- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07722754
Bevacizumab, Sintilimab, Cetuximab and Irinotecan in Refractory RAS Wild-type Metastatic Colorectal Cancer: BOND-4 Trial (BOND-4)
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
Studieoversikt
Status
Intervensjon / Behandling
Detaljert 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 (mCR) 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, programmed death-1 (PD-1) 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 11% in the control arm and 26% in the experimental arm, with a one-sided alpha of 0.05 and power of 80%, the required sample size is approximately 160 to account for 5% dropout.
Studietype
Registrering (Antatt)
Fase
- Fase 2
Kontakter og plasseringer
Studiekontakt
- Navn: Jian Xiao, MD
- Telefonnummer: 86-20-83525975
- E-post: xiaojian@gdph.org.cn
Studer Kontakt Backup
- Navn: Xiaoru Lin
- Telefonnummer: 86-20-83525975
- E-post: ruya16128@163.com
Studiesteder
-
-
Guangdong
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Guangzhou, Guangdong, Kina, 510060
- Rekruttering
- Guangdong Provincial People's Hospital
-
Ta kontakt med:
- Xiaoru Lin, Bachelor
- Telefonnummer: 80510 81884713
- E-post: ruya16128@163.com
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
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
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / 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
|
|
Eksperimentell: 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
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
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 |
Tiltaksbeskrivelse |
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
|
Samarbeidspartnere og etterforskere
Etterforskere
- Hovedetterforsker: Jian Xiao, MD, Guangdong Provincial People's Hospital
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Patologiske prosesser
- Neoplasmer etter nettsted
- Neoplasmer
- Tarmsykdommer
- Gastrointestinale neoplasmer
- Neoplasmer i fordøyelsessystemet
- Sykdommer i fordøyelsessystemet
- Gastrointestinale sykdommer
- Kolorektale neoplasmer
- Intestinale neoplasmer
- Kolonsykdommer
- Neoplastiske prosesser
- Patologiske tilstander, tegn og symptomer
- Kolon neoplasmer
- Neoplasma Metastase
- Aminosyrer, peptider og proteiner
- Proteiner
- Heterocykliske forbindelser
- Camptothecin
- Alkaloider
- Antistoffer, monoklonalt, humanisert
- Antistoffer, monoklonalt
- Antistoffer
- Immunoglobuliner
- Immunoproteiner
- Blodproteiner
- Serumglobuliner
- Globuliner
- Bevacizumab
- Irinotekan
- Cetuximab
- Sintilimab
Andre studie-ID-numre
- KY2024-373-03
Plan for individuelle deltakerdata (IPD)
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Legemiddel- og utstyrsinformasjon, studiedokumenter
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