TP53 Mutation Predicts Worse Survival and Earlier Local Progression in Patients with Hepatocellular Carcinoma Treated with Transarterial Embolization.

IF 3.4 4区 医学 Q2 ONCOLOGY Current oncology Pub Date : 2025-01-18 DOI:10.3390/curroncol32010051
Ken Zhao, Anita Karimi, Luke Kelly, Elena Petre, Brett Marinelli, Erica S Alexander, Vlasios S Sotirchos, Joseph P Erinjeri, Anne Covey, Constantinos T Sofocleous, James J Harding, William Jarnagin, Carlie Sigel, Efsevia Vakiani, Etay Ziv, Hooman Yarmohammadi
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Abstract

The aim of this study was to evaluate associations between TP53 status and outcomes after transarterial embolization (TAE) for the treatment of patients with hepatocellular carcinoma (HCC). This single-institution study included patients from 1/2014 to 6/2022 who underwent TAE of HCC and genomic analysis of tumoral tissue. The primary outcome was overall survival (OS) with relation to TP53 status, and the secondary outcome was the time to progression. Survival analysis was performed using the Kaplan-Meier method. The time to progression with death or the last patient contact without progression as competing risks were used to obtain a cumulative incidence function, and the association with TP53 status was evaluated using the Gray test. In total, 75 patients (63 men) with a median age of 70.0 (IQR 62.0-76.3) years were included. Of these, 26/75 (34.7%) patients had TP53-mutant HCC. Patients with TP53-mutant HCC had a significantly worse median OS of 15.2 (95% CI, 9.5-29.3) months, versus 31.2 (95% CI, 21.2-52.4) months as the median OS (p = 0.023) for TP53 wild-type HCC. Competing risk analysis showed a shorter time to local hepatic progression (at the site of the previously treated tumor) after TAE in patients with TP53-mutant HCC. The cumulative incidences of local progression at 6 and 12 months for TP53-mutant HCC were 65.4% and 84.6%, versus 40.8% and 55.1% for TP53 wild-type HCC (p = 0.0072). A TP53 mutation may predict a worse overall survival and a shorter time to local progression in HCC patients treated with TAE.

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经动脉栓塞治疗的肝细胞癌患者TP53突变预示更差的生存和更早的局部进展
本研究的目的是评估经动脉栓塞(TAE)治疗肝细胞癌(HCC)患者后TP53状态与预后之间的关系。这项单机构研究纳入了2014年1月至2022年6月期间接受HCC TAE和肿瘤组织基因组分析的患者。主要终点是与TP53状态相关的总生存期(OS),次要终点是进展时间。采用Kaplan-Meier法进行生存分析。以死亡至进展的时间或作为竞争风险的最后一次患者接触无进展的时间来获得累积发生率函数,并使用Gray检验评估与TP53状态的关联。共纳入75例患者(63例男性),中位年龄为70.0 (IQR 62.0-76.3)岁。其中,26/75(34.7%)患者为tp53突变型HCC。TP53突变型HCC患者的中位生存期明显更差,为15.2 (95% CI, 9.5-29.3)个月,而TP53野生型HCC患者的中位生存期为31.2 (95% CI, 21.2-52.4)个月(p = 0.023)。竞争风险分析显示,在tp53突变型HCC患者中,TAE后局部肝脏进展(在先前治疗过的肿瘤部位)的时间更短。TP53突变型HCC 6个月和12个月局部进展的累积发生率分别为65.4%和84.6%,而TP53野生型HCC为40.8%和55.1% (p = 0.0072)。在接受TAE治疗的HCC患者中,TP53突变可能预示着更差的总生存期和更短的局部进展时间。
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来源期刊
Current oncology
Current oncology ONCOLOGY-
CiteScore
3.30
自引率
7.70%
发文量
664
审稿时长
1 months
期刊介绍: Current Oncology is a peer-reviewed, Canadian-based and internationally respected journal. Current Oncology represents a multidisciplinary medium encompassing health care workers in the field of cancer therapy in Canada to report upon and to review progress in the management of this disease. We encourage submissions from all fields of cancer medicine, including radiation oncology, surgical oncology, medical oncology, pediatric oncology, pathology, and cancer rehabilitation and survivorship. Articles published in the journal typically contain information that is relevant directly to clinical oncology practice, and have clear potential for application to the current or future practice of cancer medicine.
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