The treatment outcome of multiple myeloma patients ineligible for hematopoietic transplantation-a single institutional experience in Taiwan

被引:7
作者
Huang, Tzu-Chuan [1 ]
Chen, Jia-Hong [1 ,5 ]
Wu, Yi-Ying [1 ,4 ]
Chang, Ping-Ying [1 ]
Dai, Ming-Shen [1 ]
Chao, Tsu-Yi [1 ,2 ]
Kao, Woei-Yau [1 ,3 ]
Chen, Yeu-Chin [1 ]
Ho, Ching-Liang [1 ]
机构
[1] Triserv Gen Hosp, Natl Def Med Ctr, Dept Med, Div Hematol Oncol, Taipei 114, Taiwan
[2] Taipei Med Univ, Shuang Ho Hosp, Div Hematol Oncol, Dept Med, Taipei, Taiwan
[3] Buddhist Tzu Chi Gen Hosp, Dept Med, Div Hematol Oncol, Taipei Branch, Taipei, Taiwan
[4] Natl Def Med Ctr, Grad Inst Life Sci, Taipei, Taiwan
[5] Taipei Med Univ, Grad Inst Clin Med, Coll Med, Taipei, Taiwan
关键词
Multiple myeloma; Hematopoietic transplantation; Bortezomib; Infection; Overall survival; ELDERLY-PATIENTS; STAGING SYSTEM; HERPES-ZOSTER; THALIDOMIDE; DEXAMETHASONE; BORTEZOMIB; MELPHALAN; PREDNISONE; ACYCLOVIR; SURVIVAL;
D O I
10.1007/s00277-014-2165-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiple myeloma (MM) is characterized by the neoplastic proliferation of monoclonal plasma cells in the bone marrow and results in complications. In Taiwan, melphalan and several novel agents are used to treat myeloma patients who are not candidate for hematopoietic stem cell transplant (HSCT). This retrospective study aimed to evaluate the characteristics, treatment outcome, and prognostic factors of MM patients who were ineligible for HSCT at our institution from October 2000 until November 2012. A total of 101 MM patients were reviewed. The median age was 71.0 years, and median overall survival (OS) was 22.0 months. Most of patients were diagnosed as IgG-type myeloma (55.4 %). The initial presentations included anemia (89.1 %), skeletal events (49.5 %), severe renal insufficiency (30.7 %), and hypercalcemia (28.7 %). With regard to the frontline therapy, thalidomide/steroid was the most common. Infection was the leading cause of death and adverse effects. Treatment with bortezomib, almost in the second- or third-line setting, was associated with longer median OS (35.5 months) and the median time to progression (TTP) (6.0 months). Bortezomib treatment, chemotherapy, International Staging System (ISS) stage I, and better performance status significantly correlated with survival benefit. In the bortezomib-treated subgroup, better treatment response caused excellent median OS (67.7 months) and also significantly delayed TTP. Therefore, this current analysis concluded a median OS of 22 months in myeloma patients ineligible for HSCT at our institution during the past 10 years. The use of bortezomib with better treatment response also achieved significantly better median OS and TTP.
引用
收藏
页码:107 / 115
页数:9
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