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HK2、PKM2和LDHA对西妥昔单抗治疗转移性结直肠癌疗效的影响。

Effect of HK2, PKM2 and LDHA on Cetuximab efficacy in metastatic colorectal cancer.

作者信息

Wang Haohua, Peng Roujun, Chen Xiuxing, Jia Rui, Huang Chunyue, Huang Yuanyuan, Xia Liangping, Guo Guifang

机构信息

VIP Region, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong 510060, P.R. China.

State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong 510060, P.R. China.

出版信息

Oncol Lett. 2018 Apr;15(4):5553-5560. doi: 10.3892/ol.2018.8005. Epub 2018 Feb 8.

Abstract

Although hexokinase (HK) 2, pyruvate kinase muscle (PKM) isozyme 2 and lactate dehydrogenase (LDH) A predict the efficacy of medicines in various solid tumors, their ability to predict the efficacy of cetuximab in metastatic colorectal cancer (mCRC) remains unclear. mCRC patients with pathological specimens who received cetuximab and chemotherapy from 2005 to 2015 in the present institution were enrolled. Immunohistochemistry was used to detect HK2, PKM2 and LDHA expression. SPSS20 was used for statistical analysis. A total of 68 patients were included; 33 received cetuximab plus chemotherapy as first-line therapy, and the rest, as second- or later-line therapy. HK2 expression levels were increased in cancer compared with normal tissue (75.4% vs. 40%; P<0.001), however PKM2 (P=0.243) and LDHA (P=0.067) expression levels were not. For progression-free survival (PFS) with first-line cetuximab plus chemotherapy, patients with high HK2 expression exhibited longer PFS compared with those with low HK2 expression (23.9 months vs. 6.9 months; P=0.021). However, this positive association was absent in 35 cases administered first-line chemotherapy alone (13.4 months vs. 13.5 months; P=0.539). LDHA expression was associated with the PFS of patients receiving first-line chemotherapy (18.3 and 10.1 months for high and low expression, respectively; P=0.005), whereas this association was absent in cetuximab plus chemotherapy cases (19.9 months vs. 12 months; P=0.522). Furthermore, high LDHA expression correlated with high overall response rate (ORR) (72.2% vs. 15.4%, P=0.006) for chemotherapy, however not disease control rate (DCR) (P=0.074). Neither DCR nor ORR were associated with HK2 expression. PKM2 expression did not affect PFS, DCR or ORR. LDHA expression (P=0.005), pathological differentiation (P=0.019) and synchronous/metachronous metastasis (P=0.014) were independent predictive factors of PFS for all first-line patients, and tumor differentiation (P=0.002) was associated with overall survival (OS) in multivariate analysis. HK2, PKM2 and LDHA did not impact OS. It was concluded that HK2 expression was increased in colorectal cancer tissue and may predict cetuximab efficacy and LDHA for chemotherapy treatment of mCRC.

摘要

尽管己糖激酶(HK)2、丙酮酸激酶肌肉型(PKM)同工酶2和乳酸脱氢酶(LDH)A可预测多种实体瘤的药物疗效,但其预测西妥昔单抗在转移性结直肠癌(mCRC)中疗效的能力仍不明确。本研究纳入了2005年至2015年在本机构接受西妥昔单抗和化疗且有病理标本的mCRC患者。采用免疫组织化学法检测HK2、PKM2和LDHA的表达。使用SPSS20进行统计分析。共纳入68例患者;33例接受西妥昔单抗联合化疗作为一线治疗,其余患者接受二线或更晚线治疗。与正常组织相比,癌组织中HK2表达水平升高(75.4%对40%;P<0.001),而PKM2(P=0.243)和LDHA(P=0.067)表达水平未升高。对于一线西妥昔单抗联合化疗的无进展生存期(PFS),HK2高表达患者的PFS长于HK2低表达患者(23.9个月对6.9个月;P=0.021)。然而,在35例仅接受一线化疗的患者中不存在这种正相关(13.4个月对13.5个月;P=0.539)。LDHA表达与接受一线化疗患者的PFS相关(高表达和低表达患者分别为18.3个月和10.1个月;P=0.005),而在西妥昔单抗联合化疗病例中不存在这种相关性(19.9个月对12个月;P=0.522)。此外,高LDHA表达与化疗的高总缓解率(ORR)相关(72.2%对15.4%,P=0.006),但与疾病控制率(DCR)无关(P=0.074)。DCR和ORR均与HK2表达无关。PKM2表达不影响PFS、DCR或ORR。对于所有一线患者,LDHA表达(P=0.005)、病理分化(P=0.019)和同时性/异时性转移(P=0.014)是PFS的独立预测因素,在多因素分析中肿瘤分化(P=0.002)与总生存期(OS)相关。HK2、PKM2和LDHA不影响OS。结论是,结直肠癌组织中HK2表达升高,可能预测西妥昔单抗疗效,而LDHA可预测mCRC化疗疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/133f/5840691/985ef4b46808/ol-15-04-5553-g00.jpg

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