Trastuzumab Deruxtecan versus Trastuzumab Emtansine for Breast Cancer

被引:669
作者
Cortes, J. [1 ,2 ]
Kim, S. -B [3 ]
Chung, W. -P [9 ]
Im, S. -A [4 ]
Park, Y. H. [6 ,7 ]
Hegg, R. [14 ]
Kim, M. H. [8 ]
Tseng, L. -M [10 ]
Petry, V [15 ]
Chung, C. -F [11 ]
Iwata, H. [17 ]
Hamilton, E. [18 ]
Curigliano, G. [19 ,20 ]
Xu, B. [21 ]
Huang, C. -S [12 ,13 ]
Kim, J. H. [5 ]
Chiu, J. W. Y. [22 ]
Pedrini, J. L. [16 ]
Lee, C. [23 ]
Liu, Y. [23 ]
Cathcart, J. [23 ]
Bako, E. [23 ]
Verma, S. [24 ]
Hurvitz, S. A. [25 ,26 ]
机构
[1] Int Breast Canc Ctr, Quironsalud Grp, Sci Dept, Med Scientia Innovat Res, Barcelona, Spain
[2] Univ Europea Madrid, Fac Biomed & Hlth Sci, Dept Med, Madrid, Spain
[3] Univ Ulsan, Asan Med Ctr, Coll Med, Ulsan, South Korea
[4] Seoul Natl Univ Hosp, Canc Res Inst, Seoul, South Korea
[5] Seoul Natl Univ, Bundang Hosp, Seoul, South Korea
[6] Seoul Natl Univ, Coll Med, Seoul, South Korea
[7] Samsung Med Ctr, Seoul, South Korea
[8] Yonsei Univ, Severance Hosp, Yonsei, South Korea
[9] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Oncol, Tainan, Taiwan
[10] Natl Yang Ming Chiao Tung Univ, Taipei Vet Gen Hosp, Coll Med, Dept Surg, Taipei, Taiwan
[11] Natl Taiwan Univ Hosp, Koo Fdn, Sun Yat Sen Canc Ctr, Taipei, Taiwan
[12] Natl Taiwan Univ Hosp, Taipei, Taiwan
[13] Natl Taiwan Univ, Coll Med, Taipei, Taiwan
[14] Clin Pesquisas & Ctr Estudos Oncol Ginecol & Mama, Sao Paulo, Brazil
[15] Inst Canc Estado Sao Paulo Octavio Frias Oliveira, Sao Paulo, Brazil
[16] Hosp Nossa Senhora Conceicao, Porto Alegre, RS, Brazil
[17] Aichi Canc Ctr Hosp, Nagoya, Aichi, Japan
[18] Tennessee Oncol, Sarah Cannon Res Inst, Nashville, TN USA
[19] Univ Milan, Dept Oncol & Hematol Oncol, Milan, Italy
[20] European Inst Oncol, Div Early Drug Dev, Ist Ricovero & Cura Carattere Sci, Milan, Italy
[21] Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, Beijing, Peoples R China
[22] Univ Hong Kong, Hong Kong, Peoples R China
[23] Daiichi Sankyo, Basking Ridge, NJ USA
[24] AstraZeneca, Gaithersburg, MD USA
[25] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[26] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
关键词
ANTIBODY-DRUG CONJUGATE; LUNG-DISEASE ILD; DS-8201A; PERTUZUMAB; DOCETAXEL;
D O I
10.1056/NEJMoa2115022
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Trastuzumab emtansine is the current standard treatment for patients with human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer whose disease progresses after treatment with a combination of anti-HER2 antibodies and a taxane. METHODS We conducted a phase 3, multicenter, open-label, randomized trial to compare the efficacy and safety of trastuzumab deruxtecan (a HER2 antibody-drug conjugate) with those of trastuzumab emtansine in patients with HER2-positive metastatic breast cancer previously treated with trastuzumab and a taxane. The primary end point was progression-free survival (as determined by blinded independent central review); secondary end points included overall survival, objective response, and safety. RESULTS Among 524 randomly assigned patients, the percentage of those who were alive without disease progression at 12 months was 75.8% (95% confidence interval [CI], 69.8 to 80.7) with trastuzumab deruxtecan and 34.1% (95% CI, 27.7 to 40.5) with trastuzumab emtansine (hazard ratio for progression or death from any cause, 0.28; 95% CI, 0.22 to 0.37; P<0.001). The percentage of patients who were alive at 12 months was 94.1% (95% CI, 90.3 to 96.4) with trastuzumab deruxtecan and 85.9% (95% CI, 80.9 to 89.7) with trastuzumab emtansine (hazard ratio for death, 0.55; 95% CI, 0.36 to 0.86; prespecified significance boundary not reached). An overall response (a complete or partial response) occurred in 79.7% (95% CI, 74.3 to 84.4) of the patients who received trastuzumab deruxtecan and in 34.2% (95% CI, 28.5 to 40.3) of those who received trastuzumab emtansine. The incidence of drug-related adverse events of any grade was 98.1% with trastuzumab deruxtecan and 86.6% with trastuzumab emtansine, and the incidence of drug-related adverse events of grade 3 or 4 was 45.1% and 39.8%, respectively. Adjudicated drug-related interstitial lung disease or pneumonitis occurred in 10.5% of the patients in the trastuzumab deruxtecan group and in 1.9% of those in the trastuzumab emtansine group; none of these events were of grade 4 or 5. CONCLUSIONS Among patients with HER2-positive metastatic breast cancer previously treated with trastuzumab and a taxane, the risk of disease progression or death was lower among those who received trastuzumab deruxtecan than among those who received trastuzumab emtansine. Treatment with trastuzumab deruxtecan was associated with interstitial lung disease and pneumonitis.
引用
收藏
页码:1143 / 1154
页数:12
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