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Imaging and angiogenesis of malignant lymphoma with dynamic MRI, H-MRS, P-MRS and FDG-PET/CT for staging, mid treatment assessment and outcome.

Imaging and angiogenesis of malignant lymphoma with dynamic MRI, H-MRS, P-MRS and FDG-PET/CT for staging, mid treatment assessment and outcome. - CILA

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35043
Enrollment
30
Registered
2010-06-17
Start date
2010-09-06
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

cancer of the lynphatic system Malignant lymphoma

Interventions

None listed

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • >= 18 years. • WHO performance status: 0-3 (see appendix 1) • Karnofsky score >= 80 (see appendix 2) • Biopsy proven de novo or relapsed malignant lymphoma of any histological subtype. Relapsed patients who participated in this study during an earlier line of treatment may be re-entered in the study when fulfilling the inclusion criteria. • Sufficient biopsy material present to perform anti-CD34 staining and subsequent MVD assessment.

Exclusion criteria

Exclusion criteria: • Other active malignancy (less than 5 years in complete remission) except skin carcinoma (non-melanoma). • HIV positive patients. • Patients with contra-indications for contrast enhanced MR exams: o Claustrophobia, o Cardiac pacemaker or pacemaker wiring in situ, o Cerebral clips or metal artificial cardiac valves, o Ossicle prosthesis o Renal failure • Pregnancy or breastfeeding . • No staging FDG-PET/CT available. • Inability of giving informed consent.

Design outcomes

Primary

MeasureTime frame
Correlation between DCE-MRI and MVD of malignant lymphoma tissue. Correlation between MRS and response to treatment. Correlation between MRS and vascularisation.

Secondary

MeasureTime frame
Evaluation of the correlation between FDG-PET/CT parameters, DCE-MRI parameters and the changes during treatment.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)