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KRAS 突变数量在转移性结直肠癌中的预后及预测价值

Prognostic and predictive value of KRAS mutation number in metastatic colorectal cancer.

作者信息

Ucar Gokhan, Ergun Yakup, Aktürk Esen Selin, Acikgoz Yusuf, Dirikoc Merve, Esen İrfan, Bal Öznur, Uncu Doğan

机构信息

Department of Medical Oncology, Ankara City Hospital, Ankara.

Department of Internal Medicine, Yenimahalle Training and Education Hospital, Ankara, Turkey.

出版信息

Medicine (Baltimore). 2020 Sep 25;99(39):e22407. doi: 10.1097/MD.0000000000022407.

Abstract

Colorectal cancer (CRC) is the third most common cancer in the world and is the second leading cause of cancer-related deaths. Several mutations are involved in the development of CRC. The prognostic significance of the KRAS mutation has been discussed in many studies. We aimed to investigate the prognostic significance of the number of KRAS mutations in metastatic CRC (mCRC).Patients with mutations in the KRAS gene were included in the study. They were divided into 2 groups as single mutation and multiple mutations in the KRAS gene.For the study, 425 CRC patients were screened. KRAS mutation was positive in 191 patients (45%). One hundred ninety-one patients were included in the study, 171 patients (90%) had single mutations and 20 patients (10%) had multiple mutations. Median progression-free survival was 12.8 months in patients with multiple mutations, while it was 8.8 months in patients with single mutations (P: .05). The median overall survival of patients with multiple mutations was 40.7 months, while it was 22.7 months for patients with single mutations (P = .01)We found that the presence of multiple mutations in KRAS mutant patients was associated with better overall survival and progression-free survival than a single mutation.

摘要

结直肠癌(CRC)是全球第三大常见癌症,也是癌症相关死亡的第二大主要原因。几种突变参与了结直肠癌的发生发展。许多研究都讨论了KRAS突变的预后意义。我们旨在研究转移性结直肠癌(mCRC)中KRAS突变数量的预后意义。

KRAS基因发生突变的患者被纳入研究。他们被分为两组,即KRAS基因单突变组和多突变组。

为进行该研究,对425例结直肠癌患者进行了筛查。191例患者(45%)KRAS突变呈阳性。191例患者被纳入研究,其中171例患者(90%)为单突变,20例患者(10%)为多突变。多突变患者的无进展生存期中位数为12.8个月,而单突变患者为8.8个月(P = 0.05)。多突变患者的总生存期中位数为40.7个月,而单突变患者为22.7个月(P = 0.01)。

我们发现,KRAS突变患者中多突变的存在与单突变相比,与更好的总生存期和无进展生存期相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ba0/7523797/5fc89f1525f2/medi-99-e22407-g002.jpg

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