Lung-resistance-related protein expression is a negative predictive factor for response to conventional low but not to intensified dose alkylating chemotherapy in multiple myeloma

被引:66
作者
Raaijmakers, HGP
Izquierdo, MAI
Lokhorst, HM
de Leeuw, C
Belien, JAM
Bloem, AC
Dekker, AW
Scheper, RJ
Sonneveld, P
机构
[1] Univ Utrecht Hosp, Dept Haematol G03647, NL-3508 GA Utrecht, Netherlands
[2] Univ Utrecht Hosp, Dept Immunol, Utrecht, Netherlands
[3] Univ Hosp Dijkzigt, Dept Haematol, NL-3015 GD Rotterdam, Netherlands
[4] Univ Hosp Vrije, Dept Pathol, Amsterdam, Netherlands
关键词
D O I
10.1182/blood.V91.3.1029.1029_1029_1036
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study was undertaken to assess the significance of lung-resistance related protein (LRP) expression in plasma cells from untreated multiple myeloma (MM) patients and to determine whether LRP was associated with a poor response and survival in patients treated with different dose regimens of melphalan. Seventy untreated patients received conventional oral dose melphalan (0.25 mg/kg, day 1 to 4) combined with prednisone (MP) or intravenous intermediate-IDM; 70 mg/m(2)) or high-(140 mg/m(2)) dose Melphalan (HDM). LRP expression was assessed with immunocytochemistry using the LRP-56 monoclonal antibody, LRP expression was found in 47% of patients. In the MP treated patients, LRP expression was a significant prognostic factor regarding response induction (P < .05), event free survival (P < .003), and overall survival(P < .001). In the intensified dose melphalan treated patients LRP did not have a prognostic value. The response rates of LRP-positive patients to MP and IDM/HDM were 18% versus 81%, respectively (P < .0001). We conclude that LRP is frequently expressed in untreated MM patients and is an independent predictor for response and survival in patients treated with MP. Pretreatment assessment of LRP identifies a subpopulation of patients with a poor probability of response to conventional dose melphalan. Dose intensification of melphalan is likely to overcome LRP-mediated resistance. (C) 1998 by The American Society of Hematology.
引用
收藏
页码:1029 / 1036
页数:8
相关论文
共 35 条
[31]  
SCHEPER RJ, 1993, CANCER RES, V53, P1475
[32]   EARLY MULTIDRUG RESISTANCE, DEFINED BY CHANGES IN INTRACELLULAR DOXORUBICIN DISTRIBUTION, INDEPENDENT OF P-GLYCOPROTEIN [J].
SCHUURHUIS, GJ ;
BROXTERMAN, HJ ;
DELANGE, JHM ;
PINEDO, HM ;
VANHEIJNINGEN, THM ;
KUIPER, CM ;
SCHEFFER, GL ;
SCHEPER, RJ ;
VANKALKEN, CK ;
BAAK, JPA ;
LANKELMA, J .
BRITISH JOURNAL OF CANCER, 1991, 64 (05) :857-861
[33]  
SLOVAK ML, 1988, CANCER RES, V48, P2793
[34]   CLINICAL MODULATION OF MULTIDRUG-RESISTANCE IN MULTIPLE-MYELOMA - EFFECT OF CYCLOSPORINE ON RESISTANT TUMOR-CELLS [J].
SONNEVELD, P ;
SCHOESTER, M ;
DELEEUW, K .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (08) :1584-1591
[35]   THE HUMAN MULTIDRUG RESISTANCE-ASSOCIATED PROTEIN MRP IS A PLASMA-MEMBRANE DRUG-EFFLUX PUMP [J].
ZAMAN, GJR ;
FLENS, MJ ;
VANLEUSDEN, MR ;
DEHAAS, M ;
MULDER, HS ;
LANKELMA, J ;
PINEDO, HM ;
SCHEPER, RJ ;
BAAS, F ;
BROXTERMAN, HJ ;
BORST, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) :8822-8826