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[癌细胞与骨的相遇。癌症治疗引起的骨质流失:CTIBL]

[Encounter of cancer cells with bone. Cancer treatment-induced bone loss : CTIBL].

作者信息

Takahashi Shunji

机构信息

Department of Medical Oncology, Cancer Institute Hospital, Japanese Fonundation for Cancer Research.

出版信息

Clin Calcium. 2011 Mar;21(3):447-53.

Abstract

Various cancer treatments can cause gonadal dysfunction and bone loss. Especially, endocrine therapies for breast cancer or prostate cancer carry a significant risk of cancer treatment-induced bone loss (CTIBL) . LHRH agonist- or chemotherapy-induced premature menopause in premenopausal breast cancer patients, aromatase inhibitor in postmenopausal breast cancer patients, and LHRH agonist with or without anti-androgen in prostate cancer patients may cause bone loss of 5% or more within several years. Oral or intravenous bisphosphonates are effective for prevention of CTIBL, and RANKL antibody (denosumab) is also effective. During treatment, physicians should follow bone mineral density and avoid QOL impairment due to osoteoporosis.

摘要

各种癌症治疗都可能导致性腺功能障碍和骨质流失。特别是,乳腺癌或前列腺癌的内分泌治疗具有引发癌症治疗所致骨质流失(CTIBL)的重大风险。绝经前乳腺癌患者使用促性腺激素释放激素(LHRH)激动剂或化疗导致的过早绝经、绝经后乳腺癌患者使用芳香化酶抑制剂,以及前列腺癌患者使用LHRH激动剂联合或不联合抗雄激素药物,都可能在数年内导致5%或更多的骨质流失。口服或静脉注射双膦酸盐对预防CTIBL有效,抗核因子κB受体活化因子配体(RANKL)抗体(地诺单抗)也有效。在治疗期间,医生应监测骨矿物质密度,并避免因骨质疏松导致生活质量受损。

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