Bone metastases: Pathogenesis, treatment, and rationale for use of resorption inhibitors Journal Article


Authors: Scher, H. I.; Yagoda, A.
Article Title: Bone metastases: Pathogenesis, treatment, and rationale for use of resorption inhibitors
Abstract: Tumors in bone are usually metastatic, with breast, prostate, and lung tumors accounting for more than 80 percent of clinically manifest lesions. Untreated, such metastases can produce the symptoms that most concern cancer patients-pain, pathologic fractures, and paralysis through epidural cord compression. Recent advances in the understanding of the metastatic cascade and the regulation of bone formation and resorption provide unique therapeutic approaches for prevention and treatment of these lesions. This article reviews the prevalence, distribution, diagnosis, and treatment of metastatic cancer in the skeleton, as well as the processes involved in the development of such metastases, the local mediators responsible for some of the destructive changes in bone, and their pathologic results. In addition to considering some of the conventional therapeutic approaches, a rationale for the use of bone resorption inhibitors, such as the diphosphonates (bisphosphonates), is presented for the prevention and amelioration of the pathologic consequences of skeletal metastases. © 1987.
Keywords: bone neoplasms; bone tumor; osteolysis; prednisone; review; multimodality cancer therapy; bone metastasis; pathophysiology; combined modality therapy; metabolism; metastasis; pain; bisphosphonic acid derivative; calcitonin; drug effect; spinal cord compression; short survey; drug therapy; diphosphonates; bone resorption; clodronic acid; mithramycin; fractures, spontaneous; etidronic acid; pathologic fracture; human; support, non-u.s. gov't; support, u.s. gov't, p.h.s.
Journal Title: The American Journal of Medicine
Volume: 82
Issue: 2 Suppl. 1
ISSN: 0002-9343
Publisher: Elsevier Inc.  
Date Published: 1987-02-23
Start Page: 6
End Page: 28
Language: English
DOI: 10.1016/0002-9343(87)90483-9
PUBMED: 3548343
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 5 February 2021 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Howard Scher
    1130 Scher
  2. Alan Yagoda
    51 Yagoda