Mayo Clinic consensus statement for the use of bisphosphonates in multiple myeloma

被引:165
作者
Lacy, Martha Q.
Dispenzieri, Angela
Gertz, Morie A.
Greipp, Philip R.
Gollbach, Kimberly L.
Hayman, Suzanne R.
Kumar, Shaji
Lust, John A.
Rajkumar, S. Vincent
Russell, Stephen J.
Witzig, Thomas E.
Zeldenrust, Steven R.
Dingli, David
Bergsagel, P. Lief
Fonseca, Rafael
Reeder, Craig B.
Stewart, A. Keith
Roy, Vivek
Dalton, Robert J.
Carr, Alan B.
Kademani, Deepak
Keller, Eugene E.
Vilozzi, Christopher V.
Kyle, Robert A.
机构
[1] Mayo Clin & Mayo Fdn, Coll Med, Div Hematol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Coll Med, Dept Dent Specialties, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Coll Med, Div Oral Diagnosis & Oral & Maxillofacial Surg, Rochester, MN 55905 USA
[4] Mayo Clin, Coll Med, Div Hematol Oncol, Scottsdale, AZ USA
[5] Mayo Clin, Coll Med, Div Hematol Oncol, Jacksonville, FL USA
[6] Mayo Hlth Syst, Div Med Oncol, Mankato, MN USA
关键词
D O I
10.4065/81.8.1047
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bisphosphonates are effective in the prevention and treatment of bone disease in multiple myeloma (MM). Osteonecrosis of the jaw is increasingly recognized as a serious complication of long-term bisphosphonate therapy. Issues such as the choice of bisphosphonate and duration of therapy have become the subject of intense debate given patient safety concerns. We reviewed available data concerning the use of bisphosphonates in MM. Guidelines for the use of bisphosphonates in MM were developed by a multidisciplinary panel consisting of hematologists, dental specialists, and nurses specializing in the treatment of MM. We conclude that intravenous pamidronate and intravenous zoledronic acid are equally effective and superior to placebo in reducing skeletal, complications. Pamidronate is favored over zoledronic acid until more data are available on the risk of complications (osteonecrosis of the jaw). We recommend discontinuing bisphosphonates after 2 years of therapy for patients who achieve complete response and/or plateau phase. For patients whose disease is active, who have not achieved a response, or who have threatening bone disease beyond 2 years, therapy can be decreased to every 3 months. These guidelines were developed in the interest of patient safety and will be reexamined as new data emerge regarding risks and benefits.
引用
收藏
页码:1047 / 1053
页数:7
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