Effects of paraprotein heavy and light chain types and free light chain load on survival in myeloma: an analysis of patients receiving conventional-dose chemotherapy in Medical Research Council UK multiple myeloma trials

被引:68
作者
Drayson, Mark
Begum, Gulnaz
Basu, Supratik
Makkuni, Sudhaker
Dunn, Janet
Barth, Nicola
Child, J. Anthony
机构
[1] Univ Birmingham, Div Immun & Infect, Sch Med, Canc Res UK Clin Trials Unit,Royal Wolverhampton, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Dept Haematol, Birmingham, W Midlands, England
[3] Univ Birmingham, Div Canc Studies, Birmingham, W Midlands, England
[4] Univ Leeds, Clin Trials Res Unit, Leeds, W Yorkshire, England
关键词
D O I
10.1182/blood-2006-03-008953
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
While investigating 2592 patients enrolled in multicenter myeloma trials, we found light chain-only (LCO) patients had worse median survival times (1.9 years) than patients with IgA and IgG paraproteins (2.3 and 2.5 years, respectively) (P < .001). However, IgA and IgG patients with levels of LC excretion similar to those of LCO patients also had poor survival times because of renal failure, resulting in worse survival during induction therapy and at relapse with no difference in progression-free survival between LCO and IgG patients. LC excretion was higher for lambda than for kappa types, but there was no difference in survival between the 2 LC types when stratified for level of LC excretion, indicating that care of renal function is vital to improving the survival of any patient with LC excretion. LCO patients were younger (P = .001), had worse performance status (P = .001), and had more lytic lesions (P < .001), perhaps reflecting late and missed diagnoses in younger and older LCO patients, respectively. No differences were observed between IgA and IgG patients in presentation characteristics, response, or survival from disease progression. The worse survival of IgA patients was attributed to shorter progression-free survival (median, 1.2 vs 1.6 years; P < .001), which is important for maintenance therapy.
引用
收藏
页码:2013 / 2019
页数:7
相关论文
共 35 条
[1]   Early mortality after diagnosis of multiple myeloma: Analysis of patients entered onto the United Kingdom Medical Research Council trials between 1980 and 2002 - Medical Research Council Adult Leukaemia Working Party [J].
Augustson, BM ;
Begum, G ;
Dunn, JA ;
Barth, NJ ;
Davies, F ;
Morgan, G ;
Behrens, J ;
Smith, A ;
Child, JA ;
Drayson, MT .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (36) :9219-9226
[2]   EVIDENCE THAT THE CLONOGENIC CELL IN MULTIPLE-MYELOMA ORIGINATES FROM A PRE-SWITCHED BUT SOMATICALLY MUTATED B-CELL [J].
BAKKUS, MHC ;
VANRIET, I ;
VANCAMP, B ;
THIELEMANS, K .
BRITISH JOURNAL OF HAEMATOLOGY, 1994, 87 (01) :68-74
[3]   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
[4]   Renal failure in multiple myeloma -: Presenting features and predictors of outcome in 94 patients from a single institution [J].
Bladé, J ;
Fernández-Llama, P ;
Bosch, F ;
Montoliu, J ;
Lens, XM ;
Montoto, S ;
Cases, A ;
Darnell, A ;
Rozman, C ;
Montserrat, E .
ARCHIVES OF INTERNAL MEDICINE, 1998, 158 (17) :1889-1893
[5]  
Blade J, 2001, Hematol J, V2, P272, DOI 10.1038/sj.thj.6200115
[6]  
Bradwell AR, 2001, CLIN CHEM, V47, P673
[7]   Serum test for assessment of patients with Bence Jones myeloma [J].
Bradwell, AR ;
Carr-Smith, HD ;
Mead, GP ;
Harvey, TC ;
Drayson, MT .
LANCET, 2003, 361 (9356) :489-491
[8]   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
[9]  
Goranova V, 1999, Folia Med (Plovdiv), V41, P164
[10]   International staging system for multiple myeloma [J].
Greipp, PR ;
San Miguel, J ;
Durie, BGM ;
Crowley, JJ ;
Barlogie, B ;
Bladé, J ;
Boccadoro, M ;
Child, JA ;
Harousseau, JL ;
Kyle, RA ;
Lahuerta, JJ ;
Ludwig, H ;
Morgan, G ;
Powles, R ;
Shimizu, K ;
Shustik, C ;
Sonneveld, P ;
Tosi, P ;
Turesson, I ;
Westin, J .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (15) :3412-3420