Ruiterkamp Jetske, Voogd Adri C, Tjan-Heijnen Vivianne C G, Bosscha Koop, van der Linden Yvette M, Rutgers Emiel J Th, Boven Epie, van der Sangen Maurice J C, Ernst Miranda F
Department of Surgery, Máxima Medical Center, Veldhoven, The Netherlands.
BMC Surg. 2012 Apr 2;12:5. doi: 10.1186/1471-2482-12-5.
Five percent of all patients with breast cancer have distant metastatic disease at initial presentation. Because metastatic breast cancer is considered to be an incurable disease, it is generally treated with a palliative intent. Recent non-randomized studies have demonstrated that (complete) resection of the primary tumor is associated with a significant improvement of the survival of patients with primary metastatic breast cancer. However, other studies have suggested that the claimed survival benefit by surgery may be caused by selection bias. Therefore, a randomized controlled trial will be performed to assess whether breast surgery in patients with primary distant metastatic breast cancer will improve the prognosis.
Randomization will take place after the diagnosis of primary distant metastatic breast cancer. Patients will either be randomized to up front surgery of the breast tumor followed by systemic therapy or to systemic therapy, followed by delayed local treatment of the breast tumor if clinically indicated.Patients with primary distant metastatic breast cancer, with no prior treatment of the breast cancer, who are 18 years or older and fit enough to undergo surgery and systemic therapy are eligible. Important exclusion criteria are: prior invasive breast cancer, surgical treatment or radiotherapy of this breast tumor before randomization, irresectable T4 tumor and synchronous bilateral breast cancer. The primary endpoint is 2-year survival. Quality of life and local tumor control are among the secondary endpoints.Based on the results of prior research it was calculated that 258 patients are needed in each treatment arm, assuming a power of 80%. Total accrual time is expected to take 60 months. An interim analysis will be performed to assess any clinically significant safety concerns and to determine whether there is evidence that up front surgery is clinically or statistically inferior to systemic therapy with respect to the primary endpoint.
The SUBMIT study is a randomized controlled trial that will provide evidence on whether or not surgery of the primary tumor in breast cancer patients with metastatic disease at initial presentation results in an improved survival.
NCT01392586.
所有乳腺癌患者中,5%在初次就诊时即有远处转移疾病。由于转移性乳腺癌被认为是一种无法治愈的疾病,通常采用姑息性治疗。最近的非随机研究表明,(完整)切除原发性肿瘤与原发性转移性乳腺癌患者的生存率显著提高相关。然而,其他研究表明,手术所宣称的生存获益可能是由选择偏倚导致的。因此,将进行一项随机对照试验,以评估原发性远处转移性乳腺癌患者的乳房手术是否会改善预后。
在诊断原发性远处转移性乳腺癌后进行随机分组。患者将被随机分为两组,一组先进行乳腺肿瘤的前期手术,然后进行全身治疗;另一组先进行全身治疗,如果临床有指征,则随后进行乳腺肿瘤的延迟局部治疗。符合条件的患者为年龄在18岁及以上、未曾接受过乳腺癌治疗、适合接受手术和全身治疗的原发性远处转移性乳腺癌患者。重要的排除标准包括:既往有浸润性乳腺癌、随机分组前对该乳腺肿瘤进行过手术治疗或放疗、无法切除的T4肿瘤以及同步双侧乳腺癌。主要终点是2年生存率。生活质量和局部肿瘤控制是次要终点。根据先前研究的结果,假设检验效能为80%,每个治疗组需要258例患者。预计总入组时间为60个月。将进行中期分析,以评估任何具有临床意义的安全性问题,并确定是否有证据表明在主要终点方面,前期手术在临床或统计学上劣于全身治疗。
SUBMIT研究是一项随机对照试验,将为初次就诊时患有转移性疾病的乳腺癌患者的原发性肿瘤手术是否能提高生存率提供证据。
NCT01392586