Gartrell, Benjamin A.
AU - Sankin, Alex
AU - Tripathi, Abhishek
AU - Zakopoulou, Roubini
AU - Bamias, Aristotelis
AU - Murgic, Jure
AU - Fröbe, Ana
AU - Rodriguez-Vida, Alejo
AU - Drakaki, Alexandra
AU - Liu, Sandy
AU - Kumar, Vivek
AU - Lorenzo, Giuseppe Di
AU - Joshi, Monika
AU - Velho, Pedro Isaacsson
AU - Buznego, Lucia Alonso
AU - Duran, Ignacio
AU - Moses, Marcus
AU - Barata, Pedro
AU - Sonpavde, Guru
AU - Yu, Evan Y.
AU - Wright, Jonathan L.
AU - Grivas, Petros
AU - Khaki, Ali Raza
N1 - Funding Information: R. Talukder, L. Carril-Ajuria, J. Park, V. Santos, J. Jain, M. Devitt, A. Nelson, E. Shreck, B. A. Gartrell, Sankin, R.Zakopoulou, J. Murgic, Frobe, V. Kumar and M. Moses have no conflicts of interest to declare. D Makrakis and LNDiamantopoulos acknowledge the support of Kure It Cancer Research. D. Castellano received travel support from Pfizer, BMS,Astellas, Roche, GSK, Bayer and Ipsen, and acted as advisor for Pfizer, BMS, Exelixis, Astellas, Roche, GSK, Bayer, Ipsen,Pierre-Fabre, MSD, Astra Zeneca, Novartis, AAA and Eisai, Eusa. I. De Kouchkovsky received Merit Award funds from theASCO Foundation. V. Koshkin received grants/contracts from Endocyte, Nektar, Clovis, Jannsen and Taiho, and consulting feesfrom Astra Zeneca, Clovis, Jansen, Pfizer, EMD Serono, Seattle Genetics / Astellas and Dendreon, and payment/honoraria forspeaking/lectures from Seattle Genetics / Astellas. A. Alva received grants/contracts from Arcus Biosciences, AstraZenecaPharmaceuticals, LP Bristol-Myers Squibb Company, Eisai Inc., Esanik, Ionnis, Merck & Co., Inc. and Prometheus, consultingfees from Bristol-Myers Squibb Company, EMD Serono, Merck & Co., Inc., and Pfizer Inc., and had a leadership/fiduciary rolein ASCO TAPUR/CRC. M. A. Bilen has acted as a paid consultant for and/or as a member of the advisory boards of Exelixis,Bayer, BMS, Eisai, Pfizer, AstraZeneca, Janssen, Genomic Health, Nektar and Sanofi, and has received grants to his institutionfrom Xencor, Bayer, Bristol-Myers Squibb, Genentech/Roche, Seattle Genetics, Incyte, Nektar, AstraZeneca, TriconPharmaceuticals, Peleton Therapeutics and Pfizer for work performed outside of the present study. T. Stewart served as anadvisor for Seagen/Astellas. R. R. McKay received research funding from Bayer, Pfizer and Tempus, serves on the AdvisoryBoard for AstraZeneca, Bayer, Bristol Myers Squibb, Calithera, Exelixis, Janssen, Merck, Novartis, Pfizer, Sanofi, Tempus andMyovant, is a consultant for Dendreon and Vividion, and serves on the molecular tumour board at Caris. N. Agarwal served asadvisory/consultant for Astellas, Astra Zeneca, Aveo, Bayer, Bristol Myers Squibb, Calithera, Clovis, Eisai, Eli Lilly, EMDSerono, Exelixis, Foundation Medicine, Genentech, Janssen, Merck, MEI Pharma, Nektar, Novartis, Pfizer, Pharmacyclics andSeattle Genetics. Y. Zakharia served as advisor to BMS, Amgen, Roche Diagnostics, Novartis, Janssen, Eisai, Exelixis, CastleBioscience, Array, Bayer, Pfizer, Clovis and EMD Serono. R. Morales-Barrera received payment/honoraria for lectures fromSanofi Aventis, AstraZeneca, Merck Sharp & Dohme, Astellas, BMS, Pfizer and Roche, and support for travel from Roche,Sanofi Aventis, Astellas, Janssen, Merck Sharp & Dohme, Bayer and Pfizer. M. Grant received honoraria for work in preparingcase studies from Keynote 426 trial from MSD UK. M. Lythgoe received an educational grant from Bayer to attend ASCO GU2020. D. J. Pinato received consulting fees from DaVolterra, H3B, EISAI, Roche and MiNa Therapeutics, payment forlectures/speaking from ViiV Healthcare, Bayer Healthcare, EISAI, Roche, travel support from BMS, MSD and Roche, andparticipated in an advisory board for AZ, EISAI and Roche. He also acknowledges the infrastructure support provided byImperial Experimental Cancer Medicine Centre, Cancer Research UK Imperial Centre, the Imperial College Healthcare NHSTrust Tissue Bank and the Imperial College BRC. C. J. Hoimes received grants/contracts from Astellas, BioNTech, Eisai, Merck&Co, BMS, Genentech/ Roche and Seagen, consulting fees from Merck &Co, BMS, Genentech/Roche and Seagen,payment/honoraria for lectures from Eisai, Merck &Co, BMS, Genentech/Roche and Seagen, travel support from BioNTech andGenentech/Roche and participated as an advisor for Seagen and Merck & Co. A. Tripathi received grants/contracts from EMDSerono, Bayer, Clovis Oncology, Aravive Inc., WindMIL Therapeutics and Corvus Pharmaceuticals, and served as an advisor forFoundation Medicine and Pfizer, Genzyme, EMD Serono, Exelixis. A. Bamias received grants/contracts from Pfizer, BMS,Astra Zeneca, Ipsen, and served as advisor and received payment/honoraria for lectures from BMS, Ipsen, MSD. A. Rodriguez-Vida received grants/contracts from Takeda, Pfizer and Merck, consulting fees from MSD, Pfizer, BMS, Astellas, Janssen, Bayer,Clovis, Ipsen and Roche, and payment for speaking from Pfizer, MSD, Astellas BMS, Janssen, Astra Zeneca, Roche, Bayer,Ipsen and Sanofi Aventis. A. Drakaki served as advisor and received consulting fees from Merck, Genentech/Roche, AstraZeneca, PACT Pharma, NEKTAR and SeaGen, travel support from Astra Zeneca for attending ASCO GU 2019, andparticipated in a Data Safety Monitoring Board for Nektar. S. Liu received payment/honoraria for speaking/lecture fromExelixis, EMD-Serono and Merck. G. Di Lorenzo served as advisor/on the Data Safety Monitoring Board for Janssen, Astellas,Ipsen and Pfizer. M. Joshi received research grants from Astra Zeneca and Pfizer. P. Isaacson-Velho received grants from ASCOConquer Cancer Foundation, consulting fees from Bayer, Astellas and AstraZeneca, payment for lectures and travel support fromAstellas, Pfizer, AstraZeneca, Merck, MSD, Janssen and BMS, and served as an advisor for Astellas, Pfizer and AstraZeneca. I.Duran received grants from Astra Zeneca and Roche, payments for lectures from Bristol-Myers Squibb, MSD Ipsen, Roche-Genentech, Janssen, Astellas Pharma, EUSA Pharma, Bayer and Novartis, travel support from Astra-Zeneca, Ipsen and Pfizer,and served as advisor for Bristol-Myers Squibb, Ipsen, Roche-Genentech, Astellas Pharma, Immunomedics, Seattle Genetics andPharmacyclics. P. Barrata received grants from Seattle Genetics, BlueEarth Diagnostics, Nektar and AstraZeneca, and served asadvisor for Exelixis, Caris, Bayer, Janssen, EMD/Serono, Pfizer, Astellas, Dendreon, Clovis and Sanofi. G. Sonpavde receivedgrants from Sanofi, AstraZeneca, Immunomedics/Gilead, QED, Predicine and BMS, payment for lectures/manuscriptwriting/educational events from Physicians Education Resource (PER), Onclive, Research to Practice, Medscape (alleducational), and Uptodate, is Editor of Elsevier Practice Update Bladder Cancer Center of Excellence, and has received travelsupport from BMS (2019), AstraZeneca (2018). He has served as advisor for BMS, Genentech, EMD Serono, Merck, Sanofi,Seattle Genetics/Astellas, Astrazeneca, Exelixis, Janssen, Bicycle Therapeutics, Pfizer, Immunomedics/Gilead, Scholar Rock, G1Therapeutics, Mereo, and in steering committees for studies for BMS, Bavarian Nordic, Seattle Genetics, QED, G1 Therapeutics(all unpaid), and AstraZeneca, EMD Serono, Debiopharm (paid). E. Y. Yu received grants from Merck and Genentech,consulting fees from Merck and AstraZeneca, and travel support from Merck, he also acknowledges the support of the SeattleTranslational Tumor Research Program at Fred Hutchinson Cancer Research Center.. J. L. Wright has received grants fromNucleix, Inc, Altor Biosci, Merck, SWOG and National Institutes of Health, royalties/licences from UpToDate, and consultingfees from Sanofi-Genzyme, he also acknowledges the support of the Seattle Translational Tumor Research Program at FredHutchinson Cancer Research Center.. P. Grivas’ institution has received grants from Bavarian Nordic, Bristol Myers Squibb,Clovis Oncology, Debiopharm, EMD Serono, GlaxoSmithKline, Immunomedics, Kure It Cancer Research, Merck & Co., MiratiTherapeutics, Pfizer, QED Therapeutics, and consulting fees from AstraZeneca, Astellas Pharma, Bayer, Bristol Myers Squibb,Clovis Oncology, Dyania Health, Driver, EMD Serono, Exelixis, Foundation Medicine, Genentech/Roche, Genzyme,GlaxoSmithKline, Guardant Health, Heron Therapeutics, Immunomedics/Gilead, Infinity Pharmaceuticals, Janssen, Merck &Co., Mirati Therapeutics, Pfizer, QED Therapeutics, Regeneron Pharmaceuticals, Seattle Genetics and 4D Pharma PLC in thelast 3 years, he also acknowledges the support of the Seattle Translational Tumor Research Program at Fred Hutchinson CancerResearch Center. A. R. Khaki temporarily owned stocks of Sanofi & Merck in the last 3 years, he also was supported by theNational Cancer Institute under training grant T32CA009515. EY Yu, JL Wright and P Grivas acknowledge the support of theSeattle Translational Tumor Research Program at Fred Hutchinson Cancer Research Center. Publisher Copyright: © 2021
PY - 2022/4
Y1 - 2022/4
N2 - Background: Immune checkpoint inhibitors (ICI) improve overall survival (OS) in patients with locally advanced, unresectable, or metastatic urothelial carcinoma (aUC), but response rates can be modest. We compared outcomes between patients with and without prior intravesical Bacillus Calmette-Guerin (BCG), who received ICI for aUC, hypothesizing that prior intravesical BCG would be associated with worse outcomes. Patients and Methods: We performed a retrospective cohort study across 25 institutions in US and Europe. We compared observed response rate (ORR) using logistic regression; progression-free survival (PFS) and OS using Kaplan-Meier and Cox proportional hazards. Analyses were stratified by treatment line (first line/salvage) and included multivariable models adjusting for known prognostic factors. Results: A total of 1026 patients with aUC were identified; 614, 617, and 638 were included in ORR, OS, PFS analyses, respectively. Overall, 150 pts had history of prior intravesical BCG treatment. ORR to ICI was similar between those with and without prior intravesical BCG exposure in both first line and salvage settings (adjusted odds radios 0.55 [P= .08] and 1.65 [P= .12]). OS (adjusted hazard ratios 1.05 [P= .79] and 1.13 [P= .49]) and PFS (adjusted hazard ratios 1.12 [P= .55] and 0.87 [P= .39]) were similar between those with and without intravesical BCG exposure in first line and salvage settings. Conclusion: Prior intravesical BCG was not associated with differences in response and survival in patients with aUC treated with ICI. Limitations include retrospective nature, lack of randomization, presence of selection and confounding biases. This study provides important preliminary data that prior intravesical BCG exposure may not impact ICI efficacy in aUC.
AB - Background: Immune checkpoint inhibitors (ICI) improve overall survival (OS) in patients with locally advanced, unresectable, or metastatic urothelial carcinoma (aUC), but response rates can be modest. We compared outcomes between patients with and without prior intravesical Bacillus Calmette-Guerin (BCG), who received ICI for aUC, hypothesizing that prior intravesical BCG would be associated with worse outcomes. Patients and Methods: We performed a retrospective cohort study across 25 institutions in US and Europe. We compared observed response rate (ORR) using logistic regression; progression-free survival (PFS) and OS using Kaplan-Meier and Cox proportional hazards. Analyses were stratified by treatment line (first line/salvage) and included multivariable models adjusting for known prognostic factors. Results: A total of 1026 patients with aUC were identified; 614, 617, and 638 were included in ORR, OS, PFS analyses, respectively. Overall, 150 pts had history of prior intravesical BCG treatment. ORR to ICI was similar between those with and without prior intravesical BCG exposure in both first line and salvage settings (adjusted odds radios 0.55 [P= .08] and 1.65 [P= .12]). OS (adjusted hazard ratios 1.05 [P= .79] and 1.13 [P= .49]) and PFS (adjusted hazard ratios 1.12 [P= .55] and 0.87 [P= .39]) were similar between those with and without intravesical BCG exposure in first line and salvage settings. Conclusion: Prior intravesical BCG was not associated with differences in response and survival in patients with aUC treated with ICI. Limitations include retrospective nature, lack of randomization, presence of selection and confounding biases. This study provides important preliminary data that prior intravesical BCG exposure may not impact ICI efficacy in aUC.
KW - BCG
KW - Bladder cancer
KW - Immunotherapy
KW - Outcomes
KW - Urinary tract neoplasms
UR - http://www.scopus.com/inward/record.url?scp=85123348408&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85123348408&partnerID=8YFLogxK
U2 - 10.1016/j.clgc.2021.12.012
DO - 10.1016/j.clgc.2021.12.012
M3 - Article
C2 - 35078711
AN - SCOPUS:85123348408
SN - 1558-7673
VL - 20
SP - 165
EP - 175
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
IS - 2
ER -