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化疗药物栓剂给药联合放疗用于直肠癌治疗

Suppository administration of chemotherapeutic drugs with concomitant radiation for rectal cancer.

作者信息

Pokorny R M, Wrightson W R, Lewis R K, Paris K J, Hofmeister A, LaRocca R, Myers S R, Ackerman D, Galandiuk S

机构信息

Price Institute of Surgical Research and Department of Surgery, University of Louisville School of Medicine, Kentucky 40292, USA.

出版信息

Dis Colon Rectum. 1997 Dec;40(12):1414-20. doi: 10.1007/BF02070704.

Abstract

PURPOSE

Preoperative radiation with combined chemotherapy is effective in shrinking advanced rectal cancer locally and facilitating subsequent surgery. Suppository delivery of 5-fluorouracil is associated with less toxicity and higher rectal tissue concentrations than intravenous administration. This prompted us to evaluate suppository and intravenous administration of 5-fluorouracil and mitomycin C with concomitant radiation to determine associated toxicity.

METHODS

Rectal, liver, lymph node, and lung tissue and systemic and portal blood were collected serially from male Sprague Dawley rats to determine drug concentrations following suppository or intravenous delivery of 5-fluorouracil or mitomycin C. Thirty-six animals were randomly assigned to treatment groups and received 5-fluorouracil suppositories, mitomycin C suppositories, or an equivalent intravenous dose of 5-fluorouracil or mitomycin C 30 minutes before radiation therapy. Before and 3, 6, 10, and 15 days following this treatment, blood was collected, colonoscopy was performed, and rectal tissue was harvested for histologic examination.

RESULTS

Mitomycin C suppository was significantly less toxic compared with intravenous delivery, and higher rectal tissue concentrations were observed from 10 to 30 minutes (P < 0.05). Compared with intravenous 5-fluorouracil administration and radiation, 5-fluorouracil suppository and radiation resulted in additive myelosuppression at day 6 (P < 0.05) with rapid recovery.

CONCLUSIONS

5-Fluorouracil and mitomycin C suppository delivery combined with radiation causes less systemic toxicity and is more effective than intravenous administration.

摘要

目的

术前放疗联合化疗可有效局部缩小晚期直肠癌并便于后续手术。与静脉给药相比,5-氟尿嘧啶栓剂给药的毒性更小且直肠组织浓度更高。这促使我们评估5-氟尿嘧啶和丝裂霉素C的栓剂及静脉给药联合同步放疗的相关毒性。

方法

从雄性Sprague Dawley大鼠身上连续采集直肠、肝脏、淋巴结和肺组织以及全身和门静脉血,以测定5-氟尿嘧啶或丝裂霉素C栓剂或静脉给药后的药物浓度。36只动物被随机分配至治疗组,并在放疗前30分钟接受5-氟尿嘧啶栓剂、丝裂霉素C栓剂或等效静脉剂量的5-氟尿嘧啶或丝裂霉素C。在该治疗前以及治疗后3、6、10和15天,采集血液、进行结肠镜检查并获取直肠组织进行组织学检查。

结果

与静脉给药相比,丝裂霉素C栓剂的毒性显著更小,且在10至30分钟时观察到更高的直肠组织浓度(P < 0.05)。与静脉给予5-氟尿嘧啶并放疗相比,5-氟尿嘧啶栓剂与放疗在第6天导致相加性骨髓抑制(P < 0.05),但恢复迅速。

结论

5-氟尿嘧啶和丝裂霉素C栓剂给药联合放疗导致的全身毒性更小,且比静脉给药更有效。

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