Trastuzumab Deruxtecan in Previously Treated HER2-Low Advanced Breast Cancer

被引:1443
作者
Modi, Shanu [1 ,37 ]
Jacot, William [2 ]
Yamashita, Toshinari [4 ]
Sohn, Joohyuk [8 ]
Vidal, Maria [14 ]
Tokunaga, Eriko [5 ]
Tsurutani, Junji [6 ]
Ueno, Naoto T. [20 ]
Prat, Aleix [14 ,15 ,16 ,17 ]
Chae, Yee Soo [12 ]
Lee, Keun Seok [13 ]
Niikura, Naoki [7 ]
Park, Yeon Hee [9 ]
Xu, Binghe [21 ]
Wang, Xiaojia [22 ]
Gil-Gil, Miguel [18 ]
Li, Wei [23 ]
Pierga, Jean-Yves [3 ]
Im, Seock-Ah [10 ]
Moore, Halle C. F. [27 ]
Rugo, Hope S. [28 ,29 ]
Yerushalmi, Rinat
Zagouri, Flora [30 ]
Gombos, Andrea [31 ]
Kim, Sung-Bae [11 ]
Liu, Qiang [24 ]
Luo, Ting [25 ]
Saura, Cristina [19 ]
Schmid, Peter [32 ]
Sun, Tao [26 ]
Gambhire, Dhiraj [34 ]
Yung, Lotus [34 ]
Wang, Yibin [34 ]
Singh, Jasmeet
Vitazka, Patrik [34 ]
Meinhardt, Gerold [34 ]
Harbeck, Nadia [35 ,36 ]
Cameron, David A. [33 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Montpellier, France
[2] Univ Montpellier, Inst Canc Montpellier, INSERM Un 1194, Montpellier, France
[3] Univ Paris Cite, Inst Curie, Paris, France
[4] Kanagawa Canc Ctr, Yokohama, Japan
[5] Natl Hosp Org, Kyushu Canc Ctr, Fukuoka, Japan
[6] Showa Univ Hosp, Tokyo, Japan
[7] Tokai Univ, Sch Med, Isehara, Japan
[8] Yonsei Univ Hlth Syst, Yonsei Canc Ctr, Seoul, South Korea
[9] Samsung Med Ctr, Seoul, South Korea
[10] Seoul Natl Univ, Seoul Natl Univ Hosp, Seoul Natl Univ Coll Med, Canc Res Inst, Seoul, South Korea
[11] Univ Ulsan Coll Med, Asan Med Ctr, Seoul, South Korea
[12] Kyungpook Natl Univ, Chilgok Hosp, Daegu, South Korea
[13] Natl Canc Ctr, Goyang, South Korea
[14] Hosp Clin Barcelona, Dept Med Oncol, Barcelona, Spain
[15] Inst Invest Biomed August Pi i Sunyer, Translat Genom & Targeted Therapies Solid Tumors, Barcelona, Spain
[16] Univ Barcelona, Dept Med, Barcelona, Spain
[17] Inst Oncol IOB Quiron Salud, Breast Canc Unit, Barcelona, Spain
[18] Hosp Duran i Reynals, Inst Catala Oncol lHospitalet, Barcelona, Spain
[19] Vall dHebron Univ Hosp, Vall dHebron Inst Oncol, Barcelona, Spain
[20] Univ Texas MD, Anderson Canc Ctr, Houston, TX USA
[21] Chinese Acad Med Sci, Canc Hosp, Peking Union Med Coll, Beijing, Peoples R China
[22] Zhejiang Canc Hosp, Hangzhou, Peoples R China
[23] First Hosp Jilin Univ, Changchun, Peoples R China
[24] Sun Yat sen Univ, Sun Yat sen Mem Hosp, Guangzhou, Peoples R China
[25] Sichuan Univ, West China Hosp, Chengdu, Peoples R China
[26] Liaoning Canc Hosp & Inst, Shenyang, Peoples R China
[27] Cleveland Clin Fdn, Cleveland Hts, OH USA
[28] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA USA
[29] Tel Aviv Univ, Rabin Med Ctr, Tel Aviv, Israel
[30] Alexandra Reg Gen Hosp, Athens, Greece
[31] Inst Jules Bordet, Brussels, Belgium
[32] Queen Mary Univ London, London, England
[33] Univ Edinburgh, Inst Genet & Canc, Edinburgh Canc Ctr, Edinburgh, Scotland
[34] Daiichi Sankyo, Basking Ridge, NJ USA
[35] Ludwig Maximilian Univ Hosp, Breast Ctr, Dept Obstet & Gynecol, Munich, Germany
[36] Ludwig Maximilian Univ Hosp, Comprehens Canc Ctr Munich, Munich, Germany
[37] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10065 USA
关键词
ANTIBODY-DRUG CONJUGATE; DS-8201A; ERIBULIN; PALBOCICLIB; INHIBITOR; LETROZOLE;
D O I
10.1056/NEJMoa2203690
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Among breast cancers without human epidermal growth factor receptor 2 (HER2) amplification, overexpression, or both, a large proportion express low levels of HER2 that may be targetable. Currently available HER2-directed therapies have been ineffective in patients with these "HER2-low " cancers. METHODS We conducted a phase 3 trial involving patients with HER2-low metastatic breast cancer who had received one or two previous lines of chemotherapy. (Low expression of HER2 was defined as a score of 1+ on immunohistochemical [IHC] analysis or as an IHC score of 2+ and negative results on in situ hybridization.) Patients were randomly assigned in a 2:1 ratio to receive trastuzumab deruxtecan or the physician's choice of chemotherapy. The primary end point was progression-free survival in the hormone receptor-positive cohort. The key secondary end points were progression-free survival among all patients and overall survival in the hormone receptor-positive cohort and among all patients. RESULTS Of 557 patients who underwent randomization, 494 (88.7%) had hormone receptor-positive disease and 63 (11.3%) had hormone receptor-negative disease. In the hormone receptor-positive cohort, the median progression-free survival was 10.1 months in the trastuzumab deruxtecan group and 5.4 months in the physician's choice group (hazard ratio for disease progression or death, 0.51; P < 0.001), and overall survival was 23.9 months and 17.5 months, respectively (hazard ratio for death, 0.64; P=0.003). Among all patients, the median progression-free survival was 9.9 months in the trastuzumab deruxtecan group and 5.1 months in the physician's choice group (hazard ratio for disease progression or death, 0.50; P < 0.001), and overall survival was 23.4 months and 16.8 months, respectively (hazard ratio for death, 0.64; P=0.001). Adverse events of grade 3 or higher occurred in 52.6% of the patients who received trastuzumab deruxtecan and 67.4% of those who received the physician's choice of chemotherapy. Adjudicated, drug-related interstitial lung disease or pneumonitis occurred in 12.1% of the patients who received trastuzumab deruxtecan; 0.8% had grade 5 events. CONCLUSIONS In this trial involving patients with HER2-low metastatic breast cancer, trastuzumab deruxtecan resulted in significantly longer progression-free and overall survival than the physician's choice of chemotherapy. (Funded by Daiichi Sankyo and AstraZeneca; DESTINY-Breast04 ClinicalTrials.gov number, .)
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收藏
页码:9 / 20
页数:12
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