- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning 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
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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.
Studietyp
Inskrivning (Beräknad)
Fas
- Fas 2
Kontakter och platser
Studiekontakt
- Namn: Jian Xiao, MD
- Telefonnummer: 86-20-83525975
- E-post: xiaojian@gdph.org.cn
Studera Kontakt Backup
- Namn: Xiaoru Lin
- Telefonnummer: 86-20-83525975
- E-post: ruya16128@163.com
Studieorter
-
-
Guangdong
-
Guangzhou, Guangdong, Kina, 510060
- Rekrytering
- Guangdong Provincial People's Hospital
-
Kontakt:
- Xiaoru Lin, Bachelor
- Telefonnummer: 80510 81884713
- E-post: ruya16128@163.com
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Beskrivning
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
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / 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
|
|
Experimentell: 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
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Objective Response Rate
Tidsram: 12 months
|
the proportion of participants who achieved a complete or partial response according to RECIST 1.1
|
12 months
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Progression-free Survival
Tidsram: 12 months
|
the interval from randomization to first disease progression or death from any cause or last follow-up
|
12 months
|
|
Overall Survival
Tidsram: 18 months
|
the interval from randomization to death from any cause or last follow-up
|
18 months
|
|
Adverse Events
Tidsram: 18 months
|
reported according to NCI Common Terminology Criteria for Adverse Events 5.0
|
18 months
|
Samarbetspartners och utredare
Utredare
- Huvudutredare: Jian Xiao, MD, Guangdong Provincial People's Hospital
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
- Patologiska processer
- Neoplasmer efter plats
- Neoplasmer
- Tarmsjukdomar
- Gastrointestinala neoplasmer
- Neoplasmer i matsmältningssystemet
- Matsmältningssystemets sjukdomar
- Gastrointestinala sjukdomar
- Kolorektala neoplasmer
- Intestinala neoplasmer
- Kolonsjukdomar
- Neoplastiska processer
- Patologiska tillstånd, tecken och symtom
- Kolonneoplasmer
- Neoplasma Metastas
- Aminosyror, peptider och proteiner
- Proteiner
- Heterocykliska föreningar
- Camptotecin
- Alkaloider
- Antikroppar, monoklonal, humaniserad
- Antikroppar, monoklonal
- Antikroppar
- Immunglobuliner
- Immunoproteiner
- Blodproteiner
- Serumglobuliner
- Globuliner
- Bevacizumab
- Irinotekan
- Cetuximab
- sintilimab
Andra studie-ID-nummer
- KY2024-373-03
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Läkemedels- och apparatinformation, studiedokument
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