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Real-world practice of conversion surgery for unresectable hepatocellular carcinoma - a single center data of 26 consecutive patients

Abstract:
AIM: To understand the proportion of uHCC (unresectable hepatocellular carcinoma) patients who achieve successful conversion resection in a high-volume setting with state of the art treatment options. METHODS: , 2022. Conversion rate, clinicopathological features, response to systemic and/or loco-regional therapy and surgical outcomes were analyzed. RESULTS: A total of 1,904 HCC patients were identified, with 1672 patients receiving anti-HCC treatment. 328 patients were considered up-front resectable. Of the remaining 1344 uHCC patients, 311 received loco-regional treatment, 224 received systemic treatment, and the remainder (809) received combination systemic plus loco-regional treatment. Following treatment, one patient from the systemic group and 25 patients from the combination group were considered to have resectable disease. A high objective response rate (ORR) was observed in these converted patients (42.3% under RECIST v1.1 and 76.9% under mRECIST criteria). The disease control rate (DCR) reached 100%. 23 patients underwent curative hepatectomy. Major post-operative morbidity was equivalent in the both groups (P=0.76). Pathologic complete response (pCR) was 39.1%. During conversion treatment, grade 3 or higher treatment-related adverse events (TRAEs) were observed in 50% of patients. The median follow-up time was 12.9 months (range, 3.9~40.6) from index diagnosis and 11.4 months (range, 0.9~26.9) from resection. Three patients experienced disease recurrence following conversion surgery. CONCLUSIONS: By intensive treatment, a small sub-group of uHCC patients (2%) may potentially be converted to curative resection. Loco-regional combined with systemic modality was relative safe and effective in the conversion therapy. Short-term outcomes are encouraging, but long-term follow-up in a larger patient population are required to fully understand the utility of this approach.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1186/s12885-023-10955-7

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Role:
Author
ORCID:
0000-0001-9780-9049
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Author
ORCID:
0000-0002-7614-4591
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ORCID:
0000-0001-7529-2587
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Author
ORCID:
0000-0002-6571-1079


Publisher:
BioMed Central
Journal:
BMC Cancer More from this journal
Volume:
23
Issue:
1
Pages:
465-465
Article number:
465
Publication date:
2023-05-20
DOI:
EISSN:
1471-2407
ISSN:
1471-2407


Language:
English
Keywords:
Pubs id:
1344462
Local pid:
pubs:1344462
Source identifiers:
W4377138075
Deposit date:
2026-05-08
ARK identifier:
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