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周剂量紫杉醇联合LFP方案治疗晚期食管癌的临床观察

The Clinical Observation of Weekly Paclitaxel Combined with LFP for Treating Advanced Esophageal Carcinoma
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摘要 目的 评价周剂量紫杉醇(PTX)联合氟脲嘧啶(5-Fu)、顺铂(DDP)和醛氢叶酸(CF)组成PLFP方案治疗晚期食管癌的临床疗效和毒副反应。方法 16例Ⅲ、Ⅳ期晚期食管癌,给予周剂量PTX+LFP(CF+5-Fu+DDP),即PTX 80 mg/m^2,iv gtt qw,连续2周;DDP 80 mg/m^2,iv gtt,d3-5;5-Fu 500 mg/m^2,iv gtt,d1-5;CF100 mg/次,iv gtt,在5-Fu前2 h内给药,d1-5,21 d为1周期,2周期后按UICC标准评价近期疗效和毒副反应。结果 全组16例,全都可评价疗效,总有效率56.3%,11例初治组有效率为63.6%,其中CR 1例。5例复治组有效率为40%。毒副反应主要为剂量限制性毒性,表现为Ⅱ~Ⅲ度为主的骨髓抑制。结论 周剂量紫杉醇联合氟脲嘧啶、顺铂和醛氢叶酸组成的PLFP方案可能是治疗晚期食管癌较好的化疗方案,值得进一步观察。 Objective To evaluate the efficacy and toxicity of weekly paelitaxel(PTX) combined with 5-fluorouracil(5-Fu) , DDP and CF as alternative chemotherapy for patients with advanced esophageal carcinoma. Methods Sixteen patients were enrolled in the study. Each was treated as follows: PTX 80 mg/m^2 infusion per week for two weeks; DDP 80 mg/m^2 infusion , d1-3 or d1-5 ; 5-Fu 500 mg/m^2 infusion, d1-5 ; CF 100 mg/d infusion 2 hours before 5-Fu infusion, d1- 5; After 2 consecutive treatment course, each for 21 days, evaluation of the short-term efficacy and adverse effects was carried out. Results The overall response rate were 43.8% . The response rates of 11 patients in primary treatment were 63.6% ( 1 ease CR) and that of relapse treatment was 40% . The dose-limited toxicity was mild and mainly expressed as bone marrow depression(grade Ⅱ -Ⅲ ). Conclusions Weekly paclitaxel(PTX) combined with 5-fluorouracil(5-Fu) , DDP and CF as alternative chemotherapy is encouraging for patients with advanced esophageal carcinoma.
出处 《肿瘤基础与临床》 2007年第5期403-405,共3页 journal of basic and clinical oncology
关键词 食管肿瘤 紫杉醇 氟脲嘧啶 顺铂 醛氢叶酸 化疗 esophageal neoplasm paelitaxel 5-fluorouracil cisplatin leucovorin chemotherapy
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  • 1中国肿瘤防治研究办公室卫生部统计信息中心.中国试点市、县恶性肿瘤的发病与死亡[M].北京:中国医药科技出版社,2002.28-34.
  • 2Richel DJ,Vervenne WL.Systemic treatment of esophageal cancer[J].Eur Gastroenterol Hepatol,2004,16(3):249-254.
  • 3Polee MB,Eskens FA,van der Burg ME,et al.Phase Ⅱ study of bi-weekly administration of paclitaxel and cisplatin in patients with advanced oesophageal cancer[J].Br J Cancer,2002,86(5):669-673.
  • 4周际昌.实用肿瘤内科学[M].2版.北京:人民卫生出版社,2002:343-346.
  • 5肖毅军,陈小兵,罗素霞.紫杉醇每周疗法联合LFP方案治疗34例晚期食管癌[J].肿瘤学杂志,2004,10(6):422-424. 被引量:9

二级参考文献9

  • 1[1]Kingston DG, Samaranayake G, Lvey CA. The chemistry of Taxol, a clinically useful anticancer agent [J]. J Nat Prod, 1990, 53(1): 1-5.
  • 2[2]Klauber N, Parangi S, Flynn E, et al. Inhibition of angio genesis and breast cancer in mice by the microtubule inhibitors 2-Methoxyestradiol and paclitaxel [J]. Cancer Res, 1997, 57(1): 81-84.
  • 3[3]Ajani JA, Ilson DH, Dangherty K, et al. Activity of taxol in patients with sqamous cell carcinoma and adenocarcinoma of the esophagus [J]. J Natl Cancer Inst, 1994, 86 (4): 1086-1090.
  • 4[4]Ajani JA. Contributions of chemotherapy in the treatment of carcinoma of the esophagus: results and commentary[J]. J Semin Oncol, 1994, 21(4): 474-479.
  • 5[5]Ilson DH, Ajani J, Bhalla K, et al. Phase Ⅱ trial of paclitaxel, fluorouracil, and cisplatin in patients with advanced carcinoma of the esophagus [J]. J Clin Oncol, 1998, 16(5):1826-1831.
  • 6[6]Murad AM, Tinoeo LA, Guimares RC, et al. Paclitaxel (T) plus 5-fluorouracil (5-Fu): a novel and very active regimen for advanced gastric cancer (Agastric cancer). A phase Ⅱ trial [J]. Proc Annu Meet Am Soe Clin Oncol,1997, 16(A): 1063-1065.
  • 7[7]Perej EA, Vogel CL, Irwin DH, et al. Multicenter phase Ⅱ trial of weekly paclitaxel in women with metastasis breast cancer [J]. J Clin Oncol, 2001, 19(22): 4216-4220.
  • 8[8]Murad AM. Phase Ⅱ trial of combination of paelitaxel and 5-Fluorouracil in the treatment of advanced gastric cancer [J]. South Am J Cancer, 1998, 2(1): 35-39.
  • 9[9]Bisse MC, Nohnek G, Sandeftnk GJ. et al. Doeetaxel (Taxotere): a review of preclinical and clinical experience [J]. Anticancer Drugs, 1995, 6: 339-342.

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