Servicio de Geriatría. Hospital Universitario Ramón y Cajal, IRYCIS. Madrid, Spain.
Unité d'oncogériatrie. Service de gériatrie. Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon. Pierre-Bénite, France.
Semin Oncol. 2024 Jun-Aug;51(3-4):95-105. doi: 10.1053/j.seminoncol.2024.01.003. Epub 2024 Feb 22.
This study describes characteristics, toxicity and survival in old patients with HR+/HER2-breast cancer (BC) treated with CDK4/6 inhibitors. Retrospective observational study that included patients ≥ 75 years with HR+/HER2-BC treated with CDK4/6 inhibitors between 2017 and 2021. Patients' general and cancer-related data were collected. Comprehensive Geriatric Assessment scales were gathered. Adverse events reported before each cycle were included. At the end of the follow-up period, mortality was retrospectively registered from medical records. All 19 patients (94.7% women, median age 77.9 ± 10.1) were at risk of frailty (G8 ≤ 14) and malnutrition (MNA-SF ≤ 11). Most were independent (52.7% Lawton ≥ 6), had no cognitive impairment (89.5%, MMSE ≥ 24), poor physical performance (70%, SPPB < 8; 62.5% TUG ≥ 12'') and polypharmacy (72.2%). Almost half had stage IV disease (47.1%). Palbociclib+letrozole was the most frequently prescribed treatment (36.8%). All patients developed some toxicity (94.7% hematologic, 36.8% renal) but except one, grade ≤ 2. Over the 42-month follow-up period, 10 reported progression and 8 died. The median survival time was 19.9 ± 3.4 months. Five months after starting treatment, the probability of survival was 73%. At 30 months, 53% of patients survived. We found a high risk of frailty and drug toxicity in this small sample. Most patients presented hematologic toxicity but to a low degree. The probability of survival increases with treatment.
这项研究描述了接受 CDK4/6 抑制剂治疗的 HR+/HER2-乳腺癌(BC)老年患者的特征、毒性和生存情况。这是一项回顾性观察研究,纳入了 2017 年至 2021 年期间接受 CDK4/6 抑制剂治疗的年龄≥75 岁的 HR+/HER2-BC 患者。收集了患者的一般和癌症相关数据,并收集了全面的老年评估量表。纳入了每个周期前报告的不良事件。在随访结束时,从病历中回顾性登记了死亡率。所有 19 名患者(94.7%为女性,中位年龄 77.9±10.1 岁)均有衰弱风险(G8≤14)和营养不良(MNA-SF≤11)。大多数患者是独立的(52.7%的 Lawton≥6),无认知障碍(89.5%,MMSE≥24),身体状况较差(70%,SPPB<8;62.5%,TUG≥12''),且服用多种药物(72.2%)。近一半患者处于 IV 期疾病(47.1%)。哌柏西利+来曲唑是最常开的处方治疗(36.8%)。所有患者均出现某种毒性(94.7%为血液学毒性,36.8%为肾脏毒性),但除 1 例外,均为≤2 级。在 42 个月的随访期间,有 10 例报告疾病进展,8 例死亡。中位生存时间为 19.9±3.4 个月。治疗开始后 5 个月,生存率为 73%。30 个月时,53%的患者存活。我们在这个小样本中发现了高衰弱风险和药物毒性。大多数患者出现血液学毒性,但程度较低。随着治疗,生存率增加。