Real-World Systemic Treatment Patterns after Atezolizumab and Bevacizumab in Patients with Hepatocellular Carcinoma in the United States

Author:

Singal Amit G.1,Özgürdal Kirhan2ORCID,Fan Xiaozhou3ORCID,Vassilev Zdravko3ORCID,Pan Xiaoyun4,Multani Jasjit K.5,Chen Chi-Chang6,Zhou Zifan6,He Jing7,Pisa Federica8

Affiliation:

1. Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

2. Medical Affairs Oncology, Bayer Consumer Care AG, 4052 Basel, Switzerland

3. Oncology RWE, Bayer HealthCare Pharmaceuticals Inc., Whippany, NJ 07981, USA

4. Global Outcomes Research Department, Bayer HealthCare Pharmaceuticals Inc., Whippany, NJ 07981, USA

5. Health Economics and Outcomes Research, Real World Evidence Solutions, IQVIA US, Falls Church, VA 22042, USA

6. Health Economics and Outcomes Research, Real World Evidence Solutions, IQVIA US, Wayne, PA 19087, USA

7. Advanced Analytics, IQVIA US, Plymouth Meeting, PA 19462, USA

8. Real World Evidence Oncology, Bayer AG, 13342 Berlin, Germany

Abstract

Real-world (RW) evidence is needed to evaluate atezolizumab plus bevacizumab (atezo + bev) utilization for hepatocellular carcinoma (HCC) in clinical practice. This retrospective cohort study used administrative claims databases to evaluate treatment patterns in individuals with HCC ≥18 years of age who were initiated on atezo + bev between June 2020 and June 2022. The endpoints of this study were the proportion of individuals who discontinued atezo + bev and received subsequent systemic therapies, time to discontinuation (TTD), and time to next treatment. Overall, 825 individuals were eligible (median age 67 years; 80% male). Over a median follow-up of 15.3 months, most (72%) discontinued atezo + bev, with a median TTD of 3.5 months. A minority (19%) received subsequent therapies, with the most common second-line agents being lenvatinib (6%), cabozantinib (4%), and nivolumab (4%). The median time from index to next treatment post-atezo + bev was 5.4 months. Further research is needed to identify the patients who are most likely to benefit from atezo + bev as well as later-line HCC therapies to optimize overall survival.

Funder

Bayer HealthCare Pharmaceuticals

Publisher

MDPI AG

Subject

Cancer Research,Oncology

Reference36 articles.

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