Ahari Daniel, Wilkinson Mark, Ali Nisha, Taxiarchi Vicky P, Dave Rajiv V, Gandhi Ashu
Wythenshawe Hospital and Nightingale Breast Cancer Centre, Manchester University Foundation Trust, Manchester M23 9LT, UK.
Centre for Women's Mental Health, Division of Psychology and Mental Health, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PL, UK.
Cancers (Basel). 2024 Sep 4;16(17):3072. doi: 10.3390/cancers16173072.
The monarchE study added the CDK4/6 inhibitor abemaciclib to the care of women with oestrogen-positive (ER+) breast cancers. Eligibility required meeting monarchE criteria-either >3 positive axillary nodes, or 1-3 positive sentinel nodes (SNB+) with tumour size >50 mm or grade 3 cancers. Women were advised to proceed to completion axillary node clearance (cANC) if size/grade criteria were not fulfilled for >3 positive nodes to be identified. However, cANC is associated with significant morbidity, conflicting with the potential benefits of abemaciclib. We analysed data of 229 consecutive women (2016-2022) with ER+ breast cancer and SNB+ who proceeded to cANC, keeping with contemporary treatment guidelines. We used this cohort to assess numbers that, under national guidance in place currently, would be advised to undergo cANC solely to check eligibility for abemaciclib treatment. Using monarchE criteria, 90 women (39%) would have accessed abemaciclib based on SNB+ and size/grade, without cANC. In total, 139 women would have been advised to proceed to cANC to check eligibility, with only 15/139 (11%) having >3 positive nodes after sentinel node biopsy and cANC. The remaining 124 (89%) would have undergone cANC but remained ineligible for abemaciclib. Size, age, grade, and Ki67 did not predict >3 nodes at cANC. Following cANC, a large majority of women with ER+, <50 mm, and grade 1-2 tumours remain ineligible for abemaciclib yet are subject to significant morbidity including lifelong lymphoedema risk. The monarchE authors state that 15 women need abemaciclib therapy for 1 to clinically benefit. Thus, in our cohort, 139 women undergoing cANC would lead to one woman benefitting.
MONARCH E研究在雌激素阳性(ER+)乳腺癌女性的治疗中加入了CDK4/6抑制剂阿贝西利。入选要求符合MONARCH E标准,即腋窝淋巴结转移阳性个数>3个,或前哨淋巴结活检1-3个阳性(SNB+)且肿瘤大小>50 mm或为3级癌症。若不符合>3个阳性淋巴结的大小/分级标准,则建议女性进行腋窝淋巴结清扫术(cANC)以确定是否有>3个阳性淋巴结。然而,cANC会带来显著的发病率,这与阿贝西利的潜在益处相冲突。我们分析了229例连续的(2016-2022年)ER+乳腺癌且进行了cANC的SNB+女性的数据,遵循当代治疗指南。我们利用该队列评估在当前国家指南下,仅为检查阿贝西利治疗资格而建议进行cANC的人数。根据MONARCH E标准,90名女性(39%)基于SNB+以及大小/分级情况可使用阿贝西利,而无需进行cANC。总共139名女性会被建议进行cANC以检查资格,在前哨淋巴结活检和cANC后,只有15/139(11%)有>3个阳性淋巴结。其余124名(89%)进行了cANC但仍不符合阿贝西利治疗资格。大小、年龄、分级和Ki67不能预测cANC时>3个淋巴结的情况。在cANC后,绝大多数ER+、<50 mm且为1-2级肿瘤的女性仍不符合阿贝西利治疗资格,但却要承受包括终身淋巴水肿风险在内的显著发病率。MONARCH E研究的作者指出,15名女性需要接受阿贝西利治疗才能获得1例临床获益。因此,在我们的队列中,139名接受cANC的女性只会使1名女性获益。