Usefulness of bone metabolic markers in the diagnosis and follow-up of bone metastasis from lung cancer

被引:58
作者
Aruga, A
Koizumi, M
Hotta, R
Takahashi, S
Ogata, E
机构
[1] CANC INST HOSP,DEPT NUCL MED,TOSHIMA KU,TOKYO 171,JAPAN
[2] CANC INST HOSP,DEPT RADIOL,TOSHIMA KU,TOKYO 171,JAPAN
[3] CANC INST HOSP,DEPT CHEMOTHERAPY,TOSHIMA KU,TOKYO 171,JAPAN
[4] CANC INST HOSP,DEPT INTERNAL MED,TOSHIMA KU,TOKYO 171,JAPAN
关键词
lung cancer; bone metastasis; ICTP; fDPD; BAL;
D O I
10.1038/bjc.1997.458
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ninety-one lung cancer patients were evaluated to determine the usefulness of bone metabolic markers in the diagnosis and follow-up of bone metastases and also to investigate their clinical usefulness as an adjunct to bone scintigraphy. Both bone resorption markers, ICTP and fDPD, and bone formation markers, Al-p, BAL, PICP and BGP, were evaluated in 47 patients with and 44 without bone metastasis. The patients with bone metastasis were classified according to the bone metastatic burden, and they were also separately classified into groups according to the course of the bone metastasis. ICTP, fDPD, Al-p and BAL were significantly elevated (P < 0.001) in patients with bone metastasis, but PICP and BGP were not. Receiver-operating characteristic (ROC) curves of these markers revealed that ICTP was most highly correlated with the diagnosis of bone metastasis. The sensitivity of ICTP (71.4%) and fDPD (61.0%) were good with high specificity. T scores of ICTP, fDPD and BAL tended to be higher at higher grades of bone metastasis. T-scores of ICTP, fDPD and BAL were elevated in the newly diagnosed cases and progressed cases, but the T-scores of ICTP and fDPD in those cases were higher than that of BAL. In the follow-up study, ICTP was well correlated with uncontrolled or controlled bone metastasis. Thus, bone resorption markers, especially ICTP, could be a good indicator of the progression and multiplicity of disease, and it could help in the follow-up and in the monitoring of therapy for bone metastasis from lung cancer.
引用
收藏
页码:760 / 764
页数:5
相关论文
共 14 条
[1]  
ABRAMS HL, 1950, CANCER, V3, P74, DOI 10.1002/1097-0142(1950)3:1<74::AID-CNCR2820030111>3.0.CO
[2]  
2-7
[3]   Markers of type I collagen degradation and synthesis in the monitoring of treatment response in bone metastases from breast carcinoma [J].
Blomqvist, C ;
Risteli, L ;
Risteli, J ;
Virkkunen, P ;
Sarna, S ;
Elomaa, I .
BRITISH JOURNAL OF CANCER, 1996, 73 (09) :1074-1079
[4]   PRELIMINARY-RESULTS OF THE USE OF URINARY-EXCRETION OF PYRIDINIUM CROSS-LINKS FOR MONITORING METASTATIC BONE-DISEASE [J].
COLEMAN, RE ;
HOUSTON, S ;
JAMES, I ;
RODGER, A ;
RUBENS, RD ;
LEONARD, RCF ;
FORD, J .
BRITISH JOURNAL OF CANCER, 1992, 65 (05) :766-768
[5]   SERUM CONCENTRATION OF THE CROSS-LINKED CARBOXYTERMINAL TELOPEPTIDE OF TYPE-I COLLAGEN (ICTP) IS A USEFUL PROGNOSTIC INDICATOR IN MULTIPLE-MYELOMA [J].
ELOMAA, I ;
VIRKKUNEN, P ;
RISTELI, L ;
RISTELI, J .
BRITISH JOURNAL OF CANCER, 1992, 66 (02) :337-341
[6]   ASSESSMENT OF BONE-RESORPTION WITH A NEW MARKER OF COLLAGEN DEGRADATION IN PATIENTS WITH METABOLIC BONE-DISEASE [J].
GARNERO, P ;
GINEYTS, E ;
RIOU, JP ;
DELMAS, PD .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (03) :780-785
[7]   BONE METABOLIC MARKERS IN BONE METASTASES [J].
KOIZUMI, M ;
YAMADA, Y ;
TAKIGUCHI, T ;
NOMURA, E ;
FURUKAWA, M ;
KITAHARA, T ;
YAMASHITA, T ;
MAEDA, H ;
TAKAHASHI, S ;
AIBA, K ;
OGATA, E .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1995, 121 (9-10) :542-548
[8]   Dissociation of bone formation markers in bone metastasis of prostate cancer [J].
Koizumi, M ;
Maeda, H ;
Yoshimura, K ;
Yamauchi, T ;
Kawai, T ;
Ogata, E .
BRITISH JOURNAL OF CANCER, 1997, 75 (11) :1601-1604
[9]   TYPE-I COLLAGEN DEGRADATION PRODUCT (ICTP) GIVES INFORMATION ABOUT THE NATURE OF BONE METASTASES AND HAS PROGNOSTIC VALUE IN PROSTATE-CANCER [J].
KYLMALA, T ;
TAMMELA, TLJ ;
RISTELI, L ;
RISTELI, J ;
KONTTURI, M ;
ELOMAA, I .
BRITISH JOURNAL OF CANCER, 1995, 71 (05) :1061-1064
[10]   Correlation between bone metabolic markers and bone scan in prostatic cancer [J].
Maeda, H ;
Koizumi, M ;
Yoshimura, K ;
Yamauchi, T ;
Kawai, T ;
Ogata, E .
JOURNAL OF UROLOGY, 1997, 157 (02) :539-543