Avelumab in Combination with Axitinib as First-Line Treatment in Patients with Advanced Hepatocellular Carcinoma: Results from the Phase 1b VEGF Liver 100 Trial

被引:59
作者
Kudo, Masatoshi [1 ]
Motomura, Kenta [2 ]
Wada, Yoshiyuki [3 ]
Inaba, Yoshitaka [4 ]
Sakamoto, Yasunari [5 ]
Kurosaki, Masayuki [6 ]
Umeyama, Yoshiko [7 ]
Kamei, Yoichi [7 ]
Yoshimitsu, Junichiro [7 ]
Fujii, Yosuke [7 ]
Aizawa, Mana [7 ]
Robbins, Paul B. [8 ]
Furuse, Junji [9 ]
机构
[1] Kindai Univ, Fac Med, Osaka, Japan
[2] Aso Iizuka Hosp, Fukuoka, Japan
[3] Kyushu Med Ctr, Fukuoka, Japan
[4] Aichi Canc Ctr Hosp, Nagoya, Aichi, Japan
[5] Natl Canc Ctr, Tokyo, Japan
[6] Musashino Red Cross Hosp, Tokyo, Japan
[7] Pfizer R&D Japan, Tokyo, Japan
[8] Pfizer, San Diego, CA USA
[9] Kyorin Univ, Fac Med, Tokyo, Japan
关键词
Hepatocellular carcinoma; Immune checkpoint inhibitor; Vascular endothelial growth factor receptor tyrosine kinase inhibitor; Avelumab; Axitinib; JAVELIN SOLID TUMOR; KEY PREDICTIVE FACTORS; CELL-CARCINOMA; SUBGROUP ANALYSIS; JAPANESE PATIENTS; 2ND-LINE TREATMENT; OPEN-LABEL; EFFICACY; SORAFENIB; SAFETY;
D O I
10.1159/000514420
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Combining an immune checkpoint inhibitor with a targeted antiangiogenic agent may leverage complementary mechanisms of action for the treatment of advanced/metastatic hepatocellular carcinoma (aHCC). Avelumab is a human anti-PD-L1 IgG1 antibody with clinical activity in various tumor types; axitinib is a selective tyrosine kinase inhibitor of vascular endothelial growth factor receptors 1, 2, and 3. We report the final analysis from VEGF Liver 100 (NCT03289533), a phase 1b study evaluating safety and efficacy of avelumab plus axitinib in treatment-naive patients with aHCC. Methods: Eligible patients had confirmed aHCC, no prior systemic therapy, >= 1 measurable lesion, Eastern Cooperative Oncology Group performance status <= 1, and Child-Pugh class A disease. Patients received avelumab 10 mg/kg intravenously every 2 weeks plus axitinib 5 mg orally twice daily until progression, unacceptable toxicity, or withdrawal. Endpoints included safety and investigator-assessed objective response per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 and modified RECIST (mRECIST) for HCC. Results: Twenty-two Japanese patients were enrolled and treated with avelumab plus axitinib. The minimum follow-up was 18 months as of October 25, 2019 (data cutoff). Grade 3 treatment-related adverse events (TRAEs) occurred in 16 patients (72.7%); the most common (>= 3 patients) were hypertension (n = 11 [50.0%]), palmar-plantar erythrodysesthesia syndrome (n = 5 [22.7%]), and decreased appetite (n = 3 [13.6%]). No grade 4 TRAEs or treatment-related deaths occurred. Ten patients (45.5%) had an immune-related AE (irAE) of any grade; 3 patients (13.6%) had an infusion-related reaction (IRR) of any grade, and no grade >= 3 irAE and IRR were observed. The objective response rate was 13.6% (95% CI: 2.9-34.9%) per RECIST 1.1 and 31.8% (95% CI: 13.9-54.9%) per mRECIST for HCC. Conclusion: Treatment with avelumab plus axitinib was associated with a manageable toxicity profile and showed antitumor activity in patients with aHCC.
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收藏
页码:249 / 259
页数:11
相关论文
共 41 条
[1]  
[Anonymous], FDA APPR AT PLUS BEV
[2]  
EUROPEAN COMMISSION
[3]  
[Anonymous], BAV AV PRESCR INF
[4]  
[Anonymous], TARGETED ONCOL
[5]  
[Anonymous], 2020, BAV AV SUMM PROD CHA
[6]  
[Anonymous], Cancer today
[7]  
[Anonymous], 2019, News release
[8]  
[Anonymous], 2014, INL AX PACK INS
[9]   Antibody-Dependent Cellular Cytotoxicity Activity of a Novel Anti-PD-L1 Antibody Avelumab (MSB0010718C) on Human Tumor Cells [J].
Boyerinas, Benjamin ;
Jochems, Caroline ;
Fantini, Massimo ;
Heery, Christopher R. ;
Gulley, James L. ;
Tsang, Kwong Yok ;
Schlom, Jeffrey .
CANCER IMMUNOLOGY RESEARCH, 2015, 3 (10) :1148-1157
[10]   Efficacy and safety of sorafenib in patients in the Asia-Pacific region with advanced hepatocellular carcinoma: a phase III randomised, double-blind, placebo-controlled trial [J].
Cheng, Ann-Lii ;
Kang, Yoon-Koo ;
Chen, Zhendong ;
Tsao, Chao-Jung ;
Qin, Shukui ;
Kim, Jun Suk ;
Luo, Rongcheng ;
Feng, Jifeng ;
Ye, Shenglong ;
Yang, Tsai-Sheng ;
Xu, Jianming ;
Sun, Yan ;
Liang, Houjie ;
Liu, Jiwei ;
Wang, Jiejun ;
Tak, Won Young ;
Pan, Hongming ;
Burock, Karin ;
Zou, Jessie ;
Voliotis, Dimitris ;
Guan, Zhongzhen .
LANCET ONCOLOGY, 2009, 10 (01) :25-34