Danzi M, Lewin M R, Cruse J P, Clark C G
Gut. 1983 Nov;24(11):1041-7. doi: 10.1136/gut.24.11.1041.
The effects of combination chemotherapy with 5FU and BCNU on rats with dimethylhydrazine (DMH)-induced colon cancer were investigated in a long term survival study. Eighty Wistar rats received a colon cancer producing regimen on DMH (40 mg/kg body weight/week, subcutaneously for 10 weeks). After presenting with signs of colonic disease, all rats underwent diagnostic laparotomy and colonoscopy when colon tumours were located, measured and the extent of the disease staged. Only animals with tumours (n = 63) were included and allocated to one of three tumour stages. Stage A (n = 17), had colonic tumours without serosal involvement; stage B (n = 28) had serosal involvement without metastases; stage C (n = 18) had serosal involvement with lymphadenopathy and/or metastases. Each group was randomly allocated into two subgroups, one serving as untreated controls while the other received 5FU (300 mg/m2 weekly intragastrically for life) together with BCNU (40 mg/m2 intraperitoneally on days 0, 42 and 84). The effect of chemotherapy on tumour growth was measured sequentially by colonoscopy. Animals were observed until death and necropsied, when colon carcinoma was histologically confirmed and survival analysed. The results indicate that chemotherapy significantly prolongs the survival of rats with the least advanced disease (stage A) but was of no benefit to rats with locally advanced or metastatic disease (stages B and C). Furthermore, chemotherapy was associated with a significant reduction in tumour size. Survival analyses in untreated animals show that the laparotomy staging system adopted provides accurate prognostic information. This study shows that DMH-induced colon tumours are chemosensitive, and suggests that this animal model may be a valuable testing ground for new chemotherapeutic agents.
在一项长期生存研究中,研究了5-氟尿嘧啶(5FU)和卡莫司汀(BCNU)联合化疗对二甲基肼(DMH)诱导的结肠癌大鼠的影响。80只Wistar大鼠接受了DMH诱导结肠癌的方案(40mg/kg体重/周,皮下注射10周)。出现结肠疾病体征后,所有大鼠均接受诊断性剖腹术和结肠镜检查,确定结肠肿瘤的位置、测量肿瘤大小并对疾病范围进行分期。仅纳入有肿瘤的动物(n = 63),并将其分为三个肿瘤分期之一。A期(n = 17),结肠肿瘤无浆膜侵犯;B期(n = 28),有浆膜侵犯但无转移;C期(n = 18),有浆膜侵犯伴淋巴结病和/或转移。每组随机分为两个亚组,一组作为未治疗的对照组,另一组接受5FU(300mg/m²每周经胃内给药,持续终身)联合BCNU(在第0、42和84天腹腔注射40mg/m²)。通过结肠镜检查依次测量化疗对肿瘤生长的影响。观察动物直至死亡并进行尸检,组织学确诊结肠癌并分析生存率。结果表明,化疗显著延长了疾病最不严重(A期)大鼠的生存期,但对局部晚期或转移性疾病(B期和C期)大鼠没有益处。此外,化疗与肿瘤大小的显著减小有关。未治疗动物的生存分析表明,所采用的剖腹术分期系统可提供准确的预后信息。本研究表明,DMH诱导的结肠肿瘤对化疗敏感,并表明该动物模型可能是新型化疗药物的有价值的试验场。