Stadler Zsofia K
Clinical Genetics Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USA.
Hematol Oncol Clin North Am. 2015 Feb;29(1):29-41. doi: 10.1016/j.hoc.2014.09.008.
Colorectal tumors exhibiting defective DNA mismatch repair (MMR-D)/microsatellite instability (MSI-H) form a distinct subgroup of CRCs associated with important clinical and pathologic features. The identification of MMR-D/MSI-H may impact CRC prognosis, prediction of response to chemotherapeutic agents, and may necessitate the need for genetic assessment for Lynch syndrome. Oncologists remain at the forefront of diagnosing, treating, and managing patients with MMR-D/MSI-H CRC and ensuring that the clinical care of these patients reflect our evolving understanding of this unique CRC subtype.
表现出DNA错配修复缺陷(MMR-D)/微卫星高度不稳定(MSI-H)的结直肠肿瘤构成了与重要临床和病理特征相关的结直肠癌独特亚组。MMR-D/MSI-H的识别可能影响结直肠癌的预后、对化疗药物反应的预测,并且可能需要对林奇综合征进行基因评估。肿瘤学家在诊断、治疗和管理MMR-D/MSI-H结直肠癌患者以及确保这些患者的临床护理反映我们对这种独特结直肠癌亚型不断发展的认识方面处于前沿位置。