Verwaal Vic J, van Ruth Serge, de Bree Eeclo, van Sloothen Gooike W, van Tinteren Harm, Boot Henk, Zoetmulder Frans A N
Department of Surgery, Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital, Amsterdam, the Netherlands.
J Clin Oncol. 2003 Oct 15;21(20):3737-43. doi: 10.1200/JCO.2003.04.187.
To confirm the findings from uncontrolled studies that aggressive cytoreduction in combination with hyperthermic intraperitoneal chemotherapy (HIPEC) is superior to standard treatment in patients with peritoneal carcinomatosis of colorectal cancer origin.
Between February 1998 and August 2001, 105 patients were randomly assigned to receive either standard treatment consisting of systemic chemotherapy (fluorouracil-leucovorin) with or without palliative surgery, or experimental therapy consisting of aggressive cytoreduction with HIPEC, followed by the same systemic chemotherapy regime. The primary end point was survival.
After a median follow-up period of 21.6 months, the median survival was 12.6 months in the standard therapy arm and 22.3 months in the experimental therapy arm (log-rank test, P =.032). The treatment-related mortality in the aggressive therapy group was 8%. Most complications from HIPEC were related to bowel leakage. Subgroup analysis of the HIPEC group showed that patients with 0 to 5 of the 7 regions of the abdominal cavity involved by tumor at the time of the cytoreduction had a significantly better survival than patients with 6 or 7 affected regions (log-rank test, P <.0001). If the cytoreduction was macroscopically complete (R-1), the median survival was also significantly better than in patients with limited (R-2a), or extensive residual disease (R-2b; log-rank test, P <.0001).
Cytoreduction followed by HIPEC improves survival in patients with peritoneal carcinomatosis of colorectal origin. However, patients with involvement of six or more regions of the abdominal cavity, or grossly incomplete cytoreduction, had still a grave prognosis.
证实非对照研究的结果,即积极的细胞减灭术联合腹腔内热灌注化疗(HIPEC)在结直肠癌源性腹膜癌患者中优于标准治疗。
1998年2月至2001年8月期间,105例患者被随机分配接受标准治疗或实验性治疗。标准治疗包括全身化疗(氟尿嘧啶-亚叶酸),可选择是否进行姑息性手术;实验性治疗包括积极的细胞减灭术联合HIPEC,随后采用相同的全身化疗方案。主要终点是生存率。
中位随访期为21.6个月后,标准治疗组的中位生存期为12.6个月,实验性治疗组为22.3个月(对数秩检验,P = 0.032)。积极治疗组的治疗相关死亡率为8%。HIPEC的大多数并发症与肠漏有关。HIPEC组的亚组分析显示,细胞减灭术时腹腔7个区域中0至5个区域受肿瘤累及的患者生存率明显高于6个或7个区域受累的患者(对数秩检验,P < 0.0001)。如果细胞减灭术在宏观上是完全的(R-1),中位生存期也明显优于有限残留(R-₂a)或广泛残留疾病(R-₂b)的患者(对数秩检验,P < 0.0001)。
细胞减灭术联合HIPEC可提高结直肠癌源性腹膜癌患者的生存率。然而,腹腔6个或更多区域受累或细胞减灭术明显不完全的患者预后仍然很差。