Bone resorption predicts for skeletal complications in metastatic bone disease

被引:122
作者
Brown, JE
Thomson, CS
Ellis, SP
Gutcher, SA
Purohit, OP
Coleman, RE [1 ]
机构
[1] Weston Pk Hosp, Canc Res Ctr, Acad Unit Clin Oncol, Sheffield S10 2SJ, S Yorkshire, England
[2] Weston Pk Hosp, Trent Canc Registry, Sheffield S10 2SJ, S Yorkshire, England
关键词
metastatic bone disease; bone markers; N-telopeptide; Ntx; skeletal-related events;
D O I
10.1038/sj.bjc.6601437
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Relationships between the rate of bone resorption (measured by urinary N-telopeptide (Ntx) excretion) and a range of skeletal complications have been evaluated in patients with metastatic bone disease. A total of 12 1 patients had monthly measurements of Ntx during treatment with bisphosphonates. All skeletal-related events, plus hospital admissions for bone pain and death during the period of observation, were recorded. Data were available for 12 1 patients over the first 3-month period of monitoring (0-3 months) and 95 patients over the second 3-month period (4-6 months). N-telopeptide levels were correlated with the number of skeletal-related events and/or death (r = 0.62, P < 0.001 for 0-3 months and r = 0.46, P < 0.001 for 4-6 months, respectively). Patients with baseline Ntx values greater than or equal to100 nmol mmol(-1) creatinine (representing clearly accelerated bone resorption) were 19.48 times (95% CI 7.55, 50.22) more likely to experience a skeletal-related event/death during the first 3 months than those with Ntx < 100 (P < 0.001). In a multivariate logistic regression model, Ntx was highly predictive for events/death. This study is the first to indicate a strong correlation between the rate of bone resorption and the frequency of skeletal complications in metastatic bone disease. N-telopeptide appears useful in the prediction of patients most likely to experience skeletal complications and thus benefit from bisphosphonate treatment.
引用
收藏
页码:2031 / 2037
页数:7
相关论文
共 24 条
[1]  
ALI SM, 2000, P AM SOC CLIN ONCOL, V19
[2]  
Armitage P., 2001, STAT METHODS MED RES, V4th
[3]  
Berenson JR, 2001, CANCER, V91, P1191, DOI 10.1002/1097-0142(20010401)91:7<1191::AID-CNCR1119>3.0.CO
[4]  
2-0
[5]   THE CLINICAL COURSE OF BONE METASTASES FROM BREAST-CANCER [J].
COLEMAN, RE ;
RUBENS, RD .
BRITISH JOURNAL OF CANCER, 1987, 55 (01) :61-66
[6]   The usefulness of bone turnover in predicting the response to transdermal estrogen therapy in postmenopausal osteoporosis [J].
Gonnelli, S ;
Cepollaro, C ;
Pondrelli, C ;
Martini, S ;
Monaco, R ;
Gennari, C .
JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 (04) :624-631
[7]  
Greenfield DM, 2000, BONE MARKERS BIOCH C, P225
[8]  
HANSON DA, 1992, J BONE MINER RES, V7, P1251
[9]   Pharmacoeconomic issues in bisphosphonate treatment of metastatic bone disease [J].
Hillner, BE .
SEMINARS IN ONCOLOGY, 2001, 28 (04) :64-68
[10]   Efficacy of pamidronate in reducing skeletal complications in patients with breast cancer and lytic bone metastases [J].
Hortobagyi, GN ;
Theriault, RL ;
Porter, L ;
Blayney, D ;
Lipton, A ;
Sinoff, C ;
Wheeler, H ;
Simeone, JF ;
Seaman, J ;
Knight, RD ;
Heffernan, M ;
Reitsma, DJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (24) :1785-1791