Body J J, Bartl R, Burckhardt P, Delmas P D, Diel I J, Fleisch H, Kanis J A, Kyle R A, Mundy G R, Paterson A H, Rubens R D
Institut J. Bordet, Université Libre de Bruxelles, Brussels, Belgium.
J Clin Oncol. 1998 Dec;16(12):3890-9. doi: 10.1200/JCO.1998.16.12.3890.
The purpose of this article is to review the recent data on bisphosphonate use in oncology and to provide some guidelines on the indications for their use in cancer patients.
The group consensus reached by experts on the rationale for the use of bisphosphonates in cancer patients and their current indications for the treatment of tumor-induced hypercalcemia and metastatic bone pain in advanced disease and for the prevention of the complications of multiple myeloma and of metastatic bone disease are reviewed.
Bisphosphonates are potent inhibitors of tumor-induced osteoclast-mediated bone resorption. They now constitute the standard treatment for cancer hypercalcemia, for which we recommend a dose of 1,500 mg of clodronate or 90 mg of pamidronate; the latter compound is more potent and has a longer lasting effect. Intravenous bisphosphonates exert clinically relevant analgesic effects in patients with metastatic bone pain. Regular pamidronate infusions can also achieve a partial objective response by conventional International Union Against Cancer criteria and enhance the objective response rate to chemotherapy. In breast cancer, the prolonged administration of oral clodronate 1,600 mg daily reduces the frequency of morbid skeletal events by more than one fourth, whereas monthly pamidronate infusions of 90 mg for only 1 year in addition to chemotherapy reduce by more than one third the frequency of all skeletal-related events. The use of bisphosphonates to prevent bone metastases remains experimental. Last, bisphosphonates in addition to chemotherapy are superior to chemotherapy alone in patients with stages II and III multiple myeloma and can reduce the skeletal morbidity rate by approximately one half.
Bisphosphonate use is a major therapeutic advance in the management of the skeletal morbidity caused by metastatic breast cancer or multiple myeloma, although many questions remain unanswered, notably regarding the optimal selection of patients and the duration of treatment.
本文旨在回顾双膦酸盐在肿瘤学领域的最新应用数据,并为癌症患者使用双膦酸盐提供一些指征指导。
回顾了专家就癌症患者使用双膦酸盐的理论依据及其目前在治疗晚期疾病的肿瘤诱导性高钙血症和转移性骨痛以及预防多发性骨髓瘤和转移性骨病并发症方面的指征所达成的小组共识。
双膦酸盐是肿瘤诱导的破骨细胞介导的骨吸收的有效抑制剂。它们现已成为癌症高钙血症的标准治疗药物,对于此我们推荐使用1500mg氯膦酸盐或90mg帕米膦酸盐;后一种化合物效力更强且作用持续时间更长。静脉注射双膦酸盐对转移性骨痛患者具有临床相关的镇痛作用。定期输注帕米膦酸盐还可根据传统的国际抗癌联盟标准实现部分客观缓解,并提高化疗的客观缓解率。在乳腺癌中,每日口服1600mg氯膦酸盐的长期给药可使病理性骨骼事件的发生率降低超过四分之一,而除化疗外每月输注90mg帕米膦酸盐仅1年可使所有骨骼相关事件的发生率降低超过三分之一。使用双膦酸盐预防骨转移仍处于试验阶段。最后,在II期和III期多发性骨髓瘤患者中,双膦酸盐联合化疗优于单纯化疗,可使骨骼发病率降低约一半。
双膦酸盐的使用是转移性乳腺癌或多发性骨髓瘤所致骨骼疾病管理方面的一项重大治疗进展,尽管许多问题仍未得到解答,尤其是关于患者的最佳选择和治疗持续时间。