Utilization patterns of immune checkpoint inhibitors (ICI) for non-small cell lung cancer (NSCLC) within the veterans health administration (VHA).

Authors

Drew Moghanaki

Drew Moghanaki

Atlanta Veterans Affairs Health Care System, Decatur, GA

Drew Moghanaki , Renjian Jiang , David Gutman , Abigail Burns , Vidula Sukhatme , William Stokes , Suresh S. Ramalingam , Vikas Sukhatme , Madhusmita Behera

Organizations

Atlanta Veterans Affairs Health Care System, Decatur, GA, Winship Research Informatics, Winship Cancer Institute of Emory University, Atlanta, GA, Atlanta VA Health Care System, Decatur, GA, Morningside Center for Innovative and Affordable Medicine, Emory Woodruff Health Sciences Center, Atlanta, GA, Emory University School of Medicine, Atlanta, GA, Winship Cancer Institute, Emory University Hospital, Atlanta, GA, Winship Cancer Institute of Emory University, Atlanta, GA

Research Funding

Other
Morningside Center for Innovative and Affordable Medicine, Emory Woodruff Health Sciences Center

Background: ICI are used routinely for treatment of lung cancer. We investigated the utilization of PD-1/PD-L1 inhibitors for NSCLC in the VHA. Methods: The VHA Corporate Data Warehouse was queried for data on ICI utilization in NSCLC [IRB #00113521]. The first date of any ICI dispensed was January 6, 2015 and therefore this investigation evaluated all patients diagnosed with NSCLC between 2015 –2019. Results: A total of 27,586 Veterans were diagnosed with NSCLC during the study period with demographics: 76.3% Caucasian, 16.3% black; 97.0% male; median age 71 years. Stage distribution was 27.9%, 7.9%, 15.8%, and 27.0% for stage I, II, III, or IV, respectively. A total of 3,990 patients were identified to have received any ICI, representing 20.1% of patients diagnosed with stage IV; 159 patients received more than one ICI. The median time from stage IV diagnosis to receipt of ICI was 5 months (IQR: 2-9 months). ICI was dispensed in 83.7% for duration of < 1 year, 13.3% for 1-2 years, and 3% for > = 2 years. The median duration of ICI receipt (with IQR in months): Nivolumab = 2.0 (0.5-5.5), Pembrolizumab = 2.1 (0.3-5.9), Durvalumab = 5.1 (1.8-9.2), and Atezolizumab = 0.3 (0.1-2.1). Multivariable analyses demonstrated female, not married, 0 comorbidity, and higher stage (II-IV) were independently associated with shorter time to receipt of ICI. Conclusions: The use of ICI for NSCLC is increasing within this integrated healthcare system and commonly prescribed within 5 months of stage IV diagnosis. Further investigations of this cohort using available clinical, pharmaceutical, and genomic data within the VHA present an opportunity to enhance our understanding of the efficacy of ICI for NSCLC.

20152016201720182019Totalmedian time
stage IV Dx to ICI
median duration
of ICI in stage IV
nivo97
(90.7%)
517 (89.3%)456 (48.3%)389 (29.8%)180
(17.1%)
1,639
(41.1%)
7 months2.1 months
pembro10
(9.3%)
65
(11.2%)
451 (47.8%)664 (50.9%)629
(59.6%)
1,819
(45.6%)
2 months2.1 months
durva0
(0%)
0
(0%)
9
(1.0%)
260 (19.9%)291
(27.6%)
560
(14.0%)
4 months2.8 months
atezo0
(0%)
5
(0.9%)
55
(5.8%)
37
(2.8%)
33
(3.1%)
130
(3.3%)
8 months1.4 months
unique pts with any ICI1075799441305105539005 months2.8 months

Frequency of patients receiving ICI per calendar year.

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Abstract Details

Meeting

2020 ASCO Virtual Scientific Program

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 38: 2020 (suppl; abstr e21630)

DOI

10.1200/JCO.2020.38.15_suppl.e21630

Abstract #

e21630

Abstract Disclosures

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