Trastuzumab Rezetecan + Bevacizumab vs. TAS-102 + Bevacizumab in Pretreated mCRC With HER2 Low/Moderate Expression or HER2 Positivity With RAS/BRAF Mutation
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).
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Studientyp
Studientyp
Einschreibung (Geschätzt)
Einschreibung
Phase
Phase
- Phase 2
Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
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.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
|---|---|
|
Experimental: Trastuzumab Rezetecan + Bevacizumab
|
Trastuzumab rezetecan , Q2W; bevacizumab 5 mg/kg IV on Day 1, Q2W. |
|
Aktiver Komparator: 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. |
Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Objective Response Rate (ORR)
Zeitfenster: 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
|
Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Progression-Free Survival (PFS)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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)
|
Mitarbeiter und Ermittler
Sponsor
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Studienbeginn
Primärer Abschluss (Geschätzt)
Primärer Abschluss
Studienabschluss (Geschätzt)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
- Neubildungen nach Standort
- Neubildungen
- Darmerkrankungen
- Gastrointestinale Neubildungen
- Neoplasmen des Verdauungssystems
- Erkrankungen des Verdauungssystems
- Magen-Darm-Erkrankungen
- Darmtumoren
- Rektale Erkrankungen
- Darmerkrankungen
- Kolorektale Neubildungen
- Heterocyclische Verbindungen, 1-Ring
- Heterocyclische Verbindungen
- Nukleinsäuren, Nukleotide und Nukleoside
- Pyrimidin -Nucleoside
- Pyrimidine
- Nukleoside
- Desoxyribonukleoside
- Thymidin
- Trifluridin
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- MA-CRC-II-028
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .