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. 2023 Sep 20;11(9):e007366. doi: 10.1136/jitc-2023-007366

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© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/.

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CONSORT (Consolidated Standards of Reporting Trials) diagram and study design. AE, adverse event; BCLC, Barcelona Clinic Liver Cancer; CBC, complete blood count; ECOG, Eastern Cooperative Oncology Group; HCC, hepatocellular carcinoma; NE, not estimable; ORR, objective response rate; OS, overall survival; pCR, pathological complete response (no viable tumor cells in the resection specimens, including completely resected primary tumors, tumor thrombosis, and lymph nodes); PD-1, programmed cell death protein-1; PFS, progression-free survival; PS, performance status; pNR, pathological non-response (> 50% viable tumor cells in the primary tumor or appearance of new lesions); pPR, pathological partial response (≤50% viable tumor cells in the primary tumor).