Korolewicz James Alexander, Scheiner Bernhard, Fulgenzi Claudia A M, D'Alessio Antonio, Cortellini Alessio, Pascual Chynna, Mehan Aman, Partridge Sarah, Gujral Dorothy M, Mohammed Waleed, Mohammed Oreoluwa, Grzesiak Aneta, Booker Lauren, Cleator Susan, Pokrovska Tzveta, Saleem Waqar, Rackie James, Needham Yasmine, Krell Jonathan, McNeish Iain, Tookman Laura, Park Won-Ho Edward, Asif Muzamil, Evans Joanne S, Pinato David J
Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK.
Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
Chemotherapy. 2024;69(4):205-211. doi: 10.1159/000539109. Epub 2024 Apr 27.
As tumour response rates are increasingly demonstrated in early-phase cancer trials (EPCT), optimal patient selection and accurate prognostication are paramount. Hammersmith Score (HS), a simple prognostic index derived on routine biochemical measures (albumin <35 g/L, lactate dehydrogenase >450 IU/L, sodium <135 mmol/L), is a validated predictor of response and survival in EPCT participants. HS has not been validated in the cancer immunotherapy era.
We retrospectively analysed characteristics and outcomes of unselected referrals to our early-phase unit (12/2019-12/2022). Independent predictors for overall survival (OS) were identified from univariable and multivariable models. HS was calculated for 66 eligible trial participants and compared with the Royal Marsden Score (RMS) to predict OS. Multivariable logistic regression and C-index was used to compare predictive ability of prognostic models.
Of 212 referrals, 147 patients were screened and 82 patients treated in EPCT. Prognostic stratification by HS identifies significant difference in median OS, and HS was confirmed as a multivariable predictor for OS (HR: HS 1 vs. 0 2.51, 95% CI: 1.01-6.24, p = 0.049; HS 2/3 vs. 0: 10.32, 95% CI: 2.15-49.62, p = 0.004; C-index 0.771) with superior multivariable predictive ability than RMS (HR: RMS 2 vs. 0/1 5.46, 95% CI: 1.12-26.57, p = 0.036; RMS 3 vs. 0/1 6.83, 95% CI: 1.15-40.53, p < 0.001; C-index 0.743).
HS is a validated prognostic index for patients with advanced cancer treated in the context of modern EPCTs, independent of tumour burden. HS is a simple, inexpensive prognostic tool to optimise referral for EPCT.
随着早期癌症试验(EPCT)中肿瘤缓解率的日益显现,最佳患者选择和准确预后至关重要。哈默史密斯评分(HS)是一种基于常规生化指标(白蛋白<35 g/L、乳酸脱氢酶>450 IU/L、钠<135 mmol/L)得出的简单预后指数,是EPCT参与者缓解和生存的有效预测指标。HS在癌症免疫治疗时代尚未得到验证。
我们回顾性分析了未经筛选转诊至我们早期治疗单元(2019年12月至2022年12月)的患者的特征和结局。从单变量和多变量模型中确定总生存(OS)的独立预测因素。为66名符合条件的试验参与者计算HS,并与皇家马斯登评分(RMS)进行比较以预测OS。使用多变量逻辑回归和C指数比较预后模型的预测能力。
在212例转诊患者中,147例患者接受了筛选,82例患者在EPCT中接受了治疗。HS进行的预后分层显示中位OS存在显著差异,HS被确认为OS的多变量预测因素(HR:HS 1 vs. 0 2.51,95% CI:1.01 - 6.24,p = 0.049;HS 2/3 vs. 0:10.32,95% CI:2.15 - 49.62,p = 0.004;C指数0.771),其多变量预测能力优于RMS(HR:RMS 2 vs. 0/1 5.46,95% CI:1.12 - 26.57,p = 0.036;RMS 3 vs. 0/1 6.83,95% CI:1.15 - 40.53,p < 0.001;C指数0.743)。
HS是现代EPCT背景下晚期癌症患者的有效预后指标,与肿瘤负荷无关。HS是一种简单、廉价的预后工具,可优化EPCT的转诊。