Trastuzumab in combination with chemotherapy versus chemotherapy alone for treatment of HER2-positive advanced gastric or gastro-oesophageal junction cancer (ToGA): a phase 3, open-label, randomised controlled trial

被引:1352
作者
Bang, Yung-Jue [1 ]
Van Cutsem, Eric [2 ]
Feyereislova, Andrea [3 ]
Chung, Hyun C. [4 ]
Shen, Lin [5 ]
Sawaki, Akira [6 ]
Lordick, Florian [7 ]
Ohtsu, Atsushi [8 ]
Omuro, Yasushi [9 ]
Satoh, Taroh [10 ]
Aprile, Giuseppe [11 ]
Kulikov, Evgeny [12 ]
Hill, Julie [13 ]
Lehle, Michaela [3 ]
Ruschoff, Josef [14 ]
Kang, Yoon-Koo [15 ]
机构
[1] Seoul Natl Univ, Coll Med, Seoul 110744, South Korea
[2] Univ Hosp Gasthuisberg, B-3000 Leuven, Belgium
[3] F Hoffmann La Roche, Basel, Switzerland
[4] Yonsei Univ, Coll Med, Canc Metastasis Res Ctr, Yonsei Canc Ctr, Seoul, South Korea
[5] Peking Univ, Beijing Canc Hosp, Beijing 100871, Peoples R China
[6] Aichi Canc Ctr, Aichi, Japan
[7] Natl Centrum Tumorerkrankungen, Heidelberg, Germany
[8] East Hosp, Natl Canc Ctr, Kashiwa, Chiba, Japan
[9] Komagome Gen Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Tokyo, Japan
[10] Kinki Univ, Sch Med, Osaka 589, Japan
[11] Azienda Osped Univ, Udine, Italy
[12] Reg Clin Oncol Dispensary, Ryazan, Russia
[13] Roche Prod Ltd, Dee Why, NSW, Australia
[14] Targos Mol Pathol, Kassel, Germany
[15] Asan Med Ctr, Seoul, South Korea
关键词
METASTATIC BREAST-CANCER; ADJUVANT CHEMOTHERAPY; GENE AMPLIFICATION; 1ST-LINE THERAPY; SUPPORTIVE CARE; III TRIAL; PLUS; HER2; FLUOROURACIL; PROGNOSIS;
D O I
10.1016/S0140-6736(10)61121-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Trastuzumab, a monoclonal antibody against human epidermal growth factor receptor 2 (HER2; also known as ERBB2), was investigated in combination with chemotherapy for first-line treatment of HER2-positive advanced gastric or gastro-oesophageal junction cancer. Methods ToGA (Trastuzumab for Gastric Cancer) was an open-label, international, phase 3, randomised controlled trial undertaken in 122 centres in 24 countries. Patients with gastric or gastro-oesophageal junction cancer were eligible for inclusion if their tumours showed overexpression of HER2 protein by immunohistochemistry or gene amplification by fluorescence in-situ hybridisation. Participants were randomly assigned in a 1:1 ratio to receive a chemotherapy regimen consisting of capecitabine plus cisplatin or fluorouracil plus cisplatin given every 3 weeks for six cycles or chemotherapy in combination with intravenous trastuzumak Allocation was by block randomisation stratified by Eastern Cooperative Oncology Group performance status, chemotherapy regimen, extent of disease, primary cancer site, and measurability of disease, implemented with a central interactive voice recognition system. The primary endpoint was overall survival in all randomised patients who received study medication at least once. This trial is registered with ClinicalTrials.gov, number NCT01041404. Findings 594 patients were randomly assigned to study treatment (trastuzumab plus chemotherapy, n=298; chemotherapy alone, n=296), of whom 584 were included in the primary analysis (n=294; n=290). Median follow-up was 18.6 months (IQR 11-25) in the trastuzumab plus chemotherapy group and 17.1 months (9-25) in the chemotherapy alone group. Median overall survival was 13 8 months (95% Cl 1.2-16) in those assigned to trastuzumab plus chemotherapy compared with 11.1 months (10-13) in those assigned to chemotherapy alone (hazard ratio 0.74; 95% Cl 0.60-0.91; p=0.0046). The most common adverse events in both groups were nausea (trastuzumab plus chemotherapy, 197 [67%] vs chemotherapy alone, 184 [63%]), vomiting (147 [50%] vs 134 [46%]), and neutropenia (157 [53%] vs 165 [57%])} Rates of overall grade 3 or 4 adverse events (201 [68%] vs 198 [68%]) and cardiac adverse events (17 [6%] vs 18 [6%]) did not differ between groups Interpretation Trastuzumab in combination with chemotherapy can be considered as a new standard option for patients with HER2-positive advanced gastric or gastro-oesophageal junction cancer.
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收藏
页码:687 / 697
页数:11
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