Back to Search Start Over

Safety and Efficacy of Atezolizumab-Bevacizumab in Real World: The First Indian Experience.

Authors :
Kulkarni, Anand V.
Krishna, Vamsi
Kumar, Karan
Sharma, Mithun
Patodiya, Bharat
Khan, Arif
Shaik, Sameer
Pasumarthy, Ashirwad
Chhabra, Prateek
Kumar Da, Pramod
Saraswat, Vivek A.
Rao, Padaki N.
Reddy, Duvvur N.
Source :
Journal of Clinical & Experimental Hepatology. Jul2023, Vol. 13 Issue 4, p618-623. 6p.
Publication Year :
2023

Abstract

Atezolizumab-bevacizumab (atezo/bev) combination is a recommended first-line systemic therapy for unresectable hepatocellular carcinoma (uHCC). There are no studies from India reporting the safety and efficacy of this drug in real-world settings where most patients present in an advanced stage. In this retrospective study from two centers in India, we included patients with uHCC who received atezo/bev as first-line systemic therapy. Comparison of overall survival (OS) among the different Child–Turcotte–Pugh (CTP) classes was the primary objective, while progression-free survival (PFS), radiologic response, and adverse events to the therapy were secondary objectives. The median age of the 67 patients who received atezo/bev therapy was 61 (29–82) years, and 86% were males. Nonalcoholic steatohepatitis (55.2%) was the commonest cause of cirrhosis, and most patients belonged to BCLC-C (74.6%%). There were 24 patients in CTP A, 36 in CTP B, and 7 in CTP C. The median OS was 12 (95%CI, 8.16–15.83) months in the cohort. The median OS in CTP class A, B, and C was 21 (95%CI, 0–42.06) months, 9 (95%CI, 5.46–12.53) months, and 4 (95%CI, 2.14–5.85) months, respectively (P < 0.001). The median PFS in the whole cohort was 8 (95%CI, 6.03–9.96) months. The median PFS in Child A, B, and C was 18 (95%CI, 0.16–35.84) months, 8 (95%CI, 6.14–9.85) months, and 2 (95%CI, 1.77–2.23) months (P < 0.001). On mRECIST evaluation, 12.9% had achieved a complete response, 25.8% had a partial response, 27.41% had stable disease, and the rest had progressed. The objective response rate was 38.7%, and the disease control rate was 66.12%. Of the 64% who developed adverse events, 13.43% discontinued the drug. The incidence of grade ≥3 events was significantly higher in CTP C (85.7%) compared to CTP A (12.5%) and CTP B (14%) (P < 0.001). Atezolizumab-bevacizumab is safe and effective in uHCC in real-world settings. Candidate selection is of utmost importance in treating uHCC with atezolizumab-bevacizumab to achieve a good response. Current evidence strongly suggests limited use of atezolizumab-bevacizumab in patients with CTP C, and such individuals should not be considered for this combination therapy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09736883
Volume :
13
Issue :
4
Database :
Academic Search Index
Journal :
Journal of Clinical & Experimental Hepatology
Publication Type :
Academic Journal
Accession number :
164582869
Full Text :
https://doi.org/10.1016/j.jceh.2023.02.003