Prevention of Cardiotoxicities With Traditional and Novel Chemotherapeutic Agents

被引:6
|
作者
Sharalaya Z. [1 ]
Collier P. [1 ]
机构
[1] Robert and Suzanne Tomsich Department of Cardiovascular Medicine, Sydell and Arnold Miller Family Heart and Vascular Institute, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Desk J1-5, Cleveland, 44195, OH
关键词
Anthracycline; Cardiomyopathy; Cardiotoxicity; Chemotherapy; Heart failure; Novel chemotherapeutics; Prevention;
D O I
10.1007/s11897-018-0400-1
中图分类号
学科分类号
摘要
Purpose of Review: This review will discuss strategies to prevent cardiotoxicity associated with chemotherapeutics. Forty years ago, investigators identified dose-dependent cardiotoxicity related to anthracycline-based regimens. Over recent decades, the development of more selective, mechanism-based chemotherapeutics has been associated with both on-target and off-target adverse cardiovascular sequelae. Recent Findings: Strategies to prevent or attenuate cardiotoxicities include limitation of anthracycline dose, appropriate patient selection, referral/access to cardio-oncology programs, early recognition of cardiac side effects, active cardio-surveillance, cardio-protective medical therapy, treatment-specific concerns, and follow-up. The importance of accurate diagnosis of cardiotoxicity is important as false-positive testing may result in inappropriate holding or stopping potentially life-saving chemotherapy. Data to support use of cardio-protective medical therapy to prevent chemotherapy-related cardiotoxicity is modest at best, limited by marginal effect size, small patient numbers, and short follow-up. Summary: The rapid growth in cardio-oncology clinics may facilitate larger multi-center randomized controlled trials in this area. © 2018, Springer Science+Business Media, LLC, part of Springer Nature.
引用
收藏
页码:260 / 269
页数:9
相关论文
共 50 条
  • [21] Natural Products and Chemotherapeutic Agents on Cancer: Prevention vs. Treatment
    Wang, Chong-Zhi
    Zhang, Zhiyu
    Anderson, Samantha
    Yuan, Chun-Su
    AMERICAN JOURNAL OF CHINESE MEDICINE, 2014, 42 (06): : 1555 - 1558
  • [22] CHEMOTHERAPEUTIC AGENTS
    OTTO, GF
    JOURNAL OF THE AMERICAN VETERINARY MEDICAL ASSOCIATION, 1969, 154 (04) : 387 - &
  • [23] CHEMOTHERAPEUTIC AGENTS
    LOURIE, EM
    ANNUAL REVIEW OF MICROBIOLOGY, 1947, 1 : 237 - 262
  • [24] Interactions of radiation with novel chemotherapeutic agents: Taxanes and nucleoside analogs
    Milas, L
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1997, 39 (02): : 131 - 131
  • [25] Inhibitors of calpain as novel chemotherapeutic agents for prostate cancer.
    Eilon, GF
    Gu, J
    Hara, K
    Jacobs, JW
    CLINICAL CANCER RESEARCH, 1999, 5 : 3789S - 3789S
  • [26] Discovery of novel chemotherapeutic agents and identification of new mechanisms of action
    Takada, Mamoru
    Yamada, Hideyuki
    Takano, Shigetsugu
    Ohtsuka, Masayuki
    CANCER SCIENCE, 2023, 114 : 81 - 81
  • [27] The use of combinatorial chemistry methodologies to discover novel chemotherapeutic agents
    Edwards, Paul J.
    DRUG DISCOVERY TODAY, 2009, 14 (1-2) : 108 - 110
  • [28] Hsp90 inhibitors as novel cancer chemotherapeutic agents
    Neckers, L
    TRENDS IN MOLECULAR MEDICINE, 2002, 8 (04) : S55 - S61
  • [29] Compounds with potentialities as novel chemotherapeutic agents in leishmaniasis at preclinical level
    Gonzalez-Matos, Maikel
    Aguado, Mirtha Elisa
    Izquierdo, Maikel
    Monzote, Lianet
    Gonzalez-Bacerio, Jorge
    EXPERIMENTAL PARASITOLOGY, 2024, 260
  • [30] Novel ceramide analogs as potential chemotherapeutic agents in breast cancer
    Struckhoff, AP
    Bittman, R
    Burow, ME
    Clejan, S
    Elliott, S
    Hammond, T
    Tang, Y
    Beckman, BS
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2004, 309 (02): : 523 - 532