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裸鼠肝脏中人类结肠肿瘤的抗转移术中化疗

Antimetastatic intraoperative chemotherapy of human colon tumors in the livers of nude mice.

作者信息

Rashidi B, An Z, Sun F X, Moossa A R, Hoffman R M

机构信息

AntiCancer, Inc., San Diego, California 92111, USA.

出版信息

Clin Cancer Res. 2000 Jun;6(6):2464-8.

Abstract

We have developed a new antimetastatic chemotherapeutic strategy for combination with hepatic resection of human colon cancers in a high-metastasis nude mouse model. The new procedure involves i.p. administration of 5-fluorouracil (5-FU) 2 h before hepatic resection of the human colon tumors, with therapy continued postoperatively for 4 consecutive days. We termed this strategy neo-neoadjuvant chemotherapy. The regime significantly prolonged animal survival compared with preoperative 5-FU neoadjuvant therapy, 5-FU postoperative adjuvant therapy, surgery alone, 5-FU without surgery, or the untreated control. The median survival of neo-neoadjuvant i.p. 5-FU-treated group was 81 days, compared with 27 days for the control group (P < 0.009). The median survival of animals in the neoadjuvant group was 37 days (P < 0.021 compared with the control group). There was also a significant difference between the median survival of neo-neoadjuvant, and the neoadjuvant group (P < 0.031). When all animals in the control group had died, 70% of animals with neo-neoadjuvant and 60% of animals with neoadjuvant 5-FU were still alive (P < 0.003 and P < 0.011, respectively). When all animals with neoadjuvant 5-FU treatment had died, 70% of animals with neo-neoadjuvant treatment were still alive (P < 0.003). Survival of all other treatment groups, including 5-FU without surgery, surgery alone, and adjuvant postoperative chemotherapy, was not significantly different from the untreated control group. Two animals in the neo-neoadjuvant group were free of tumors when sacrificed at days 154 and 165 post surgery. Whereas 100% of animals in the control, 90% in the 5-FU alone, 70% in the surgery alone, 60% in the 5-FU adjuvant, and 40% in the neoadjuvant groups had metastases in the lymph nodes draining the liver, only 10% of animals in the neo-neoadjuvant group had metastases. These data suggest that the neo-neoadjuvant therapy increased survival by preventing metastasis of cancer cells not removed in the liver resection procedure. The results of this study indicate that the neo-neoadjuvant treatment strategy for resection of colon cancer liver metastasis should be explored clinically.

摘要

我们已开发出一种新的抗转移化疗策略,用于在高转移裸鼠模型中与人类结肠癌肝切除术联合使用。新方法包括在人类结肠肿瘤肝切除术前2小时腹腔注射5-氟尿嘧啶(5-FU),术后连续4天继续治疗。我们将此策略称为新辅助化疗。与术前5-FU新辅助治疗、5-FU术后辅助治疗、单纯手术、未手术的5-FU治疗或未治疗的对照组相比,该方案显著延长了动物生存期。新辅助腹腔注射5-FU治疗组的中位生存期为81天,而对照组为27天(P<0.009)。新辅助组动物的中位生存期为37天(与对照组相比,P<0.021)。新辅助组与新辅助治疗组的中位生存期之间也存在显著差异(P<0.031)。当对照组所有动物死亡时,新辅助组70%的动物和新辅助5-FU组60%的动物仍存活(分别为P<0.003和P<0.011)。当所有接受新辅助5-FU治疗的动物死亡时,新辅助治疗组70%的动物仍存活(P<0.003)。所有其他治疗组,包括未手术的5-FU治疗、单纯手术和术后辅助化疗,其生存期与未治疗的对照组无显著差异。新辅助组有两只动物在术后第154天和165天处死时无肿瘤。对照组100%的动物、单纯5-FU组90%的动物、单纯手术组70%的动物、5-FU辅助组60%的动物以及新辅助组40%的动物在引流肝脏的淋巴结中有转移,而新辅助组只有10%的动物有转移。这些数据表明,新辅助治疗通过预防肝切除术中未切除的癌细胞转移来提高生存期。本研究结果表明,结肠癌肝转移切除的新辅助治疗策略应进行临床探索。

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