Wheeler Scott R, Shi Chanjuan, Holt Jonathan A, Vnencak-Jones Cindy L
1 Department of Pathology, Microbiology and Immunology, 2 Department of Bioinformatics, Vanderbilt University Medical Center, Nashville, TN 37211, USA.
J Gastrointest Oncol. 2016 Jun;7(3):E64-71. doi: 10.21037/jgo.2016.01.07.
Patients with Lynch syndrome often present with multiple synchronous or metachronous colorectal cancers (CRCs). The presence of multiple CRCs with distinct genetic profiles and driver mutations could complicate treatment as each cancer may respond differently to therapy. Studies of sporadic CRCs suggested that synchronous tumors have distinct etiologies, but could not rule out differences in genetic background. The presence of multiple cancers in a patient with a predisposing mutation provides an opportunity to profile synchronous cancers in the same genetic background. Here, we describe the case of a patient with Lynch syndrome that presented with six synchronous CRCs. Microsatellite instability (MSI) and genomic profiling indicated that each lesion had a unique pattern of instability and a distinct profile of affected genes. These findings support the idea that in Lynch syndrome, synchronous CRCs can develop in parallel with distinct mutation profiles and that these differences may inform treatment decisions.
林奇综合征患者常出现多个同时性或异时性结直肠癌(CRC)。多个具有不同基因特征和驱动突变的结直肠癌的存在可能使治疗复杂化,因为每种癌症对治疗的反应可能不同。散发性结直肠癌的研究表明,同时性肿瘤有不同的病因,但不能排除基因背景的差异。携带易感突变的患者出现多种癌症,为在相同基因背景下分析同时性癌症提供了机会。在此,我们描述了一例患有林奇综合征且出现六个同时性结直肠癌的患者病例。微卫星不稳定性(MSI)和基因组分析表明,每个病变都有独特的不稳定性模式和受影响基因的不同特征。这些发现支持了这样一种观点,即在林奇综合征中,同时性结直肠癌可具有不同的突变特征并行发生,且这些差异可能为治疗决策提供依据。