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TOPO-1在转移性结直肠癌组织中的表达及与伊立替康化疗的相关性研究 被引量:2

Correlation of TOPO-1 expression with irinotecan therapy in patients with metastatic colorectal cancer
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摘要 目的探讨拓扑异构酶1(topoisomerase1,TOPO-1)在转移性结直肠癌组织中的表达,并分析其与伊立替康(CPT-11)化疗疗效的相关性。方法经病理活检证实为转移性结直肠癌初诊者98例,均接受FOLFIRI方案一线化疗,化疗前检测肿瘤组织TOPO-1的表达水平,分析TOPO-1表达水平与近期疗效的关系,并观察远期疗效。结果 TOPO-1表达水平与转移性结直肠癌的临床特征无明显相关性(P>0.05)。高表达组患者RR为52.2%(24/46),低表达组RR为28.8%(15/52),差异有统计学意义(P<0.05)。TOPO-1高表达组中位PFS为9.5个月(8~12个月),低表达组为8.0个月(7~9个月),差异有统计学意义(P=0.002)。结论 TOPO-1高表达转移性结直肠癌患者可从伊立替康化疗中获得更高的近期疗效和更长的无疾病进展生存时间,可能对伊立替康化疗更敏感。 Objective To explore TOPO-1 expression in patients with metastatic colorectal cancer. Methods TOPO-1 expression was detected by immunohistochemistry in 98 cases of metastatic colorectal cancer before receiving FOLFIRI chemotherapy, and investigate its association with short-term efficacy of chemotherapy.The long-term efficacy of chemotherapy was evaluated. Results TOPO-1 expression showed no obvious correlation with clinico-pathological characteristics (t≥0.05). The patients showing high and low TOPO-1 expression showed significant difference between response rate (52.2% vs 28.8% ,P〈0.05 )and median progression-free survival (9.5 months vs 8.0 months,P=0.002). Conclusion Irinotecan showed a tendency toward higher response rate and longer median survival for treating metastatic colorectal cancer patients with high expression of TOPO-1.
出处 《中国癌症防治杂志》 CAS 2017年第5期383-387,共5页 CHINESE JOURNAL OF ONCOLOGY PREVENTION AND TREATMENT
基金 国家自然科学基金资助项目(81260340) 广西自然科学基金资助项目(2013GXNSFAA019263)
关键词 结直肠肿瘤 转移性结直肠癌 拓扑异构酶1 伊立替康 化疗 Colorectal neoplasms Metastatic colorectal cancer Topoisomerase-1 Irinotecan Chemotherapy
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  • 1Rustum YM, Cao S. New drugs in therapy of colorectal cancer:preclinical studies. Semin Oncol, 1999, 26: 612-620.
  • 2Sahz LB, Cox JV, Blanke C, et al. CPT-11 plus fluorouracil and leucovorin for metastatic colorectal cancer. N Engl J Med, 2000, 343:905-914.
  • 3Maiello E, Gebbia V, Giuliani F, et al. 5-Fluorouracil and folinic acid with or without CPT-11 in advanced colorectal cancer patients: a multicenter randomized phase Ⅱ study of the southern Italy oncology group. Ann Oncol, 2000, 11: 1045-1051.
  • 4Miller AB, Hoogstraten MB, Staquet M, et al. Reporting result of cancer treatment. Cancer, 1981, 47: 207-210.
  • 5Johnston PG, Hang CM, Henry S, et al. Production and characterization of monoclonal antibodies that localize human thymidilate synthase in the cytoplasm of human cells and tissue. Cancer Res, 1991,51 : 6668-6676.
  • 6Xu JM, Azzafiti A, Tommasi S, et al. Combination of 5-fluorouracil and irinotecan on modulation of thymidylate synthase and topoisomerase I expression and cell cycle regulation in human colon cancer Lovo ceils:clinical relevance. Clin Colorectal Cancer, 2002, 2: 182-188.
  • 7Leichman CG, Lenz H.l, Leichman L, et al. Quantitation of intratumoral thymidylate synthase expression predicts for disseminated colorectal cancer response and resistance to protracted-infusion fluorouracil and weekly leucovorin. J Clin Oncol, 1997, 10: 3223-3229.
  • 8Goldwasser F, Shimizu T, Jackman J, et al. Correlations between S and G2 arrest and the cytotoxicity of camptothecin in human colon carcinoma cells. Cancer Res, 1996, 56: 4430-1437.
  • 9Saltz L, Danenberg K, Paty P, et al. High thymidylate synthase(TS) expression does not preclude activity of CPT-11 in colorectal cancer (CRC). Proc Am Soc Clin Oncol, 1998, 17: 281.
  • 10Kanavaros P, Stefanaki K, Valassiadou K, et al. Expression of p53,p21/waf, bcl-2, bax, Rb and Ki-67 proteins in colorectal adenocarcinomas.Med Oncol, 1999, 16: 23-30.

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