Pan-Cancer Survival Impact of Immune Checkpoint Inhibitors in a National Healthcare System

被引:0
|
作者
Miller, Sean R. [1 ,2 ]
Schipper, Matthew [3 ]
Fritsche, Lars G. [3 ,4 ]
Jiang, Ralph [3 ]
Strohbehn, Garth [5 ,6 ,7 ,8 ]
Otles, Erkin [9 ]
Mcmahon, Benjamin H. [10 ]
Crivelli, Silvia [11 ]
Zamora-Resendiz, Rafael [11 ]
Ramnath, Nithya [6 ,7 ]
Yoo, Shinjae [12 ]
Dai, Xin [12 ]
Sankar, Kamya [13 ]
Edwards, Donna M. [1 ,2 ]
Allen, Steven G. [1 ,2 ]
Green, Michael D. [1 ,2 ]
Bryant, Alex K. [1 ,2 ]
机构
[1] Vet Affairs Ann Arbor Healthcare Syst, Dept Radiat Oncol, Ann Arbor, MI 48105 USA
[2] Univ Michigan, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Biostat, Ann Arbor, MI USA
[4] Univ Michigan, Ctr Stat Genet, Ann Arbor, MI USA
[5] Vet Affairs Ctr Clin Management Res, Ann Arbor, MI 48105 USA
[6] Vet Affairs Ann Arbor Healthcare Syst, Dept Med, Div Med Oncol, Ann Arbor, MI USA
[7] Univ Michigan, Dept Med, Div Hematol Oncol, Ann Arbor, MI USA
[8] Univ Michigan, Rogel Canc Ctr, Ann Arbor, MI USA
[9] Univ Michigan, Med Sch, Med Scientist Training Program, Ann Arbor, MI USA
[10] Los Alamos Natl Lab, Theoret Biol & Biophys, Los Alamos, NM 87545 USA
[11] Lawrence Berkeley Natl Lab, Appl Math & Computat Res Div, Berkeley, CA USA
[12] Brookhaven Natl Lab, Computat Sci Initiat, Upton, NY 11973 USA
[13] Cedars Sinai Med Ctr, Samuel Oschin Comprehens Canc Inst, Dept Med, Div Med Oncol, Los Angeles, CA USA
来源
CANCER MEDICINE | 2024年 / 13卷 / 21期
关键词
check point control; clinical cancer research; clinical observations; immune checkpoint inhibitors; SQUAMOUS-CELL CARCINOMA; OPEN-LABEL; UROTHELIAL CARCINOMA; 1ST-LINE TREATMENT; PLUS CHEMOTHERAPY; 2ND-LINE THERAPY; SINGLE-ARM; NIVOLUMAB; PEMBROLIZUMAB; IPILIMUMAB;
D O I
10.1002/cam4.70379
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The cumulative, health system-wide survival benefit of immune checkpoint inhibitors (ICIs) is unclear, particularly among real-world patients with limited life expectancies and among subgroups poorly represented on clinical trials. We sought to determine the health system-wide survival impact of ICIs. Methods We identified all patients receiving PD-1/PD-L1 or CTLA-4 inhibitors from 2010 to 2023 in the national Veterans Health Administration (VHA) system (ICI cohort) and all patients who received non-ICI systemic therapy in the years before ICI approval (historical control). ICI and historical control cohorts were matched on multiple cancer-related prognostic factors, comorbidities, and demographics. The effect of ICI on overall survival was quantified with Cox regression incorporating matching weights. Cumulative life-years gained system-wide were calculated from the difference in adjusted 5-year restricted mean survival times. Results There were 27,322 patients in the ICI cohort and 69,801 patients in the historical control cohort. Among ICI patients, the most common cancer types were NSCLC (46%) and melanoma (10%). ICI demonstrated a large OS benefit in most cancer types with heterogeneity across cancer types (NSCLC: adjusted HR [aHR] 0.56, 95% confidence interval [CI] 0.54-0.58, p < 0.001; urothelial: aHR 0.91, 95% CI 0.83-1.01, p = 0.066). The relative benefit of ICI was stable across patient age, comorbidity, and self-reported race subgroups. Across VHA, 15,859 life-years gained were attributable to ICI within 5-years of treatment, with NSCLC contributing the most life-years gained. Conclusion We demonstrated substantial increase in survival due to ICIs across a national health system, including in patient subgroups poorly represented on clinical trials.
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页数:12
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