大肠癌肝转移肝移植前的局部强化治疗:新颖的移植前治疗方案

IF 4.7 2区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Liver Transplantation Pub Date : 2024-12-01 Epub Date: 2024-06-05 DOI:10.1097/LVT.0000000000000417
Chase J Wehrle, Masato Fujiki, Andrea Schlegel, Melis Uysal, Anastasia Sobotka, Maureen Whitsett Linganna, Jamak Modaresi Esfeh, Suneel Kamath, Mazhar Khalil, Alejandro Pita, Jae-Keun Kim, David C H Kwon, Charles Miller, Koji Hashimoto, Federico Aucejo
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引用次数: 0

摘要

背景:我们描述了一种治疗结直肠肝转移(CRLM)的新型肝移植前(LT)方法,该方法可在患者接受移植前改善肿瘤生物学监测并减轻疾病负担:方法:纳入在克利夫兰诊所接受LT治疗的CRLM患者。所述方案包括强化局部治疗和全身化疗,目的是使 PET 扫描和 CEA 显示的疾病负担最小。检测不到疾病或治疗引起的不可逆转的肝损伤的患者将接受移植手术:在接受评估的27名患者中,有9名患者接受了肝移植(33.3%)。中位随访时间为 700 天。七名患者(77.8%)接受了活体肝移植。其中五人未发现疾病,四人患有治疗诱发的肝硬化。移植前治疗包括化疗(9例)+/-贝伐单抗(6例)和/或抗EGFR(6例)。肝移植前化疗周期中位数=16(范围10-40)。肝脏定向治疗包括钇-90(5例)、消融(4例)、切除(4例)和HAI-泵(3例)。3名患者在LT治疗后复发。精算的1年和2年无复发生存率分别为75%(6/8)和60%(3/5)。复发发生在肺部(n=1)、肝脏移植物(n=1)和肺部+主动脉旁结节(n=1)。LT前可检测到疾病的患者RFS降低(P=0.04)。所有复发患者的肝脏移植组织学肿瘤均存活。接受我们方案治疗的患者(16 例)与非候选者(11 例)相比,无论移植情况如何,生存率都有所提高(P=0.01):结论:通过积极的移植前肝脏导向治疗和对未检测到疾病或治疗引起肝损伤的患者进行移植,可帮助预防肿瘤复发。
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Intensive locoregional therapy before liver transplantation for colorectal cancer liver metastasis: A novel pretransplant protocol.

We describe a novel pre-liver transplant (LT) approach in colorectal liver metastasis, allowing for improved monitoring of tumor biology and reduction of disease burden before committing a patient to transplantation. Patients undergoing LT for colorectal liver metastasis at Cleveland Clinic were included. The described protocol involves intensive locoregional therapy with systemic chemotherapy, aiming to reach minimal disease burden revealed by positron emission tomography scan and carcinoembryonic Ag. Patients with no detectable disease or irreversible treatment-induced liver injury undergo transplant. Nine patients received liver transplant out of 27 who were evaluated (33.3%). The median follow-up was 700 days. Seven patients (77.8%) received a living donor LT. Five had no detectable disease, and 4 had treatment-induced cirrhosis. Pretransplant management included chemotherapy (n = 9) +/- bevacizumab (n = 6) and/or anti-EGFR (n = 6). The median number of pre-LT cycles of chemotherapy was 16 (range 10-40). Liver-directed therapy included Yttrium-90 (n = 5), ablation (n = 4), resection (n = 4), and hepatic artery infusion pump (n = 3). Three patients recurred after LT. Actuarial 1- and 2-year recurrence-free survival were 75% (n = 6/8) and 60% (n = 3/5). Recurrence occurred in the lungs (n = 1), liver graft (n = 1), and lungs+para-aortic nodes (n = 1). Patients with pre-LT detectable disease had reduced RFS ( p = 0.04). All patients with recurrence had histologically viable tumors in the liver explant. Patients treated in our protocol (n = 16) demonstrated improved survival versus those who were not candidates (n = 11) regardless of transplant status ( p = 0.01). A protocol defined by aggressive pretransplant liver-directed treatment and transplant for patients with the undetectable disease or treatment-induced liver injury may help prevent tumor recurrence.

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来源期刊
Liver Transplantation
Liver Transplantation 医学-外科
CiteScore
7.40
自引率
6.50%
发文量
254
审稿时长
3-8 weeks
期刊介绍: Since the first application of liver transplantation in a clinical situation was reported more than twenty years ago, there has been a great deal of growth in this field and more is anticipated. As an official publication of the AASLD, Liver Transplantation delivers current, peer-reviewed articles on liver transplantation, liver surgery, and chronic liver disease — the information necessary to keep abreast of this evolving specialty.
期刊最新文献
Management of the liver transplant candidate with high cardiac risk: Multidisciplinary best practices and recommendations. An international, multicenter, survey-based analysis of practice and management of acute liver failure. Utility of scores to predict alcohol use after liver transplant: Take them with a grain of salt. Intensive locoregional therapy before liver transplantation for colorectal cancer liver metastasis: A novel pretransplant protocol. Association of psychosocial risk factors and liver transplant evaluation outcomes in metabolic dysfunction-associated steatotic liver disease.
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