Health Equity in Patients Receiving Durvalumab for Unresectable Stage III Non-Small Cell Lung Cancer in the US Veterans Health Administration

Author:

Moore Amanda M12ORCID,Nooruddin Zohra2ORCID,Reveles Kelly R123ORCID,Koeller Jim M12ORCID,Whitehead Jennifer M23,Franklin Kathleen3,Datta Paromita23ORCID,Alkadimi Munaf23ORCID,Brannman Lance4ORCID,Cotarla Ion5ORCID,Frankart Andrew J6ORCID,Mulrooney Tiernan5ORCID,Jones Xavier13,Frei Christopher R123ORCID

Affiliation:

1. Division of Pharmacotherapy, College of Pharmacy, The University of Texas at Austin , San Antonio, TX , USA

2. Pharmacotherapy Education and Research Center, Department of Medicine, Long School of Medicine, University of Texas Health San Antonio , San Antonio, TX , USA

3. Research Service, Audie L. Murphy Memorial Veterans Hospital Division, South Texas Veterans Health Care System , San Antonio, TX , USA

4. Oncology Business Unit , Global Medical Affairs, AstraZeneca Pharmaceuticals, Gaithersburg, MD , USA

5. Oncology Business Unit , US Medical Affairs, AstraZeneca Pharmaceuticals, Gaithersburg, MD , USA

6. Department of Radiation Oncology, University of Cincinnati , Cincinnati, OH , USA

Abstract

Abstract Background Real-world evidence is limited regarding the relationship between race and use of durvalumab, an immunotherapy approved for use in adults with unresectable stage III non-small cell lung cancer (NSCLC) post-chemoradiotherapy (CRT). This study aimed to evaluate if durvalumab treatment patterns differed by race in patients with unresectable stage III NSCLC in a Veterans Health Administration (VHA) population. Materials and Methods This was a retrospective analysis of White and Black adults with unresectable stage III NSCLC treated with durvalumab presenting to any VHA facility in the US from January 1, 2017, to June 30, 2020. Data captured included baseline characteristics and durvalumab treatment patterns, including treatment initiation delay (TID), interruption (TI), and discontinuation (TD); defined as CRT completion to durvalumab initiation greater than 42 days, greater than 28 days between durvalumab infusions, and more than 28 days from the last durvalumab dose with no new durvalumab restarts, respectively. The number of doses, duration of therapy, and adverse events were also collected. Results A total of 924 patients were included in this study (White = 726; Black = 198). Race was not a significant factor in a multivariate logistic regression model for TID (OR, 1.39; 95% CI, 0.81-2.37), TI (OR, 1.58; 95% CI, 0.90-2.76), or TD (OR, 0.84; 95% CI, 0.50-1.38). There were also no significant differences in median (interquartile range [IQR]) number of doses (White: 15 [7-24], Black: 18 [7-25]; P = .25) or median (IQR) duration of therapy (White: 8.7 months [2.9-11.8], Black: 9.8 months [3.6-12.0]; P = .08), although Black patients were less likely to experience an immune-related adverse event (28% vs. 36%, P = .03) and less likely to experience pneumonitis (7% vs. 14%, P < .01). Conclusion Race was not found to be linked with TID, TI, or TD in this real-world study of patients with unresectable stage III NSCLC treated with durvalumab at the VHA.

Funder

National Center for Advancing Translational Sciences

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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