Berenson J R, Lichtenstein A, Porter L, Dimopoulos M A, Bordoni R, George S, Lipton A, Keller A, Ballester O, Kovacs M J, Blacklock H A, Bell R, Simeone J, Reitsma D J, Heffernan M, Seaman J, Knight R D
West Los Angeles Veterans Affairs Medical Center, CA 90073, USA.
N Engl J Med. 1996 Feb 22;334(8):488-93. doi: 10.1056/NEJM199602223340802.
Skeletal complications are a major clinical manifestation of multiple myeloma. These complications are caused by soluble factors that stimulate osteoclasts to resorb bone. Bisphosphonates such as pamidronate inhibit osteoclastic activity and reduce bone resorption.
Patients with stage III multiple myeloma and at least one lytic lesion received either placebo or pamidronate (90 mg) as a four-hour intravenous infusion given every four weeks for nine cycles in addition to antimyeloma therapy. The patients were stratified according to whether they were receiving first-line (stratum 1) or second-line (stratum 2) antimyeloma chemotherapy at entry into the study. Skeletal events (pathologic fracture, irradiation of or surgery on bone, and spinal cord compression), hypercalcemia (symptoms or a serum calcium concentration > or = 12 mg per deciliter [3.0 mmol per liter]), bone pain, analgesic-drug use, performance status, and quality of life were assessed monthly.
Among 392 treated patients, the efficacy of treatment could be evaluated in 196 who received pamidronate and 181 who received placebo. The proportion of patients who had any skeletal events was significantly lower in the pamidronate group (24 percent) than in the placebo group (41 percent, P < 0.001), and the reduction was evident in both stratum 1 (P = 0.04) and stratum 2 (P = 0.004). The patients who received pamidronate had significant decreases in bone pain and no deterioration in performance status and quality of life. Pamidronate was tolerated well.
Monthly infusions of pamidronate provide significant protection against skeletal complications and improve the quality of life of patients with stage III multiple myeloma.
骨骼并发症是多发性骨髓瘤的主要临床表现。这些并发症由刺激破骨细胞吸收骨质的可溶性因子引起。帕米膦酸等双膦酸盐可抑制破骨细胞活性并减少骨质吸收。
III期多发性骨髓瘤且至少有一处溶骨性损害的患者,除接受抗骨髓瘤治疗外,每四周接受一次安慰剂或帕米膦酸(90毫克)静脉输注,持续4小时,共九个周期。患者根据进入研究时接受一线(第1层)或二线(第2层)抗骨髓瘤化疗进行分层。每月评估骨骼事件(病理性骨折、骨骼照射或手术以及脊髓压迫)、高钙血症(症状或血清钙浓度≥12毫克/分升[3.0毫摩尔/升])、骨痛、镇痛药使用、体能状态和生活质量。
在392例接受治疗的患者中,可对196例接受帕米膦酸治疗的患者和181例接受安慰剂治疗的患者进行疗效评估。帕米膦酸组发生任何骨骼事件的患者比例(24%)显著低于安慰剂组(41%,P<0.001),在第1层(P=0.04)和第2层(P=0.004)中降低均明显。接受帕米膦酸治疗的患者骨痛显著减轻,体能状态和生活质量没有恶化。帕米膦酸耐受性良好。
每月输注帕米膦酸可显著预防骨骼并发症,并改善III期多发性骨髓瘤患者的生活质量。