Sebagh Mylène, Allard Marc-Antoine, Bosselut Nelly, Dao Myriam, Vibert Eric, Lewin Maïté, Lemoine Antoinette, Cherqui Daniel, Adam René, Sa Cunha Antonio
AP-HP Hôpital Paul Brousse, Department of Pathology, Villejuif, France.
Inserm U1193, Paris-Sud University, Villejuif, France.
Oncotarget. 2016 Apr 19;7(16):21591-600. doi: 10.18632/oncotarget.7809.
In patients receiving preoperative chemotherapy, colorectal liver metastases (CLM) are expected to demonstrate a similar behaviour because of similar organ microenvironment and tumour cell chemosensitivity. We focused on the occurrence of pathological and genetic heterogeneity within CLM.
Patients resected for multiple CLM between 2004 and 2011 after > three cycles of chemotherapy were included. Pathological heterogeneity was arbitrarily defined as a > 50% difference in the percentage of remaining tumour cells between individual CLM. In patients with pathological heterogeneity, the mutational genotyping (KRAS, NRAS, BRAF and PIK3CA) was determined from the most heterogeneous CLM.
Pathological heterogeneity was observed in 31 of 157 patients with multiple CLM (median = 4, range, 2-32) (19.7%). In 72.4% of them, we found a concordance of the mutation status between the paired CLM: both wild-type in 55%, and both mutated in 17.2%. We observed a discordance of the mutation status of 27.6% between CLM: one mutated and the other wild-type. The mutated CLM was the less florid one in 75% of patients with genetic heterogeneity.
Pathological heterogeneity is present in 19.7% of patients with multiple CLM. Genetic heterogeneity is present in 27.6% of patients with pathological heterogeneity. Heterogeneity could refine guide management for tissue sampling.
在接受术前化疗的患者中,由于器官微环境和肿瘤细胞化学敏感性相似,结直肠癌肝转移(CLM)预计会表现出相似的行为。我们关注CLM内病理和基因异质性的发生情况。
纳入2004年至2011年间接受三个以上化疗周期后因多发CLM接受手术切除的患者。病理异质性被任意定义为各个CLM之间剩余肿瘤细胞百分比差异>50%。在存在病理异质性的患者中,从最具异质性的CLM中确定突变基因分型(KRAS、NRAS、BRAF和PIK3CA)。
157例多发CLM患者中有31例观察到病理异质性(中位数 = 4,范围2 - 32)(19.7%)。其中72.4%的患者,我们发现配对CLM之间的突变状态一致:55%均为野生型,17.2%均为突变型。我们观察到CLM之间突变状态不一致的情况占27.6%:一个突变而另一个野生型。在75%存在基因异质性的患者中,突变的CLM表现为不那么活跃。
19.7%的多发CLM患者存在病理异质性。27.6%存在病理异质性的患者存在基因异质性。异质性可为组织采样的管理提供更精确的指导。