Early lymphocyte recovery predicts longer survival after autologous peripheral blood stem cell transplantation in multiple myeloma

被引:51
作者
Kim, H.
Sohn, H-J
Kim, S.
Lee, J-S
Kim, W-K
Suh, C.
机构
[1] Univ Ulsan, Dept Internal Med, ASAN Med Ctr, Coll Med,Div Oncol, Seoul 138736, South Korea
[2] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Div Hematol Oncol, Ulsan 680749, South Korea
关键词
lymphocyte; multiple myeloma; survival; peripheral blood stem cell transplantation;
D O I
10.1038/sj.bmt.1705373
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
To understand the prognostic value of lymphocyte recovery after autologous peripheral blood stem cell transplantation (APBSCT), we performed a retrospective study of 59 newly diagnosed multiple myeloma (MM) patients who underwent frontline APBSCT. Conditioning regimens were melphalan 100 mg/m(2) for 2 days. Following APBSCT, all patients showed complete or partial response. Median follow-up time was 29.57 months and median recovery of absolute lymphocyte count (ALC) >= 1000/mm(3) was 23 days. Univariate analysis revealed that significant predictors of overall survival (OS) included bone marrow (BM) plasma cells <= 40% at diagnosis (P = 0.0243) and recovery of ALC >= 1000/mm(3) by day +23 (P = 0.0156). Positive predictors for progression-free survival (PFS) were BM plasma cells <= 40% at diagnosis (P = 0.0134) and recovery of ALC >= 1000/mm3 by day +23 (P + 0.0243). Absolute neutrophil count >= 1000/mm3 on day +12 was marginally significant for OS and PFS (P = 0.0821 and P = 0.1153, respectively). Multivariate analysis showed that ALC >= 1000/mm(3) on day +23 independently predicted OS (P = 0.031) and prolonged PFS (P = 0.011), and that serum beta 2-microglobulin was marginally significant for prolonged OS (P = 0.066). In conclusion, ALC recovery was an independent predictor of both OS and PFS in MM.
引用
收藏
页码:1037 / 1042
页数:6
相关论文
共 33 条
[1]   A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma [J].
Attal, M ;
Harousseau, JL ;
Stoppa, AM ;
Sotto, JJ ;
Fuzibet, JG ;
Rossi, JF ;
Casassus, P ;
Maisonneuve, H ;
Facon, T ;
Ifrah, N ;
Payen, C ;
Bataille, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (02) :91-97
[2]   Treatment of multiple myeloma [J].
Barlogie, B ;
Shaughnessy, J ;
Tricot, G ;
Jacobson, J ;
Zangari, M ;
Anaissie, E ;
Walker, R ;
Crowley, J .
BLOOD, 2004, 103 (01) :20-32
[3]   Hypodiploidy and 22q11 rearrangements at diagnosis are associated with poor prognosis in patients with multiple myeloma [J].
Calasanz, MJ ;
Cigudosa, JC ;
Odero, MD ;
GarciaFoncillas, J ;
Marin, J ;
Ardanaz, MT ;
Rocha, E ;
Gullon, A .
BRITISH JOURNAL OF HAEMATOLOGY, 1997, 98 (02) :418-425
[4]   The t(4;14) is associated with poor prognosis in myeloma patients undergoing autologous stem cell transplant [J].
Chang, H ;
Sloan, S ;
Li, D ;
Zhuang, LH ;
Yi, QL ;
Chen, CI ;
Reece, D ;
Chun, K ;
Stewart, AK .
BRITISH JOURNAL OF HAEMATOLOGY, 2004, 125 (01) :64-68
[5]   High-dose chemotherapy with hematopoietic stem-cell rescue for multiple myeloma [J].
Child, JA ;
Morgan, GJ ;
Davies, FE ;
Owen, RG ;
Bell, SE ;
Hawkins, K ;
Brown, J ;
Drayson, MT ;
Selby, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (19) :1875-1883
[6]   Outcomes for reduced-intensity allogeneic transplantation for multiple myeloma:: an analysis of prognostic factors from the Chronic Leukaemia Working Party of the EBMT [J].
Crawley, C ;
Lalancette, M ;
Szydlo, R ;
Gilleece, M ;
Peggs, K ;
Mackinnon, S ;
Juliusson, G ;
Ahlberg, L ;
Nagler, A ;
Shimoni, A ;
Sureda, A ;
Boiron, JM ;
Einsele, H ;
Chopra, R ;
Carella, A ;
Cavenagh, J ;
Gratwohl, A ;
Garban, F ;
Zander, A ;
Björkstrand, B ;
Niederwieser, D ;
Gahrton, G ;
Apperley, JF .
BLOOD, 2005, 105 (11) :4532-4539
[7]   Dendritic cells - Dendritic cell recovery after autologous stem cell transplantation [J].
Damiani, D ;
Stocchi, R ;
Masolini, P ;
Michelutti, A ;
Sperotto, A ;
Geromin, A ;
Skert, C ;
Cerno, M ;
Michieli, M ;
Baccarani, M ;
Fanin, R .
BONE MARROW TRANSPLANTATION, 2002, 30 (05) :261-266
[8]  
Desikan R, 2000, BLOOD, V95, P4008
[9]   Both hypodiploidy and deletion of chromosome 13 independently confer poor prognosis in multiple myeloma [J].
Fassas, ABT ;
Spencer, T ;
Sawyer, J ;
Zangari, M ;
Lee, CK ;
Anaissie, E ;
Muwalla, F ;
Morris, C ;
Barlogie, B ;
Tricot, G .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 118 (04) :1041-1047
[10]  
Hernandez MD, 1998, MED CLIN-BARCELONA, V110, P768