PO.CTP01.03 · 进行中的临床试验
一项关于过去五年内有癌症病史患者肝移植结局的前瞻性观察性注册研究:评估肝移植资格
A prospective observational registry study on transplantation of liver outcomes in patients with a history of cancer within the past five years: Evaluating eligibility for liver transplantation
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摘要 Abstract
中文摘要
背景:肝移植(LT)当前的禁忌症之一是既往有肝外恶性肿瘤病史。有恶性肿瘤病史的候选者必须已接受确定性治疗,并在被考虑接受LT之前证明有充分的无瘤生存。为既往有恶性肿瘤的患者进行移植的挑战源于免疫抑制治疗下恶性肿瘤复发风险增加,以及在供体池有限的情况下对器官公平分配的担忧。研究表明,实体器官移植,尤其是在肾移植受者中,与移植前恶性肿瘤的高复发率相关。然而,LT不同于肾移植,它所需的免疫抑制水平较低,可能降低恶性肿瘤复发的风险。与肾衰竭不同(透析可作为过渡性治疗),肝衰竭患者没有等效的长期管理策略。因此,LT的最佳时机至关重要。在既往有肝外恶性肿瘤的患者中,肿瘤学缓解所需的等待期可能延迟LT资格。然而,在此期间,疾病进展可能导致出现额外的禁忌症,最终使LT无法进行并抵消其潜在获益。近期对一个关于移植前恶性肿瘤患者的大型公共数据库的分析表明,双肺移植(DLT)后的总生存率与无恶性肿瘤病史患者所观察到的相当。目前,针对肺局限性恶性肿瘤的双肺移植注册研究(DREAM)正在进行,纳入了一个因呼吸衰竭接受DLT、且过去五年内有恶性肿瘤病史的患者队列。本前瞻性观察性注册研究旨在更好地理解在Northwestern Medicine临床项目中,5年内有恶性肿瘤病史的患者接受肝移植的长期结局。本研究将评估标准化的患者选择和术后管理方法对该人群肝移植后长期生存的影响。将监测其临床病程,包括总生存、无病生存和移植物失功。
方法:这是一项针对肝衰竭且过去五年内有癌症病史、并符合Northwestern Medicine及参与中心肝移植纳入标准的患者的前瞻性观察性注册试验。将对转诊至Northwestern Medicine、正在接受肝移植且患有以下疾病的患者进行评估和筛查以纳入本注册研究:纳入疾病:1. 过去5年内有既往已治疗的非肝原发癌病史(处于缓解期)的肝衰竭患者 2. 合并活动性原发癌、在LT后接受根治性切除的肝衰竭患者。临床试验注册号:入组始于2025年8月18日。截至2025年11月18日,试验开放并持续招募参与者。
查看英文原文 English abstract
Background: One of the current contraindications to LT is a prior history of extrahepatic malignancy. Candidates with a history of malignancy must have undergone definitive treatment and demonstrated adequate tumor-free survival before being considered for LT. The challenge of transplanting patients with a prior malignancy arises from the increased risk of malignancy recurrence under immunosuppressive therapy and concerns regarding equitable organ allocation given the limited donor pool. Studies have shown that solid organ transplantation, particularly in kidney transplant recipients, is associated with a high recurrence rate of pretransplant malignancies. However, LT differs from kidney transplantation in that it requires lower levels of immunosuppression, potentially reducing the risk of malignancy recurrence. Unlike kidney failure, where dialysis can serve as a bridging therapy, there is no equivalent long-term management strategy for patients with liver failure. The optimal timing of LT is therefore critical. In patients with a prior extrahepatic malignancy, the necessary waiting period for oncologic remission may delay LT eligibility. However, during this period, disease progression may result in the development of additional contraindications, ultimately precluding LT and negating its potential benefits. A recent analysis of a large public database on patients with pretransplant malignancies demonstrates comparable overall survival rates following double lung transplantation (DLT) to those observed in patients without a history of malignancy. Currently, the Double Lung Transplant Registry for Lung-Limited Malignancies (DREAM) is underway, including a cohort of patients undergoing DLT for respiratory failure with a history of malignancy within the past five years. This prospective observational registry aims to better understand the long-term outcomes in patients undergoing liver transplantation with a history of malignancy within 5 years in the clinical programs at Northwestern Medicine. The study will assess the impact of a standardized approach to patient selection and postoperative management on long-term survival following liver transplantation in this population. Their clinical course, including overall survival, disease-free survival, and graft failure, will be monitored.
Methods: This is a prospective observational registry trial for patients with liver failure who have a history of cancer within the last five years, and who meet the inclusion criteria for liver transplantation at Northwestern Medicine and participating centers. Patients referred to Northwestern Medicine who are undergoing liver transplantation and have the following diseases will be assessed and screened for this registry: Diseases included: 1. Liver failure patients with a history of previously treated non-liver primary cancer within the last 5 years (in remission) 2. Liver failure patients with concomitant active primary cancer who undergo curative resection after LT. Clinical trial registry number : Enrollment began 8/18/25. Trial is open and continues to enroll participants as of 11/18/25.
利益披露 Disclosure
Y. Chae,
AbbVie ).
Bristol Myers Squibb ).
Biodesix ).
Freenome ).
Predicine ).
Regeneron Other, consulting fees, payments, and/or honoraria.
Roche/Genentech Other, consulting fees, payments, and/or honoraria.
AstraZeneca Other, consulting fees, payments, and/or honoraria.
Foundation Medicine Other, consulting fees, payments, and/or honoraria.
Neogenomics Other, consulting fees, payments, and/or honoraria.
Guardant Health Other, consulting fees, payments, and/or honoraria.
Boehringer Ingelheim Other, consulting fees, payments, and/or honoraria.
Biodesix Other, consulting fees, payments, and/or honoraria.
ImmuneOncia Other, consulting fees, payments, and/or honoraria.
Lilly Oncology Other, consulting fees, payments, and/or honoraria.
Merck Other, consulting fees, payments, and/or honoraria.
Takeda Other, consulting fees, payments, and/or honoraria.
Lunit Other, consulting fees, payments, and/or honoraria.
Jazz Pharmaceutical Other, consulting fees, payments, and/or honoraria.
Tempus Other, consulting fees, payments, and/or honoraria.
R. S. S. Min, None..
L. Chung, None..
L. Herbert, None..
J. Liskh, None..
S. Kim, None..
D. Shin, None..
H. Lee, None..
C. Moore, None..
S. Eswaran, None..
D. Hughes, None..
J. Boike, None..
A. Cheung, None..
D. Ganger, None..
J. Crismale, None..
T. Lee, None..
L. M. Kulik, None.
S. Thaker,
Madrigal Other, Advisory Board.
Ipsen Advisory Board.
T. Demir, None..
A. Duarte-Rojo, None.