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TRANsplantation vs reSECTion After Conversion Therapy for Initially Unresectable Colorectal Liver Metastases (TRANSECT)

2026年7月16日 更新者:Niguarda Hospital

TRANsplantation vs reSECTion After Conversion Therapy for Initially Unresectable

The TRANSECT trial is a prospective randomized study designed to evaluate the role of liver transplantation (LT) versus radical local treatment (hepatic resection and/or ablation) in patients with initially unresectable colorectal liver metastases (CRLM) converted to resectability after conversion therapy.

Liver metastases are the leading cause of mortality in colorectal cancer patients. Although hepatic resection combined with chemotherapy remains the standard curative-intent treatment, only a minority of patients are eligible for upfront surgery. Advances in modern conversion chemotherapy have substantially increased the proportion of patients who can subsequently undergo curative local treatment. However, liver resection after intensive chemotherapy is still associated with high rates of intrahepatic recurrence, risk of R1 resections, chemotherapy-induced liver injury, and the need for complex surgical procedures carrying considerable morbidity and mortality. In parallel, recent studies investigating LT for unresectable CRLM, including the TRANSMET trial, demonstrated highly promising oncological outcomes, with 5-year overall survival rates exceeding 50% in selected patients.

Based on these findings, the TRANSECT trial hypothesizes that LT may represent a more effective therapeutic strategy also in patients initially deemed unresectable but subsequently converted to resectability, by completely removing the hepatic metastatic niche.

TRANSECT is a single-center, randomized, open-label, proof-of-concept trial. Patients with liver-only CRLM initially assessed as unresectable by a dedicated multidisciplinary tumor board and subsequently converted to resectability after systemic therapy will be randomized to either LT or hepatic resection and/or ablation. The primary endpoint is 3-year intention-to-treat overall survival (OS). Secondary endpoints include perioperative morbidity and mortality, disease-free survival, treatment adherence, quality of life, and exploratory translational analyses including radiomics and circulating tumor DNA assessment.

A total of 70 patients (35 per arm) will be enrolled, with an estimated overall study duration of 5 years. TRANSECT represents the first randomized trial directly comparing LT and liver-directed surgery in patients with initially unresectable CRLM converted to resectability after systemic therapy, with the aim of redefining curative treatment strategies in this selected patient population.

調査の概要

詳細な説明

Liver metastases represent the leading cause of mortality in patients with colorectal cancer. Although hepatic resection combined with systemic therapy remains the standard curative-intent treatment, a substantial proportion of patients present with disease that is initially unresectable at diagnosis.

Over the last years, advances in systemic chemotherapy and targeted therapies have significantly increased conversion-to-resectability rates in patients with initially unresectable colorectal liver metastases. As systemic therapies continue to improve, the number of patients achieving conversion from initially unresectable to potentially resectable disease is expected to progressively increase, making this clinical scenario increasingly relevant in daily practice.

However, surgical treatment after conversion therapy remains associated with important oncological and surgical challenges. A complete radiological response does not necessarily correspond to a complete pathological response, with the possible persistence of microscopic residual disease and a consequent risk of intrahepatic recurrence. In addition, prolonged exposure to chemotherapy may result in liver toxicity and impairment of the residual liver parenchyma, increasing the complexity of surgical strategies required to achieve radical resection and raising the risk of post-hepatectomy liver failure.

In this context, liver transplantation may represent an alternative therapeutic strategy that could overcome some of the limitations of resective surgery by completely replacing the metastatic liver and eradicating both macroscopic and microscopic residual disease.

This is a single-center, prospective, randomized, open-label, proof-of-concept study designed to compare liver transplantation with radical local treatment in patients with colorectal liver metastases initially unresectable and subsequently converted to resectability following systemic therapy.

Patient evaluation will be performed through a centralized multidisciplinary assessment involving hepatobiliary surgeons, transplant surgeons, oncologists, and radiologists with specific expertise in the management of colorectal liver metastases. All cases will be discussed within a multidisciplinary tumor board with centralized imaging review both at diagnosis and after systemic therapy in order to define initial unresectability and subsequent potential conversion to resectability in a standardized manner.

The definition of unresectability will consider anatomical, oncological, and functional criteria, including the possibility of achieving complete radical (R0) resection, the predicted future liver remnant volume, the need for complex surgical procedures, and the presence of factors associated with increased surgical or oncological risk. Similarly, conversion to resectability will be defined according to the possibility of achieving radical local treatment with curative intent following systemic therapy.

All patients will undergo centralized radiological reassessment with contrast-enhanced CT scan and MRI; FDG-PET imaging will be performed when clinically indicated. During systemic treatment, radiological reassessments will be performed periodically to monitor oncological response, confirm the absence of extrahepatic disease, and evaluate eligibility for radical local treatment.

Eligible patients will receive induction systemic therapy according to institutional clinical practice and, in case of conversion to resectability and maintenance of eligibility criteria, will be randomized in a 1:1 ratio to one of the two treatment strategies provided by the protocol:

  • liver transplantation;
  • radical local treatment consisting of hepatic resection with or without ablative procedures.

In the liver transplantation arm, patients will continue systemic therapy until being listed for liver transplantation or until a transplantation date is established. If transplantation is not performed within two months after listing, patients will undergo repeat clinical, radiological, and biochemical reassessment, including imaging studies and tumor marker evaluation. In the presence of disease progression or increased tumor marker levels, patients may be temporarily suspended from the transplant waiting list and started on additional systemic therapy, followed by reassessment according to protocol-defined criteria. In the case of disease control, patients may be reconsidered for the transplant pathway. Otherwise, treatment will continue according to standard clinical practice.

In the surgical arm, radical local treatment will consist of hepatic resection with or without ablative procedures, according to multidisciplinary evaluation and the surgical strategy considered most appropriate to achieve complete disease control.

The study includes the evaluation of oncological, perioperative, and treatment adherence outcomes, in addition to exploratory translational analyses including radiomic characteristics, quality of life, and circulating biomarkers.

Patients will undergo clinical, laboratory, and radiological follow-up according to the study protocol and institutional clinical practice in order to monitor disease recurrence, oncological outcomes, and treatment safety.

研究の種類

介入

入学 (推定)

70

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria screening phase (before randomization):

  • Signed screening phase informed consent.
  • Age >18.
  • Performance status score of Eastern Cooperative Oncology Group (PS-ECOG) 0-1
  • Adequate organ functions.
  • Liver-limited Metastatic Disease Confirmed as Unresectable by Colorectal Oncology Multidisciplinary Tumor Board (MTB).
  • Histologically documented adenocarcinoma of the colon or intra-peritoneal rectum
  • Absence of extra-hepatic disease demonstrated by contrast-enhanced CT + MRI and, in clinically indicated (clinical suspicion or elevated biomarkers), FDG-PET.
  • No previous systemic treatment for unresectable disease.
  • No previous systemic treatment for primary tumor resection
  • Recurrence occurring beyond six months after completion of adjuvant treatment.
  • MMR proficient cancer (MSS) regardless of RAS mutational status, BRAF-WT except for BRAF V600E-mut treated and responding to anti-BRAF + cytotoxic therapy.

Exclusion criteria:

  • Absolute contraindication to liver transplant.
  • Other malignancies in the previous 5 years excluding non melanoma skin-cancers or in situ disease.
  • Hereditary CRC syndromes including FAP and Lynch syndrome.
  • Previous extrahepatic metastatic localization or locoregional tumor recurrence.
  • Extra-peritoneal cancers.
  • BRAFV600E-mut patients non-responder to 1st line anti-BRAF + cytotoxic therapy (Elez et al NEJM 2025, ref. 8)

Randomization inclusion criteria:

  • Signed randomization phase informed consent.
  • CEA < 80 ng/ml or decrease in CEA level at least 50% from baseline (TRANSMET criteria (5)).
  • Conversion to resectability according to MTB discussion during first 6 months of induction chemotherapy.
  • Sustained objective response defined as stable disease (SD), partial response (PR) or complete response (CR) according to Response Evaluation Criteria in Solid Tumors (RECIST) criteria (19), under chemotherapy, for at least 3 months.
  • Surgical resection of the primary tumor with a high oncological standard, as outlined in The American Society of Colon and Rectal Surgeons Clinical Practice Guidelines for the Management of Colon Cancer (20), ensuring safe margins of resection and adequate TNM staging.
  • Histologically confirmed primary tumor with achievement of R0 resection.
  • Three months interval from primary tumor resection to randomization in patients staged up to pT3b and pN1.
  • Only metachronous metastases are eligible in pT4a and/or pN2 primary. For pT4a tumors, a minimum disease-free interval of 6 months from primary tumor resection is required before randomization.
  • Absence of local recurrence and extra-hepatic disease demonstrated by contrast-enhanced CT + MRI and, in clinically indicated (clinical suspicion or elevated biomarkers), FDG-PET.
  • PS-ECOG 0-1.
  • Adequate organ functions.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Transplantation
Participants randomized to this arm will undergo liver transplantation after successful conversion to resectability following systemic therapy. In case of disease progression during the waiting period, patients may receive additional systemic therapy and be re-evaluated for transplant eligibility. In case of loss of eligibility, the patient will undergo the best standard of care (including resection). Post-transplant management will follow standard institutional protocols, including immunosuppressive therapy and oncologic follow-up.
Orthotopic liver transplantation performed in patients with colorectal liver metastases after successful conversion to resectability following systemic therapy. Eligibility for transplantation is confirmed through multidisciplinary evaluation and restaging. Patients continue systemic therapy after randomization until listing for transplantation or until the date of the procedure is established. Postoperative management includes standard immunosuppressive therapy and oncologic follow-up according to institutional protocols
アクティブコンパレータ:Resection
Participants randomized to this arm will undergo radical local treatment consisting of hepatic resection with or without ablative techniques after successful conversion to resectability following systemic therapy. The surgical approach will be determined based on tumor characteristics and institutional standards, with the goal of achieving complete tumor removal (R0 resection). Perioperative management and postoperative care will follow standard clinical practice
Liver resection with or without ablative techniques in patients with colorectal liver metastases after successful conversion to resectability following systemic therapy. Patients continue systemic therapy after randomization until the surgical procedure is performed, according to protocol. The surgical strategy is determined by a multidisciplinary team with the aim of achieving complete tumor removal (R0 resection). Perioperative and postoperative management follow standard institutional practice

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Overall Survival (OS)
時間枠:3 years
Overall survival will be measured from the date of randomization to death from any cause and analyzed according to the intention-to-treat principle.
3 years

二次結果の測定

結果測定
メジャーの説明
時間枠
Disease-Free Survival (DFS)
時間枠:Up to 3 years
Disease-free survival is defined as the time from the date of treatment (liver transplantation or hepatic resection ± ablation) to the date of tumor recurrence or death from any cause, whichever occurs first.
Up to 3 years
Perioperative Morbidity
時間枠:90 days after treatment
Assessment of postoperative complications occurring within 90 days after liver transplantation or hepatic resection + ablation, graded according to standard clinical classifications.
90 days after treatment
Perioperative Mortality
時間枠:90 days after treatment
All-cause mortality occurring within 90 days after liver transplantation or hepatic resection + ablation
90 days after treatment

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Stefano Di Sandro, MD、ASST Grande Ospedale Metropolitano Niguarda

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年6月1日

一次修了 (推定)

2029年6月15日

研究の完了 (推定)

2031年6月15日

試験登録日

最初に提出

2026年5月14日

QC基準を満たした最初の提出物

2026年5月22日

最初の投稿 (実際)

2026年5月26日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月17日

QC基準を満たした最後の更新が送信されました

2026年7月16日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

After request to the PI and evaluation of the research intent.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

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