Bone-Specific Alkaline Phosphatase Levels among Patients with Multiple Myeloma Receiving Various Therapy Options

被引:6
|
作者
Cetin, Guven [1 ]
Eskazan, Ahmet Emre [2 ]
Ar, M. Cem [3 ]
Aydin, Seniz Ongoren [4 ]
Ferhanoglu, Burhan [4 ]
Soysal, Teoman [4 ]
Baslar, Zafer [4 ]
Aydin, Yildiz [4 ]
机构
[1] Bezmialem Vakif Univ, Fac Med, Dept Internal Med, Div Hematol, Istanbul, Turkey
[2] Diyarbakir Training & Res Hosp, Diyarbakir, Turkey
[3] Istanbul Training & Res Hosp, Istanbul, Turkey
[4] Istanbul Univ, Cerrahpasa Fac Med, Dept Internal Med, Div Hematol, Istanbul, Turkey
关键词
Multiple myeloma; Bone-specific alkaline phosphatase; Bortezomib; Thalidomide; BIOCHEMICAL MARKERS; KAPPA-B; BORTEZOMIB; DEXAMETHASONE; DISEASE; GROWTH; COMBINATION; THALIDOMIDE; PREDNISONE; METABOLISM;
D O I
10.4274/tjh.2013.0004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: This study aimed to investigate the impact of the different therapy regimens used in multiple myeloma (MM) on bone-specific alkaline phosphatase (BALP) levels. Materials and Methods: One hundred and thirteen patients with MM were included in the study. Patients were grouped according to the regimens they received, as follows: group 1, melphalan and prednisolone (MP); group 2, vincristine, adriablastin, and dexamethasone (VAD); group 3, thalidomide plus dexamethasone; and group 4, bortezomib plus dexamethasone. BALP levels were measured before treatment and at the third and sixth months of treatment. A fifth group consisted of patients in the post-treatment remission period at study entry (no-treatment group). Results: The BALP levels at the third and sixth months of the treatment were significantly higher than the pre-treatment levels in the bortezomib and the no-treatment groups, whereas no significant difference was observed in the MP, VAD, and thalidomide groups. Conclusion: Considering that BALP is a surrogate marker of bone formation, our study suggests efficiently leads to the improvement of bone disease in myeloma than other treatment options.
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页码:374 / 380
页数:7
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