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Trastuzumab Rezetecan + Bevacizumab vs. TAS-102 + Bevacizumab in Pretreated mCRC With HER2 Low/Moderate Expression or HER2 Positivity With RAS/BRAF Mutation

3 novembre 2026 aggiornato da: Ying Yuan, MD, Second Affiliated Hospital, Zhejiang University, School of Medicine

Trastuzumab Rezetecan or Trifluridine/Tipiracil in Combination With Bevacizumab in Patients With HER2 Low-to-Moderate Expressing or HER2-Positive RAS/BRAF-Mutant Metastatic Colorectal Cancer Refractory to Prior Chemotherapy: A Randomized Controlled Study

This is a randomized, open-label, study designed to evaluate the efficacy and safety of trastuzumab rezetecan plus bevacizumab versus trifluridine/tipiracil (FTD/TPI; TAS-102) plus bevacizumab in patients with metastatic colorectal cancer (mCRC) who have failed prior standard chemotherapy with fluoropyrimidines, oxaliplatin and irinotecan and whose tumors show HER2 low-to-moderate expression (IHC 2+ and ISH-negative, or IHC 1+) or HER2 positivity (IHC 3+ or IHC 2+ and ISH-positive) with a concomitant RAS or BRAF mutation.

86 eligible participants will be randomized in a 1:1 ratio to the experimental arm (trastuzumab rezetecan plus bevacizumab) or the control arm (trifluridine/tipiracil [TAS-102] plus bevacizumab). Randomization will be stratified by HER2 expression level (high vs. low-to-moderate) and by RAS/BRAF status (wild-type vs. mutant).

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

86

Fase

  • Fase 2

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria

  • Age ≥ 18 years; male or female.
  • Histologically or cytologically confirmed unresectable locally advanced or metastatic colorectal cancer.
  • Failure of prior therapy with fluoropyrimidines (e.g., 5-FU, capecitabine), oxaliplatin and irinotecan; participants with dMMR/MSI-H tumors must also have failed prior anti-PD-1/PD-L1 antibody therapy. Treatment failure is defined as:a) Disease progression (including metastasis or recurrence) during treatment;b) Disease progression within 6 months after the last dose of neoadjuvant or adjuvant therapy (including maintenance therapy);c) Permanent discontinuation of a fluoropyrimidine, oxaliplatin or irinotecan due to unacceptable non-hematologic toxicity or severe hypersensitivity, such that, in the investigator's judgment, the drug cannot be re-administered.
  • Able to provide a tumor tissue sample for HER2 expression testing;
  • HER2 low-to-moderate expression (IHC 2+ and FISH-negative, or IHC 1+), or HER2 positive (IHC 3+, or IHC 2+ and FISH-positive) with a RAS or BRAF mutation.
  • At least one measurable lesion according to RECIST v1.1; the measurable lesion must not have received prior radiotherapy or other local therapy (a lesion located within a previously irradiated field may be selected as a target lesion if progression has been documented).
  • ECOG performance status of 0-1.
  • Life expectancy ≥ 12 weeks.
  • Adequate major organ function as specified below (no administration of any blood products or cell growth factors is permitted within 14 days prior to screening laboratory tests):1) Adequate bone marrow reserve: absolute neutrophil count ≥ 1.5 × 10^9/L, platelets ≥ 100 × 10^9/L, hemoglobin ≥ 9 g/dL;2) Hepatic: serum albumin ≥ 3.0 g/dL, total bilirubin ≤ 1.5 × ULN, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × ULN; in the presence of liver metastases, ALT and/or AST ≤ 5 × ULN;3) Renal: serum creatinine ≤ 1.5 × ULN or creatinine clearance ≥ 60 mL/min (Cockcroft-Gault); if urinalysis shows urine protein ≥ ++, 24-hour urine protein must be documented as ≤ 1.0 g;4) Coagulation: activated partial thromboplastin time (APTT) and international normalized ratio (INR) ≤ 1.5 × ULN (participants receiving a stable dose of anticoagulant therapy, such as low-molecular-weight heparin or warfarin, with INR within the intended therapeutic range of the anticoagulant may be screened).
  • Fertile participants (male and female) must agree to use a highly effective method of contraception with their partner during the study and for at least 7 months after the last dose of study drug; women of childbearing potential must have a negative serum pregnancy test within 7 days prior to the first administration of study drug.
  • Voluntary participation in this study, signed informed consent, good compliance, and willingness to cooperate with follow-up.

Exclusion Criteria

  • Prior receipt of any of the following:1) Prior receipt of an anti-HER2 antibody-drug conjugate containing exatecan or an exatecan derivative as a topoisomerase I inhibitor, e.g., Enhertu (DS-8201a; trastuzumab deruxtecan); 2) Receipt of the last dose of anticancer therapy within 4 weeks before the first dose of study drug, including chemotherapy, radiotherapy, biotherapy, targeted therapy or immunotherapy; Chinese herbal medicine with anticancer indications within 2 weeks before the first dose of study drug; 3) Receipt of any unapproved investigational drug or treatment within 4 weeks before the first dose of study drug; 4) Requirement for systemic corticosteroids (greater than 10 mg/day prednisone equivalent) or other immunosuppressive agents within 2 weeks before the first dose of study drug; exceptions include the use of corticosteroids for local inflammation and for prophylaxis of allergy, nausea and vomiting; 5) Major surgery or severe trauma within 4 weeks before the first dose of study drug, or elective surgery planned during the study period; a traumatic minor procedure (e.g., needle biopsy) within 7 days before the first dose.
  • History of hypersensitivity to monoclonal antibodies or to any of the formulation excipients of trastuzumab rezetecan.
  • Toxicities from prior anticancer therapy that have not recovered to CTCAE v5.0 grade ≤ 1 (except toxicities judged by the investigator to carry no safety risk, e.g., alopecia) or to the level specified in the inclusion/exclusion criteria; participants who have received immune checkpoint inhibitors and have type 1 diabetes mellitus or hypothyroidism that is stable on hormone replacement therapy are eligible.
  • History of or current leptomeningeal metastasis; presence of active brain metastasis, defined as untreated and/or symptomatic disease, or disease requiring corticosteroids or antiepileptic drugs to control related symptoms. Participants who have received surgery or radiotherapy are eligible if screening imaging shows no evidence of progression for at least 4 weeks and symptoms have resolved (except residual signs or symptoms related to CNS treatment), corticosteroids have not been required for at least 2 weeks, and acute toxicities related to prior therapy have recovered.
  • Uncontrolled pleural effusion, pericardial effusion or ascites requiring repeated drainage.
  • Within 28 days before the first dose of study drug: inability to swallow, chronic diarrhea, gastroenteritis, intestinal obstruction, gastrointestinal perforation, ulcerative colitis or inflammatory bowel disease, or any other disease or condition that may affect oral administration or absorption of the study drug.
  • Bleeding tendency, high bleeding risk, coagulation disorder or thrombotic tendency, including but not limited to: imaging evidence that the tumor has invaded a major vessel, or, in the investigator's judgment, a high likelihood that the tumor will invade a major vessel during the study and cause fatal massive bleeding; grade > 1 pulmonary hemorrhage or grade > 2 bleeding at other sites within 4 weeks before enrollment; bleeding tendency (e.g., active peptic ulcer), or current treatment with thrombolytic or anticoagulant agents such as warfarin, heparin or their analogues.
  • Presence of a non-healing wound (severe, non-healing or dehisced), active peptic ulcer, or untreated fracture.
  • History of immunodeficiency, including a positive HIV test, or other acquired or congenital immunodeficiency disease, or a history of organ transplantation or allogeneic bone marrow transplantation.
  • Unexplained fever greater than 38.5 °C during screening or before the first dose (participants with tumor-related fever, as judged by the investigator, may be enrolled); severe infection (CTCAE grade > 2) within 4 weeks before the first dose of study drug, e.g., severe pneumonia, bacteremia or infectious complications requiring hospitalization; baseline chest imaging showing active pulmonary inflammation, or signs and symptoms of infection requiring oral or intravenous antibiotic therapy within 2 weeks before the first dose of study drug, except for prophylactic antibiotic use.
  • Known or suspected interstitial pneumonitis; other severe pulmonary disease significantly impairing respiratory function within 3 months before the first dose, including but not limited to idiopathic pulmonary fibrosis, organizing pneumonia/bronchiolitis obliterans, severe COPD, and severe obstructive or restrictive ventilatory dysfunction. Participants who developed grade ≥ 3 interstitial or immune-mediated pneumonitis during prior immune checkpoint inhibitor therapy, or who permanently discontinued such therapy because of interstitial or immune-mediated pneumonitis, are not eligible for this study.
  • Active hepatitis B (HBV DNA ≥ 500 IU/mL); hepatitis C (HCV antibody positive with HCV-RNA above the lower limit of detection of the assay).
  • Clinically significant cardiovascular disease, such as severe/unstable angina pectoris, symptomatic congestive heart failure (NYHA ≥ class II), clinically significant supraventricular or ventricular arrhythmia requiring treatment or intervention, arterial or venous thrombosis within 6 months before the first dose (except thromboses judged by the investigator to be not clinically significant, e.g., transient thrombosis caused by PICC line placement), acute coronary syndrome, myocardial infarction, cerebrovascular accident (including transient ischemic attack), or other grade ≥ 3 cardiovascular or cerebrovascular events; QTcF greater than 450 ms (male) or greater than 470 ms (female) on 12-lead ECG at rest; left ventricular ejection fraction < 50%; clinically uncontrolled hypertension.
  • Other malignancy within the past 5 years, except cured basal cell carcinoma of the skin and carcinoma in situ of the cervix.
  • Pregnant or breastfeeding women.
  • Any other factor that, in the investigator's judgment, may result in the participant's forced early termination from the study, such as other serious disease (including psychiatric disease) requiring concomitant treatment, severe laboratory abnormalities, or family or social factors that may affect the participant's safety or the collection of study data.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Trastuzumab Rezetecan + Bevacizumab

Trastuzumab rezetecan , Q2W; bevacizumab 5 mg/kg IV on Day 1, Q2W.

Comparatore attivo: Trifluridine/Tipiracil (TAS-102) + Bevacizumab

TAS-102 35 mg/m2 orally twice daily (BID) on Days 1-5 of each cycle (maximum single dose 80 mg); bevacizumab 5 mg/kg IV on Day 1, Q2W. Each cycle is 2 weeks.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Objective Response Rate (ORR)
Lasso di tempo: From the date of randomization until the date of first documented disease progression or death from any cause, whichever occurs first, assessed up to approximately 24 months
From the date of randomization until the date of first documented disease progression or death from any cause, whichever occurs first, assessed up to approximately 24 months

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
Progression-Free Survival (PFS)
Lasso di tempo: From randomization until disease progression or death from any cause, assessed up to approximately 24 months
From randomization until disease progression or death from any cause, assessed up to approximately 24 months
Overall Survival (OS)
Lasso di tempo: From randomization until death from any cause, assessed up to approximately 36 months
From randomization until death from any cause, assessed up to approximately 36 months
Number of participants with treatment-emergent adverse events (TEAEs) as assessed by CTCAE v5.0
Lasso di tempo: From the first dose of study treatment through 30 days after the last dose (approximately 24 months)
From the first dose of study treatment through 30 days after the last dose (approximately 24 months)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 dicembre 2026

Completamento primario (Stimato)

1 dicembre 2029

Completamento dello studio (Stimato)

1 dicembre 2030

Date di iscrizione allo studio

Primo inviato

20 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

3 novembre 2026

Primo Inserito (Effettivo)

9 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

9 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 novembre 2026

Ultimo verificato

1 ottobre 2026

Maggiori informazioni

Termini relativi a questo studio

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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