Caires-Lima Rafael, Cayres Karolina, Protásio Bruno, Caires Inacelli, Andrade Júlia, Rocha Lucila, Takahashi Tiago Kenji, Hoff Paulo M, de Castro Gilberto, Mak Milena Perez
Medical Oncology, Instituto do Cancer do Estado de Sao Paulo, Sao Paulo 01246-000, Brazil.
Ecancermedicalscience. 2018 Apr 30;12:831. doi: 10.3332/ecancer.2018.831. eCollection 2018.
Although patients with incurable disease and Eastern Cooperative Oncology Group performance status (ECOG-PS ≥ 2) are underrepresented in clinical trials, they are frequently offered palliative chemotherapy (pCT) in daily clinical practice in order to improve symptoms and quality of life. In this case-control retrospective analysis, our goal was to identify factors associated with poorer survival and lack of benefit of pCT in this population.
We evaluated 2,514 patients who died between August 2011 and July 2012 in an academic cancer care institution and its hospice. A total of 301 patients with solid tumours and ECOG-PS ≥ 2 at prescription of pCT were selected for this case-control retrospective analysis. Cases were defined as patients who survived less than 90 days after the first cycle of first line pCT, and controls were those who had a longer survival.
142 cases and 159 controls were included. Cases were more likely to experience grade ≥ 3 toxicity (43% versus 28%; = 0.005), die of toxicity (16% versus 6%; < 0.001) and not be offered best supportive care (BSC) only (47% versus 71%; < 0.001). Median overall survival was 204 among controls and 34 days in cases (hazard ratio = 0.177; 95%, confidence interval = 0.015-0.033, < 0.001). Logistic regression analysis identified ECOG-PS > 2 (odds ratio (OR) = 2.3, = 0.044) and serum creatinine (sCr) > 1 mg/dL (OR = 11.2, < 0.001) as independent predictors of 90-day mortality.
The independent predictors of short survival (less than 3 months) after initiation of pCT in this population were ECOG-PS > 2 and elevated sCr. Therefore, patient selection is crucial, as pCT may be deleterious in ECOG-PS ≥ 2 pts.
尽管患有不治之症且东部肿瘤协作组体能状态(ECOG-PS≥2)的患者在临床试验中的代表性不足,但在日常临床实践中,他们常接受姑息性化疗(pCT)以改善症状和生活质量。在这项病例对照回顾性分析中,我们的目标是确定该人群中与较差生存及pCT无获益相关的因素。
我们评估了2011年8月至2012年7月间在一家学术性癌症护理机构及其临终关怀机构死亡的2514例患者。本病例对照回顾性分析共选取了301例在开具pCT处方时患有实体瘤且ECOG-PS≥2的患者。病例定义为一线pCT首个周期后存活少于90天的患者,对照为存活时间更长的患者。
纳入142例病例和159例对照。病例更有可能经历≥3级毒性反应(43%对28%;P = 0.005)、死于毒性反应(16%对6%;P < 0.001)且未仅接受最佳支持治疗(BSC)(47%对71%;P < 0.001)。对照的中位总生存期为204天,病例为34天(风险比 = 0.177;95%置信区间 = 0.015 - 0.033,P < 0.001)。逻辑回归分析确定ECOG-PS > 2(比值比(OR) = 2.3,P = 0.044)和血清肌酐(sCr)> 1 mg/dL(OR = 11.2,P < 0.001)为90天死亡率的独立预测因素。
该人群中开始pCT后短期生存(少于3个月)的独立预测因素为ECOG-PS > 2和sCr升高。因此,患者选择至关重要,因为pCT对ECOG-PS≥2的患者可能有害。