Poziotinib in Non-Small-Cell Lung Cancer Harboring HER2 Exon 20 Insertion Mutations After Prior Therapies: ZENITH20-2 Trial

被引:116
作者
Le, Xiuning [1 ]
Cornelissen, Robin [2 ]
Garassino, Marina [3 ]
Clarke, Jeffrey M. [4 ]
Tchekmedyian, Nishan [5 ]
Goldman, Jonathan W. [6 ]
Leu, Szu-Yun [7 ]
Bhat, Gajanan [7 ]
Lebel, Francois [7 ]
Heymach, John, V [1 ]
Socinski, Mark A. [8 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[2] Erasmus MC, Med Oncol, Rotterdam, Netherlands
[3] Ist Nazl Tumori Milano Fdn IRCCS, Med Thorac Oncol, Milan, Italy
[4] Duke Univ, Med Oncol, Med Ctr, Durham, NC USA
[5] Pacific Shores Med Grp, Med Oncol, Irvine, CA USA
[6] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[7] Spectrum Pharmaceut, Res & Dev, Irvine, CA USA
[8] AdventHlth Canc Inst, Thorac Oncol, 2501 N Orange Ave,Suite 689, Orlando, FL 32804 USA
关键词
TYROSINE KINASE INHIBITOR; PHASE-II TRIAL; ANTITUMOR-ACTIVITY; 1ST-LINE TREATMENT; SOMATIC MUTATIONS; OPEN-LABEL; EGFR; DOMAIN; HM781-36B; DACOMITINIB;
D O I
10.1200/JCO.21.01323
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE Insertion mutations in Erb-b2 receptor tyrosine kinase 2 gene (ERBB2 or HER2) exon 20 occur in 2%-5% of non-small-cell lung cancers (NSCLCs) and function as an oncogenic driver. Poziotinib, a tyrosine kinase inhibitor, was evaluated in previously treated patients with NSCLC with HER2 exon 20 insertions. METHODS ZENITH20, a multicenter, multicohort, open-label phase II study, evaluated poziotinib in patients with advanced or metastatic NSCLC. In cohort 2, patients received poziotinib (16 mg) once daily. The primary end point was objective response rate evaluated by independent review committee (RECIST v1.1); secondary outcome measures were disease control rate, duration of response, progression-free survival, and safety and tolerability. Quality of life was assessed. RESULTS Between October 2017 and March 2021, 90 patients with a median of two prior lines of therapy (range, 1-6) were treated. With a median follow-up of 9.0 months, objective response rate was 27.8% (95% CI, 18.9 to 38.2); 25 of 90 patients achieved a partial response. Disease control rate was 70.0% (95% CI, 59.4 to 79.2). Most patients (74%) had tumor reduction (median reduction 22%). Median progression-free survival was 5.5 months (95% CI, 3.9 to 5.8); median duration of response was 5.1 months (95% CI, 4.2 to 5.5). Clinical benefit was seen regardless of lines and types of prior therapy, presence of central nervous system metastasis, and types of HER2mutations. Grade 3 or higher treatment-related adverse events included rash (48.9%), diarrhea (25.6%), and stomatitis (24.4%). Most patients had poziotinib dose reductions (76.7%), with median relative dose intensity of 71.5%. Permanent treatment discontinuation because of treatment-related adverse events occurred in 13.3% of patients. CONCLUSION Poziotinib demonstrates antitumor activity in previously treated patients with HER2 exon 20 insertion NSCLC. (C) 2021 by American Society of Clinical Oncology
引用
收藏
页码:710 / 718
页数:10
相关论文
共 38 条
[1]   THE EUROPEAN-ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER QLQ-C30 - A QUALITY-OF-LIFE INSTRUMENT FOR USE IN INTERNATIONAL CLINICAL-TRIALS IN ONCOLOGY [J].
AARONSON, NK ;
AHMEDZAI, S ;
BERGMAN, B ;
BULLINGER, M ;
CULL, A ;
DUEZ, NJ ;
FILIBERTI, A ;
FLECHTNER, H ;
FLEISHMAN, SB ;
DEHAES, JCJM ;
KAASA, S ;
KLEE, M ;
OSOBA, D ;
RAZAVI, D ;
ROFE, PB ;
SCHRAUB, S ;
SNEEUW, K ;
SULLIVAN, M ;
TAKEDA, F .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (05) :365-376
[2]   THE EORTC QLQ-LC13 - A MODULAR SUPPLEMENT TO THE EORTC CORE QUALITY-OF-LIFE QUESTIONNAIRE (QLQ-C30) FOR USE IN LUNG-CANCER CLINICAL-TRIALS [J].
BERGMAN, B ;
AARONSON, NK ;
AHMEDZAI, S ;
KAASA, S ;
SULLIVAN, M .
EUROPEAN JOURNAL OF CANCER, 1994, 30A (05) :635-642
[3]   Antitumor activity of HM781-36B, a highly effective pan-HER inhibitor in erlotinib-resistant NSCLC and other EGFR-dependent cancer models [J].
Cha, Mi Young ;
Lee, Kwang-Ok ;
Kim, Mira ;
Song, Ji Yeon ;
Lee, Kyu Hang ;
Park, Jongmin ;
Chae, Yun Jung ;
Kim, Young Hoon ;
Suh, Kwee Hyun ;
Lee, Gwan Sun ;
Park, Seung Bum ;
Kim, Maeng Sup .
INTERNATIONAL JOURNAL OF CANCER, 2012, 130 (10) :2445-2454
[4]   Activating HER2 mutations as emerging targets in multiple solid cancers [J].
Connell, Claire M. ;
Doherty, Gary J. .
ESMO OPEN, 2017, 2 (05)
[5]   Clinical activity of afatinib (BIBW 2992) in patients with lung adenocarcinoma with mutations in the kinase domain of HER2/neu [J].
De Greve, J. ;
Teugels, E. ;
Geers, C. ;
Decoster, L. ;
Galdermans, D. ;
De Mey, J. ;
Everaert, H. ;
Umelo, I. ;
In't Veld, P. ;
Schallier, D. .
LUNG CANCER, 2012, 76 (01) :123-127
[6]   Afatinib in NSCLC With HER2 Mutations: Results of the Prospective, Open-Label Phase II NICHE Trial of European Thoracic Oncology Platform (ETOP) [J].
Dziadziuszko, Rafal ;
Smit, Egbert F. ;
Dafni, Urania ;
Wolf, Juergen ;
Wasag, Bartosz ;
Biernat, Wojciech ;
Finn, Stephen P. ;
Kammler, Roswitha ;
Tsourti, Zoi ;
Rabaglio, Manuela ;
Ruepp, Barbara ;
Roschitzki-Voser, Heidi ;
Stahel, Rolf A. ;
Felip, Enriqueta ;
Peters, Solange .
JOURNAL OF THORACIC ONCOLOGY, 2019, 14 (06) :1086-1094
[7]   Mutation Variants and Co-Mutations as Genomic Modifiers of Response to Afatinib in HER2-Mutant Lung Adenocarcinoma [J].
Fang, Wenfeng ;
Zhao, Shen ;
Liang, Ying ;
Yang, Yunpeng ;
Yang, Lin ;
Dong, Xiaorong ;
Zhang, Li ;
Tang, Yong ;
Wang, Shoufeng ;
Yang, Yang ;
Ma, Xiaoyan ;
Wang, Minghui ;
Wang, Wenjing ;
Zhao, Songhui ;
Wang, Kai ;
Gao, Song ;
Zhang, Li .
ONCOLOGIST, 2020, 25 (03) :E545-E554
[8]   A Phase II Trial of Poziotinib in EGFR and HER2 exon 20 Mutant Non-Small Cell Lung Cancer (NSCLC) [J].
Heymach, J. ;
Negrao, M. ;
Robichaux, J. ;
Carter, B. ;
Patel, A. ;
Altan, M. ;
Gibbons, D. ;
Fossella, F. ;
Simon, G. ;
Lam, V. ;
Blumenschein, G. ;
Tsao, A. ;
Kurie, J. ;
Mott, F. ;
Jenkins, D. ;
Mack, D. ;
Feng, L. ;
Roeck, B. ;
Yang, Z. ;
Papadimitrakopoulou, V. ;
Elamin, Y. .
JOURNAL OF THORACIC ONCOLOGY, 2018, 13 (10) :S323-S324
[9]   HER kinase inhibition in patients with HER2-and HER3-mutant cancers [J].
Hyman, David M. ;
Piha-Paul, Sarina A. ;
Won, Helen ;
Rodon, Jordi ;
Saura, Cristina ;
Shapiro, Geoffrey I. ;
Juric, Dejan ;
Quinn, David I. ;
Moreno, Victor ;
Doger, Bernard ;
Mayer, Ingrid A. ;
Boni, Valentina ;
Calvo, Emiliano ;
Loi, Sherene ;
Lockhart, Albert C. ;
Erinjeri, Joseph P. ;
Scaltriti, Maurizio ;
Ulaner, Gary A. ;
Patel, Juber ;
Tang, Jiabin ;
Beer, Hannah ;
Selcuklu, S. Duygu ;
Hanrahan, Aphrothiti J. ;
Bouvier, Nancy ;
Melcer, Myra ;
Murali, Rajmohan ;
Schram, Alison M. ;
Smyth, Lillian M. ;
Jhaveri, Komal ;
Li, Bob T. ;
Drilon, Alexander ;
Harding, James J. ;
Iyer, Gopa ;
Taylor, Barry S. ;
Berger, Michael F. ;
Cutler, Richard E., Jr. ;
Xu, Feng ;
Butturini, Anna ;
Eli, Lisa D. ;
Mann, Grace ;
Farrell, Cynthia ;
Lalani, Alshad S. ;
Bryce, Richard P. ;
Arteaga, Carlos L. ;
Meric-Bernstam, Funda ;
Baselga, Jose ;
Solit, David B. .
NATURE, 2018, 554 (7691) :189-194
[10]   Antitumor Activity of HM781-36B, Alone or in Combination with Chemotherapeutic Agents, in Colorectal Cancer Cells [J].
Kang, Mi Hyun ;
Moon, Sung Ung ;
Sung, Ji Hea ;
Kim, Jin Won ;
Lee, Keun Wook ;
Lee, Hye Seung ;
Lee, Jong Seok ;
Kim, Jee Hyun .
CANCER RESEARCH AND TREATMENT, 2016, 48 (01) :355-364