Observational real world data with palbociclib associated to hormone therapy for advanced breast carcinoma.

Teresa Sampedro-Gimeno, Rubén Pampín-Sánchez, Francisco Javier Barbazán-Vázquez, Virginia Reguero-Cuervo, Virginia Galeazzi-Martínez, Ignacio Pelaez-Fernández
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Abstract

Objective: Cyclin-dependent kinase 4/6 inhibitors have a synergistic effect  in combination with endocrine therapy. This combination is used as first and  subsequent-line treatment for advanced luminal breast carcinoma because it  increases progression-free survival. We analysed clinical course and toxicity  in patients treated with palbociclib in our hospital and determined potential  associations between these variables and clinicopathological variables.

Method: Observational retrospective study including patients with advanced  or metastatic breast cancer treated with palbociclib plus endocrine therapy at  the Hospital Universitario de Cabueñes between 2017 and 2020. We  analysed clinicopathological variables, toxicity, and survival. Results: In total, 72 women and 1 man (median age: 63 years) received palbociclib plus an  aromatase inhibitor or fulvestrant. When used as firstline treatment,  progression-free survival was 22 months, and as second and subsequent-line treatment, progression-free survival was 13 months. Adverse effects (mainly haematological) were experienced by nearly all any patient, although delays  and dose adjustments were common (61.7% and 42.7%, respectively).  Performance status alone had a significant impact on progression-free  survival (22 months in patients with ECOG 0 vs 12 months in patients with  ECOG ≥ 1; P = 0.021).

Conclusions: Disease stage, age, and performance status do not limit the  use of treatment with palbociclib, nor its combination with aromatase inhibitors or fulvestrant for first or subsequent-line treatment.  Toxicity is easily managed. Real-world results are equivalent to those  published to date.

帕博西尼与晚期乳腺癌激素治疗相关的观察性真实世界数据。
目的:细胞周期蛋白依赖性激酶4/6抑制剂联合内分泌治疗具有协同作用。这一组合被用作晚期腔内乳腺癌的一线和后续治疗,因为它增加了无进展生存期。我们分析了我院接受帕博西尼治疗的患者的临床病程和毒性,并确定了这些变量与临床病理变量之间的潜在关联。方法:观察性回顾性研究,纳入2017年至2020年在Cabueñes Universitario医院接受帕博西尼联合内分泌治疗的晚期或转移性乳腺癌患者。我们分析了临床病理变量、毒性和生存率。结果:总共有72名女性和1名男性(中位年龄:63岁)接受了帕博西尼加芳香酶抑制剂或氟维司汀。作为一线治疗,无进展生存期为22个月,作为二线及后续治疗,无进展生存期为13个月。几乎所有患者都经历了不良反应(主要是血液学),尽管延迟和剂量调整很常见(分别为61.7%和42.7%)。运动状态本身对无进展生存期有显著影响(ECOG为0的患者为22个月,ECOG≥1的患者为12个月;P = 0.021)。结论:疾病分期、年龄和运动状态不限制帕博西尼治疗的使用,也不限制帕博西尼与芳香酶抑制剂或氟维司汀联合进行一线或后续治疗。毒性很容易控制。实际结果与迄今为止发表的结果相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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