Department of Medical Oncology, Klinikum Grosshadern, University of Munich, Munich, Germany.
Clin Colorectal Cancer. 2011 Dec;10(4):317-24. doi: 10.1016/j.clcc.2011.03.027. Epub 2011 May 12.
Mortality rates in published irinotecan-based trials range between 1.7% and 5.0%. This analysis aimed to evaluate clinical and histopathologic factors associated with 60-day mortality in first-line therapy for metastatic colorectal cancer (mCRC).
Sixty-day all-cause and disease-specific mortality rates from 479 patients who participated in a randomized phase III study comparing FUFIRI (5-fluorouracil [5-FU], leucovorin, irinotecan) (n = 238) vs. mIROX (modified irinotecan plus oxaliplatin (n = 241) were evaluated for association with prognostic factors such as platelet counts, alkaline phosphatase (AP) levels, white blood cell (WBC) counts, hemoglobin values, lactate dehydrogenase (LDH) levels, carcinoembryonic antigen (CEA) levels, and several other baseline parameters using univariate and multivariate logistic regression analyses applied to patients combined from both treatment groups.
The all-cause 60-day mortality rate was 5.0% (24/479). Thirteen patients (5.5%) in the FUFIRI arm died within the first 60 days of treatment compared with 11 (4.6%) patients in the mIROX arm (P = .68). Among the 24 patients in both treatment arms, mortality was qualified as disease related in 15 (63%) patients and treatment related in 7 (29%) patients (P = .695). In multivariate analyses, high LDH levels (P = .010) and an elevated WBC count (P = .006) remained as significant independent prognostic factors. Low Karnofsky performance status (KPS) showed a strong trend but failed to reach statistical significance (P = .057) as did AP levels and the number of metastatic sites.
In this study 63% of the early deaths were disease related, whereas only 29% were possibly related to study medication. Independent prognostic factors for early mortality were LDH levels and WBC counts. KPS showed a strong trend in the multivariate analysis. Future investigation may consider LDH levels and WBC counts for exclusion criteria.
已发表的伊立替康为基础的试验中死亡率在 1.7%至 5.0%之间。本分析旨在评估转移性结直肠癌(mCRC)一线治疗中与 60 天死亡率相关的临床和组织病理学因素。
对参加一项比较 FUFIRI(5-氟尿嘧啶[5-FU]、亚叶酸、伊立替康)(n=238)与 mIROX(改良伊立替康加奥沙利铂(n=241)的随机 III 期研究的 479 名患者的 60 天全因和疾病特异性死亡率进行评估,使用单变量和多变量逻辑回归分析与预后因素相关,如血小板计数、碱性磷酸酶(AP)水平、白细胞(WBC)计数、血红蛋白值、乳酸脱氢酶(LDH)水平、癌胚抗原(CEA)水平和其他一些基线参数,应用于两个治疗组的患者。
全因 60 天死亡率为 5.0%(24/479)。FUFIRI 组有 13 名患者(5.5%)在治疗的前 60 天内死亡,而 mIROX 组有 11 名患者(4.6%)(P=0.68)。在两个治疗组的 24 名患者中,15 名(63%)患者的死亡与疾病相关,7 名(29%)患者的死亡与治疗相关(P=0.695)。多变量分析中,高 LDH 水平(P=0.010)和白细胞计数升高(P=0.006)仍然是显著的独立预后因素。低卡氏功能状态(KPS)评分有很强的趋势,但未达到统计学意义(P=0.057),AP 水平和转移部位数量也是如此。
在这项研究中,63%的早期死亡与疾病相关,而只有 29%可能与研究药物相关。早期死亡率的独立预后因素是 LDH 水平和白细胞计数。KPS 在多变量分析中显示出很强的趋势。未来的研究可能会考虑 LDH 水平和白细胞计数作为排除标准。