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Validation of Immunotherapy Response Score as Predictive of Pan-solid Tumor Anti-PD-1/PD-L1 Benefit.
Bulen, Benjamin J; Khazanov, Nickolay A; Hovelson, Daniel H; Lamb, Laura E; Matrana, Marc; Burkard, Mark E; Yang, Eddy Shih-Hsin; Edenfield, William J; Claire Dees, Elizabeth; Onitilo, Adedayo A; Buchschacher, Gary L; Miller, Alan M; Parsons, Benjamin M; Wassenaar, Timothy R; Suga, Jennifer M; Siegel, Robert D; Irvin, William; Nair, Suresh; Slim, Jennifer N; Misleh, Jamal; Khatri, Jamil; Masters, Gregory A; Thomas, Sachdev; Safa, Malek M; Anderson, Daniel M; Mowers, Jonathan; Dusenbery, Anna C; Drewery, Stephanie; Plouffe, Komal; Reeder, Travis; Vakil, Hana; Patrias, Lynnae; Falzetta, Amanda; Hamilton, Ryan; Kwiatkowski, Kat; Johnson, D Bryan; Rhodes, Daniel R; Tomlins, Scott A.
Afiliación
  • Bulen BJ; Strata Oncology, Ann Arbor, Michigan.
  • Khazanov NA; Strata Oncology, Ann Arbor, Michigan.
  • Hovelson DH; Strata Oncology, Ann Arbor, Michigan.
  • Lamb LE; Strata Oncology, Ann Arbor, Michigan.
  • Matrana M; Ochsner Cancer Institute, New Orleans, Louisiana.
  • Burkard ME; University of Wisconsin Carbone Cancer Center, Madison, Wisconsin.
  • Yang ES; O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham School of Medicine, Birmingham, Alabama.
  • Edenfield WJ; Prisma Health Greenville Memorial Hospital, Greenville, Carolina.
  • Claire Dees E; UNC Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina.
  • Onitilo AA; Cancer Care and Research Center, Marshfield Clinic Research Institute, Marshfield, Wisconsin.
  • Buchschacher GL; Kaiser Permanente Southern California, Los Angeles, California.
  • Miller AM; Translational Drug Development, Scottsdale, Arizona.
  • Parsons BM; Gundersen Health System, La Crosse, Wisconsin.
  • Wassenaar TR; UW Health Cancer Center at ProHealth Care, Waukesha, Wisconsin.
  • Suga JM; Kaiser Permanente Northern California, Vallejo, California.
  • Siegel RD; Bon Secours St. Francis Cancer Center, Greenville, Carolina.
  • Irvin W; Bon Secours Cancer Institute, Midlothian, Virginia.
  • Nair S; Lehigh Valley Topper Cancer Institute, Allentown, Pennsylvania.
  • Slim JN; MultiCare Regional Cancer Center - Tacoma, Washington.
  • Misleh J; The US Oncology Network, Newark, Delaware.
  • Khatri J; ChristianaCare Oncology Hematology, Newark, Delaware.
  • Masters GA; Medical Oncology Hematology Consultants, Helen F Graham Cancer Center and Research Institute, Newark, Delaware.
  • Thomas S; Kaiser Permanente Northern California, Oakland, California.
  • Safa MM; Kettering Health, Kettering, Ohio.
  • Anderson DM; Metro-Minnesota Community Oncology Research Consortium, St. Louis Park, Minnesota.
  • Mowers J; Strata Oncology, Ann Arbor, Michigan.
  • Dusenbery AC; Strata Oncology, Ann Arbor, Michigan.
  • Drewery S; Strata Oncology, Ann Arbor, Michigan.
  • Plouffe K; Strata Oncology, Ann Arbor, Michigan.
  • Reeder T; Strata Oncology, Ann Arbor, Michigan.
  • Vakil H; Strata Oncology, Ann Arbor, Michigan.
  • Patrias L; Strata Oncology, Ann Arbor, Michigan.
  • Falzetta A; Strata Oncology, Ann Arbor, Michigan.
  • Hamilton R; Strata Oncology, Ann Arbor, Michigan.
  • Kwiatkowski K; Strata Oncology, Ann Arbor, Michigan.
  • Johnson DB; Strata Oncology, Ann Arbor, Michigan.
  • Rhodes DR; Strata Oncology, Ann Arbor, Michigan.
  • Tomlins SA; Strata Oncology, Ann Arbor, Michigan.
Cancer Res Commun ; 3(7): 1335-1349, 2023 07.
Article en En | MEDLINE | ID: mdl-37497337
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.

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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Cancer Res Commun Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Cancer Res Commun Año: 2023 Tipo del documento: Article
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