Department of Surgical Oncology, Unit 1484, The University of Texas MD Anderson Cancer Center, Houston, USA.
Ann Surg Oncol. 2013 Aug;20(8):2493-500. doi: 10.1245/s10434-012-2864-7. Epub 2013 Feb 3.
Patients with colorectal liver metastases (CLM) are increasingly treated with preoperative chemotherapy. Chemotherapy associated liver injury is associated with postoperative hepatic insufficiency (PHI) and mortality. The adequate minimum future liver remnant (FLR) volume in patients treated with extensive chemotherapy remains unknown.
All patients with standardized FLR > 20 %, who underwent extended right hepatectomy for CLM from 1993-2011, were divided into three cohorts by chemotherapy duration: no chemotherapy (NC, n = 30), short duration (SD, ≤12 weeks, n = 78), long duration (LD, >12 weeks, n = 86). PHI and mortality were compared by using uni-/multivariate analyses. Optimal FLR for LD chemotherapy was determined using a minimum p-value approach.
A total of 194 patients met inclusion criteria. LD chemotherapy was significantly associated with PHI (NC + SD 3.7 vs. LD 16.3%, p = 0.006). Ninety-day mortality rates were 0 % in NC, 1.3 % in SD, and 2.3% in LD patients, respectively (p = 0.95). In patients with FLR > 30 %, PHI occurred in only two patients (both LD, 2/20, 10 %), but all patients with FLR > 30 % survived. The best cutoff of FLR for preventing PHI after chemotherapy >12 weeks was estimated as >30 %. Both LD chemotherapy (odds ratio [OR] 5.4, p = 0.004) and FLR ≤ 30 % (OR 6.3, p = 0.019) were independent predictors of PHI.
Preoperative chemotherapy >12 weeks increases the risk of PHI after extended right hepatectomy. In patients treated with long-duration chemotherapy, FLR > 30 % reduces the rate of PHI and may provide enough functional reserve for clinical rescue if PHI develops.
越来越多的结直肠癌肝转移(CLM)患者接受术前化疗。化疗相关肝损伤与术后肝不全(PHI)和死亡率相关。接受广泛化疗的患者的足够最小未来肝残留(FLR)体积仍不清楚。
所有接受标准化 FLR > 20%的患者,1993-2011 年接受 CLM 扩大右肝切除术,根据化疗时间分为三组:无化疗(NC,n=30)、短时间(SD,≤12 周,n=78)、长时间(LD,>12 周,n=86)。使用单变量/多变量分析比较 PHI 和死亡率。使用最小 p 值方法确定 LD 化疗的最佳 FLR。
共有 194 名患者符合纳入标准。LD 化疗与 PHI 显著相关(NC+SD 为 3.7%,LD 为 16.3%,p=0.006)。NC、SD 和 LD 患者的 90 天死亡率分别为 0%、1.3%和 2.3%(p=0.95)。FLR>30%的患者中仅 2 例发生 PHI(均为 LD,2/20,10%),但所有 FLR>30%的患者均存活。化疗>12 周后预防 PHI 的最佳 FLR 截断值估计为>30%。LD 化疗(优势比 [OR] 5.4,p=0.004)和 FLR≤30%(OR 6.3,p=0.019)均是 PHI 的独立预测因子。
12 周的术前化疗增加了扩大右肝切除术治疗后 PHI 的风险。在接受长疗程化疗的患者中,FLR>30%可降低 PHI 发生率,如果发生 PHI,可为临床抢救提供足够的功能储备。