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Brachytherapy Followed by Nivolumab Prior to Surgery in Rectal Cancer (IMPERIA)

8 juni 2026 bijgewerkt door: Dr. Te Vuong

Pilot Evaluation of the Immunogenic Potentiation of Neo-adjuvant Brachytherapy Followed by Nivolumab Immunotherapy Without Chemotherapy in Stage II/III Locally Advanced Mismatch Repair Proficient Rectal Cancer

This is a small Phase II study testing whether targeted internal radiation treatment (HDREBT) followed by two doses of the immunotherapy drug Nivolumab is safe, practical, and potentially effective before patients undergo surgery (TME) to remove rectal cancer.

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Geschat)

10

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Quebec
      • Montreal, Quebec, Canada, H3T 1E2
        • Jewish General Hospital
        • Contact:

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  1. Age ≥18 years at the time of consent.
  2. Histologically confirmed rectal adenocarcinoma arising within 5 to 15 cm of the anal verge as measured by sigmoidoscopy or MRI.
  3. Rectal cancer staging:

    1. Clinical Stage cT2 or cT3 based on high resolution pelvic MRI;
    2. No evidence of distant metastases (cM0) on contrast -enhanced CT of chest, abdomen and pelvis (or PET/CT if clinically indicated);
    3. Disease deemed technically resectable with curative intent by multidisciplinary tumor board (MDT)*. No radiologic evidence of unresectable local disease (e.g., tumor fixation or invasion of adjacent unresectable structures).
  4. At least one of the following adverse prognostic features observed on baseline MRI:

    1. Node-positive disease (cN+);
    2. Threatened mesorectal fascia (MRF) defined as distance from tumor to mesorectal fascia < 1mm on pelvic MRI;
    3. Extramural venous invasion (EMVI+).
  5. Proficient mismatch repair (pMMR) status, as determined by immunohistochemistry and/or microsatellite instability-low (MSI-L) status by next-generation sequencing
  6. Planned management includes neoadjuvant therapy with radiotherapy followed by curative-intent TME.
  7. Prior external beam pelvic radiation for other malignancy (prostate, gynecology, lymphoma, bladder) are acceptable, provided the colorectal surgeon deems the patient as a candidate for TME surgery.
  8. ECOG performance status of 0-2
  9. Adequate organ function, defined by:

    1. Absolute Neutrophil Count (ANC) ≥ 1.5 x 109/L
    2. Platelets ≥ 100 x 109/L
    3. Hemoglobin ≥ 90 g/L
    4. Estimated creatinine clearance ≥ 30 mL/min
    5. Total bilirubin ≤ 1.5 x ULN (except for patients with Gilbert's syndrome who may only be included with total bilirubin ≤ 3.0 x ULN)
    6. Aspartate transaminase (AST) ≤ 3.0 x ULN
    7. Alanine transaminase (ALT) ≤ 3.0 x ULN
    8. INR ≤ 1.5 ULN
    9. aPTT and PT ≤ 1.5 ULN
    10. Albumin ≥ 25 g/L
  10. Ability to understand, willing to provide written informed consent, and to comply with study requirements.

Exclusion Criteria:

  1. Prior anticancer therapy for rectal cancer.
  2. Contraindication to safe MRI imaging.
  3. Evidence of bowel obstruction on MRI or clinical evaluation.
  4. Evidence of distant metastasis.
  5. Medical or surgical contraindications to major pelvic surgery
  6. Active autoimmune disease requiring systemic immunosuppressive therapy.
  7. Active/uncontrolled infection. Infectious screening for HIV, Hepatitis B (HBV), Hepatitis C (HBC) and tuberculosis will be performed at screening:

    1. Participants who are hepatitis B surface antigen (HBsAg) positive are eligible if they have received HBV anti-viral therapy for at least 4 weeks; and have undetectable HBV viral load prior to starting treatment. Participants should remain on anti-viral therapy throughout study intervention and follow local guidelines for HBV anti-viral therapy post completion of study intervention.
    2. Participants with a history of HCV infection are eligible if HCV viral load is undetectable at screening. Note: Participants must have completed curative anti-viral therapy at least 4 weeks prior to start of treatment.
    3. HIV-infected participants must have well-controlled HIV on antiretroviral treatment (ART), defined as:

    i. have a CD4+ T-cell count ≥ 0.35 x109 cells/L at the time of screening. ii. must have achieved and maintained virologic suppression defined as confirmed HIV ribonucleic acid (RNA) level below 50 or the LLOQ (below the limit of detection) using the locally available assay at the time of screening and for at least 12 weeks before screening.

    iii. must not have had any AIDS-defining opportunistic infections within the past 12 months.

    iv. must have been on a stable regimen, without changes in drugs or dose modification, for at least 4 weeks before start of treatment and agree to continue ART throughout the study.

  8. Known allergy or hypersensitivity to nivolumab or any of its excipients.
  9. Patients with other psychiatric, social or severe or uncontrolled medical conditions that in the opinion of the investigator may compromise their compliance with the protocol or may represent an unacceptable risk to their safety (e.g. uncontrolled diabetes, active or uncontrolled infection, uncontrolled clinically significant cardiovascular disease).
  10. Requirement for prohibited concomitant medication, as outlined in section 8.4 within 14 days prior to first brachytherapy treatment.
  11. Treatment with other investigational agents (defined as not used in accordance with the approved indication) within 28 days of first neo-adjuvant treatment.
  12. Patients who are pregnant or breastfeeding or WOCBP not employing an effective method of birth control.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Brachytherapy (HDREBT) followed by nivolumab and total mesorectal excision
HDREBT (26 Gy delivered in 4 fractions over Days 1-4) followed by up to 2 doses of nivolumab (3 mg/kg mg IV every 2 weeks starting at 7-14 days post HDREBT). Surgical resection of tumor (6-8 weeks post HDREBT)
2 doses of nivolumab 3 mg/kg mg IV every 2 weeks
26 Gy in 4 fractions Administered over Days 1-4 as per institutional standard
Targeted to take place 6-8 weeks post completion of HDREBT (maximum 12 weeks)

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Pathologic complete response (pCR)
Tijdsspanne: This is assessed at the time of total mesorectal excision surgery, occurring approximately 12 weeks after enrollment.
This is assessed at the time of total mesorectal excision surgery, occurring approximately 12 weeks after enrollment.

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Incidence and severity of adverse events, as per CTCAE criteria v6.0
Tijdsspanne: From time of first treatment through 90 days following last treatment with nivolumab
From time of first treatment through 90 days following last treatment with nivolumab
Assess feasibility of treatment sequence
Tijdsspanne: This is assessed from the time of enrollment until the time of surgery, approximately 12 weeks after enrolment.
Completion of treatment of all treatment modalities within protocol-defined timeframes (brachytherapy, immunotherapy and surgery)
This is assessed from the time of enrollment until the time of surgery, approximately 12 weeks after enrolment.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

1 juli 2026

Primaire voltooiing (Geschat)

1 december 2028

Studie voltooiing (Geschat)

1 december 2030

Studieregistratiedata

Eerst ingediend

2 juni 2026

Eerst ingediend dat voldeed aan de QC-criteria

8 juni 2026

Eerst geplaatst (Werkelijk)

12 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

12 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

8 juni 2026

Laatst geverifieerd

1 juni 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

ONBESLIST

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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