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Trained immunity induced by BCG in urothelial carcinoma

Trained immunity induced by BCG in urothelial carcinoma - Tribute

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON47732
Enrollment
80
Registered
2018-09-26
Start date
2018-06-20
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-muscle invasive bladder cancer

Interventions

bladder cancer
immunotherapy

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Presence of high-grade Ta or T1 urothelial carcinoma of the bladder with or without carcinoma in situ; tumor can be primary or recurrent 2. Able to communicate in Dutch, and read and understand the patient information and informed consent form and fill out questionnaires 3. Signed and dated informed consent form 4. Complete resection of (visible) tumor at start of BCG therapy as determined via re-TURT or negative cystoscopy/cytology (at most 6 weeks prior to BCG therapy initiation)

Exclusion criteria

Exclusion criteria: 1. Any previous intravesical BCG therapy 2. Presence of primary CIS only 3. Presence of histopathologically proven muscle-invasive urothelial carcinoma of the bladder at first or re-TUR surgical specimens 4. Presence of tumor stage cN1 of cM1 as assessed by CT-thorax/abdomen 5. Presence of any upper urinary tract tumors 6. Histology subtype of resected tumor is not predominant urothelial carcinoma 7. Presence of another malignancy other than basal cell carcinoma of the skin or prostate cancer under active surveillance 8. Presence of pregnancy or lactation 9. Presence of active tuberculosis, any form of immunodeficiency (e.g. HIV + serology, transplant recipients) and/or any other contraindication of BCG therapy 10. Patients who have received any systemic cytostatic agents within the last 3 months 11. Patients younger than 18 and older than 85 years of age 12. Patients with uncontrollable urinary tract infection

Design outcomes

Primary

MeasureTime frame
Study parameters include (i) histone 3 lysine 4 (H3K4) trimethylation (me3), H3K9me3, and H3K27 acetylation levels at the TNF-*, IL-6 and IL1-b promoters in circulating monocytes during BCG treatment; (ii) TNF-*, IL-6 and IL-1b levels produced by ex vivo stimulated monocytes during treatment, (iii) DNA variant genotypes and molecular bladder tumor subtypes, (iv) CyPRIT score, (v) (time to) tumor recurrence.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)