中华病理学杂志
中華病理學雜誌
중화병이학잡지
Chinese Journal of Pathology
2011年
4期
220-226
,共7页
林莉%闵敏%毕成峰%王晓卿%罗添友%赵莎%张文燕%刘卫平
林莉%閔敏%畢成峰%王曉卿%囉添友%趙莎%張文燕%劉衛平
림리%민민%필성봉%왕효경%라첨우%조사%장문연%류위평
胃肠肿瘤%淋巴瘤,B细胞%免疫表型分型%预后
胃腸腫瘤%淋巴瘤,B細胞%免疫錶型分型%預後
위장종류%림파류,B세포%면역표형분형%예후
Gastrointestinal neoplasms%Lymphoma,B-cell%Immunophenotyping%Prognosis
目的 了解原发胃肠道弥漫性大B细胞淋巴瘤的免疫分型,并比较Choi、Tally和Hans 分型及其与预后的关系.方法 复习90例原发胃肠道弥漫性大B细胞淋巴瘤患者的临床及病理资料并进行随访,应用Kaplan-Meier法、Log-rank检验和Cox比例风险回归模型对临床资料、实验室检测结果 进行生存分析及单因素和多因素预后分析.免疫表型检测采用EnVision和EliVision法,选用的抗体有CD20、CD3ε、CDl0、bcl-6、MUM-1、CD5、bcl-2、GCET1、FOXP1、LMO2、BLIMP1和Ki-67等.结果 (1)年龄为27~83岁,中位年龄58岁,男女比为1.31:1;胃肿瘤58例,占64.4%(58/90);肠肿瘤32例,占35.6%(32/90).(2)肿瘤细胞均表达CD20抗原,均不表达CD3ε和CD5;CD10、bcl-6、MUM-1(30%/80%阈值)的表达率分别为17.8%(16/90)、75.6%(68/90)、52.2%(47/90)/43.3%(39/90),GCET1、FOXP1、LMO2的表达率分别为50.0%(45/90)、45.6%(41/90)、23.3%(21/90),bcl-2、BLIMP1的表达率分别为42.2%(38/90)、8.9%(8/90),Ki-67阳性指数20%~95%,中位数为80%.Hans分型:51.1%为生发中心B细胞型(GCB型),48.9%为非GCB型;Choi分型:55.6%为GCB型,44.4%为活化B细胞(ABC)型;Tally分型:34.4%为GCB型,65.6%为非GCB型.(3)67.8%(61/90)的患者接受化疗,68.9%(62/90)的患者接受手术.患者的2、3和5年总体生存率分别为58.5%、52.8%和49.8%,CHOP方案(环磷酰胺+多柔比星+长春新碱+泼尼松)治疗组的2、3和5年总体生存率分别为68.5%、61.2%和52.9%.结论 Hans和Choi分型各亚型比例差别不大,Tally分型中非GCB型较GCB型比例增高.三种分型的各亚型均存在GCB型优于非GCB/ABC型的趋势.Log-rank检验单因素分析提示乳酸脱氢酶(LDH)水平、国际预后指数(IPI)、化疗、手术、B症状、病变数量、临床分期对预后有影响.Cox比例风险回归模型多因素分析提示Hans分型、Choi分型、化疗、手术、LDH和Lugano分期是独立的预后因素.
目的 瞭解原髮胃腸道瀰漫性大B細胞淋巴瘤的免疫分型,併比較Choi、Tally和Hans 分型及其與預後的關繫.方法 複習90例原髮胃腸道瀰漫性大B細胞淋巴瘤患者的臨床及病理資料併進行隨訪,應用Kaplan-Meier法、Log-rank檢驗和Cox比例風險迴歸模型對臨床資料、實驗室檢測結果 進行生存分析及單因素和多因素預後分析.免疫錶型檢測採用EnVision和EliVision法,選用的抗體有CD20、CD3ε、CDl0、bcl-6、MUM-1、CD5、bcl-2、GCET1、FOXP1、LMO2、BLIMP1和Ki-67等.結果 (1)年齡為27~83歲,中位年齡58歲,男女比為1.31:1;胃腫瘤58例,佔64.4%(58/90);腸腫瘤32例,佔35.6%(32/90).(2)腫瘤細胞均錶達CD20抗原,均不錶達CD3ε和CD5;CD10、bcl-6、MUM-1(30%/80%閾值)的錶達率分彆為17.8%(16/90)、75.6%(68/90)、52.2%(47/90)/43.3%(39/90),GCET1、FOXP1、LMO2的錶達率分彆為50.0%(45/90)、45.6%(41/90)、23.3%(21/90),bcl-2、BLIMP1的錶達率分彆為42.2%(38/90)、8.9%(8/90),Ki-67暘性指數20%~95%,中位數為80%.Hans分型:51.1%為生髮中心B細胞型(GCB型),48.9%為非GCB型;Choi分型:55.6%為GCB型,44.4%為活化B細胞(ABC)型;Tally分型:34.4%為GCB型,65.6%為非GCB型.(3)67.8%(61/90)的患者接受化療,68.9%(62/90)的患者接受手術.患者的2、3和5年總體生存率分彆為58.5%、52.8%和49.8%,CHOP方案(環燐酰胺+多柔比星+長春新堿+潑尼鬆)治療組的2、3和5年總體生存率分彆為68.5%、61.2%和52.9%.結論 Hans和Choi分型各亞型比例差彆不大,Tally分型中非GCB型較GCB型比例增高.三種分型的各亞型均存在GCB型優于非GCB/ABC型的趨勢.Log-rank檢驗單因素分析提示乳痠脫氫酶(LDH)水平、國際預後指數(IPI)、化療、手術、B癥狀、病變數量、臨床分期對預後有影響.Cox比例風險迴歸模型多因素分析提示Hans分型、Choi分型、化療、手術、LDH和Lugano分期是獨立的預後因素.
목적 료해원발위장도미만성대B세포림파류적면역분형,병비교Choi、Tally화Hans 분형급기여예후적관계.방법 복습90례원발위장도미만성대B세포림파류환자적림상급병리자료병진행수방,응용Kaplan-Meier법、Log-rank검험화Cox비례풍험회귀모형대림상자료、실험실검측결과 진행생존분석급단인소화다인소예후분석.면역표형검측채용EnVision화EliVision법,선용적항체유CD20、CD3ε、CDl0、bcl-6、MUM-1、CD5、bcl-2、GCET1、FOXP1、LMO2、BLIMP1화Ki-67등.결과 (1)년령위27~83세,중위년령58세,남녀비위1.31:1;위종류58례,점64.4%(58/90);장종류32례,점35.6%(32/90).(2)종류세포균표체CD20항원,균불표체CD3ε화CD5;CD10、bcl-6、MUM-1(30%/80%역치)적표체솔분별위17.8%(16/90)、75.6%(68/90)、52.2%(47/90)/43.3%(39/90),GCET1、FOXP1、LMO2적표체솔분별위50.0%(45/90)、45.6%(41/90)、23.3%(21/90),bcl-2、BLIMP1적표체솔분별위42.2%(38/90)、8.9%(8/90),Ki-67양성지수20%~95%,중위수위80%.Hans분형:51.1%위생발중심B세포형(GCB형),48.9%위비GCB형;Choi분형:55.6%위GCB형,44.4%위활화B세포(ABC)형;Tally분형:34.4%위GCB형,65.6%위비GCB형.(3)67.8%(61/90)적환자접수화료,68.9%(62/90)적환자접수수술.환자적2、3화5년총체생존솔분별위58.5%、52.8%화49.8%,CHOP방안(배린선알+다유비성+장춘신감+발니송)치료조적2、3화5년총체생존솔분별위68.5%、61.2%화52.9%.결론 Hans화Choi분형각아형비례차별불대,Tally분형중비GCB형교GCB형비례증고.삼충분형적각아형균존재GCB형우우비GCB/ABC형적추세.Log-rank검험단인소분석제시유산탈경매(LDH)수평、국제예후지수(IPI)、화료、수술、B증상、병변수량、림상분기대예후유영향.Cox비례풍험회귀모형다인소분석제시Hans분형、Choi분형、화료、수술、LDH화Lugano분기시독립적예후인소.
Objective To study the immunophenotype and prognostic significance of primary gastrointestinal diffuse large B-cell Iymphoma, with reference to Hans, Choi and Tally algorithms. Methods The clinicopathologic features and follow-up data in 90 cases of primary gastrointestinal diffuse large B-cell lymphoma were analyzed by Kaplan-Meier method, Log-rank test and Cox regression model.Immunohistochemistry was carried out using EliVision and EnVision methods for CD20, CD3ε, CD10,bcl-6, MUM-1, CDS, bcl-2, GCET1, FOXP1, LMO2,BLIMP1 and Ki-67. Results The age of patients studied, 64. 4% (58/90) involved the stomach and 35.6% (32/90) involved the intestine. The immunohistochemical findings were as follows: 100% positivity for CD20, 0% for CD3ε and CD5, 17.8% (16/90) for CD10, 75.6% (68/90) for bcl-6, 52. 2% (47/90) for MUM-1 (cut off was 30%), 43.3%(39/90) for MUM-1 (cut off was 80%), 50.0% (45/90) for GCET1, 45.6% (41/90) for FOXP1,23.3%(21/90) for LMO2, 42.2% (38/90) for bcl-2 and 8.9% (8/90) for BLIMP1. The Ki-67 index ranged from 20% to95% (median =80%). According to Hans algorithm, 51.1% of the cases belonged to germinal center B-cell (GCB) subtype and 48.9% belonged to non-GCB subtype. In contrast, Choi algorithm classified 55.6% cases as GCB subtype and 44. 4% as activated B-cell (ABC) subtype.According to Tally algorithm, 34. 4% were of GCB subtype and 65.6% of non-GCB subtype. Most of the patients (67. 8% ,61/90) received chemotherapy and 68.9% (62/90) underwent surgical resection. The overall 2, 3 and 5-year survival rates were 58. 5%, 52. 8% and 49. 8%, respectively. The overall 2, 3 and 5-year survival rates in the CHOP therapy group were 68.5%, 61.2% and 52. 9%, respectively.Conclusions There is no significant difference in ratio between the GCB and non-GCB/ABC subtypes by Hans and Choi algorithms. The non-GCB subtype seems to be more prevalent according to Tally algorithm.Although there is no significant difference in survival between GCB and non-GCB/ABC subtypes by the 3algorithms, GCB subtype tends to show a better survival. In univariate analysis, LDH level, international prognostic index, chemotherapy, surgical resection, B symptoms, number of involved sites and clinical stage are found to have prognostic significance. In multivariate analysis, Choi algorithm, Tally algorithm,chemotherapy, surgical resection, LDH level and clinical stage are independent prognostic factors.