Osteoporosis due to cancer treatment: Pathogenesis and management

被引:277
作者
Pfeilschifter, J
Diel, IJ
机构
[1] Ruhr Univ Bochum, Berufsgenossenschaftliche Kliniken Bergmannsheil, Dept Internal Med, D-4630 Bochum, Germany
[2] Heidelberg Univ, Dept Obstet Gynecol, Heidelberg, Germany
关键词
D O I
10.1200/JCO.2000.18.7.1570
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Many therapeutic regimens in cancer treatment carry the risk of causing or favoring the development of osteoporosis. Therapies in which hypogonadism may occur are most relevant in this respect. Prompt hormone replacement therapy is indicated in these patients. In patients in whom this is undesirable because of a hormone-dependent tumor, the risk of osteoporosis should be assessed by means of osteodensitometry, and prophylactic or therapeutic measures should be instituted if necessary. Early intervention improves outcome because osteoporosis therapy is most effective in preventing deterioration of bone mass. There remains much uncertainty in assessing the risk of combination chemotherapy with regard to the development of osteoporosis. Negative effects on the skeleton have, however, been demonstrated far individual drugs, such as methotrexate and ifosfamide, Negative effects of the tumor itself on bone metabolism may aggravate the degree of osteoporosis, Detailed data and long-term experience to assess the risk are urgently needed in this area and constitute an important research topic for the coming years and decades. This review discusses the mast prevalent mechanisms of osteoporosis caused by cancer treatment and outlines therapeutic strategies for the prevention and treatment of therapy-induced bone loss. (C) 2000 by American Society of Clinical Oncology.
引用
收藏
页码:1570 / 1593
页数:24
相关论文
共 305 条
[1]  
ABE O, 1992, LANCET, V339, P71
[2]   Intermittent etidronate therapy to prevent corticosteroid-induced osteoporosis [J].
Adachi, JD ;
Bensen, WG ;
Brown, J ;
Hanley, D ;
Hodsman, A ;
Josse, R ;
Kendler, DL ;
Lentle, B ;
Olszynski, W ;
SteMarie, LG ;
Tenenhouse, A ;
Chines, AA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (06) :382-387
[3]  
ADACHI JD, 1994, J RHEUMATOL, V21, P1922
[4]   THE ACUTE-PHASE RESPONSE AFTER BISPHOSPHONATE ADMINISTRATION [J].
ADAMI, S ;
BHALLA, AK ;
DORIZZI, R ;
MONTESANTI, F ;
ROSINI, S ;
SALVAGNO, G ;
LOCASCIO, V .
CALCIFIED TISSUE INTERNATIONAL, 1987, 41 (06) :326-331
[5]   Adverse effects of bisphosphonates - A comparative review [J].
Adami, S ;
Zamberlan, N .
DRUG SAFETY, 1996, 14 (03) :158-170
[6]   ESTROGEN REPLACEMENT THERAPY FOR PREVENTION OF OSTEOPOROSIS AFTER OOPHORECTOMY [J].
AITKEN, JM ;
HART, DM ;
LINDSAY, R .
BMJ-BRITISH MEDICAL JOURNAL, 1973, 3 (5879) :515-518
[7]  
AKBER J, 1988, AM J PEDIAT HEMATOL, V10, P258
[8]   THYROID-HORMONES AND BONE [J].
ALLAIN, TJ ;
MCGREGOR, AM .
JOURNAL OF ENDOCRINOLOGY, 1993, 139 (01) :9-18
[9]  
Appelbaum FR, 1997, J RHEUMATOL, V24, P41
[10]   CHEMOTHERAPY-INDUCED PREMATURE OVARIAN FAILURE - MECHANISMS AND PREVENTION [J].
ATAYA, K ;
MOGHISSI, K .
STEROIDS, 1989, 54 (06) :607-626