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Bevacizumab, Sintilimab, Cetuximab and Irinotecan in Refractory RAS Wild-type Metastatic Colorectal Cancer: BOND-4 Trial (BOND-4)

20. juli 2026 opdateret af: Guangdong Provincial People's Hospital

A Randomized, Multi-center, Open-label Phase II Trial of Irinotecan and Cetuximab With or Without the Combination of Bevacizumab and Sintilimab in RAS Wild-type, Irinotecan-refractory Metastatic Colorectal Cancer

Primary endpoint: objective response rate Secondary endpoints: PFS, OS and adverse events

Studieoversigt

Detaljeret beskrivelse

This randomized, multi-center, open-label phase II trial studies the efficacy and safety of irinotecan and cetuximab with or without bevacizumab plus sintilimab in the treatment for RAS wild-type metastatic colorectal cancer in third- or later-line setting.

Patients with refractory mCRC have limited treatment options after failure of standard chemotherapies and anti-angiogenic agents. The BOND-3 trial showed that adding bevacizumab to cetuximab and irinotecan may improve outcomes in this setting. Meanwhile, immune checkpoint inhibitors have demonstrated activity in MSI-high tumors but have limited efficacy in MSS mCRC. Preclinical and clinical evidence suggests that anti-VEGF therapy can modulate the tumor immune microenvironment and may synergize with PD-1 blockade. This study therefore tests whether the quadruple combination (bevacizumab + sintilimab + cetuximab + irinotecan) can improve objective response rate compared with cetuximab and irinotecan alone in this heavily pretreated population.

The primary efficacy analysis will be conducted on the intention-to-treat population. Assuming an ORR of 10% in the control arm and 30% in the experimental arm, with a two-sided alpha of 0.05 and power of 80%, the required sample size is approximately 70 patients per arm (total 140), and we enroll 160 to account for 10-15% dropout.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

160

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

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  • Ældre voksen

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Ingen

Beskrivelse

Inclusion Criteria:

  • Metastatic and unresectable colorectal adenocarcinom;
  • RAS wild-type and MSS tumor;
  • Measurable lesions;
  • Failed to at least two lines of standard treatment containing fluoropyrimidine, irinotecan and bevacizumab;
  • Eastern Cooperative Oncology Group performance status 2 or less;
  • White blood cell≥ 3*10^9/L, neutrophil≥ 1.5*10^9/Lplatelet count≥75*10^9/L, hemoglobin≥60g/L;
  • Total serum bilirubin≤upper limit of normal (ULN), alanine aminotransferase and aspartate aminotransferase ≤ 2.5*ULN or ≤5*ULN for subjects with liver metastasis;
  • Creatinine ≤ ULN or creatinine clearance ≥ 80 mL/min;
  • Urinary protein negative or 24-hour urinary protein ≤ 2g;
  • Activated partial thromboplastin time≤ULN and international normalized ratio≤1.5;
  • Any major surgery ≥ 4 weeks and any minor surgery ≥ 1 week and fully recovered from the procedure;
  • Life expectancy > 3 months;
  • Provide fully informed written consent;

Exclusion Criteria:

  • Other aggressive malignancies within 3 years (Exceptions: non-melanoma skin cancer or carcinoma-in-situ of the cervix that has been treated);
  • Allergy or intolerance to any of the study drugs;
  • Human immunodeficiency virus positive;
  • Concurrent anti-cancer therapy including radiation therapy, chemotherapy, targeted agents or biological agents not otherwise specified within two weeks;
  • Malignant bowel obstruction;
  • Prior treatment with PD-1 antibody;
  • Autoimmune diseases;
  • Significant bleeding events or pre-existing bleeding diathesis within 6 months (unless the source of bleeding has been resected);
  • Gastrointestinal perforation within 12 months;
  • Serious or non-healing wound, ulcer, or bone fracture;
  • Blood pressure >= 160/90 mmHg after active anti-hypertensive therapy;
  • Arterial or venous thrombotic or embolic events within 6 months (including but not limited to transient ischemic attack, cerebrovascular accident, unstable angina or myocardial infarction);
  • Uncontrolled illness including active infection, symptomatic congestive heart failure, cardiac arrhythmia, respiratory failure, symptomatic pulmonary fibrosis, interstitial pneumonitis or psychiatric illness that may interfere with the conduct of the study;
  • Known or suspected brain or central nervous system (CNS) metastases, or carcinomatous meningitis;
  • Any of the following: pregnant, nursing, childbearing potential but unwilling to employ contraception.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: CI Arm
Cetuximab: 250mg/m^2/week with a loading dose of 400mg/m^2; Irinotecan: 125mg/m^2 on D1 and D8 every three weeks.
250mg/m^2/week with a loading dose of 400mg/m^2
125mg/m^2 on D1 and D8 every three weeks
Eksperimentel: CIBS Arm
Cetuximab: 250mg/m^2/week with a loading dose of 400mg/m^2; Irinotecan: 125mg/m^2 on D1 and D8 every three weeks; Bevacizumab: 7.5mg/kg every three weeks ; Sintilimab: 200mg every three weeks.
250mg/m^2/week with a loading dose of 400mg/m^2
125mg/m^2 on D1 and D8 every three weeks
7.5mg/kg every three weeks
200mg every three weeks

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Objective Response Rate
Tidsramme: 12 months
the proportion of participants who achieved a complete or partial response according to RECIST 1.1
12 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Progression-free Survival
Tidsramme: 12 months
the interval from randomization to first disease progression or death from any cause or last follow-up
12 months
Overall Survival
Tidsramme: 18 months
the interval from randomization to death from any cause or last follow-up
18 months
Adverse Events
Tidsramme: 18 months
reported according to NCI Common Terminology Criteria for Adverse Events 5.0
18 months

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Jian Xiao, MD, Guangdong Provincial People's Hospital

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. august 2026

Primær færdiggørelse (Anslået)

31. juli 2028

Studieafslutning (Anslået)

31. januar 2029

Datoer for studieregistrering

Først indsendt

20. juli 2026

Først indsendt, der opfyldte QC-kriterier

20. juli 2026

Først opslået (Faktiske)

23. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

23. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

20. juli 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

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INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Ingen

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