Nordlinger Bernard, Sorbye Halfdan, Glimelius Bengt, Poston Graeme J, Schlag Peter M, Rougier Philippe, Bechstein Wolf O, Primrose John N, Walpole Euan T, Finch-Jones Meg, Jaeck Daniel, Mirza Darius, Parks Rowan W, Collette Laurence, Praet Michel, Bethe Ullrich, Van Cutsem Eric, Scheithauer Werner, Gruenberger Thomas
Centre Hospitalier Universitaire Ambroise Paré, Assistance Publique Hôpitaux de Paris, Departments of Surgery and Oncology, Boulogne-Billancourt, France.
Lancet. 2008 Mar 22;371(9617):1007-16. doi: 10.1016/S0140-6736(08)60455-9.
Surgical resection alone is regarded as the standard of care for patients with liver metastases from colorectal cancer, but relapse is common. We assessed the combination of perioperative chemotherapy and surgery compared with surgery alone for patients with initially resectable liver metastases from colorectal cancer.
This parallel-group study reports the trial's final data for progression-free survival for a protocol unspecified interim time-point, while overall survival is still being monitored. 364 patients with histologically proven colorectal cancer and up to four liver metastases were randomly assigned to either six cycles of FOLFOX4 before and six cycles after surgery or to surgery alone (182 in perioperative chemotherapy group vs 182 in surgery group). Patients were centrally randomised by minimisation, adjusting for centre and risk score. The primary objective was to detect a hazard ratio (HR) of 0.71 or less for progression-free survival. Primary analysis was by intention to treat. Analyses were repeated for all eligible (171 vs 171) and resected patients (151 vs 152). This trial is registered with ClinicalTrials.gov, number NCT00006479.
In the perioperative chemotherapy group, 151 (83%) patients were resected after a median of six (range 1-6) preoperative cycles and 115 (63%) patients received a median six (1-8) postoperative cycles. 152 (84%) patients were resected in the surgery group. The absolute increase in rate of progression-free survival at 3 years was 7.3% (from 28.1% [95.66% CI 21.3-35.5] to 35.4% [28.1-42.7]; HR 0.79 [0.62-1.02]; p=0.058) in randomised patients; 8.1% (from 28.1% [21.2-36.6] to 36.2% [28.7-43.8]; HR 0.77 [0.60-1.00]; p=0.041) in eligible patients; and 9.2% (from 33.2% [25.3-41.2] to 42.4% [34.0-50.5]; HR 0.73 [0.55-0.97]; p=0.025) in patients undergoing resection. 139 patients died (64 in perioperative chemotherapy group vs 75 in surgery group). Reversible postoperative complications occurred more often after chemotherapy than after surgery (40/159 [25%] vs 27/170 [16%]; p=0.04). After surgery we recorded two deaths in the surgery alone group and one in the perioperative chemotherapy group.
Perioperative chemotherapy with FOLFOX4 is compatible with major liver surgery and reduces the risk of events of progression-free survival in eligible and resected patients.
单纯手术切除被视为结直肠癌肝转移患者的标准治疗方法,但复发很常见。我们评估了围手术期化疗与手术联合应用相较于单纯手术治疗初治可切除结直肠癌肝转移患者的效果。
这项平行组研究报告了该试验在一个未明确规定的中期时间点的无进展生存期最终数据,总生存期仍在监测中。364例经组织学证实为结直肠癌且肝转移灶最多为四处的患者被随机分为两组,一组在手术前和手术后各接受六个周期的FOLFOX4化疗,另一组仅接受手术治疗(围手术期化疗组182例,手术组182例)。患者通过最小化法进行中心随机分组,并根据中心和风险评分进行调整。主要目标是检测无进展生存期的风险比(HR)为0.71或更低。主要分析采用意向性治疗。对所有符合条件的患者(171例对171例)和接受手术的患者(151例对152例)重复进行分析。该试验已在ClinicalTrials.gov注册,编号为NCT00006479。
在围手术期化疗组中,151例(83%)患者在术前接受了中位数为六个周期(范围1 - 6个周期)的化疗,115例(63%)患者在术后接受了中位数为六个周期(1 - 8个周期)的化疗。手术组中有152例(84%)患者接受了手术。随机分组患者中,3年时无进展生存率的绝对提高为7.3%(从28.1%[95.66%CI 21.3 - 35.5]提高到35.4%[28.1 - 42.7];HR 0.79[0.62 - 1.02];p = 0.058);符合条件的患者中为8.1%(从28.1%[21.2 -
36.6]提高到36.2%[28.7 - 43.8];HR 0.77[0.60 - 1.00];p = 0.041);接受手术的患者中为9.2%(从33.2%[25.3 - 41.2]提高到42.4%[34.0 - 50.5];HR 0.73[0.55 - 0.97];p = 0.025)。139例患者死亡(围手术期化疗组64例,手术组75例)。化疗后可逆性术后并发症的发生率高于手术组(40/159[25%]对27/170[16%];p = 0.04)。手术后,我们记录到单纯手术组有2例死亡,围手术期化疗组有1例死亡。
FOLFOX4围手术期化疗与大型肝脏手术兼容,并降低了符合条件和接受手术患者的无进展生存事件风险。