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利塞膦酸盐治疗骨Paget病病变的改善:一项放射学研究。

Improvement of pagetic bone lesions with risedronate treatment: a radiologic study.

作者信息

Brown J P, Chines A A, Myers W R, Eusebio R A, Ritter-Hrncirik C, Hayes C W

机构信息

Le Centre Hospitalier Universitaire de Quebec, Sainte-Foy, Canada.

出版信息

Bone. 2000 Mar;26(3):263-7. doi: 10.1016/s8756-3282(99)00271-9.

Abstract

Risedronate is a potent pyridinyl bisphosphonate in clinical development for treatment and prevention of osteoporosis, and has been recently approved for treatment of Paget's disease in the United States. An open-label study was conducted to determine the effect of risedronate treatment on pagetic bone lesions in patients with moderate to severe Paget's disease (mean serum alkaline phosphatase levels [ALP] approximately seven times the upper limit of normal). Patients were treated with 30 mg/day oral risedronate for 84 days followed by a 112-day nontreatment period. This 196-day cycle was repeated once in patients whose ALP did not normalize or who experienced relapse, defined as a > or =25% increase in ALP from the lowest value measured. Radiographs of affected anatomical sites in 26 patients were collected at baseline, 6 months, and/or 12 months. Eleven patients received one course and 15 patients received two courses of treatment. Radiographs were examined by a skeletal radiologist who was blinded to their time sequence. Changes in pagetic lesions were categorized as "improved," "deteriorated," or "no change." Between baseline and 6 months, 16 patients improved and 3 deteriorated; at 12 months, 11 patients improved and 2 deteriorated. Most lesions remained unchanged between 6 and 12 months. Improvements were noted in all skeletal sites (tibia, femur, humerus, forearm, pelvis, spine, and skull), but were most pronounced in weight-bearing long bones. In weight-bearing bones, nine lesions had osteolytic fronts. Of these, seven improved and two remained unchanged at 6 months; at 12 months, all but one lesion (which improved) remained unchanged. This radiographic assessment demonstrates that oral risedronate, 30 mg/day in one or two 3-month courses, is highly effective for improving bone lesions in patients with Paget's disease. Risedronate treatment had no deleterious effect on osteolytic lesions in weight-bearing bones; indeed, the majority of lesions with osteolytic fronts were improved after 6 months of risedronate treatment.

摘要

利塞膦酸盐是一种强效吡啶基双膦酸盐,正处于治疗和预防骨质疏松症的临床研发阶段,最近在美国已被批准用于治疗佩吉特病。开展了一项开放标签研究,以确定利塞膦酸盐治疗对中重度佩吉特病患者(平均血清碱性磷酸酶水平[ALP]约为正常上限的7倍)的佩吉特骨病变的影响。患者口服利塞膦酸盐30毫克/天,持续84天,随后为112天的非治疗期。对于ALP未恢复正常或出现复发(定义为ALP较所测最低值升高≥25%)的患者,重复这个196天的周期一次。在基线、6个月和/或12个月时收集了26例患者受累解剖部位的X光片。11例患者接受了一个疗程的治疗,15例患者接受了两个疗程的治疗。由一位对X光片时间顺序不知情的骨骼放射科医生对X光片进行检查。佩吉特病病变的变化分为“改善”、“恶化”或“无变化”。在基线和6个月之间,16例患者病情改善,3例恶化;在12个月时,11例患者病情改善,2例恶化。大多数病变在6至12个月之间保持不变。在所有骨骼部位(胫骨、股骨、肱骨、前臂、骨盆、脊柱和颅骨)均观察到病情改善,但在负重长骨中最为明显。在负重骨中,有9处病变有溶骨前沿。其中,7处病变在6个月时改善,2处保持不变;在12个月时,除1处病变(改善)外,其余均保持不变。这项影像学评估表明,每日30毫克、为期1个或2个3个月疗程的口服利塞膦酸盐对改善佩吉特病患者的骨病变非常有效。利塞膦酸盐治疗对负重骨的溶骨病变没有有害影响;事实上,大多数有溶骨前沿的病变在利塞膦酸盐治疗6个月后得到改善。

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