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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Nine-week trastuzumab treatment versus 52-week trastuzumab treatment for HER2-positive early-stage breast cancer.
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Nine-week trastuzumab treatment versus 52-week trastuzumab treatment for HER2-positive early-stage breast cancer.

机译:HER2阳性早期乳腺癌的9周曲妥珠单抗治疗与52周曲妥珠单抗治疗相比。

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Trastuzumab is known to be effective for early and advanced stages of breast cancer but optimal duration for early-stage breast cancer (EBC) is not well known. We evaluated the efficacy and toxicity of 9- and 52-week trastuzumab therapy for EBC retrospectively.In this multicenter study, the medical records of all patients with EBC were analyzed in 8 centers retrospectively. Totally consecutive, 479 female patients who received trastuzumab in the adjuvant treatment were evaluated for disease-free survival (DFS), overall survival (OS), efficacy, and toxicity.There were 181 (37.8?%) and 298 (62.2?%) patients in the 9- and 52-week trastuzumab groups, respectively. Median follow-up was 30.6?months (5.7-68.9) in the 9-week trastuzumab group and 29.3?months (5.9-59.6) in the 52-week trastuzumab group. Thirty-six month DFS was 90 and 85?% (P?=?0.132) in the 9- and 52-week trastuzumab treatment groups, respectively, and 36-month OS was 96 and 97?% in the 9- and 52-week trastuzumab groups, respectively (P?=?0.779). Symptomatic cardiotoxicity was observed in 1 (0.6?%) patient in the 9-week trastuzumab group and in 4 (1.3?%) patients in the 52-week trastuzumab group.In this study, similar outcomes were found in the 9- and 52-week trastuzumab treatment groups.
机译:曲妥珠单抗已知对乳腺癌的早期和晚期有效,但是对于早期乳腺癌(EBC)的最佳持续时间尚不为人所知。我们回顾性评估了9周和52周曲妥珠单抗治疗EBC的疗效和毒性。在这项多中心研究中,回顾性分析了8个中心的所有EBC患者的病历。对总共479例接受曲妥珠单抗辅助治疗的女性患者的无病生存期(DFS),总生存期(OS),疗效和毒性进行了评估,分别为181(37.8%)和298(62.2%)。分别在9周和52周的曲妥珠单抗组接受治疗的患者。曲妥珠单抗9周组中位随访时间为30.6个月(5.7-68.9),曲妥珠单抗52周组中位随访时间为29.3个月(5.9-59.6)。在为期9周和52周的曲妥珠单抗治疗组中,36个月的DFS分别为90%和85%(P?=?0.132),在9周和52周的36个月OS为96%和97%。每周曲妥珠单抗组(P≥0.779)。在第9周的曲妥珠单抗组中有1名(0.6%)患者出现心脏毒性,在第52周的曲妥珠单抗组中有4名(1.3%)患者出现心脏毒性。在这项研究中,在9周和52周中发现了类似的结果。周曲妥珠单抗治疗组。

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