Survival of Trial-Like and Non–Trial-Like Patients With Immunotherapy in Advanced Hepatocellular Carcinoma in Real World: A Collaborative Multicenter Indian Study (IMHEP)

Author:

Ramaswamy Anant1ORCID,Kulkarni Anand2ORCID,John George1,Rauthan Amit3ORCID,Patil Shekhar4,Duseja Ajay5ORCID,Talwar Vineet6ORCID,Rajappa Senthil J.7,Ghadyalpatil Nikhil8,Wadhawan Manav9,Shukla Akash10,Krishna Vamshi M.11ORCID,Srinivas Sujay1ORCID,Taneja Sunil1ORCID,Sravani K. Mary5,Rathi Sahaj8,Bhargava Prabhat5ORCID,Ostwal Vikas1ORCID

Affiliation:

1. Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Parel, India,

2. Hepatology and Liver Transplantation, Asian Institute of Gastroenterology, Gachibowli, India

3. Manipal Hospital, Bangalore, India

4. HCG Group of Hospital, Bangalore, India

5. Department of Hepatology, Post Graduate Institute of Medical Education and Research, Chandigarh, India

6. Department of Medical Oncology, Rajiv Gandhi Cancer Institute and Research Centre, Rohini, India

7. Basavatarakam Indo American Cancer Hospital & RI, Banjara Hills, Hyderabad, India

8. Yashoda Hospital, Hyderabad, India

9. Gastroenterology & Hepatology, Dr B. L. Kapur Memorial Hospital, (A Unit of Lahore Hospital Society), New Delhi, India

10. Department of Gastroenterology, Seth GSMC & KEM Hospital, Mumbai, India

11. Medical Oncology and Hematology, Institute of Oncology AIG Hospitals, Hyderabad, India

Abstract

PURPOSE Immune checkpoint inhibitors (ICIs) is the initial line of management in advanced hepatocellular carcinoma (HCC), but survivals in the real world are not known. MATERIALS AND METHODS A retrospective study of patients with advanced HCC receiving ICIs (as first-line therapy or as later lines of therapy) across 11 Indian institutions was conducted. Patients were divided into either cohort 1 (trial-like receiving ICI as first-line therapy), with a Child Pugh score (CTP) of ≤6, an Eastern Cooperative Oncology Group performance status (ECOG PS) of 0/1, and no VP4 (main portal vein thrombosis [MPVT]) or cohort 2 (trial unlike) who did not satisfy at least one of the above criteria. The primary end point was 12-month overall survival (OS). RESULTS Between January 2017 and January 2022, 133 patient data were analyzed. The presence of MPVT was seen in 33 patients (25%). The ICIs used were atezolizumab-bevacizumab, nivolumab, and pembrolizumab in 89 (66%), 44 (33%), and one (1%) patients, respectively. With a median follow-up of 13.8 months, the 12-month OS for the entire cohort was 33.4% (95% CI, 23.6 to 43.2). Patients in cohort 1 (n = 31) had a significantly improved OS compared with patients in cohort 2 (n = 102; 12-month OS, 57.9% [95% CI, 38.5 to 77.3] v 24% [95% CI, 13.4 to 34.6]; P = .005). Patients with CTP A as compared with CTP B (9.7 v 4.3 months; P < .001) and an ECOG PS of 0/1 as compared with a PS of ≥2 (8.7 v 7.2 months; P = .04) and without MPVT (9.4 v 4.0; P < .001) had superior survivals. CONCLUSION Patients with advanced HCC in the real world, trial-like have survivals in consonance with trial data, whereas patients with features excluding them from trials, such as main portal vein thrombosis, poor ECOG PS, and child Pugh B status, have markedly inferior survivals, despite good tolerance to immunotherapy.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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