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长春地辛与MER在结直肠癌中的评估。

Evaluation of vindesine and MER in colorectal cancer.

作者信息

Bedikian A Y, Valdivieso M, Maroun J, Gutterman J U, Hersh E M, Bodey G P

出版信息

Cancer. 1980 Aug 1;46(3):463-7. doi: 10.1002/1097-0142(19800801)46:3<463::aid-cncr2820460307>3.0.co;2-p.

DOI:10.1002/1097-0142(19800801)46:3<463::aid-cncr2820460307>3.0.co;2-p
PMID:6249481
Abstract

Vindesine, a derivative of vinblastine, was administered to 39 patients with advanced colorectal cancer refractory to 5-fluorouracil alone or in combination with other chemotherapeutic agents. The initial dose of vindesine was 4 mg/m2 administered intravenously (IV) over 30 minutes every two weeks. Tumor regression of more than 50% was seen in 2 and stable disease in 13 of 33 patients evaluable for response. Prior treatment with vincristine did not seem to influence response to vindesine. The median survival time was four months. The major toxic effect of vindesine was peripheral neuropathy, which occurred in 35% of patients who received two or more courses of treatment. Methanol extract residue of BCG (MER) was administered IV to 20 of 39 patients receiving vindesine without randomization in order to evaluate toxicities associated with IV MER. The most common toxic reactions to MER were fever and chills, while malaise and headaches were less common. Transient respiratory distress associated with appearance of reticulonodular pulmonary infiltrates occurred in 1 patient. Thus, MER at a dose of less than 1 mg/m2 did not seem to significantly influence the response rate to vindesine or the survival of patients. However, it appeared to ameliorate the myelosuppression caused by vindesine.

摘要

长春地辛是长春碱的衍生物,对39例单用5-氟尿嘧啶或联合其他化疗药物治疗无效的晚期结直肠癌患者进行了治疗。长春地辛的初始剂量为4mg/m²,每两周静脉注射(IV)30分钟。在可评估反应的33例患者中,2例出现超过50%的肿瘤消退,13例病情稳定。先前使用长春新碱治疗似乎不影响对长春地辛的反应。中位生存时间为4个月。长春地辛的主要毒性作用是周围神经病变,在接受两个或更多疗程治疗的患者中,35%出现该症状。为了评估与静脉注射卡介苗甲醇提取物残渣(MER)相关的毒性,在未进行随机分组的情况下,对39例接受长春地辛治疗的患者中的20例静脉注射了MER。对MER最常见的毒性反应是发热和寒战,而不适和头痛则较少见。1例患者出现与网状结节状肺浸润相关的短暂呼吸窘迫。因此,剂量小于1mg/m²的MER似乎不会显著影响长春地辛的反应率或患者的生存率。然而,它似乎改善了长春地辛引起的骨髓抑制。

相似文献

1
Evaluation of vindesine and MER in colorectal cancer.长春地辛与MER在结直肠癌中的评估。
Cancer. 1980 Aug 1;46(3):463-7. doi: 10.1002/1097-0142(19800801)46:3<463::aid-cncr2820460307>3.0.co;2-p.
2
Sequential phase II studies of chemotherapy for colorectal cancer with 5-fluorouracil and vindesine with or without methyl-1,3 cis(2 chloroethyl)-1-nitrosourea.采用5-氟尿嘧啶和长春地辛联合或不联合甲基-1,3-顺式(2-氯乙基)-1-亚硝基脲对结直肠癌进行化疗的序贯II期研究。
Am J Clin Oncol. 1982 Aug;5(4):421-7. doi: 10.1097/00000421-198208000-00013.
3
Phase II evaluation of vindesine in the treatment of colorectal and esophageal tumors.长春地辛治疗结直肠癌和食管癌的II期评估。
Cancer Chemother Pharmacol. 1979;2(4):263-6. doi: 10.1007/BF00257192.
4
Broad phase II study of vindesine.
Cancer Treat Rep. 1981 Sep-Oct;65(9-10):877-9.
5
Initial clinical studies of vindesine.长春地辛的初步临床研究。
Cancer Treat Rep. 1981 Sep-Oct;65(9-10):873-5.
6
Phase II study of vindesine in patients with advanced breast cancer.
Cancer Treat Rep. 1982 Sep;66(9):1729-32.
7
Phase I evaluation of vindesine in children: a Southwest Oncology Group pilot study.长春地辛在儿童中的I期评估:西南肿瘤协作组的一项试点研究。
Med Pediatr Oncol. 1980;8(3):243-50. doi: 10.1002/mpo.2950080306.
8
Vindesine in the treatment of refractory breast cancer: improvement in therapeutic index with continuous 5-day infusion.
Cancer Treat Rep. 1981 Sep-Oct;65(9-10):775-9.
9
Therapeutic efficacy and pharmacokinetics of vindesine and vindesine-cisplatin in previously treated patients with non-small cell lung carcinoma.
Cancer Chemother Pharmacol. 1983;10(2):104-8. doi: 10.1007/BF00446219.
10
Treatment of advanced breast cancer with mitomycin C combined with vinblastine or vindesine.
J Clin Oncol. 1983 Dec;1(12):772-5. doi: 10.1200/JCO.1983.1.12.772.

引用本文的文献

1
Cardiotoxicity of chemotherapeutic agents: incidence, treatment and prevention.化疗药物的心脏毒性:发生率、治疗与预防
Drug Saf. 2000 Apr;22(4):263-302. doi: 10.2165/00002018-200022040-00002.
2
Vindesine: phase II evaluation in colon cancer and description of its platelet stimulating activity.
Cancer Chemother Pharmacol. 1982;9(1):41-4. doi: 10.1007/BF00296760.