Clinical efficacy of frontline immunotherapy (IO) in ethnic-minority patients (pts) with metastatic NSCLC.

Authors

null

Matthew Lee

Montefiore-Einstein Cancer Center, The Bronx, NY

Matthew Lee , Jianyou Liu , Emily Miao , Shuai Wang , Frank Zhang , John X Wei , Julie Chung , Xiaonan Xue , Balazs Halmos , Dean Hosgood , Haiying Cheng

Organizations

Montefiore-Einstein Cancer Center, The Bronx, NY, Albert Einstein College of Medicine, Department of Epidemiology and Population Heath, Bronx, NY, Albert Einstein College of Medicine, Bronx, NY, Montefiore Einstein Center for Cancer Care, Bronx, NY, Montefiore Medical Center, Bronx, NY, Department of Medicine, Albert Einstein College of Medicine/Montefiore Medical Center, New York, NY, Department of Health Information Management, Montefiore Medical Center, Bronx, NY, Montefiore Einstein Cancer Center, Bronx, NY

Research Funding

No funding received

Background: Since minority pts have been historically underrepresented in key IO trials, knowledge on the clinical use of IO in ethnic-minority pts with non-small cell lung cancer (NSCLC) remains limited. This study aims to evaluate race/ethnicity and other demographic, socioeconomic and clinical factors of pts with metastatic NSCLC treated with first-line IO. Methods: A retrospective cohort study of 5920 pts diagnosed with lung cancer within the Montefiore Health system from 1/1/2013 to 6/1/2022 was conducted. Pts with metastatic NSCLC without EGFR or ALK alterations and underwent first-line IO use were identified. The primary endpoint was overall survival (OS) with secondary endpoints of progression-free survival (PFS) and time to discontinuation (TTD) from the start of IO. Results: In total, 248 pts were identified with median follow-up time of 10.7 months (mons), median age of 66 years and 39.1% as Non-Hispanic Black (NHB), 30.2% as Hispanic and 30.7% as non-Hispanic White (NHW). OS (p = 0.39), PFS (p = 0.29) and TTD (p = 0.98) were similar among races/ethnic groups. ECOG < 2 at the start of IO was associated with longer OS summarized in Table 1. Significantly higher PFS and TTD were noted respectively in pts with Medicare insurance and PD-L1 status (TPS>1), while lower PFS and TTD with lower BMI. These results were remained after adjusting for biological sex, smoking status, histology, and IO regimen. Conclusions: Our study demonstrates that race/ethnicity does not impact the benefits of IO. However, factors such as ECOG status impact OS, and BMI, insurance and PD-L1 significantly impact PFS and TTD. These findings help identify potential factors that can be addressed to optimize outcomes and supportive care while undergoing IO.

OS (median) (95% CI) P-value PFS (median) (95% CI) P-value TTD (median) (IQR) P-value
Age0.3 0.74 0.29
< 65 22.7(16.7-43) 7.6(5.6-12.7) 5.0(2.1-12)
>65 20.7(12.6-31.8) 7.9(6.5-11.9) 4.3(1.4-11)
GenderMale 19.7(14-31.8) 0.75 7.8(6.5-12.8) 0.32 4.9(1.9-10.5) 0.91
Female 22.7(15.4-43) 8.2(5.3-11.3) 4.4(1.4-13)
Race/EthnicityNon-Hispanic Black 26.3(14-NA) 0.39 6.7(4.1-9.7) 0.29 4.5(1.4-12.5) 0.98
Hispanic 23.5(13.9-45.7) 7.6(5.6-14.6) 4.9(2.1-11.9)
Non-Hispanic White/Others 16.8(12.8-27.7) 4.9(1.7-9.5)
Median BMI (range) 23.3 (14.2-65.8)
Underweight ( < 18.5) 12.1(8.4-NA) 0.4 6.9(3.2-23) 0.01 3.8(1.8-8.5) 0.02
Healthy (18.5-24.9) 20.2(13.9-31.8) 6.0(5-7.8) 3.7(1.3-8)
Overweight (>25) 23.5(16.4-44.7) 11.9(8.2-18.3) 7(2.6-13.6)
InsuranceCommercial 18.5(13-31.8) 0.15 7.6(5.5-11.3) 0.008
4.9(2.3-9.3) 0.04
Medicare 35.4(19.7-NA) 13.2(7.6-20.4) 5.6(2.1-14)
Medicaid 16.4(10.7-29.6) 6(4-7.9) 3.7(1.4-8.5)
ECOG< 2 37.2(20.7-NA) < .0001
12.8(8.2-17.1) < .0001
5.9(2.8-13.9) < .0001
>2 9.0(6.3-15.7) 4.6(3.4-7.6) 2.6(0.7-7.3)
PDL1< 1 19.4(10.7-45.7) 0.75 6.5 (5.3-7.3) 0.01 4.3(1.4-9) 0.05
>1 23.0(15.7-38.9) 8.7 (7.6-14.3) 5.1(1.4-11.9)

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Abstract Details

Meeting

2023 ASCO Annual Meeting

Session Type

Publication Only

Session Title

Publication Only: Lung Cancer—Non-Small Cell Metastatic

Track

Lung Cancer

Sub Track

Metastatic Non–Small Cell Lung Cancer

Citation

J Clin Oncol 41, 2023 (suppl 16; abstr e21063)

DOI

10.1200/JCO.2023.41.16_suppl.e21063

Abstract #

e21063

Abstract Disclosures

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