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Poster session 17

981P - Tyrosine kinase inhibitors vs anti-VEGF antibody, combined with anti-PD-1 inhibitors and TACE in the conversion therapy for hepatocellular carcinoma: A retrospective multicenter real-world study

Date

14 Sep 2024

Session

Poster session 17

Topics

Tumour Site

Hepatobiliary Cancers

Presenters

Qi Ling

Citation

Annals of Oncology (2024) 35 (suppl_2): S656-S673. 10.1016/annonc/annonc1595

Authors

Q. Ling1, H. Jiang2, L. Sheng2, Y. Zhang3, B. Wang1, A. Mu1, Y. Zhu1, S. Zheng1

Author affiliations

  • 1 Department Of Surgery, The First Affiliated Hospital of Medical School of Zhejiang University, 310003 - Hangzhou/CN
  • 2 Department Of Radiology, West China Hospital, Sichuan University, 610041 - Chengdu/CN
  • 3 Department Of Surgery, Zhejiang Cancer Hospital, 310022 - Hangzhou/CN

Resources

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Abstract 981P

Background

Both tyrosine kinase inhibitors (TKIs, i.g., lenvatinib and donafenib) and anti-VEGF antibody (bevacizumab) are widely used anti-angiogenesis regimens but have different pharmacokinetics and toxicity. We aimed to compare the efficacy and safety between TKIs-based triple therapy (TkiTT) and bevacizumab-based triple therapy (BevTT) during the perioperative period in patients who underwent curative surgical resection after successful conversion for initially unresectable hepatocellular carcinoma (HCC).

Methods

272 consecutive patients who were initially diagnosed as unresectable HCC and received Lenvatinib/donafenib or bevacizumab combined with anti-PD-1 antibody and transarterial chemoembolization (TACE) between January 2022 and December 2023 from three tertiary-care hospitals were screened, and those underwent radical surgical resection after successful tumor downstaging were finally included. Clinical, imaging and pathological parameters during the perioperative period were compared between TkiTT group and BevTT group.

Results

A total of 106 HCC patients successfully received radical resection after conversion. The conversion rate was 41.8% (46/110) and 37% (60/162) in TkiTT group and BevTT group, respectively (p =0.427). The patient characteristics, tumor features and conversion time did not differ significantly between the two groups (Table). BevTT group had a significantly longer drug withdrawal time than TkiTT group. The operation time, intra-operative bleeding, and post-operative liver function recovery did not differ significantly between the two groups. No major complication occurred in the two groups. The pathology showed significantly higher complete response rate in TkiTT group than that in BevTT group. Table: 981P

TkiTT BevTT P
Age (yr) 59.2±9.5 56.5±11.7 0.154
Male (n) 39 49 0.672
HBsAg positive 39 52 1.000
AFP (ng/mL) 77 18 0.377
PIVKA-II 3348 1237 0.134
BCLC staging 0.088
A 20 30
B 15 9
C 11 21
From conversion to resection (d) 95 76 0.446
From TKIs/Bev withdrawal to resection (d) 7 35

Conclusions

Both TkiTT and BevTT are effective and safe in HCC conversion therapy. TkiTT is associated with superior tumor response.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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