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Validation of Immunotherapy Response Score as Predictive of Pan-solid Tumor Anti-PD-1/PD-L1 Benefit.

Authors :
Bulen BJ
Khazanov NA
Hovelson DH
Lamb LE
Matrana M
Burkard ME
Yang ES
Edenfield WJ
Claire Dees E
Onitilo AA
Buchschacher GL
Miller AM
Parsons BM
Wassenaar TR
Suga JM
Siegel RD
Irvin W
Nair S
Slim JN
Misleh J
Khatri J
Masters GA
Thomas S
Safa MM
Anderson DM
Mowers J
Dusenbery AC
Drewery S
Plouffe K
Reeder T
Vakil H
Patrias L
Falzetta A
Hamilton R
Kwiatkowski K
Johnson DB
Rhodes DR
Tomlins SA
Source :
Cancer research communications [Cancer Res Commun] 2023 Jul 25; Vol. 3 (7), pp. 1335-1349. Date of Electronic Publication: 2023 Jul 25 (Print Publication: 2023).
Publication Year :
2023

Abstract

Immunotherapy response score (IRS) integrates tumor mutation burden (TMB) and quantitative expression biomarkers to predict anti-PD-1/PD-L1 [PD-(L)1] monotherapy benefit. Here, we evaluated IRS in additional cohorts. Patients from an observational trial (NCT03061305) treated with anti-PD-(L)1 monotherapy were included and assigned to IRS-High (-H) versus -Low (-L) groups. Associations with real-world progression-free survival (rwPFS) and overall survival (OS) were determined by Cox proportional hazards (CPH) modeling. Those with available PD-L1 IHC treated with anti-PD-(L)1 with or without chemotherapy were separately assessed. Patients treated with PD-(L)1 and/or chemotherapy (five relevant tumor types) were assigned to three IRS groups [IRS-L divided into IRS-Ultra-Low (-UL) and Intermediate-Low (-IL), and similarly assessed]. In the 352 patient anti-PD-(L)1 monotherapy validation cohort (31 tumor types), IRS-H versus IRS-L patients had significantly longer rwPFS and OS. IRS significantly improved CPH associations with rwPFS and OS beyond microsatellite instability (MSI)/TMB alone. In a 189 patient (10 tumor types) PD-L1 IHC comparison cohort, IRS, but not PD-L1 IHC nor TMB, was significantly associated with anti-PD-L1 rwPFS. In a 1,103-patient cohort (from five relevant tumor types), rwPFS did not significantly differ in IRS-UL patients treated with chemotherapy versus chemotherapy plus anti-PD-(L)1, nor in IRS-H patients treated with anti-PD-(L)1 versus anti-PD-(L)1 + chemotherapy. IRS associations were consistent across subgroups, including both Europeans and non-Europeans. These results confirm the utility of IRS utility for predicting pan-solid tumor PD-(L)1 monotherapy benefit beyond available biomarkers and demonstrate utility for informing on anti-PD-(L)1 and/or chemotherapy treatment.<br />Significance: This study confirms the utility of the integrative IRS biomarker for predicting anti-PD-L1/PD-1 benefit. IRS significantly improved upon currently available biomarkers, including PD-L1 IHC, TMB, and MSI status. Additional utility for informing on chemotherapy, anti-PD-L1/PD-1, and anti-PD-L1/PD-1 plus chemotherapy treatments decisions is shown.<br /> (© 2023 The Authors; Published by the American Association for Cancer Research.)

Details

Language :
English
ISSN :
2767-9764
Volume :
3
Issue :
7
Database :
MEDLINE
Journal :
Cancer research communications
Publication Type :
Academic Journal
Accession number :
37497337
Full Text :
https://doi.org/10.1158/2767-9764.CRC-23-0036