Maltoni Roberta, Roncadori Andrea, Balzi William, Mazza Massimiliano, Nicolini Fabio, Palleschi Michela, Ulivi Paola, Bravaccini Sara
IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", 47014 Meldola, Italy.
Biomedicines. 2024 Feb 22;12(3):498. doi: 10.3390/biomedicines12030498.
Cyclin-dependent kinase 4 and 6 (CDK4 and CDK6) inhibitors have changed the therapeutic management of hormone receptor-positive (HR+) metastatic breast cancer (mBC) by targeting the cell cycle machinery and overcoming endocrine resistance. However, a large number of patients present disease progression due to cancer cells resisting CDK4/6 inhibitors. Our research considers which clinicopathological characteristics could be useful in identifying patients who might respond to CDK4/6 inhibitors by analyzing a retrospective case series of patients with HR+ mBC who were treated with hormone therapy plus CDK4/6 inhibitors. Approximately 177 mBC patients were enrolled, of whom 66 were treated with CD4/6 inhibitors plus letrozole and 111 were treated with CDK4/6 inhibitors and fulvestrant. A multistate model was used. A low body surface area and older age were associated with an increased risk of developing neutropenia. A high Ki67 index, the presence of visceral metastases, and not having previously undergone adjuvant chemotherapy were prognostic factors of disease progression/death. As expected, some of the neutropenic patients who had previously undergone multiple lines of treatment were at a higher risk of disease progression/death. Furthermore, neutropenia status was associated with a more than doubled risk of progression/death compared to patients without neutropenia (HR = 2.311; = 0.025). Having identified certain factors that could be associated with the development of neutropenia and considering that neutropenia itself is associated with an increased risk of progression, we believe that the baseline characteristics should be taken into account to reduce cases of neutropenia and disease progression.
细胞周期蛋白依赖性激酶4和6(CDK4和CDK6)抑制剂通过靶向细胞周期机制和克服内分泌抵抗,改变了激素受体阳性(HR+)转移性乳腺癌(mBC)的治疗管理。然而,大量患者由于癌细胞对CDK4/6抑制剂产生耐药而出现疾病进展。我们的研究通过分析接受激素治疗加CDK4/6抑制剂治疗的HR+ mBC患者的回顾性病例系列,探讨哪些临床病理特征有助于识别可能对CDK4/6抑制剂有反应的患者。大约177例mBC患者入组,其中66例接受CD4/6抑制剂加来曲唑治疗,111例接受CDK4/6抑制剂和氟维司群治疗。使用了多状态模型。低体表面积和老年与发生中性粒细胞减少的风险增加相关。高Ki67指数、存在内脏转移以及未曾接受过辅助化疗是疾病进展/死亡的预后因素。正如预期的那样,一些先前接受过多线治疗的中性粒细胞减少患者疾病进展/死亡的风险更高。此外,与无中性粒细胞减少的患者相比,中性粒细胞减少状态与进展/死亡风险增加一倍以上相关(HR = 2.311;P = 0.025)。在确定了某些可能与中性粒细胞减少发生相关的因素,并考虑到中性粒细胞减少本身与进展风险增加相关后,我们认为应考虑基线特征以减少中性粒细胞减少和疾病进展的病例。