Prognostic value of Ki-67 expression in localized cutaneous malignant melanoma

被引:35
作者
Henrique, R
Azevedo, R
Bento, MJ
Domingues, JC
Silva, C
Jerónimo, C
机构
[1] Ctr Reg Porto, Portuguese Canc Inst, Dept Pathol, P-4200072 Porto, Portugal
[2] Ctr Reg Porto, Portuguese Canc Inst, Dept Epidemiol, P-4200072 Porto, Portugal
[3] Ctr Reg Porto, Portuguese Canc Inst, Dept Dermatol, P-4200072 Porto, Portugal
[4] Ctr Reg Porto, Portuguese Canc Inst, Unit Mol Pathol, P-4200072 Porto, Portugal
关键词
D O I
10.1067/mjd.2000.109282
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: The proliferative activity of some tumors is related to the development of metastatic disease and survival. Thus it could be used as a potential prognostic variable. Objective: The purpose of this study was to determine the prognostic value of the Ki-67 index and of a "proliferation-based prognostic index" (PBPI, derived as tumor thickness x Ki-67 index/100) in localized cutaneous malignant melanoma (CMM). Methods: The Ki-67 index (percent of total tumor nuclei) was determined in a series of 84 localized CMMs, with the use of the alkaline phosphatase-antialkaline phosphatase labeling method in formalin-fixed, paraffin-embedded material, and was correlated with other prognostic variables. Survival analysis was performed to determine whether the Ki-67 index and the PBPI could be predictive of metastatic spread or recurrent disease. A stratified analysis of these two parameters according to the tumor thickness was done. Results: An association among the Ki-67 index and location, Clark level, tumor thickness and stage, and prognostic index was detected. Increased Ki-67 index and PBPI were associated with poorer overall survival (P = .03 and P < .0001, respectively) and disease-free survival (P = .01 and P < .0001, respectively). However, after stratification for thickness, only the PBPI showed independent prognostic significance, restricted to tumors thicker than 4 mm (P = .03). Conclusion: The determination of the PBPI in CMM conveys prognostic information for localized thick (>4 mm) CMM, identifying two groups of patients with distinct outcome.
引用
收藏
页码:991 / 1000
页数:10
相关论文
共 44 条
[1]   MULTIFACTORIAL ANALYSIS OF MELANOMA - PROGNOSTIC HISTOPATHOLOGICAL FEATURES COMPARING CLARKS AND BRESLOWS STAGING METHODS [J].
BALCH, CM ;
MURAD, TM ;
SOONG, SJ ;
INGALLS, AL ;
HALPERN, NB ;
MADDOX, WA .
ANNALS OF SURGERY, 1978, 188 (06) :732-742
[2]   MIB-1 immunoreactivity correlates with metastatic dissemination in primary thick cutaneous melanoma [J].
Boni, R ;
Doguoglu, A ;
Burg, G ;
Muller, B ;
Dummer, R .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1996, 35 (03) :416-418
[4]  
BUTTNER P, 1995, CANCER-AM CANCER SOC, V75, P2499, DOI 10.1002/1097-0142(19950515)75:10<2499::AID-CNCR2820751016>3.0.CO
[5]  
2-8
[6]  
CLARK WH, 1969, CANCER RES, V29, P705
[7]   MODEL PREDICTING SURVIVAL IN STAGE-I MELANOMA BASED ON TUMOR PROGRESSION [J].
CLARK, WH ;
ELDER, DE ;
GUERRY, D ;
BRAITMAN, LE ;
TROCK, BJ ;
SCHULTZ, D ;
SYNNESTVEDT, M ;
HALPERN, AC .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1989, 81 (24) :1893-1904
[8]  
COSTA A, 1987, CANCER-AM CANCER SOC, V60, P2797, DOI 10.1002/1097-0142(19871201)60:11<2797::AID-CNCR2820601133>3.0.CO
[9]  
2-B
[10]   DOES DELAY IN FIXATION AFFECT THE NUMBER OF MITOTIC FIGURES IN PROCESSED TISSUE [J].
CROSS, SS ;
START, RD ;
SMITH, JHF .
JOURNAL OF CLINICAL PATHOLOGY, 1990, 43 (07) :597-599