首页> 外文期刊>The breast journal >Randomized trial comparing locoregional resection of primary tumor with no surgery in stage IV breast cancer at the presentation (Protocol MF07-01): a study of Turkish Federation of the National Societies for Breast Diseases.
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Randomized trial comparing locoregional resection of primary tumor with no surgery in stage IV breast cancer at the presentation (Protocol MF07-01): a study of Turkish Federation of the National Societies for Breast Diseases.

机译:演讲中比较了IV期乳腺癌未手术的原发灶局部切除术(协议MF07-01):土耳其国家乳腺疾病学会联合会的一项研究。

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摘要

The MF07-01 trial is a phase III randomized controlled trial which compares breast cancer patients with distant metastases at presentation who receive locoregional treatment for intact primary tumor with those who do not receive such treatment. The primary objective of the study is to assess whether locoregional treatment of the primary tumor provides a better overall survival. Secondary objectives include progression-free survival, quality-of-life, and morbidity related to locoregional treatment. Locoregional treatments consist of either mastectomy or breast conserving surgery with level I-II axillary clearance in clinically or sentinel lymph node positive patients. Radiation therapy to the whole breast follows breast conserving surgery. Standard systemic therapy is given to all patients either immediately after randomization in no-locoregional treatment arm or after surgical resection of the intact primary tumor in locoregional treatment arm. The study is conducted in Turkey as a multicenter trial with central randomization. Total accrual target is 271. The trial was activated in October 2007 and authorized centers started to recruit patients since then. ClinicalTrials.gov identifier number is NCT00557986.
机译:MF07-01试验是一项III期随机对照试验,该试验比较了就诊时患有原发灶的局部治疗的乳腺癌患者和未接受这种治疗的乳腺癌患者。该研究的主要目的是评估局部治疗原发性肿瘤是否能提供更好的总体生存率。次要目标包括与局部治疗有关的无进展生存期,生活质量和发病率。在临床或前哨淋巴结阳性患者中,局部治疗包括乳房切除术或保乳手术,I-II级腋窝清除率。保留乳房的手术是对整个乳房的放射疗法。在无局部区域的治疗组中随机分配后或局部区域的完整原发肿瘤手术切除后,立即对所有患者进行标准全身治疗。这项研究是在土耳其进行的一项多中心试验,其中有中心随机分组。总应计目标为271。该试验于2007年10月启动,自那时以来,授权中心开始招募患者。 ClinicalTrials.gov的标识号为NCT00557986。

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