Qin Shukui, Ji Jiafu, Xu Rui-Hua, Wang Wei, Tang Yong, Bi Feng, Li Jin, Wang Kang, Xu Jian-Ming, Fan Qingxia, Su Wuyun, Shen Lin
Nanjing Bayi Hospital of Nanjing University of Chinese Medicine, Nanjing, Jiangsu, People's Republic of China.
Peking University Cancer Hospital and Institute, Beijing, People's Republic of China.
Oncologist. 2021 Sep;26(9):e1567-e1580. doi: 10.1002/onco.13826. Epub 2021 Aug 3.
Real-world safety and effectiveness data for trastuzumab plus chemotherapy treatment of patients with HER2-positive metastatic gastric cancer (mGC) in China are lacking.
EVIDENCE was a prospective, multicenter, noninterventional registry study evaluating the safety and effectiveness of trastuzumab in five cohorts of Chinese patients with gastric cancer, stratified by HER2 status and trastuzumab treatment. Effectiveness was analyzed for cohorts I (HER2-positive, trastuzumab treated), II (HER2-positive, trastuzumab untreated), and IV (HER2-negative, trastuzumab untreated); trastuzumab-related adverse events (AEs) were analyzed for cohort I.
Cohorts I, II, and IV included 174, 113, and 422 patients, respectively. Most patients received first-line chemotherapy (87.6%). Median overall survival (OS1) for first-line treatment was 22.3, 17.2, and 17.4 months in cohorts I, II, and IV, respectively. After excluding patients who had surgery, respective median OS1 was 19.9, 15.3, and 12.9 months. Respective first-line progression-free survival (PFS1) was 8.2, 6.9, and 6.2 months; and respective first-line response rates (RR) were 51.7%, 18.4%, and 32.8%. Cohort I was significantly favored over cohort II for propensity score-matched first-line median OS1 (hazard ratio [HR], 0.61), PFS1 (HR, 0.64), and RR (odds ratio, 4.93). Trastuzumab-related AEs, grade 3-5 AEs, serious AEs, and AEs with a fatal outcome occurred in 23.6%, 3.4%, 2.3%, and 0.6% of cohort I patients, respectively.
Safety profiles were consistent with those known for trastuzumab and chemotherapy; trastuzumab treatment improved outcomes. Our study provides real-world data supporting first-line trastuzumab plus chemotherapy in Chinese patients with HER2-positive mGC.
This prospective, noninterventional registry study aimed to provide safety and effectiveness data for the use of trastuzumab in combination with chemotherapy in Chinese patients with HER2-positive metastatic gastric cancer (mGC) from the real-world clinical setting. Trastuzumab plus first-line chemotherapy was shown to be safe and to improve outcomes when compared with patients treated with chemotherapy alone. Trastuzumab was effective within a range of treatment regimens; subgroup analysis showed that trastuzumab paired most effectively with the XELOX regimen. This study provides real-world clinical safety and effectiveness data supporting the use of trastuzumab in the treatment of Chinese patients with HER2-positive mGC.
中国缺乏关于曲妥珠单抗联合化疗治疗HER2阳性转移性胃癌(mGC)患者的真实世界安全性和有效性数据。
EVIDENCE是一项前瞻性、多中心、非干预性注册研究,评估曲妥珠单抗在中国五组胃癌患者中的安全性和有效性,这些患者按HER2状态和曲妥珠单抗治疗情况分层。对第I组(HER2阳性,接受曲妥珠单抗治疗)、第II组(HER2阳性,未接受曲妥珠单抗治疗)和第IV组(HER2阴性,未接受曲妥珠单抗治疗)进行有效性分析;对第I组进行曲妥珠单抗相关不良事件(AE)分析。
第I组、第II组和第IV组分别纳入174例、113例和422例患者。大多数患者接受一线化疗(87.6%)。第I组、第II组和第IV组一线治疗的中位总生存期(OS1)分别为22.3个月、17.2个月和17.4个月。排除接受手术的患者后,各自的中位OS1分别为19.9个月、15.3个月和12.9个月。各自的一线无进展生存期(PFS1)分别为8.2个月、6.9个月和6.2个月;各自的一线缓解率(RR)分别为51.7%、*18.4%和32.8%。倾向评分匹配的一线中位OS1(风险比[HR],0.61)、PFS1(HR,0.64)和RR(优势比,4.93)方面,第I组显著优于第II组。第I组患者中,曲妥珠单抗相关AE、3 - 5级AE、严重AE和导致死亡的AE分别发生在23.6%、3.4%、2.3%和0.6%的患者中。
安全性特征与已知的曲妥珠单抗和化疗的特征一致;曲妥珠单抗治疗改善了预后。我们的研究提供了真实世界数据,支持中国HER2阳性mGC患者一线使用曲妥珠单抗联合化疗。
这项前瞻性、非干预性注册研究旨在从真实世界临床环境中提供曲妥珠单抗联合化疗在中国HER2阳性转移性胃癌(mGC)患者中使用的安全性和有效性数据。与单独接受化疗的患者相比,曲妥珠单抗联合一线化疗被证明是安全的且改善了预后。曲妥珠单抗在一系列治疗方案中均有效;亚组分析表明,曲妥珠单抗与XELOX方案联合最有效。本研究提供了支持曲妥珠单抗治疗中国HER2阳性mGC患者的真实世界临床安全性和有效性数据。