Predictive factors for transition to conversion therapy in hepatocellular carcinoma using atezolizumab plus bevacizumab.

Barcelona clinic liver cancer stage alfa-fetoprotein atezolizumab bevacizumab cancer-free child-Pugh score conversion therapy hepatocellular carcinoma real-world practice tumour response

Journal

Liver international : official journal of the International Association for the Study of the Liver
ISSN: 1478-3231
Titre abrégé: Liver Int
Pays: United States
ID NLM: 101160857

Informations de publication

Date de publication:
15 Mar 2024
Historique:
revised: 04 03 2024
received: 17 08 2023
accepted: 06 03 2024
medline: 15 3 2024
pubmed: 15 3 2024
entrez: 15 3 2024
Statut: aheadofprint

Résumé

To identify predictive factors associated with successful transition to conversion therapy following combination therapy with atezolizumab and bevacizumab in the treatment of unresectable hepatocellular carcinoma (HCC). In total, 188 patients with HCC, who received atezolizumab plus bevacizumab combination therapy as the first-line chemotherapy, were studied. Patients who achieved complete response (CR) with systemic chemotherapy alone were excluded. Clinical factors possibly linked to successful transition to conversion therapy and the achievement of cancer-free status were identified. Fifteen (8.0%) patients underwent conversion therapy. In the conversion group, there was a significantly higher proportion of patients with Barcelona Clinic Liver Cancer (BCLC) stage A or B (73.3% versus [vs.] 45.1%; p = .03) and tended to have lower Child-Pugh scores and alpha-fetoprotein levels. Multivariate analysis revealed that BCLC stage was a predictive factor for the implementation of conversion therapy (A or B; odds ratio 3.7 [95% CI: 1.1-13]; p = .04). Furthermore, 10 (66.7%) patients achieved cancer-free status and exhibited a smaller number of intrahepatic lesions at the start of treatment (3.5 vs. 7; p < .01), and a shorter interval between systemic chemotherapy induction and conversion therapy (131 vs. 404 days; p < .01). In addition, the rate of achieving cancer-free status by undergoing surgical resection or ablation therapy was significantly higher (p = .03). BCLC stage was the sole predictive factor for successful transition to conversion therapy when using combination therapy with atezolizumab and bevacizumab to treat HCC. Furthermore, a small number of intrahepatic lesions and early transition to conversion therapy were associated with the achievement of cancer-free status.

Sections du résumé

BACKGROUND BACKGROUND
To identify predictive factors associated with successful transition to conversion therapy following combination therapy with atezolizumab and bevacizumab in the treatment of unresectable hepatocellular carcinoma (HCC).
METHODS METHODS
In total, 188 patients with HCC, who received atezolizumab plus bevacizumab combination therapy as the first-line chemotherapy, were studied. Patients who achieved complete response (CR) with systemic chemotherapy alone were excluded. Clinical factors possibly linked to successful transition to conversion therapy and the achievement of cancer-free status were identified.
RESULTS RESULTS
Fifteen (8.0%) patients underwent conversion therapy. In the conversion group, there was a significantly higher proportion of patients with Barcelona Clinic Liver Cancer (BCLC) stage A or B (73.3% versus [vs.] 45.1%; p = .03) and tended to have lower Child-Pugh scores and alpha-fetoprotein levels. Multivariate analysis revealed that BCLC stage was a predictive factor for the implementation of conversion therapy (A or B; odds ratio 3.7 [95% CI: 1.1-13]; p = .04). Furthermore, 10 (66.7%) patients achieved cancer-free status and exhibited a smaller number of intrahepatic lesions at the start of treatment (3.5 vs. 7; p < .01), and a shorter interval between systemic chemotherapy induction and conversion therapy (131 vs. 404 days; p < .01). In addition, the rate of achieving cancer-free status by undergoing surgical resection or ablation therapy was significantly higher (p = .03).
CONCLUSION CONCLUSIONS
BCLC stage was the sole predictive factor for successful transition to conversion therapy when using combination therapy with atezolizumab and bevacizumab to treat HCC. Furthermore, a small number of intrahepatic lesions and early transition to conversion therapy were associated with the achievement of cancer-free status.

Identifiants

pubmed: 38488749
doi: 10.1111/liv.15907
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Ministry of Education, Culture, Sports, Science and Technology, Japan
ID : 22H02828
Organisme : Japan Agency for Medical Research and Development, AMED
ID : JP 23fk0210092
Organisme : Japan Agency for Medical Research and Development, AMED
ID : JP 23fk0210133
Organisme : Japan Agency for Medical Research and Development, AMED
ID : JP 23fk0310506

Informations de copyright

© 2024 The Authors. Liver International published by John Wiley & Sons Ltd.

Références

Yamashita T, Kudo M, Ikeda K, et al. REFLECT - a phase 3 trial comparing efficacy and safety of lenvatinib to sorafenib for the treatment of unresectable hepatocellular carcinoma: an analysis of Japanese subset. J Gastroenterol. 2020;55:113-122.
Fuchigami A, Imai Y, Uchida Y, et al. Therapeutic efficacy of lenvatinib for patients with unresectable hepatocellular carcinoma based on the middle-term outcome. PLoS One. 2020;15:e0231427.
Kudo M, Ueshima K, Ikeda M, et al. Final results of TACTICS: a randomized, prospective trial comparing transarterial chemoembolization plus sorafenib to transarterial chemoembolization alone in patients with unresectable hepatocellular carcinoma. Liver Cancer. 2022;11:354-367.
Peng Z, Fan W, Zhu B, et al. Lenvatinib combined with transarterial chemoembolization as first-line treatment for advanced hepatocellular carcinoma: a phase III, randomized clinical trial (LAUNCH). J Clin Oncol. 2023;41:117-127.
Shimose S, Iwamoto H, Tanaka M, et al. Alternating lenvatinib and trans-arterial therapy prolongs overall survival in patients with inter-mediate stage hepatocellular carcinoma: a propensity score matching study. Cancers (Basel). 2021;13(1):160.
Kawamura Y, Kobayashi M, Shindoh J, et al. Lenvatinib-transarterial chemoembolization sequential therapy as an effective treatment at progression during lenvatinib therapy for advanced hepatocellular carcinoma. Liver Cancer. 2020;9:756-770.
Kudo M, Ueshima K, Ikeda M, et al. Randomised, multicentre prospective trial of transarterial chemoembolisation (TACE) plus sorafenib as compared with TACE alone in patients with hepatocellular carcinoma: TACTICS trial. Gut. 2020;69:1492-1501.
Finn RS, Qin S, Ikeda M, et al. Atezolizumab plus bevacizumab in unresectable hepatocellular carcinoma. N Engl J Med. 2020;382:1894-1905.
Cheng AL, Qin S, Ikeda M, et al. Updated efficacy and safety data from IMbrave150: atezolizumab plus bevacizumab vs. sorafenib for unresectable hepatocellular carcinoma. J Hepatol. 2022;76:862-873.
Kudo M. A novel treatment strategy for patients with intermediate-stage HCC who are not suitable for TACE: upfront systemic therapy followed by curative conversion. Liver Cancer. 2021;10:539-544.
Kudo M. Atezolizumab plus bevacizumab followed by curative conversion (ABC conversion) in patients with unresectable, TACE-unsuitable intermediate-stage hepatocellular carcinoma. Liver Cancer. 2022;11:399-406.
Kudo M, Aoki T, Ueshima K, et al. Achievement of complete response and drug-free status by atezolizumab plus bevacizumab combined with or without curative conversion in patients with transarterial chemoembolization-unsuitable, intermediate-stage hepatocellular carcinoma: a multicenter proof-of-concept study. Liver Cancer. 2023;12(4):321-338. doi:10.1159/000529
Shimose S, Iwamoto H, Shirono T, et al. The impact of curative conversion therapy aimed at a cancer-free state in patients with hepatocellular carcinoma treated with atezolizumab plus bevacizumab. Cancer Med. 2023;12:12325-12335.
Zhu AX, Dayyani F, Yen CJ, et al. Alpha-fetoprotein as a potential surrogate biomarker for atezolizumab + bevacizumab treatment of hepatocellular carcinoma. Clin Cancer Res. 2022;28:3537-3545.
Hiraoka A, Kumada T, Tada T, et al. Early experience of atezolizumab plus bevacizumab treatment for unresectable hepatocellular carcinoma BCLC-B stage patients classified as beyond up to seven criteria - multicenter analysis. Hepatol Res. 2022;52:308-316.
Kudo M, Ushima K, Saeki I, et al. A phase 2, prospective, multicenter, single-arm trial of transarterial chemoembolization therapy in combination strategy with lenvatinib in patients with unresectable intermediate-stage hepatocellular carcinoma: TACTICS-L trial. Liver Cancer. 2023;13(1):99-112. doi:10.1159/000531377

Auteurs

Tatsuya Kikuchi (T)

Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama City, Japan.

Yasuto Takeuchi (Y)

Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama City, Japan.
Department of Regenerative Medicine, Center for Innovative Clinical Medicine, Okayama University Hospital, Okayama, Japan.

Kazuhiro Nouso (K)

Department of Gastroenterology, Okayama City Hospital, Okayama, Japan.

Kazuya Kariyama (K)

Department of Gastroenterology, Okayama City Hospital, Okayama, Japan.

Kenji Kuwaki (K)

Department of Gastroenterology, Okayama Saiseikai General Hospital, Okayama, Japan.

Junichi Toshimori (J)

Department of Gastroenterology, Japanese Red Cross Okayama Hospital, Okayama, Japan.

Shota Iwado (S)

Department of Gastroenterology, Hiroshima City Hospital, Hiroshima, Japan.

Akio Moriya (A)

Department of Gastroenterology, Mitoyo General Hospital, Kan'onji, Japan.

Hiroaki Hagihara (H)

Department of Gastroenterology, Sumitomo Besshi Hospital, Niihama, Japan.

Hiroyuki Takabatake (H)

Department of Gastroenterology, Kurashiki Central Hospital, Kurashiki, Japan.

Toshifumi Tada (T)

Department of Gastroenterology, Japanese Red Cross Himeji Hospital, Himeji, Japan.

Tetsuya Yasunaka (T)

Department of Gastroenterology, Fukuyama City Hospital, Fukuyama, Japan.

Masahiro Sakata (M)

Department of Gastroenterology, Fukuyama Medical Center, Fukuyama, Japan.

Masahiko Sue (M)

Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama City, Japan.

Nozomi Miyake (N)

Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama City, Japan.

Takuya Adachi (T)

Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama City, Japan.

Nozomu Wada (N)

Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama City, Japan.

Hideki Onishi (H)

Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama City, Japan.

Hidenori Shiraha (H)

Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama City, Japan.

Akinobu Takaki (A)

Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama City, Japan.

Motoyuki Otsuka (M)

Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama City, Japan.

Classifications MeSH