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临床试验/JPRN-jRCT2080221752
JPRN-jRCT2080221752已完成3 期

A Study of Pertuzumab in Addition to Chemotherapy and Herceptin (Trastuzumab) as Adjuvant Therapy in Patients With HER2-Positive Primary Breast Cancer

Chugai Pharmaceutical Co., Ltd.0 个研究点目标入组 4,800 人开始时间: 2012年3月29日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
4,800

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator)

入排标准

年龄范围
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • Adult patients. >/= 18 years of age
  • - Non-metastatic primary invasive HER2-positive carcinoma of the breast that is adequately excised, and that is either node-positive (except T0) or node-negative but with presence of at least one risk factor as defined by the protocol
  • - Eastern Cooperative Oncology Group (ECOG) performance status - The interval between definitive surgery for breast cancer and the first dose of chemotherapy must be no more than 8 weeks (56 days). The first cycle of chemotherapy must be administered within 7 days of randomization or on Day 56, whichever occurs first.
  • - Known hormone receptor status (estrogen receptor and progesterone receptor)
  • - Baseline LVEF >/= 55%
  • - Women of childbearing potential and male participants with partners of childbearing potential must agree to use effective contraception (as defined by the protocol) by the patient and/or partner for the duration of the study treatment and for at least 6 months after the last dose of study drug

排除标准

  • - History of any prior (ipsi- and/or contralateral) invasive breast cancer
  • - History of non-breast malignancies within the 5 years prior to study entry, except for carcinoma in situ of the cervix, carcinoma in situ of the colon, melanoma in situ, and basal cell and squamous cell carcinomas of the skin
  • - Any clinical T4 tumor as defined by TNM, including inflammatory breast cancer
  • - Any previous systemic chemotherapy for cancer or radiotherapy for cancer
  • - Prior use of anti-HER2 therapy for any reason or other prior biologic or immunotherapy for cancer
  • - Concurrent anti-cancer treatment in another investigational trial
  • - Serious cardiac or cardiovascular disease or condition
  • - Pregnant or lactating women

研究者

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