Progression patterns and therapeutic sequencing following immune checkpoint inhibition for hepatocellular carcinoma: An international observational study

Author:

Talbot Thomas1ORCID,D'Alessio Antonio12,Pinter Matthias3ORCID,Balcar Lorenz3ORCID,Scheiner Bernhard3ORCID,Marron Thomas U.4,Jun Tomi5,Dharmapuri Sirish4,Ang Celina4,Saeed Anwaar6,Hildebrand Hannah6,Muzaffar Mahvish7,Fulgenzi Claudia A. M.18,Amara Suneetha7,Naqash Abdul Rafeh79,Gampa Anuhya10,Pillai Anjana10,Wang Yinghong11,Khan Uqba12,Lee Pei‐Chang13,Huang Yi‐Hsiang1314ORCID,Bengsch Bertram15,Bettinger Dominik15ORCID,Mohamed Yehia I.16,Kaseb Ahmed16,Pressiani Tiziana17,Personeni Nicola217,Rimassa Lorenza217ORCID,Nishida Naoshi18,Kudo Masatoshi18ORCID,Weinmann Arndt19,Galle Peter R.19ORCID,Muhammed Ambreen1,Cortellini Alessio1,Vogel Arndt20,Pinato David J.121ORCID

Affiliation:

1. Department of Surgery & Cancer, Imperial College London Hammersmith Hospital London UK

2. Department of Biomedical Sciences Humanitas University Milan Italy

3. Division of Gastroenterology & Hepatology, Department of Internal Medicine III Medical University of Vienna Vienna Austria

4. Division of Hematology/Oncology, Department of Medicine, Tisch Cancer Institute Mount Sinai Hospital New York New York USA

5. Sema4 Stamford Connecticut USA

6. Division of Medical Oncology, Department of Medicine Kansas University Cancer Center Westwood Kansas USA

7. Division of Hematology/Oncology East Carolina University Greenville North Carolina USA

8. Department of Medical Oncology University Campus Bio‐Medico Rome Italy

9. Division of Cancer Treatment and Diagnosis National Cancer Institute Bethesda Maryland USA

10. Section of Gastroenterology Hepatology & Nutrition, the University of Chicago Medicine Chicago Illinois USA

11. Department of Gastroenterology, Hepatology & Nutrition The University of Texas MD Anderson Cancer Center Houston Texas USA

12. Division of Hematology and Oncology Weill Cornell Medicine/New York Presbyterian Hospital New York New York USA

13. Division of Gastroenterology and Hepatology, Department of Medicine Taipei Veterans General Hospital Taipei Taiwan

14. Institute of Clinical Medicine National Yang Ming Chiao Tung University School of Medicine Taipei Taiwan

15. Department of Medicine II, Faculty of Medicine Medical Center University of Freiburg, University of Freiburg Freiburg Germany

16. Department of Gastrointestinal Medical Oncology The University of Texas MD Anderson Cancer Center Houston Texas USA

17. Medical Oncology and Hematology Unit, Humanitas Cancer Center IRCCS Humanitas Research Hospital Milan Italy

18. Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka‐Sayama Japan

19. 1st Department of Internal Medicine, Gastroenterology and Hepatology University Medical Center of the Johannes Gutenberg‐University Mainz Mainz Germany

20. Department of Gastroenterology, Hepatology and Endocrinology Hannover Medical School Hannover Germany

21. Division of Oncology, Department of Translational Medicine University of Piemonte Orientale “A. Avogadro” Novara Italy

Abstract

AbstractBackground and AimsDifferent approaches are available after the progression of disease (PD) to immune checkpoint inhibitors (ICIs) for hepatocellular carcinoma (HCC), including the continuation of ICI, treatment switching to tyrosine kinase inhibitors (TKIs) and cessation of anticancer therapy. We sought to characterise the relationship between radiological patterns of progression and survival post‐ICI, also appraising treatment strategies.MethodsWe screened 604 HCC patients treated with ICIs, including only those who experienced PD by data cut‐off. We evaluated post‐progression survival (PPS) according to the treatment strategy at PD and verified its relationship with radiological patterns of progression: intrahepatic growth (IHG), new intrahepatic lesion (NIH), extrahepatic growth (EHG), new extrahepatic lesion (NEH) and new vascular invasion (nVI).ResultsOf 604 patients, 364 (60.3%) experienced PD during observation. Median PPS was 5.3 months (95% CI: 4.4–6.9; 271 events). At the data cut‐off, 165 patients (45%) received no post‐progression anticancer therapy; 64 patients (17.6%) continued ICI beyond PD. IHG (HR 1.64 [95% CI: 1.21–2.22]; p = .0013) and nVI (HR 2.15 [95% CI: 1.38–3.35]; p = .0007) were associated with shorter PPS. Multivariate models adjusted for progression patterns, treatment line and albumin‐bilirubin grade and Eastern Cooperative Oncology Group performance status at PD confirmed receipt of ICI beyond PD with (HR 0.17, 95% CI: 0.09–0.32; p < .0001) or without subsequent TKI (HR 0.39, 95% CI: 0.26–0.58; p < .0001) as predictors of prolonged PPS versus no anticancer therapy.ConclusionsICI‐TKI sequencing is a consolidated option in advanced HCC. nVI and IHG predict a poorer prognosis. Despite lack of recommendation, the continuation of ICI beyond progression in HCC is adopted clinically: future efforts should appraise which patients benefit from this approach.

Funder

European Association for the Study of the Liver

NIHR Imperial Biomedical Research Centre

Wellcome Trust

Cancer Research UK

Publisher

Wiley

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