Bisphosphonate-associated osteonecrosis of mandibular and maxillary bone - An emerging oral complication of supportive cancer therapy

被引:350
作者
Migliorati, CA
Schubert, MM
Peterson, DE
Seneda, LM
机构
[1] Nova SE Univ, Coll Dent Med, Dept Diagnost Sci, Ft Lauderdale, FL 33328 USA
[2] Univ Washington, Dept Oral Med, Sch Dent, Seattle, WA 98195 USA
[3] Seattle Canc Care Alliance, Oral Med Serv, Seattle, WA USA
[4] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[5] Univ Connecticut, Ctr Hlth, Dept Oral Hlth & Diagnost Sci, Sch Dent Med, Farmington, CT USA
[6] Univ Connecticut, Ctr Hlth, Ctr Canc, Farmington, CT USA
[7] Hosp Sirio Libanes, Ctr Oncol, Oral Med Clin, Sao Paulo, Brazil
关键词
osteonecrosis; bisphosphonates; jaws; cancer metastasis; skeletal metastasis; oral complication; osteoporosis;
D O I
10.1002/cncr.21130
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The current report presented 17 patients with cancer with bone metastases and 1 patient with osteopenia who received treatment with bisphos phonates and who subsecluently developed osteonecrosis of the mandible and/or maxilla. METHODS. The authors reviewed information on 18 patients who were referred to oral medicine or oral surgery specialists for evaluation and treatment of mandibular and/or maxitlary bone necrosis from June 2002 to September 2004. To be included in the current review, patients must have been treated with either pamidronate or zoledronic acid to control or prevent metastatic disease, or with alendronate for osteoporosis. All patients with cancer had received chemotherapy while receiving bisphosphonate management. RESULTS. The 17 patients with cancer were receiving active medical care for a malignancy. Cancer treatment included a variety of chemotherapeutic agents. They presented with metastatic disease to bone and were treated intravenously with the bisphosphonates pamidronate or zoledronic acid for a mean time of 25 months (range, 4-41 mos). There were 14 females and 4 males with a mean age of 62 years (range, 37-74 yrs). Malignancies included breast carcinoma (n = 10), multiple myeloma (n = 3), prostate carcinoma (n = 1), ovarian carcinoma (n = 1), prostate carcinoma/ lymphoma (n = 1), and breast/ovarian carcinoma (n = 1). One female patient with osteopenia received alendronate. The most common clinical osteonecrosis presentations included infection and necrotic bone in the mandible. Associated events included dental extractions, infection, and trauma. Two patients appeared to develop disease spontaneously, without any clinical or radiographic evidence of local pathology. Despite surgical intervention, antibiotic therapy, hyperbaric oxygen therapy, and topical use of chemotherapeutic mouth rinses, most of the lesions did not respond well to therapy. Discontinuation of bisphosphonate therapy did not assure heating. However, I patient with cancer healed after discontinuation of bisphosphonate therapy for 4 months. CONCLUSIONS. The findings in the patient population combined with recent literature reports suggested that bisphosphonates may contribute to the pathogenesis of the oral lesions. The risk factors and precise mechanism involved in the formation of the osteonecrosis are not known. This condition represents a new oral complication in patients with cancer and can be termed bisphosphonate-associated osteonecrosis. Lesions in patients with osteoporosis are worrisome and need to be further evaluated. (c) 2005 American Cancer Society.
引用
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页码:83 / 93
页数:11
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