Abstract
PURPOSE Durable partial response (PR) and durable stable disease (SD) are often seen in patients with hepatocellular carcinoma (HCC) receiving atezolizumab plus bevacizumab (atezo-bev).This study investigates the outcome of these patients and the histopathology of the residual tumors.PATIENTS AND The IMbrave150 study's atezo-bev group was analyzed.PR or SD per RECIST v1.1 METHODS lasting more than 6 months was defined as durable.For histologic analysis, a comparable real-world group of patients from Japan and Taiwan who had undergone resection of residual tumors after atezo-bev was investigated.RESULTS In the IMbrave150 study, 56 (77.8%) of the 72 PRs and 41 (28.5%) of the 144 SDs were considered durable.The median overall survival was not estimable for patients with durable PR and 23.7 months for those with durable SD.The median progression-free survival was 23.2 months for patients with durable PR and 13.2 months for those with durable SD.In the real-world setting, a total of 38 tumors were resected from 32 patients (23 PRs and nine SDs) receiving atezo-bev.Pathologic complete responses (PCRs) were more frequent in PR tumors than SD tumors (57.7% v 16.7%, P 5.034).PCR rate correlated with time from atezo-bev initiation to resection and was 55.6% (5 of 9) for PR tumors resected beyond 8 months after starting atezo-bev, a time practically corresponding to the durable PR definition used for IMbrave150.We found no reliable radiologic features to predict PCR of the residual tumors.CONCLUSION Durable PR patients from the atezo-bev group showed a favorable outcome, which may be partly explained by the high rate of PCR lesions.Early recognition of PCR lesions may help subsequent treatment decision.
| Original language | English |
|---|---|
| Pages (from-to) | 4060-4070 |
| Number of pages | 11 |
| Journal | Journal of Clinical Oncology |
| Volume | 42 |
| Issue number | 34 |
| DOIs | |
| State | Published - 01 12 2024 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2024 by American Society of Clinical Oncology.