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高剂量亚叶酸对5-氟尿嘧啶的生物学调节作用以及5-氟尿嘧啶与顺铂联合化疗在转移性结直肠腺癌中的应用

Biologic modulation of 5-fluorouracil with high-dose leucovorin and combination chemotherapy of 5-fluorouracil and cisplatin in metastatic colorectal adenocarcinoma.

作者信息

Petrelli N J, Madajewicz S, Herrera L, Rustum Y M, Trave F, Creaven P, Mittelman A

机构信息

Department of Surgical Oncology, Roswell Park Memorial Institute, Buffalo, NY 14263.

出版信息

NCI Monogr. 1987(5):189-92.

PMID:3501541
Abstract

The data from an ongoing 3-arm prospective study of 72 patients with advanced colorectal carcinoma is presented. The 3 regimens are as follows: Regime 1 (every 4 weeks)--5-fluorouracil (FUra) (450 mg/m2 iv bolus daily for 5 days, then 200 mg/m2 iv bolus every other day for 6 doses); regime 2 (every week for 4 weeks, then every other week)--methotrexate (MTX) (50 mg/m2 in a 4-hour infusion) followed by FUra (600 mg/m2 iv bolus); regime 3 (weekly for 6 weeks followed by a 2-week rest period)--D,L-leucovorin (D,L-CF) (500 mg/m2 in a 2-hour infusion) with FUra (600 mg/m2 iv bolus) 1 hour after the D,L-CF infusion began. All monitoring lesions except lung were documented by tissue biopsy. Thirteen of 18 patients in the FUra + D,L-CF arm were evaluable for response. Six of the 13 patients (46%) have had a partial response. The duration of the 6 responses has been 11, 8, 7, 4, 3 and 3 months. In patients with liver metastases as the monitoring lesion, a dramatic improvement in liver function tests has been seen during the first 2 courses (12 weeks) of treatment, but this was not sustained. The toxicity of FUra + D,L-CF was predominantly gastrointestinal; unlike with FUra alone, myelosuppression was not predominant.

摘要

本文展示了一项正在进行的针对72例晚期结直肠癌患者的三臂前瞻性研究的数据。三种治疗方案如下:方案1(每4周一次)——5-氟尿嘧啶(FUra)(450mg/m²静脉推注,每日1次,共5天,然后每隔日200mg/m²静脉推注,共6剂);方案2(第1至4周每周一次,之后每两周一次)——甲氨蝶呤(MTX)(50mg/m²静脉滴注4小时),随后给予FUra(600mg/m²静脉推注);方案3(每周一次,共6周,之后休息2周)——亚叶酸钙(D,L-CF)(500mg/m²静脉滴注2小时),在D,L-CF开始输注1小时后给予FUra(600mg/m²静脉推注)。除肺部外的所有监测病灶均通过组织活检记录。FUra + D,L-CF组的18例患者中有13例可评估疗效。13例患者中有6例(46%)出现部分缓解。6例缓解患者的缓解持续时间分别为11、8、7、4、3和3个月。以肝转移灶作为监测病灶的患者,在治疗的前2个疗程(12周)肝功能检查有显著改善,但未持续。FUra + D,L-CF的毒性主要为胃肠道毒性;与单用FUra不同,骨髓抑制并不突出。

相似文献

1
Biologic modulation of 5-fluorouracil with high-dose leucovorin and combination chemotherapy of 5-fluorouracil and cisplatin in metastatic colorectal adenocarcinoma.高剂量亚叶酸对5-氟尿嘧啶的生物学调节作用以及5-氟尿嘧啶与顺铂联合化疗在转移性结直肠腺癌中的应用
NCI Monogr. 1987(5):189-92.
2
Schedule-selective biochemical modulation of 5-fluorouracil: a phase II study in advanced colorectal cancer.5-氟尿嘧啶的时间选择性生化调节:晚期结直肠癌的II期研究
Clin Cancer Res. 1995 Sep;1(9):955-60.
3
A phase II trial of 5-fluorouracil and high-dose leucovorin in gastric carcinoma and a phase I trial of intraperitoneal 5-fluorouracil and leucovorin.一项关于5-氟尿嘧啶和高剂量亚叶酸在胃癌中的II期试验以及一项关于腹腔内5-氟尿嘧啶和亚叶酸的I期试验。
NCI Monogr. 1987(5):203-5.
4
A Northern California Oncology Group randomized trial of leucovorin plus 5-fluorouracil versus sequential methotrexate, 5-fluorouracil, and leucovorin in patients with advanced colorectal cancer who failed treatment with 5-fluorouracil or 5-fluorodeoxyuridine alone.
NCI Monogr. 1987(5):175-7.
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Clinical studies of biochemical modulation of 5-fluorouracil by leucovorin in patients with advanced colorectal cancer by the North Central Cancer Treatment Group and Mayo Clinic.由北中部癌症治疗组和梅奥诊所开展的关于亚叶酸对晚期结直肠癌患者5-氟尿嘧啶进行生化调节的临床研究。
NCI Monogr. 1987(5):185-8.
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Treatment of advanced colorectal and gastric adenocarcinomas with 5-fluorouracil and high-dose folinic acid.用5-氟尿嘧啶和高剂量亚叶酸治疗晚期结直肠癌和胃腺癌。
NCI Monogr. 1987(5):193-8.
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Cisplatin, etoposide, and weekly high-dose 5-fluorouracil and leucovorin infusion (PE-HDFL)--a very effective regimen with good patients' compliance for advanced gastric cancer.顺铂、依托泊苷以及每周一次的大剂量5-氟尿嘧啶和亚叶酸钙静脉输注(PE-HDFL)——一种对晚期胃癌非常有效的治疗方案,患者依从性良好。
Anticancer Res. 1998 Mar-Apr;18(2B):1267-72.
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A phase II study of weekly methotrexate, cisplatin, and 24-hour infusion of high-dose 5-fluorouracil and leucovorin (MP-HDFL) in patients with metastatic and recurrent esophageal cancer-improving toxicity profile by infusional schedule and double biochemical modulation of 5-fluorouracil.一项针对转移性和复发性食管癌患者的II期研究,采用每周一次甲氨蝶呤、顺铂以及24小时大剂量5-氟尿嘧啶和亚叶酸钙静脉输注(MP-HDFL)方案——通过输注方案和5-氟尿嘧啶的双重生化调节改善毒性反应。
Anticancer Res. 2002 Nov-Dec;22(6B):3621-7.
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Double modulation with methotrexate and L-leucovorin of weekly 24- hour fluorouracil infusion in fluorouracil-refractory colorectal cancer.
Anticancer Res. 1996 Sep-Oct;16(5B):3101-4.
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A prospective randomized trial of 5-fluorouracil versus 5-fluorouracil and high-dose leucovorin versus 5-fluorouracil and methotrexate in previously untreated patients with advanced colorectal carcinoma.一项针对既往未经治疗的晚期结直肠癌患者,比较5-氟尿嘧啶、5-氟尿嘧啶与高剂量亚叶酸钙、5-氟尿嘧啶与甲氨蝶呤疗效的前瞻性随机试验。
J Clin Oncol. 1987 Oct;5(10):1559-65. doi: 10.1200/JCO.1987.5.10.1559.

引用本文的文献

1
Experimental studies on potentiation of the antitumor activity of 5-fluorouracil with 3'-azido-3'-deoxythymidine for the gastric cancer cell line MKN28 in vivo.体内对胃癌细胞系MKN28进行5-氟尿嘧啶与3'-叠氮基-3'-脱氧胸苷联合增强抗肿瘤活性的实验研究。
Jpn J Cancer Res. 1997 Jan;88(1):97-102. doi: 10.1111/j.1349-7006.1997.tb00307.x.