Proton Pump Inhibitor Use and Efficacy of Nivolumab and Ipilimumab in Advanced Melanoma.
checkpoint inhibitors
melanoma
pooled analysis
proton pump inhibitors
Journal
Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829
Informations de publication
Date de publication:
05 May 2022
05 May 2022
Historique:
received:
02
04
2022
revised:
22
04
2022
accepted:
25
04
2022
entrez:
14
5
2022
pubmed:
15
5
2022
medline:
15
5
2022
Statut:
epublish
Résumé
The impact of proton pump inhibitors (PPIs) on clinical outcomes with first-line immune checkpoint inhibitors (ICIs) in patients with metastatic melanoma was previously analyzed in the phase II study, CheckMate 069. This retrospective analysis utilized data from three phase II/III studies of first-line ICI therapy in untreated advanced melanoma: CheckMate 066, 067, and 069. All randomized patients with PPI use ≤ 30 days before initiating study treatment were included in the PPI-use subgroup. Possible associations between baseline PPI use and efficacy were evaluated within each treatment arm of each study using multivariable modeling. Approximately 20% of 1505 randomized patients across the studies reported baseline PPI use. The median follow-up was 52.6-58.5 months. Objective response rate (ORR), progression-free survival (PFS), and overall survival analyses provided insufficient evidence of a meaningful association between PPI use and efficacy outcomes with nivolumab-plus-ipilimumab, nivolumab, or ipilimumab therapy. In five of the six ICI treatment arms, 95% confidence intervals for odds ratios or hazard ratios traversed 1. Significant associations were observed in the CheckMate 069 combination arm between PPI use and poorer ORR and PFS. This multivariable analysis found insufficient evidence to support meaningful associations between PPI use and ICI efficacy in patients with advanced melanoma.
Identifiants
pubmed: 35565428
pii: cancers14092300
doi: 10.3390/cancers14092300
pmc: PMC9103038
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : Bristol Myers Squibb
ID : N/A
Références
J Immunother Cancer. 2021 Apr;9(4):
pubmed: 33827906
Ann Transl Med. 2020 Dec;8(24):1655
pubmed: 33490167
J Oncol Pharm Pract. 2019 Apr;25(3):762-764
pubmed: 29690815
Hum Vaccin Immunother. 2021 Jan 2;17(1):55-61
pubmed: 32574106
J Immunother Cancer. 2020 Oct;8(2):
pubmed: 33037115
Science. 2018 Jan 5;359(6371):104-108
pubmed: 29302014
N Engl J Med. 2017 Oct 5;377(14):1345-1356
pubmed: 28889792
N Engl J Med. 2015 Jul 2;373(1):23-34
pubmed: 26027431
Science. 2015 Nov 27;350(6264):1079-84
pubmed: 26541610
Lancet Oncol. 2018 Nov;19(11):1480-1492
pubmed: 30361170
JAMA Oncol. 2019 Feb 1;5(2):187-194
pubmed: 30422243
Cancer Lett. 2019 Apr 10;447:41-47
pubmed: 30684593
Clin Transl Oncol. 2020 Sep;22(9):1481-1490
pubmed: 31919759
JAMA. 2004 Oct 27;292(16):1955-60
pubmed: 15507580
Gut. 2016 May;65(5):749-56
pubmed: 26719299
N Engl J Med. 2015 Jan 22;372(4):320-30
pubmed: 25399552
Lancet Oncol. 2016 Nov;17(11):1558-1568
pubmed: 27622997
Nature. 2014 Nov 27;515(7528):568-71
pubmed: 25428505
Ann Oncol. 2020 Apr;31(4):525-531
pubmed: 32115349
Melanoma Res. 2016 Dec;26(6):609-615
pubmed: 27603551
Cancer Discov. 2017 Feb;7(2):188-201
pubmed: 27903500
N Engl J Med. 2015 May 21;372(21):2006-17
pubmed: 25891304
Gut. 2016 May;65(5):740-8
pubmed: 26657899
Lung Cancer. 2019 Apr;130:10-17
pubmed: 30885328
N Engl J Med. 2019 Oct 17;381(16):1535-1546
pubmed: 31562797
Clin Cancer Res. 2020 Oct 15;26(20):5487-5493
pubmed: 32933995
Science. 2018 Jan 5;359(6371):97-103
pubmed: 29097493
Science. 2015 Nov 27;350(6264):1084-9
pubmed: 26541606
Oncotarget. 2017 Jun 16;8(35):58801-58808
pubmed: 28938598
N Engl J Med. 2016 Sep 1;375(9):819-29
pubmed: 27433843
J Clin Oncol. 2020 Nov 20;38(33):3937-3946
pubmed: 32997575
Int Immunopharmacol. 2020 Nov;88:106972
pubmed: 33182025