Lenvatinib-based treatment regimens in conversion therapy of unresectable hepatocellular carcinoma: A systematic review and meta-analysis

被引:4
作者
Li, Saixin [1 ,2 ]
Zhang, Zeyu [3 ]
Wang, Zheng [1 ,2 ]
Wang, Kenan [1 ]
Sui, Minghao [1 ]
Liu, Dongbin [1 ]
Liang, Kuo [1 ,2 ]
机构
[1] Capital Med Univ, Xuanwu Hosp, Dept Gen Surg, 45 Changchun St, Beijing 100053, Peoples R China
[2] Beijing Municipal Geriatr Med Res Ctr, Beijing 100053, Peoples R China
[3] Xuzhou Med Univ, Dept Hepatobiliary Surg, Affiliated Huaian Hosp, Huaian 223001, Jiangsu, Peoples R China
基金
北京市自然科学基金;
关键词
lenvatinib; conversion therapy; hepatocellular carcinoma; locoregional therapy; immune checkpoint inhibitor; TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION; TRANSARTERIAL CHEMOEMBOLIZATION; ANTI-PD-1; ANTIBODIES; 1ST-LINE TREATMENT; EFFICACY; PLUS; SAFETY; TACE; ANGIOGENESIS; COMBINATION;
D O I
10.3892/ol.2024.14398
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) is a malignancy associated with high morbidity and mortality rates. Conversion therapy provides patients with unresectable HCC (uHCC) the opportunity to undergo radical treatment and achieve long-term survival. Despite accumulating evidence regarding the efficacy of conversion therapy, the optimal treatment approach for such therapy remains uncertain. Lenvatinib (LEN) has shown efficacy and tolerable rates of adverse events (AEs) when applied in combination with immune checkpoint inhibitors (ICIs) or locoregional therapy (LRT) over the past decade. Therefore, the present meta-analysis was performed to systematically assess the safety and efficacy of LEN-based treatment regimens in conversion therapies for uHCC. Data on outcomes, including the conversion rate, objective response rate (ORR), disease control rate (DCR) and AE incidence in patients with uHCC, were collected. A systematic literature search was performed using MEDLINE, Embase, Web of Science and Cochrane Library databases, up to the date of September 1, 2023. In total, 16 studies, encompassing a total of 1,650 cases of uHCC, were included in the final meta-analysis. The pooled conversion rates for LEN alone, LEN + ICI, LEN + LRT and LEN + ICI + LRT were calculated to be 0.04 (95% CI, 0.00-0.07; I2=77%), 0.23 (95% CI, 0.16-0.30; I2=66%), 0.14 (95% CI, 0.10-0.18; I2=0%) and 0.35 (95% CI, 0.23-0.47; I2=88%), respectively. The pooled ORRs for LEN alone, LEN + ICI, LEN + LRT and LEN + ICI + LRT were found to be 0.45 (95% CI, 0.23-0.67; I2=96%), 0.49 (95% CI, 0.39-0.60; I2=78%), 0.43 (95% CI, 0.24-0.62; I2=88%) and 0.69 (95% CI, 0.56-0.82; I2=92%), respectively. The pooled DCRs for LEN alone, LEN + ICI, LEN + LRT and LEN + ICI + LRT were observed to be 0.77 (95% CI, 0.73-0.81; I2=23%), 0.82 (95% CI, 0.69-0.95; I2=90%), 0.67 (95% CI, 0.39-0.94; I2=94%) and 0.87 (95% CI, 0.82-0.93; I2=67%), respectively. The pooled grade >= 3 AEs for LEN alone, LEN + ICI, LEN + LRT and LEN + ICI + LRT were 0.25 (95% CI, 0.14-0.36; I2=89%), 0.43 (95% CI, 0.34-0.53; I2=23%), 0.42 (95% CI, 0.19-0.66; I2=81%) and 0.35 (95% CI, 0.17-0.54; I2=94%), respectively. These findings suggested that LEN-based combination strategies may confer efficacy and acceptable tolerability for patients with uHCC. In particular, LEN + ICI, with or without LRT, appears to represent a highly effective conversion regimen, with an acceptable conversion rate and well-characterized safety profile.
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页数:11
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共 74 条
[1]   Cabozantinib in Patients with Advanced and Progressing Hepatocellular Carcinoma [J].
Abou-Alfa, G. K. ;
Meyer, T. ;
Cheng, A. -L. ;
El-Khoueiry, A. B. ;
Rimassa, L. ;
Ryoo, B. -Y. ;
Cicin, I. ;
Merle, P. ;
Chen, Y. H. ;
Park, J. -W. ;
Blanc, J. -F. ;
Bolondi, L. ;
Klumpen, H. -J. ;
Chan, S. L. ;
Zagonel, V. ;
Pressiani, T. ;
Ryu, M. -H. ;
Venook, A. P. ;
Hessel, C. ;
Borgman-Hagey, A. E. ;
Schwab, G. ;
Kelley, R. K. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (01) :54-63
[2]   Lenvatinib: A Review in Hepatocellular Carcinoma [J].
Al-Salama, Zaina T. ;
Syed, Yahiya Y. ;
Scott, Lesley J. .
DRUGS, 2019, 79 (06) :665-674
[3]   Conversion surgery after preoperative therapy for advanced hepatocellular carcinoma in the era of molecular targeted therapy and immune checkpoint inhibitors [J].
Arita, Junichi ;
Ichida, Akihiko ;
Nagata, Rihito ;
Mihara, Yuichiro ;
Kawaguchi, Yoshikuni ;
Ishizawa, Takeaki ;
Akamatsu, Nobuhisa ;
Kaneko, Junichi ;
Hasegawa, Kiyoshi .
JOURNAL OF HEPATO-BILIARY-PANCREATIC SCIENCES, 2022, 29 (07) :732-740
[4]   Colon Cancer, Version 2.2021 [J].
Benson, Al B. ;
Venook, Alan P. ;
Al-Hawary, Mahmoud M. ;
Arain, Mustafa A. ;
Chen, Yi-Jen ;
Ciombor, Kristen K. ;
Cohen, Stacey ;
Cooper, Harry S. ;
Deming, Dustin ;
Farkas, Linda ;
Garrido-Laguna, Ignacio ;
Grem, Jean L. ;
Gunn, Andrew ;
Hecht, J. Randolph ;
Hoffe, Sarah ;
Hubbard, Joleen ;
Hunt, Steven ;
Johung, Kimberly L. ;
Kirilcuk, Natalie ;
Krishnamurthi, Smitha ;
Messersmith, Wells A. ;
Meyerhardt, Jeffrey ;
Miller, Eric D. ;
Mulcahy, Mary F. ;
Nurkin, Steven ;
Overman, Michael J. ;
Parikh, Aparna ;
Patel, Hitendra ;
Pedersen, Katrina ;
Saltz, Leonard ;
Schneider, Charles ;
Shibata, David ;
Skibber, John M. ;
Sofocleous, Constantinos T. ;
Stoffel, Elena M. ;
Stotsky-Himelfarb, Eden ;
Willett, Christopher G. ;
Gregory, Kristina M. ;
Gurski, Lisa A. .
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2021, 19 (03) :329-359
[5]   Management of Immune-Related Adverse Events in Patients Treated With Immune Checkpoint Inhibitor Therapy: American Society of Clinical Oncology Clinical Practice Guideline [J].
Brahmer, Julie R. ;
Lacchetti, Christina ;
Schneider, Bryan J. ;
Atkins, Michael B. ;
Brassil, Kelly J. ;
Caterino, Jeffrey M. ;
Chau, Ian ;
Ernstoff, Marc S. ;
Gardner, Jennifer M. ;
Ginex, Pamela ;
Hallmeyer, Sigrun ;
Chakrabarty, Jennifer Holter ;
Leighl, Natasha B. ;
Mammen, Jennifer S. ;
McDermott, David F. ;
Naing, Aung ;
Nastoupil, Loretta J. ;
Phillips, Tanyanika ;
Porter, Laura D. ;
Puzanov, Igor ;
Reichner, Cristina A. ;
Santomasso, Bianca D. ;
Seigel, Carole ;
Spira, Alexander ;
Suarez-Almazor, Maria E. ;
Wang, Yinghong ;
Weber, Jeffrey S. ;
Wolchok, Jedd D. ;
Thompson, John A. .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (17) :1714-+
[6]   Management of Hepatocellular Carcinoma A Review [J].
Brown, Zachary J. ;
Tsilimigras, Diamantis I. ;
Ruff, Samantha M. ;
Mohseni, Alireza ;
Kamel, Ihab R. ;
Cloyd, Jordan M. ;
Pawlik, Timothy M. .
JAMA SURGERY, 2023, 158 (04) :410-420
[7]   Transarterial Chemoembolization Combined With Lenvatinib Plus PD-1 Inhibitor for Advanced Hepatocellular Carcinoma: A Retrospective Cohort Study [J].
Cai, Mingyue ;
Huang, Wensou ;
Huang, Jingjun ;
Shi, Wenbo ;
Guo, Yongjian ;
Liang, Licong ;
Zhou, Jingwen ;
Lin, Liteng ;
Cao, Bihui ;
Chen, Ye ;
Zhou, Juan ;
Zhu, Kangshun .
FRONTIERS IN IMMUNOLOGY, 2022, 13
[8]   Anti-PD-1/PD-L1 immunotherapy in conversion treatment of locally advanced hepatocellular carcinoma [J].
Chen, Jiaqi ;
Zhang, Ding ;
Yuan, Ying .
CLINICAL AND EXPERIMENTAL MEDICINE, 2023, 23 (03) :579-590
[9]   Lenvatinib plus TACE with or without pembrolizumab for the treatment of initially unresectable hepatocellular carcinoma harbouring PD-L1 expression: a retrospective study [J].
Chen, Song ;
Wu, Zhiqiang ;
Shi, Feng ;
Mai, Qicong ;
Wang, Liguang ;
Wang, Fan ;
Zhuang, Wenquan ;
Chen, Xiaoming ;
Chen, Huanwei ;
Xu, Bo ;
Lai, Jiaming ;
Guo, Wenbo .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2022, 148 (08) :2115-2125
[10]   Sequential transarterial chemoembolisation and stereotactic body radiotherapy followed by immunotherapy as conversion therapy for patients with locally advanced, unresectable hepatocellular carcinoma (START-FIT) a single-arm, phase 2 trial [J].
Chiang, Chi Leung ;
Chiu, Keith Wan Hang ;
Chan, Kenneth Sik Kwan ;
Lee, Francis Ann Shing ;
Li, James Chun Bong ;
Wan, Catherine Wing Suet ;
Dai, Wing Chiu ;
Lam, Tai Chung ;
Chen, Wenqi ;
Wong, Natalie Sean Man ;
Cheung, Andy Lai Yin ;
Lee, Venus Wan Yan ;
Lau, Vince Wing Hang ;
El Helali, Aya ;
Man, Kwan ;
Kong, Feng Ming ;
Lo, Chung Mau ;
Chan, Albert Chi-Yan .
LANCET GASTROENTEROLOGY & HEPATOLOGY, 2023, 8 (02) :169-178