Impact of radiological response and pattern of progression in patients with HCC treated by atezolizumab-bevacizumab

Author:

Campani Claudia12ORCID,Vallot Ariane3,Ghannouchi Haroun4,Allaire Manon5,Evain Manon5,Sultanik Philippe5,Sidali Sabrina16,Blaise Lorraine7,Thabut Dominique58,Nahon Pierre17,Seror Olivier14,Ganne-Carrié Nathalie17,Nault Jean-Charles17ORCID,Wagner Mathilde3,Sutter Olivier4

Affiliation:

1. Cordeliers Research Center, Sorbonne University, Inserm, Paris Cité University, “Functional Genomics of Solid Tumors” team, Ligue Nationale Contre le Cancer accredited team, Labex OncoImmunology, Paris, France

2. Department of Experimental and Clinical Medicine, Internal Medicine and Hepatology Unit, University of Firenze, Florence, Italy

3. Radiology Department, AP-HP, Sorbonne University, Universitary Hospital Pitié Salpêtriére, Paris, France

4. Interventional Radiology Department, Avicenne Hospital, Paris-Seine-Saint-Denis Universitary Hospitals, AP-HP, Bobigny, France

5. Hepato-gastroenterology Department, AP-HP, Sorbonne University, Pitié Salpêtriére Universitary Hospital, Paris, France

6. Liver Unit, Paris Cité University, Beaujon Hospital, APHP, DMU DIGEST, Clichy, France

7. Liver Unit, Avicenne Hospital, Paris-Seine-Saint-Denis Universitary Hospitals, AP-HP, Bobigny, France

8. INSERM/UMR_S 938/Sorbonne University, Saint-Antoine Research Center (CRSA), Paris, France

Abstract

Background and Aims: We aim to assess the role of radiological response to atezolizumab-bevacizumab in patients with HCC to predict overall survival. Approach and Results: We retrospectively included patients with HCC treated by atezolizumab-bevacizumab in 2 tertiary centers. A retrospective blinded analysis was performed by 2 radiologists to assess Response Evaluation Criteria in Solid Tumor (RECIST 1.1) and modified RECIST (mRECIST) criteria at 12 weeks. Imaging response and treatment decisions in the multidisciplinary tumor board at 12 weeks were registered. Among 125 patients, 9.6% and 20.8% had a response, 39.2% and 35.2% had stable disease, and 51.2% and 44% had progression, according to RECIST 1.1 and mRECIST, respectively, with a substantial interobserver agreement (k coefficient=0.79). Metastasis was independently associated with a higher risk of progression. Patients classified as responders did not reach median survival, which was 16.2 and 15.9 months for patients classified as stable and 9.1 and 9.0 months for patients classified as progressors, in RECIST 1.1 and mRECIST criteria, respectively. We observed a wide variability in the identification of progression in the multidisciplinary tumor board in clinical practice compared with the blind evaluation by radiologists mainly due to discrepancy in the evaluation of the increase in size of intrahepatic lesions. The appearance of new extrahepatic lesions or vascular invasion lesions was associated with a worse overall survival (p=0.032). Conclusions: RECIST 1.1 and mRECIST criteria predict overall survival with more responders identified by mRECIST and the appearance of new extrahepatic lesion or vascular invasion was associated with a poor prognosis. A noticeable discrepancy was observed between patients classified as progressors at reviewing and the decision reached during the multidisciplinary tumor board.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hepatology

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