• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Carcinogenicity of antineoplastic agents in man.

作者信息

Rieche K

出版信息

Cancer Treat Rev. 1984 Mar;11(1):39-67. doi: 10.1016/0305-7372(84)90016-1.

DOI:10.1016/0305-7372(84)90016-1
PMID:6375862
Abstract

Review of the literature shows that: Anticancer drugs are in all probability mostly also carcinogenic. Alkylating agents such as melphalan, chlorambucil and cyclophosphamide seem to lead to the highest rate of second malignancies. Second malignancies after antitumour drugs are mostly acute leukaemias. Conditions which could influence the carcinogenicity of an antitumour drug are (a) its carcinogenic potency; (b) long-term administration; (c) the total dose used and (d) long-term survival of the patient. Irradiation and chemotherapy seem to have the greatest carcinogenic potential, e.g. in malignant lymphomas. The role of immunosuppression as a co-carcinogenic factor is difficult to estimate. Although transplant patients on anticancer drugs for immunosuppression have a higher risk of reticulosarcomas, but not of solid tumours, there is no evidence to suppose that in general immunosuppression and carcinogenicity are directly related. There is no reason to abandon intensive chemotherapy regimes if they lead to significant therapeutic results on the grounds of possible carcinogenicity of these drugs.

摘要

相似文献

1
Carcinogenicity of antineoplastic agents in man.
Cancer Treat Rev. 1984 Mar;11(1):39-67. doi: 10.1016/0305-7372(84)90016-1.
2
Second cancers following antineoplastic therapy.抗肿瘤治疗后的二次癌症。
Curr Probl Cancer. 1985 Feb;9(2):1-43. doi: 10.1016/s0147-0272(85)80033-7.
3
[Secondary carcinoma: a complication of cytostatic therapy?].[继发性癌:细胞毒性疗法的一种并发症?]
Med Klin. 1979 Oct 5;74(40):1422-30.
4
Malignancies induced by drug therapy: a review.药物治疗引起的恶性肿瘤:综述
IARC Sci Publ. 1986(78):13-27.
5
Carcinogenic effects of chemotherapeutic compounds.化疗化合物的致癌作用。
Prog Clin Biol Res. 1992;374:167-74.
6
Occurrence of second tumors in man after anticancer drug treatment.抗癌药物治疗后人类继发性肿瘤的发生情况。
Cancer Treat Rev. 1982 Sep;9(3):167-94. doi: 10.1016/s0305-7372(82)80006-6.
7
Risk of acute nonlymphocytic leukemia and preleukemia in patients treated with cyclophosphamide for non-Hodgkin's lymphomas. Comparison with results obtained in patients treated for Hodgkin's disease and ovarian carcinoma with other alkylating agents.接受环磷酰胺治疗的非霍奇金淋巴瘤患者发生急性非淋巴细胞白血病和白血病前期的风险。与接受其他烷化剂治疗的霍奇金病和卵巢癌患者的结果比较。
Ann Intern Med. 1985 Aug;103(2):195-200. doi: 10.7326/0003-4819-103-2-195.
8
Secondary malignancies following cancer chemotherapy.
Acta Oncol. 1994;33(6):591-8. doi: 10.3109/02841869409121767.
9
Second neoplasm--a complication of cancer chemotherapy.第二原发性肿瘤——癌症化疗的一种并发症。
N Engl J Med. 1977 Jul 28;297(4):213-5. doi: 10.1056/NEJM197707282970411.
10
Carcinogenic action of anticancer drugs with special reference to immunosuppression.抗癌药物的致癌作用,特别提及免疫抑制。
Cancer. 1977 Oct;40(4 Suppl):1927-9. doi: 10.1002/1097-0142(197710)40:4+<1927::aid-cncr2820400825>3.0.co;2-s.

引用本文的文献

1
Diosbulbin C, a novel active ingredient in Dioscorea bulbifera L. extract, inhibits lung cancer cell proliferation by inducing G0/G1 phase cell cycle arrest.黄独素 C,从黄药子(Dioscorea bulbifera L.)提取物中提取的一种新型活性成分,通过诱导 G0/G1 期细胞周期阻滞抑制肺癌细胞增殖。
BMC Complement Med Ther. 2023 Dec 4;23(1):436. doi: 10.1186/s12906-023-04245-9.
2
Frequency and component analysis of contaminants generated in preparation of anticancer agents using closed system drug transfer devices (CSTDs).使用密闭式药物传输装置(CSTD)制备抗癌药物时产生的污染物的频率和成分分析。
Sci Rep. 2022 Jan 7;12(1):139. doi: 10.1038/s41598-021-03780-0.
3
Intraductally administered pegylated liposomal doxorubicin reduces mammary stem cell function in the mammary gland but in the long term, induces malignant tumors.
经导管给予的聚乙二醇化脂质体阿霉素可降低乳腺中的乳腺干细胞功能,但长期来看,会诱导恶性肿瘤。
Breast Cancer Res Treat. 2012 Aug;135(1):201-8. doi: 10.1007/s10549-012-2138-x. Epub 2012 Jul 1.
4
Risk of second breast cancer in female Hodgkin's lymphoma survivors: a meta-analysis.女性霍奇金淋巴瘤幸存者罹患第二乳腺癌的风险:一项荟萃分析。
BMC Cancer. 2012 May 28;12:197. doi: 10.1186/1471-2407-12-197.
5
The anti-tumour activity of ifosfamide on heterotransplanted testicular cancer cell lines remains unaltered by the uroprotector mesna.异环磷酰胺对异种移植睾丸癌细胞系的抗肿瘤活性不受尿路保护剂美司钠的影响。
Br J Cancer. 1994 May;69(5):863-7. doi: 10.1038/bjc.1994.167.
6
Biological and environmental monitoring of occupational exposure of pharmaceutical plant workers to methotrexate.制药厂工人职业接触甲氨蝶呤的生物与环境监测
Int Arch Occup Environ Health. 1994;65(6):401-3. doi: 10.1007/BF00383251.
7
Risk of leukaemia associated with cancer chemotherapy.癌症化疗相关的白血病风险。
Br Med J (Clin Res Ed). 1985 Jan 26;290(6464):261-3. doi: 10.1136/bmj.290.6464.261.
8
Chronic myelocytic leukemia as a secondary malignant condition in a patient receiving prolonged chemotherapy for ovarian carcinoma.慢性粒细胞白血病作为一名接受卵巢癌长期化疗患者的继发性恶性疾病。
West J Med. 1985 Aug;143(2):243.
9
Sjögren's syndrome and fibrosing alveolitis complicated by pulmonary lymphoma.干燥综合征与合并肺淋巴瘤的纤维化肺泡炎。
Ann Rheum Dis. 1987 Sep;46(9):701-5. doi: 10.1136/ard.46.9.701.
10
Synthesis, antitumor activity, distribution and toxicity of 4-[4-[bis(2-chloroethyl)amino]phenyl]-1-hydroxybutane-1 1-bisphosphonic acid (BAD), a new lost derivative with increased accumulation in rat osteosarcoma.4-[4-[双(2-氯乙基)氨基]苯基]-1-羟基丁烷-1,1-双膦酸(BAD)的合成、抗肿瘤活性、分布及毒性研究,BAD是一种新型的膦酸盐衍生物,在大鼠骨肉瘤中蓄积增加
J Cancer Res Clin Oncol. 1986;111(3):209-19. doi: 10.1007/BF00389236.