Khan K H, Yap T A, Ring A, Molife L R, Bodla S, Thomas K, Zivi A, Smith A, Judson I, Banerji U, de Bono J S, Kaye S B
Drug Development Unit, The Royal Marsden NHS Foundation Trust, Sutton SM2 5PT, UK.
Gastrointestinal Cancers Unit, The Royal Marsden NHS Foundation Trust, Sutton SM2 5PT, UK.
Br J Cancer. 2016 Feb 2;114(3):262-8. doi: 10.1038/bjc.2015.477. Epub 2016 Jan 12.
This study had two aims: (a) to test the hypothesis that advanced age is associated with lower levels of tolerability and clinical benefit to experimental Phase I trial agents; (b) to assess the validity of the Royal Marsden Hospital (RMH) prognostic score as a patient selection tool in older patients.
Clinico-pathological characteristics and treatment outcomes of all patients treated consecutively from 2005 to 2009 in phase I trials at the RMH were recorded. All toxicity and clinical outcome data were compared between patients aged below and above 65 years of age.
One thousand and four patients were treated in 30 Phase I trials, with 315 (31%) patients aged 65 years and older. Grade 3-5 toxicities (22.8% vs 24.8% (P=0.52)), trial discontinuation (6% vs 4%; P=0.33), and dose interruptions (8.0% vs 8.0% (P=0.96)) were observed at similar rates in patients below and above 65 years of age, respectively. The overall response rate 5.2% vs 4.1%, progression-free survival (PFS) 1.9 vs 3.5 months and clinical benefit rate (CBR) at 6 months 15.2% vs 14.3% were comparable in both groups. To avoid bias due to the potential therapeutic benefit of abiraterone, comparisons were repeated excluding prostate cancer patients with similar results (ORR 4.6% vs 4%, PFS 1.8 vs 3.0 months, CBR at 6 months 13.5% vs 9.5%). Multivariate analysis indicated that the previously identified RMH score (including albumin and lactate dehydrogenase levels) was an accurate predictor of outcome.
Phase I clinical trials should be considered in patients with advanced cancers regardless of age, as older patients who enter these have similar safety and efficacy outcomes as their younger counterparts. The RMH prognostic score can assist in the selection of suitable older patients.
本研究有两个目的:(a)检验以下假设,即高龄与对实验性I期试验药物的耐受性水平较低及临床获益相关;(b)评估皇家马斯登医院(RMH)预后评分作为老年患者患者选择工具的有效性。
记录2005年至2009年在RMH进行的I期试验中连续治疗的所有患者的临床病理特征和治疗结果。比较65岁以下和65岁以上患者的所有毒性和临床结局数据。
1004例患者在30项I期试验中接受治疗,其中315例(31%)患者年龄在65岁及以上。65岁以下和65岁以上患者分别观察到3 - 5级毒性(22.8%对24.8%(P = 0.52))、试验中断(6%对4%;P = 0.33)和剂量中断(8.0%对8.0%(P = 0.96))的发生率相似。两组的总缓解率分别为5.2%对4.1%、无进展生存期(PFS)分别为1.9对3.5个月以及6个月时的临床获益率(CBR)分别为15.2%对14.3%相当。为避免因阿比特龙的潜在治疗益处导致的偏差,排除前列腺癌患者后重复进行比较,结果相似(ORR 4.6%对4%,PFS 1.8对3.0个月,6个月时CBR 13.5%对9.5%)。多变量分析表明,先前确定的RMH评分(包括白蛋白和乳酸脱氢酶水平)是结局的准确预测指标。
无论年龄大小,晚期癌症患者均应考虑进行I期临床试验,因为参加这些试验的老年患者与年轻患者具有相似的安全性和疗效结局。RMH预后评分可有助于选择合适的老年患者。