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

被引:19
|
作者
Kulkarni, Anand, V [1 ,5 ]
Krishna, Vamsi [2 ]
Kumar, Karan [3 ]
Sharma, Mithun [1 ]
Patodiya, Bharat [2 ]
Khan, Arif [2 ]
Shaik, Sameer [1 ]
Pasumarthy, Ashirwad [4 ]
Chhabra, Prateek [1 ]
Da, Pramod Kumar [1 ]
Saraswat, Vivek A. [3 ]
Rao, Padaki N. [1 ]
Reddy, Duvvur N. [1 ]
机构
[1] AIG Hosp, Dept Hepatol & Liver Transplantat, Hyderabad, India
[2] AIG Hosp, Dept Oncol, Hyderabad, India
[3] Mahatma Gandhi Hosp, Dept Hepatol, Jaipur, India
[4] AIG Hosp, Dept Radiol, Hyderabad, India
[5] Asian Inst Gastroenterol, Dept Hepatol & Liver Transplantat, Hyderabad, India
关键词
HCC; overall survival; progression-free survival; UNRESECTABLE HEPATOCELLULAR-CARCINOMA; PLUS BEVACIZUMAB; SORAFENIB;
D O I
10.1016/j.jceh.2023.02.003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: 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. Methods: 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. Results: 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). Conclusions: Atezolizumab-bevacizumab is safe and effective in uHCC in real-world settings. Candidate selection is of utmost importance in treating uHCC with atezolizumabbevacizumab to achieve a good response. Current evidence strongly suggests limited use of atezolizumabbevacizumab in patients with CTP C, and such individuals should not be considered for this combination therapy. ( J CLIN EXP HEPATOL 2023;13:618-623)
引用
收藏
页码:618 / 623
页数:6
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