IS POOR PROGNOSIS REALLY RELATED TO HLA-DR EXPRESSION BY MALIGNANT-MELANOMA CELLS

被引:24
作者
COLLOBY, PS
WEST, KP
FLETCHER, A
机构
[1] LEICESTER ROYAL INFIRM,DEPT HISTOPATHOL,LEICESTER LE2 7LX,ENGLAND
[2] UNIV LEICESTER,DEPT PATHOL,LEICESTER LE1 7RH,ENGLAND
关键词
MALIGNANT MELANOMA; HLA-DR; PROGNOSIS;
D O I
10.1111/j.1365-2559.1992.tb01011.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
HLA-DR expression was examined in 50 consecutive primary cutaneous malignant melanomas with a Breslow depth > 2 mm using two well-characterized monoclonal antibodies which detect fixation-resistant epitopes. In 31 of these cases (62%) a subpopulation of tumour cells was reactive, although there was considerable heterogeneity. Positive labelling did not correlate with depth but was associated with a reduced likelihood of developing early metastatic disease and a tendency for better overall survival, particularly in male patients. These findings contrast with earlier studies using cryostat sections and one study on paraffin-embedded tissue in which HLA-DR expression was shown to be a poor prognostic factor, but are consistent with the findings in other malignant tumours studied. The significance of HLA-DR expression as a marker of prognosis may depend on the type of tissue preparation, the sensitivity of the immunocytochemical techniques used and the method of assessment.
引用
收藏
页码:411 / 416
页数:6
相关论文
共 17 条
[1]   PHENOTYPIC DYNAMICS OF TUMOR PROGRESSION IN HUMAN-MALIGNANT MELANOMA [J].
BROCKER, EB ;
SUTER, L ;
BRUGGEN, J ;
RUITER, DJ ;
MACHER, E ;
SORG, C .
INTERNATIONAL JOURNAL OF CANCER, 1985, 36 (01) :29-35
[2]   A MONOCLONAL-ANTIBODY THAT DETECTS HLA-D REGION ANTIGEN IN ROUTINELY FIXED, WAX EMBEDDED SECTIONS OF NORMAL AND NEOPLASTIC LYMPHOID-TISSUES [J].
EPENETOS, AA ;
BOBROW, LG ;
ADAMS, TE ;
COLLINS, CM ;
ISAACSON, PG ;
BODMER, WF .
JOURNAL OF CLINICAL PATHOLOGY, 1985, 38 (01) :12-17
[3]   AUTOLOGOUS TUMOR-SPECIFIC CYTO-TOXIC LYMPHOCYTES-T IN THE INFILTRATE OF HUMAN METASTATIC MELANOMAS - ACTIVATION BY INTERLEUKIN-2 AND AUTOLOGOUS TUMOR-CELLS, AND INVOLVEMENT OF THE T-CELL RECEPTOR [J].
ITOH, K ;
PLATSOUCAS, CD ;
BALCH, CM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (04) :1419-1441
[4]  
KARAKOUSIS CP, 1989, CANCER-AM CANCER SOC, V64, P1432, DOI 10.1002/1097-0142(19891001)64:7<1432::AID-CNCR2820640712>3.0.CO
[5]  
2-M
[6]   CUTANEOUS MALIGNANT-MELANOMA - A FRESH OUTLOOK [J].
KERNOHAN, NM .
JOURNAL OF PATHOLOGY, 1991, 163 (04) :283-285
[7]  
MARDER RJ, 1985, LAB INVEST, V52, P497
[8]  
NATALI P, 1990, CANCER RES, V50, P1271
[9]   A PROGRESS REPORT ON THE TREATMENT OF 157 PATIENTS WITH ADVANCED CANCER USING LYMPHOKINE-ACTIVATED KILLER-CELLS AND INTERLEUKIN-2 OR HIGH-DOSE INTERLEUKIN-2 ALONE [J].
ROSENBERG, SA ;
LOTZE, MT ;
MUUL, LM ;
CHANG, AE ;
AVIS, FP ;
LEITMAN, S ;
LINEHAN, WM ;
ROBERTSON, CN ;
LEE, RE ;
RUBIN, JT ;
SEIPP, CA ;
SIMPSON, CG ;
WHITE, DE .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (15) :889-897
[10]  
RUITER DJ, 1984, CANCER RES, V44, P3930