Giuliano Armando E, Ballman Karla V, McCall Linda, Beitsch Peter D, Brennan Meghan B, Kelemen Pond R, Ollila David W, Hansen Nora M, Whitworth Pat W, Blumencranz Peter W, Leitch A Marilyn, Saha Sukamal, Hunt Kelly K, Morrow Monica
Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, California.
Alliance Statistics and Data Center, Weill Cornell Medicine/New York-Presbyterian Hospital, New York, New York.
JAMA. 2017 Sep 12;318(10):918-926. doi: 10.1001/jama.2017.11470.
The results of the American College of Surgeons Oncology Group Z0011 (ACOSOG Z0011) trial were first reported in 2005 with a median follow-up of 6.3 years. Longer follow-up was necessary because the majority of the patients had estrogen receptor-positive tumors that may recur later in the disease course (the ACOSOG is now part of the Alliance for Clinical Trials in Oncology).
To determine whether the 10-year overall survival of patients with sentinel lymph node metastases treated with breast-conserving therapy and sentinel lymph node dissection (SLND) alone without axillary lymph node dissection (ALND) is noninferior to that of women treated with axillary dissection.
DESIGN, SETTING, AND PARTICIPANTS: The ACOSOG Z0011 phase 3 randomized clinical trial enrolled patients from May 1999 to December 2004 at 115 sites (both academic and community medical centers). The last date of follow-up was September 29, 2015, in the ACOSOG Z0011 (Alliance) trial. Eligible patients were women with clinical T1 or T2 invasive breast cancer, no palpable axillary adenopathy, and 1 or 2 sentinel lymph nodes containing metastases.
All patients had planned lumpectomy, planned tangential whole-breast irradiation, and adjuvant systemic therapy. Third-field radiation was prohibited.
The primary outcome was overall survival with a noninferiority hazard ratio (HR) margin of 1.3. The secondary outcome was disease-free survival.
Among 891 women who were randomized (median age, 55 years), 856 (96%) completed the trial (446 in the SLND alone group and 445 in the ALND group). At a median follow-up of 9.3 years (interquartile range, 6.93-10.34 years), the 10-year overall survival was 86.3% in the SLND alone group and 83.6% in the ALND group (HR, 0.85 [1-sided 95% CI, 0-1.16]; noninferiority P = .02). The 10-year disease-free survival was 80.2% in the SLND alone group and 78.2% in the ALND group (HR, 0.85 [95% CI, 0.62-1.17]; P = .32). Between year 5 and year 10, 1 regional recurrence was seen in the SLND alone group vs none in the ALND group. Ten-year regional recurrence did not differ significantly between the 2 groups.
Among women with T1 or T2 invasive primary breast cancer, no palpable axillary adenopathy, and 1 or 2 sentinel lymph nodes containing metastases, 10-year overall survival for patients treated with sentinel lymph node dissection alone was noninferior to overall survival for those treated with axillary lymph node dissection. These findings do not support routine use of axillary lymph node dissection in this patient population based on 10-year outcomes.
clinicaltrials.gov Identifier: NCT00003855.
美国外科医师学会肿瘤学组Z0011(ACOSOG Z0011)试验的结果于2005年首次公布,中位随访时间为6.3年。由于大多数患者患有雌激素受体阳性肿瘤,可能在疾病后期复发,因此需要更长时间的随访(ACOSOG现在是肿瘤学临床试验联盟的一部分)。
确定仅接受保乳治疗和前哨淋巴结清扫术(SLND)而未进行腋窝淋巴结清扫术(ALND)的前哨淋巴结转移患者的10年总生存率是否不劣于接受腋窝清扫术的女性患者。
设计、地点和参与者:ACOSOG Z0011 3期随机临床试验于1999年5月至2004年12月在115个地点(学术和社区医疗中心)招募患者。ACOSOG Z0011(联盟)试验的最后随访日期为2015年9月29日。符合条件的患者为患有临床T1或T2期浸润性乳腺癌、无可触及腋窝淋巴结肿大且1或2个前哨淋巴结有转移的女性。
所有患者均计划进行肿块切除术、计划的全乳切线照射和辅助全身治疗。禁止进行第三野放疗。
主要结局为总生存率,非劣效性风险比(HR)界值为1.3。次要结局为无病生存率。
在891名随机分组的女性(中位年龄55岁)中,856名(96%)完成了试验(仅SLND组446名,ALND组445名)。中位随访9.3年(四分位间距,6.93 - 10.34年)时,仅SLND组的10年总生存率为86.3%,ALND组为83.6%(HR,0.85[单侧95%CI,0 - 1.16];非劣效性P = 0.02)。仅SLND组的10年无病生存率为80.2%,ALND组为78.2%(HR,0.85[95%CI,0.62 - 1.17];P = 0.32)。在第5年至第10年期间,仅SLND组出现1例区域复发,而ALND组未出现。两组间10年区域复发率无显著差异。
在患有T1或T2期浸润性原发性乳腺癌、无可触及腋窝淋巴结肿大且1或2个前哨淋巴结有转移的女性中,仅接受前哨淋巴结清扫术患者的1年总生存率不劣于接受腋窝淋巴结清扫术患者的总生存率。基于10年的结果,这些发现不支持在该患者群体中常规使用腋窝淋巴结清扫术。
clinicaltrials.gov标识符:NCT00003855。