Shikanai Ayana, Horimoto Yoshiya, Ishizuka Yumiko, Uomori Toshitaka, Nakai Katsuya, Arakawa Atsushi, Saito Mitsue
Department of Breast Oncology, School of Medicine, Juntendo University, Tokyo, Japan.
Department of Human Pathology, School of Medicine, Juntendo University, Tokyo, Japan.
Breast Cancer (Auckl). 2022 Jan 5;16:11782234211065148. doi: 10.1177/11782234211065148. eCollection 2022.
Resistance to endocrine therapy has been a major obstacle in the management of hormone receptor (HR)-positive metastatic breast cancer (MBC). Meanwhile, a number of treatments are available to such patients, and physicians often encounter difficulties in choosing the most appropriate treatments for individual patients. The combination of CDK 4/6 inhibitors (CDKi) and endocrine therapy has now become a standard treatment for HR-positive and human epidermal growth factor receptor 2 (HER2)-negative MBC. However, no predictive markers for CDKi-based treatments have been established. Considering their side effects and the financial burden on patients, identifying such markers is crucial.
Clinicopathological features of 107 patients with HR-positive HER2-negative MBC, who received CDKi-based treatments at our institution were retrospectively investigated. HR status in distant metastatic lesions and immunocompetent cells in peripheral blood were also studied.
Progression-free survival (PFS) was significantly shorter in patients whose primary tumour was high grade ( = 0.016) or high neutrophil-to-lymphocyte ratio (NLR) at baseline ( = 0.017). Meanwhile, there were no differences in other factors, such as expression levels of hormone receptors. Patients whose metastatic lesions were of low tumour grade or high Ki67 labelling index had longer PFS, and such trends were more obvious than primary lesions.
Our data indicate that tumour grade in primary lesion and NLR are potential predictive factors for CDKi-based treatments. Moreover, pathological assessment of metastatic lesions might also be useful.
内分泌治疗耐药一直是激素受体(HR)阳性转移性乳腺癌(MBC)治疗中的主要障碍。与此同时,这类患者有多种治疗方法可供选择,医生在为个体患者选择最合适的治疗方法时常常遇到困难。细胞周期蛋白依赖性激酶4/6抑制剂(CDKi)与内分泌治疗联合应用现已成为HR阳性且人表皮生长因子受体2(HER2)阴性MBC的标准治疗方法。然而,尚未建立基于CDKi治疗的预测标志物。考虑到其副作用和患者的经济负担,识别此类标志物至关重要。
回顾性研究了在我们机构接受基于CDKi治疗的107例HR阳性HER2阴性MBC患者的临床病理特征。还研究了远处转移病灶中的HR状态和外周血中的免疫活性细胞。
原发肿瘤为高级别(=0.016)或基线时中性粒细胞与淋巴细胞比值高(NLR)(=0.017)的患者无进展生存期(PFS)显著缩短。同时,在其他因素如激素受体表达水平方面没有差异。转移病灶为低肿瘤分级或高Ki67标记指数的患者PFS更长,且这种趋势在转移病灶中比原发病灶更明显。
我们的数据表明,原发病灶的肿瘤分级和NLR是基于CDKi治疗的潜在预测因素。此外,转移病灶的病理评估可能也有用。