SHOULD BISPHOSPHONATES BE PART OF THE STANDARD THERAPY OF PATIENTS WITH MULTIPLE-MYELOMA OR BONE METASTASES FROM OTHER CANCERS - AN EVIDENCE-BASED REVIEW

Authors
Citation
Dj. Bloomfield, SHOULD BISPHOSPHONATES BE PART OF THE STANDARD THERAPY OF PATIENTS WITH MULTIPLE-MYELOMA OR BONE METASTASES FROM OTHER CANCERS - AN EVIDENCE-BASED REVIEW, Journal of clinical oncology, 16(3), 1998, pp. 1218-1225
Citations number
42
Categorie Soggetti
Oncology
ISSN journal
0732183X
Volume
16
Issue
3
Year of publication
1998
Pages
1218 - 1225
Database
ISI
SICI code
0732-183X(1998)16:3<1218:SBBPOT>2.0.ZU;2-D
Abstract
Purpose: To review objectively the evidence for the use of bisphosphon ates for the reduction of skeletal events or the management of pain du e to multiple myeloma or bone metastases from other types of cancer. M ethods: MEDLINE was searched from 1976 onwards using the MeSH terms '' exp diphosphonates/,'' ''exp bone neoplasms/,'' ''exp multiple myeloma /,'' and ''bone metastases'' as text words. Bibliographies of reports on these topics and major medical and scientific journals were searche d. Experts in the field were approached. The question was defined and the evidence stratified in a hierarchical manner according to classifi cation of study design. There were sufficient studies to enable the us e of randomized trials only to address the questions. Effectiveness wa s defined and the evidence reviewed in a systematic manner. Results an d Conclusion: Eighteen randomized trials were identified. No meta-anal yses are available. There is level I evidence (defined as an appropria tely conducted randomized clinical trial with a statistically signific ant result) for the use of bisphosphonates to reduce both skeletal eve nts and pain in multiple myeloma and in breast cancer patients with me tastatic bone disease. There is also level I evidence for their use as part of a pain management program for bone metastases from carcinoma of the breast, lung, and prostate, and for symptomatic myeloma. The bi sphosphonates appear to be well tolerated. (C) 1998 by American Societ y of Clinical Oncology.