徐州医学院学报
徐州醫學院學報
서주의학원학보
Acta Academiae Medicinae Xuzhou
2015年
10期
667-672
,共6页
王晓杰%林晶%陈誉%师怡%杨眉%陈玲%余家密%郭增清
王曉傑%林晶%陳譽%師怡%楊眉%陳玲%餘傢密%郭增清
왕효걸%림정%진예%사이%양미%진령%여가밀%곽증청
晚期结直肠癌%KRAS野生型%PTEN%西妥昔单抗%化学治疗
晚期結直腸癌%KRAS野生型%PTEN%西妥昔單抗%化學治療
만기결직장암%KRAS야생형%PTEN%서타석단항%화학치료
advanced colorectal cancer%wild-type KRAS%PTEN%cetuximab%chemotherapy
目的:探讨PTNE蛋白表达对于西妥昔单抗联合化疗治疗转移性结直肠癌疗效的影响。方法初诊的晚期结直肠癌患者,共纳入经分子病理学证实KRAS野生型、同时接受过西妥昔单抗联合化疗的患者共51例,应用免疫组织化学法( S-P法)检测肿瘤组织中PTEN蛋白的表达。分析PTNE蛋白表达与患者临床病理特征及疗效的关系。结果51例患者中,25例患者一线接受了西妥昔单抗联合化疗,26例患者二线接受了西妥昔单抗联合化疗。25例患者获得部分缓解(PR),占49.0%;19例患者病情稳定(SD),占37.3%;疾病控制率(DCR)86.3%。中位生存时间22.0个月。 PTEN阳性表达30例(58.8%)。 PTEN表达与病理分级有关(P=0.015);PTEN阳性的患者DCR 93.3%(28/30),PTEN阴性者DCR 66.7%(14/21),PTEN表达与DCR有关(P=0.035)。单因素分析显示,不同ECOG PS评分、PTEN状态对中位总生存时间(OS)的影响差异有统计学意义(P=0.032,P=0.026);Cox多因素分析提示ECOG PS评分及PTEN状态是晚期KRAS野生型的结直肠癌患者接受西妥昔单抗治疗独立疗效预后因素。结论 KARS野生型晚期结直肠癌患者PTEN蛋白检测可能有助于预测西妥昔单抗联合化疗的疗效。
目的:探討PTNE蛋白錶達對于西妥昔單抗聯閤化療治療轉移性結直腸癌療效的影響。方法初診的晚期結直腸癌患者,共納入經分子病理學證實KRAS野生型、同時接受過西妥昔單抗聯閤化療的患者共51例,應用免疫組織化學法( S-P法)檢測腫瘤組織中PTEN蛋白的錶達。分析PTNE蛋白錶達與患者臨床病理特徵及療效的關繫。結果51例患者中,25例患者一線接受瞭西妥昔單抗聯閤化療,26例患者二線接受瞭西妥昔單抗聯閤化療。25例患者穫得部分緩解(PR),佔49.0%;19例患者病情穩定(SD),佔37.3%;疾病控製率(DCR)86.3%。中位生存時間22.0箇月。 PTEN暘性錶達30例(58.8%)。 PTEN錶達與病理分級有關(P=0.015);PTEN暘性的患者DCR 93.3%(28/30),PTEN陰性者DCR 66.7%(14/21),PTEN錶達與DCR有關(P=0.035)。單因素分析顯示,不同ECOG PS評分、PTEN狀態對中位總生存時間(OS)的影響差異有統計學意義(P=0.032,P=0.026);Cox多因素分析提示ECOG PS評分及PTEN狀態是晚期KRAS野生型的結直腸癌患者接受西妥昔單抗治療獨立療效預後因素。結論 KARS野生型晚期結直腸癌患者PTEN蛋白檢測可能有助于預測西妥昔單抗聯閤化療的療效。
목적:탐토PTNE단백표체대우서타석단항연합화료치료전이성결직장암료효적영향。방법초진적만기결직장암환자,공납입경분자병이학증실KRAS야생형、동시접수과서타석단항연합화료적환자공51례,응용면역조직화학법( S-P법)검측종류조직중PTEN단백적표체。분석PTNE단백표체여환자림상병리특정급료효적관계。결과51례환자중,25례환자일선접수료서타석단항연합화료,26례환자이선접수료서타석단항연합화료。25례환자획득부분완해(PR),점49.0%;19례환자병정은정(SD),점37.3%;질병공제솔(DCR)86.3%。중위생존시간22.0개월。 PTEN양성표체30례(58.8%)。 PTEN표체여병리분급유관(P=0.015);PTEN양성적환자DCR 93.3%(28/30),PTEN음성자DCR 66.7%(14/21),PTEN표체여DCR유관(P=0.035)。단인소분석현시,불동ECOG PS평분、PTEN상태대중위총생존시간(OS)적영향차이유통계학의의(P=0.032,P=0.026);Cox다인소분석제시ECOG PS평분급PTEN상태시만기KRAS야생형적결직장암환자접수서타석단항치료독립료효예후인소。결론 KARS야생형만기결직장암환자PTEN단백검측가능유조우예측서타석단항연합화료적료효。
Objective To determine the relationship between the level of phosphatase and tensin homolog deleted on chromosome ten ( PTEN) and the efficacy of cetuximab in combined with chemotherapy to treat metastatic colorectal canc-er ( mCRC) .Methods A total of 51 mCRC patients who were initially diagnosed in our hospital from January 2007 to December 2012 were included in the current study.They were identified as wild-type KRAS carriers and treated with cetuximab in combination with chemotherapy.Then, the levels of PTEN in tumor tissues were determined by immunohis-tochemistry ( IHC) .Results Among these patients were 25 patients who received first-line cetuximab combined with chemotherapy, and 26 patients who underwent second -line cetuximab combined with chemotherapy.The partial re-sponse (PR) rate was 49.0% (25/51).There were 19 patients with stable disease (SD).The disease control rate (DCR) was 86.3%(44/51).The median overall survival was 22.0 months.The positive expression rate of PTEN was 58.8%(30/51), which was correlated with histological grade (P=0.015).The DCR was 93.3%(28/30) for PTEN positive patients and 66.7% (14/21) for PTEN negative patients.The quantity of PTEN was related with DCR ( P=0.035).According to analysis of variance, the effects of RCOG performance status (PS) scores and PTEN level on me-dian overall survival were statistically different (P=0.032 and P=0.026, respectively).Multivariate COX regression a-nalysis showed that ECOG PS scores and PTEN level were independent prognostic factors for mCRC patients with wild-type KRAS receiving cetuximab combined with chemotherapy.Conclusion Detection of PTEN in mCRC patients with wild-type KRAS is beneficial for predicting the efficacy of cetuximab combined with chemotherapy.