中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2014年
12期
2882-2884
,共3页
徐姗%梅金红%王淳良%杨玄勇%王珊珊
徐姍%梅金紅%王淳良%楊玄勇%王珊珊
서산%매금홍%왕순량%양현용%왕산산
少突胶质细胞肿瘤%染色体%杂合性缺失%临床病理特征
少突膠質細胞腫瘤%染色體%雜閤性缺失%臨床病理特徵
소돌효질세포종류%염색체%잡합성결실%림상병리특정
Oligodendroglial tumors%Chromosome%Heterozygosity loss%Clinicopathologic feature
目的 探讨染色体1p/19q杂合性缺失与少突胶质细胞肿瘤临床病理特征的关系.方法 采用荧光免疫原位杂交技术检测73例少突胶质细胞肿瘤1p/19q杂合性缺失,并随访观察预后.结果 少突胶质细胞肿瘤年轻患者(< 60岁)1p/19q缺失高于老年患者(>60岁,P<0.01);好发部位(额、顶、枕叶)的少突胶质细胞肿瘤1p/19q缺失与其他部位比较差异无统计学意义(P>0.05),与性别及肿瘤级别均无明显相关(P>0.05);少突胶质细胞肿瘤患者存在1p/19q联合缺失的中位生存时间为74个月,5年总生存率为72%;仅存在1p缺失者中位生存时间为43个月,5年总生存率为29%;而不存在1p/19q缺失者中位生存时间39个月,5年总生存率为18%.1p/19q联合缺失者中位生存时间长于仅存在1p缺失组,差异有统计学意义(P<0.05);且1p/19q缺失组中位生存时间也长于1 p/19q未缺失组,差异有统计学意义(P<0.05).仅存在1p缺失组中位生存时间虽然长于不存在1p/19q缺失组,但差异无统计学意义(Pp>0.05).结论 少突胶质细胞肿瘤1p/19q缺失与患者年龄明显相关,与患者性别、肿瘤发生部位及肿瘤级别无明显相关;少突胶质细胞肿瘤中染色体1p/19q杂合性缺失对患者的化疗敏感性及预后有关,可以作为分子分型的标准.
目的 探討染色體1p/19q雜閤性缺失與少突膠質細胞腫瘤臨床病理特徵的關繫.方法 採用熒光免疫原位雜交技術檢測73例少突膠質細胞腫瘤1p/19q雜閤性缺失,併隨訪觀察預後.結果 少突膠質細胞腫瘤年輕患者(< 60歲)1p/19q缺失高于老年患者(>60歲,P<0.01);好髮部位(額、頂、枕葉)的少突膠質細胞腫瘤1p/19q缺失與其他部位比較差異無統計學意義(P>0.05),與性彆及腫瘤級彆均無明顯相關(P>0.05);少突膠質細胞腫瘤患者存在1p/19q聯閤缺失的中位生存時間為74箇月,5年總生存率為72%;僅存在1p缺失者中位生存時間為43箇月,5年總生存率為29%;而不存在1p/19q缺失者中位生存時間39箇月,5年總生存率為18%.1p/19q聯閤缺失者中位生存時間長于僅存在1p缺失組,差異有統計學意義(P<0.05);且1p/19q缺失組中位生存時間也長于1 p/19q未缺失組,差異有統計學意義(P<0.05).僅存在1p缺失組中位生存時間雖然長于不存在1p/19q缺失組,但差異無統計學意義(Pp>0.05).結論 少突膠質細胞腫瘤1p/19q缺失與患者年齡明顯相關,與患者性彆、腫瘤髮生部位及腫瘤級彆無明顯相關;少突膠質細胞腫瘤中染色體1p/19q雜閤性缺失對患者的化療敏感性及預後有關,可以作為分子分型的標準.
목적 탐토염색체1p/19q잡합성결실여소돌효질세포종류림상병리특정적관계.방법 채용형광면역원위잡교기술검측73례소돌효질세포종류1p/19q잡합성결실,병수방관찰예후.결과 소돌효질세포종류년경환자(< 60세)1p/19q결실고우노년환자(>60세,P<0.01);호발부위(액、정、침협)적소돌효질세포종류1p/19q결실여기타부위비교차이무통계학의의(P>0.05),여성별급종류급별균무명현상관(P>0.05);소돌효질세포종류환자존재1p/19q연합결실적중위생존시간위74개월,5년총생존솔위72%;부존재1p결실자중위생존시간위43개월,5년총생존솔위29%;이불존재1p/19q결실자중위생존시간39개월,5년총생존솔위18%.1p/19q연합결실자중위생존시간장우부존재1p결실조,차이유통계학의의(P<0.05);차1p/19q결실조중위생존시간야장우1 p/19q미결실조,차이유통계학의의(P<0.05).부존재1p결실조중위생존시간수연장우불존재1p/19q결실조,단차이무통계학의의(Pp>0.05).결론 소돌효질세포종류1p/19q결실여환자년령명현상관,여환자성별、종류발생부위급종류급별무명현상관;소돌효질세포종류중염색체1p/19q잡합성결실대환자적화료민감성급예후유관,가이작위분자분형적표준.
Objective To investigate the relationship between the loss of heterozygosity (LOH)on chromosome 1p/19q and clinicopathologic feature in oligodendroglial tumors.Methods The LOH on chromosome 1 p/19q was detected with fluorescence in situ hybridization in 73 patients with oligodendroglial tumors,and the prognosis was followed up.Results The positive rate of the LOH on chromosome 1p/19q in oligodendroglioma in younger patients (< 60 years old) was higher than in older patients (> 60 years old),(P < 0.01).There was no statistically significant difference in the LOH on chromosome 1 p/19q betwcen the oligodendroglial tumors at frontal lobe and other lobes (P > 0.05).There was no statistically significant difference in the LOH on chromosome 1p/19q in oligodendroglioma between low grade and high grade (P >0.05).There was no statistically significant difference in the LOH on chromosome 1p/19q in oligodendroglioma between males and females.The median survival time of patients with the LOH on chromosome 1 p/19q of oligodendroglioma was 74 months,and total 5-year survival rate was 72%.The median survival time in patients with 1 p LOH was 43 months,and the total 5-year survival rate was 29%.The median survival time of patients without 1 p/19q LOH was 39 months,and total 5-year survival rate was 18%.The median survival time of patients with 1p/19q LOH was significantly longer than that of those with 1 p LOH (P < 0.05).The median survival time of patients with 1 p/19q LOH was significantly longer than that of those without 1 p/19q LOH (P < 0.05).The median survival time of patients with 1 p LOH was longer than that in those without 1p/19q LOH,but there was no statistically significant difference (P>0.05).Conclusion The LOH on chromosome 1 p/19q in oligodendroglioma was obviously correlated with patients' age,but not with gender,tumor location and tumor grade.There were correlations between the LOH on chromosome 1 p/19q of oligodendroglioma and chemotherapy sensibility and prognosis.The LOH on chromosome 1p/19q of oligodendroglioma can act as the classified standard of molecular subtyping.