Department of General Surgery, Cleveland Clinic, Digestive Diseases and Surgery Institute, Cleveland, Ohio, USA.
Department of Gastroenterology, Hepatology & Nutrition, Cleveland Clinic, Digestive Diseases and Surgery Institute, Cleveland, Ohio, USA.
Liver Transpl. 2024 Dec 1;30(12):1238-1249. doi: 10.1097/LVT.0000000000000417. Epub 2024 Jun 5.
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.
我们描述了一种新的肝移植前(LT)方法,用于结直肠癌肝转移,可在将患者移植之前改善肿瘤生物学监测并降低疾病负担。克利夫兰诊所接受 LT 治疗的结直肠癌肝转移患者被纳入研究。该描述的方案包括强化局部区域治疗和全身化疗,旨在通过正电子发射断层扫描和癌胚抗原检测达到最小疾病负担。没有检测到疾病或不可逆转的治疗引起的肝损伤的患者接受移植。在 27 名接受评估的患者中,有 9 名接受了肝移植(33.3%)。中位随访时间为 700 天。7 名患者(77.8%)接受了活体供肝 LT。5 名患者无疾病检测,4 名患者存在治疗诱导性肝硬化。移植前管理包括化疗(n = 9)+/-贝伐单抗(n = 6)和/或抗 EGFR(n = 6)。化疗的中位预 LT 周期数为 16 个(范围 10-40)。肝靶向治疗包括钇 90(n = 5)、消融(n = 4)、切除(n = 4)和肝动脉输注泵(n = 3)。3 名患者在 LT 后复发。1 年和 2 年无复发生存率分别为 75%(n = 6/8)和 60%(n = 3/5)。复发发生在肺部(n = 1)、肝移植(n = 1)和肺部+主动脉旁淋巴结(n = 1)。LT 前有疾病检测的患者 RFS 降低(p = 0.04)。所有复发患者的肝移植标本中均有组织学上存活的肿瘤。在我们的方案中治疗的患者(n = 16)与不符合移植条件的患者(n = 11)相比,无论移植状态如何,生存均得到改善(p = 0.01)。对于可检测到疾病或治疗引起的肝损伤的患者,通过强化移植前肝靶向治疗和移植的方案可能有助于预防肿瘤复发。