Yonemura Yutaka, Kawamura Taiichi, Bando Etsuro, Takahashi Shigeru, Sawa Toshiharu, Yoshimitsu Yutaka, Obata Tohru, Endo Yoshio, Sasaki Takuma, Sugarbaker Paul H
Peritoneal Dissemination Program, Shizuoka Cancer Center.
Gan To Kagaku Ryoho. 2004 Oct;31(11):1723-6.
No standard treatment exists for peritoneal dissemination from gastric cancer. We reviewed our experience using a novel treatment consisting of peritonectomy and intraoperative chemo-hyperthermic peritoneal perfusion (CHPP). Records of all patients who underwent CHPP and cytoreductive surgery from 1992 to 2001 were reviewed.
Data from 107 patients (average age, 52 years) were available. P3 dissemination was found in 72 patients, and 8 and 27 patients showed P1 or P2 dissemination, respectively. Peritoneal metastasis was synchronous in 75 and metachronous in 32 patients. All patients received CHPP after cytoreductive surgery. Peritonectomy was performed in 42 patients. Complete cytoreduction (CC-0) was achieved in 47 patients (44%). Peritonectomy, resulted in CC-0 in 69% (29/42), but CC-0 was achieved in 18 of 65 (28%) patients by ordinary surgical techniques. There were 23 postoperative complications (21%) after operation. The overall operative mortality was 2.8% (3/107). Median follow-up for the entire study group was 46 months. Seventeen patients (15%) were disease-free, and 90 patients were dead at the time of analysis. Eighty-seven deaths were related to progression of disease. The median survival of all patients was 16.2 months, with an actual 5-year survival of 6%. Median survival of CHPP plus ordinary cyoreduction was 12.0 months and that after CHPP and peritonectomy was 22.8 months. Completeness of cytoreduction and peritonectomy were significant prognostic factors on univariate analysis and 5-year survival rate was 27%. Lymph node status, grade of peritoneal dissemination (P1-2 vs P3), age (>60 years vs <60 years), tumor volume of dissemination (>2.5 cm vs <2.5 cm in diameter), and histologic type (differentiated vs. poorly differentiated type) did not affect survival. The cox proportional model demonstrated that completeness of cytoreduction was the strongest prognostic factor. Patients who had an incomplete resection had 2.8-fold higher risk of dying from disease than patients who underwent complete cytoreduction. The 5-year survival after complete cytoreduction was 12%, compared with 2% for incomplete resection. Four patients lived more than 5 years. Cytoreduction was incomplete in one 5-year survivor who showed complete response to CHPP.
Complete cytoreduction using peritonectomy and CHPP may improve survival of patients with peritoneal dissemination from gastric cancer. This procedure is most appropriate for highly motivated patients who are committed to survive as long as possible.
目前尚无针对胃癌腹膜播散的标准治疗方法。我们回顾了采用一种新的治疗方法(包括腹膜切除术和术中化疗热灌注(CHPP))的经验。对1992年至2001年期间接受CHPP和细胞减灭术的所有患者的记录进行了回顾。
获得了107例患者(平均年龄52岁)的数据。72例患者发现P3播散,8例和27例患者分别表现为P1或P2播散。75例患者腹膜转移为同时性,32例为异时性。所有患者在细胞减灭术后接受CHPP。42例患者进行了腹膜切除术。47例患者(44%)实现了完全细胞减灭(CC-0)。腹膜切除术使69%(29/42)的患者实现了CC-0,但普通手术技术使65例患者中的18例(28%)实现了CC-0。术后有23例并发症(21%)。总体手术死亡率为2.8%(3/107)。整个研究组的中位随访时间为46个月。17例患者(15%)无疾病,分析时90例患者死亡。87例死亡与疾病进展相关。所有患者的中位生存期为16.2个月,实际5年生存率为6%。CHPP加普通细胞减灭术的中位生存期为12.0个月,CHPP和腹膜切除术后的中位生存期为22.8个月。单因素分析显示细胞减灭的完整性和腹膜切除术是显著的预后因素,5年生存率为27%。淋巴结状态、腹膜播散分级(P1-2与P3)、年龄(>60岁与<60岁)、播散肿瘤体积(直径>2.5 cm与<2.5 cm)以及组织学类型(高分化与低分化类型)均不影响生存。Cox比例模型表明细胞减灭的完整性是最强的预后因素。不完全切除的患者死于疾病的风险比接受完全细胞减灭的患者高2.8倍。完全细胞减灭后的5年生存率为12%,不完全切除的患者为2%。4例患者存活超过5年。1例5年生存者细胞减灭不完全,但对CHPP显示完全缓解。
采用腹膜切除术和CHPP进行完全细胞减灭可能提高胃癌腹膜播散患者的生存率。该手术最适合那些有强烈意愿尽可能长期生存的患者。