Medical Oncology 1 Unit, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.
Medical Oncology 1 Unit, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.
J Geriatr Oncol. 2021 Mar;12(2):290-297. doi: 10.1016/j.jgo.2020.09.009. Epub 2020 Sep 21.
BACKGROUND: There is poor data on the prognostic role of Comprehensive Geriatric Assessment (CGA) in older patients with metastatic renal cell carcinoma (mRCC) treated with first line Tyrosine Kinase Inhibitors (TKIs). MATERIALS AND METHODS: We retrospectively reviewed the clinical charts of mRCC patients older than 70 years treated at our Institute with first-line Sunitinib or Pazopanib for at least 6 months. Every patient received a CGA at baseline and was identified as fit, vulnerable or frail according to Balducci's Criteria. We then assessed the impact of CGA category on survival, disease control and tolerability of TKIs. RESULTS: We identified 86 eligible patients. Median age: 74.5 years, 56% males; 45.4% were fit, 37.2% vulnerable and 17.4% frail at CGA. There were no significant differences in the rate of Grade (G)1-2 and G3-4 toxicities, dose reduction rates, PFS and OS between Sunitinib and Pazopanib. Fit, vulnerable and frail patients achieved significantly different median PFS (18.9 vs 11.2 vs 5.1 months; p < 0.001) and OS (35.5 vs 14.6 vs 10.9 months; p < 0.001). Patients categorized as fit had higher chance of receiving a second-line treatment (66.6% vs 28.9% in vulnerable/frail; p = 0.002). The incidence of G3/4 events was significantly lower in the fit subgroup (19% vs 45% in vulnerable/frail; p = 0.0025). CONCLUSIONS: In our retrospective single-center experience, CGA could accurately discriminate patients with higher risk of experiencing G3/4 toxicities, shorter PFS, and lower chance of receiving a second line treatment. CGA strongly impacted on OS, independently from International mRCC Database Consortium (IMDC) classification.
背景:在接受一线酪氨酸激酶抑制剂(TKI)治疗的转移性肾细胞癌(mRCC)老年患者中,综合老年评估(CGA)的预后作用数据较差。
材料和方法:我们回顾性地审查了在我们研究所接受一线舒尼替尼或帕唑帕尼治疗至少 6 个月的 70 岁以上 mRCC 患者的临床病历。每位患者在基线时接受 CGA,并根据 Balducci 标准确定为适合、脆弱或虚弱。然后,我们评估了 CGA 类别对 TKI 生存、疾病控制和耐受性的影响。
结果:我们确定了 86 名符合条件的患者。中位年龄:74.5 岁,男性占 56%;45.4%为适合,37.2%为脆弱,17.4%为虚弱。在 G1-2 和 G3-4 毒性、剂量减少率、PFS 和 OS 方面,舒尼替尼和帕唑帕尼之间没有显著差异。适合、脆弱和虚弱的患者获得了显著不同的中位 PFS(18.9 个月比 11.2 个月比 5.1 个月;p<0.001)和 OS(35.5 个月比 14.6 个月比 10.9 个月;p<0.001)。适合组患者接受二线治疗的机会更高(66.6%比脆弱/虚弱组的 28.9%;p=0.002)。适合组的 G3/4 事件发生率明显较低(19%比脆弱/虚弱组的 45%;p=0.0025)。
结论:在我们的回顾性单中心经验中,CGA 可以准确区分出发生 G3/4 毒性、较短 PFS 和接受二线治疗机会较低的高风险患者。CGA 对 OS 的影响明显,独立于国际 mRCC 数据库联盟(IMDC)分类。
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