Manyam Bindu V, Tendulkar Rahul, Cherian Sheen, Vicini Frank, Badiyan Shahed N, Shah Chirag
Department of Radiation Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
21st Century Oncology, Michigan Healthcare Professionals, Farmington Hills, MI.
Am J Clin Oncol. 2018 Jun;41(6):526-531. doi: 10.1097/COC.0000000000000332.
PURPOSE/OBJECTIVE(S): After breast conserving surgery, adjuvant radiation therapy represents the standard of care for most patients. However, multiple options exist beyond standard fractionated whole breast irradiation including hypofractionated whole breast irradiation (HFRT), accelerated partial breast irradiation (APBI), and endocrine therapy (ET) alone, which can limit treatment duration, and potentially reduce morbidity and cost. Limited data are available on the percentage of patients eligible for these alternatives; therefore, a Surveillance Epidemiology and End Results (SEER) analysis was performed to assess candidacy for these alternative options in women with early stage breast cancer.
Women treated for breast cancer between the years of 2010 and 2012 were identified in the SEER database. Patients with unknown staging, metastatic disease, T3/T4 disease, and ≥N1 disease were excluded. Patients were defined as eligible for HFRT based on the American Society for Radiation Oncology (ASTRO) consensus guidelines and randomised trial testing intensity modulated and partial organ radiotherapy following breast conservation surgery for early breast cancer (IMPORT LOW) trial criteria, APBI based on the ASTRO, American Brachytherapy Society and the Groupe Européen de Curiethérapie of European Society for Therapeutic Radiotherapy and Oncology (GEC-ESTRO) consensus guidelines, and GEC-ESTRO APBI and IMPORT LOW trial criteria, and ET alone based on the Cancer and Leukemia Group B 9343 and Post-operative Radiotherapy in Minimum Risk Elderly II inclusion criteria.
A total of 108,484 women with early stage breast cancer who met the aforementioned inclusion criteria were identified. Of these patients, 86,896 (80.1%) were eligible for HFRT based on ASTRO consensus guidelines and 81,459 (75.0%) based on IMPORT LOW trial criteria. Regarding APBI, 44,797 (41.2%), 81,020 (74.6%), 81,020 (74.6%) were eligible according to ASTRO, ABS, GEC-ESTRO consensus guidelines, respectively, 97,301 (89.7%) patients according to the GEC-ESTRO trial criteria, and 81,459 (75.0%) patients according to the IMPORT LOW trial criteria. For ET alone, 23,006 (21.2%) were eligible according to Cancer and Leukemia Group B 9343 criteria and 42,104 (38.8%) according to Post-operative Radiotherapy in Minimum Risk Elderly II criteria.
This SEER analysis demonstrates that a substantial proportion of women with early stage breast cancer are eligible for HFRT, APBI, or ET alone after breast conserving surgery according to consensus guidelines and prospective trial criteria. With incorporation of additional pathologic, dosimetric, and chemotherapy data, quality assurance pathways may use such data to help ensure patients are receiving appropriate risk stratified treatment recommendations.
保乳手术后,辅助放疗是大多数患者的标准治疗方案。然而,除了标准分割全乳照射外,还有多种选择,包括大分割全乳照射(HFRT)、加速部分乳腺照射(APBI)以及单纯内分泌治疗(ET),这些方法可以缩短治疗时间,并有可能降低发病率和成本。关于符合这些替代方案的患者比例的数据有限;因此,进行了一项监测、流行病学和最终结果(SEER)分析,以评估早期乳腺癌女性患者采用这些替代方案的适用性。
在SEER数据库中识别出2010年至2012年间接受乳腺癌治疗的女性。排除分期不明、转移性疾病、T3/T4期疾病以及N1期及以上疾病的患者。根据美国放射肿瘤学会(ASTRO)共识指南以及早期乳腺癌保乳手术后调强和部分器官放疗的随机试验(IMPORT LOW)试验标准,将符合条件的患者定义为适合HFRT;根据ASTRO、美国近距离放射治疗学会以及欧洲治疗放射肿瘤学会(GEC-ESTRO)的共识指南,以及GEC-ESTRO APBI和IMPORT LOW试验标准,定义为适合APBI;根据癌症与白血病B组9343试验以及低风险老年患者术后放疗II纳入标准,定义为适合单纯ET。
共识别出108,484例符合上述纳入标准的早期乳腺癌女性患者。在这些患者中,根据ASTRO共识指南,86,896例(80.1%)适合HFRT;根据IMPORT LOW试验标准,81,459例(75.0%)适合。关于APBI,根据ASTRO、美国近距离放射治疗学会、GEC-ESTRO共识指南,分别有44,797例(41.2%)、81,020例(74.6%)、81,020例(74.6%)适合;根据GEC-ESTRO试验标准,97,301例(89.7%)患者适合;根据IMPORT LOW试验标准,81,459例(75.0%)患者适合。对于单纯ET,根据癌症与白血病B组9343标准,23,006例(21.2%)适合;根据低风险老年患者术后放疗II标准,42,104例(38.8%)适合。
这项SEER分析表明,根据共识指南和前瞻性试验标准,相当一部分早期乳腺癌女性患者在保乳手术后适合HFRT、APBI或单纯ET。纳入更多的病理、剂量学和化疗数据后,质量保证途径可以利用这些数据,以帮助确保患者获得适当的风险分层治疗建议。