Danish Elder Lymphoma Patient Hematopoietic Investigation

Lymphoma Clinical Trial

— DELPHI  

Official title:

Chemotherapy-induced Genomic Damage in Elderly Patients With Lymphoma: Prevalence, Evolution, and Clinical Consequences

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05245487
• Other study ID #: DELPHI
• Status: Recruiting
• Start date: January 1, 2022
• Est. completion date: January 1, 2035

Study information

• Verified date: April 2023
• Source: Rigshospitalet, Denmark
• Contact: Simon Husby, MD PhD
• Phone: +45 3545 6060
• Email: simon.husby.01[@]regionh.dkZZZZZZ
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Every year approximately 300 Danish patients die from lymphoma. The median age at diagnosis is 70 years. Lymphoma can be efficiently treated with chemotherapy, and potentially cured. However, sufficient treatment is often hampered by toxicity, especially in elderly patients. It is also well known that the main risk factor for dying of lymphoma is age. New biologically targeted therapies with fewer side effects are becoming available for lymphoma treatment, however it is currently difficult to delineate which patients benefit from chemotherapy and which should be treated with novel expensive therapies. Recently, it has been discovered that chemotherapy can provoke growth of patient blood cells with DNA mutations. This leads to increased rates of treatment side effects and excess mortality. These defects have so far only been examined in younger patients below 70 years of age, where they are found in roughly 10% of patients. It remains unknown to what extent elderly individuals are affected, but the investigators hypothesize that the proportion and negative effects are much larger. Therefore, the investigators propose to investigate the frequency and evolution of these DNA mutations during chemotherapy in a prospective study of patients, who are either above 60 years of age and previously treated with chemotherapy for lymphoma in a nation-wide collaboration. By using blood samples, advanced genetic analyses and patient-reported questionnaires, the investigators will study - The prevalence of these mutations and their consequences for patient wellbeing, treatment side effects (such as anemia, infections etc.) and mortality - The kinetics of these mutations during and after treatment, and explore possible evolutionary patterns of the inferred damages The investigators expect to include 300 patients in the study and that the first results will be ready in a timeframe of 4 years. The investigators hope to obtain new insights in the risk factors for physiological and mental health in lymphoma patients and thereby pave the way for improvements in wellbeing and survival of this underserved population.

Description:

DELPHI is prospective nationwide observational study investigating blood mutations in patients with lymphoma. Inclusion criteria: - Diagnosis of B-cell Non-Hodgkin lymphoma - In need of systemic treatment with second (2.) or higher line of active therapy for lymphoma - 60 years of age or older (no age maximum) Exclusion criteria: - Unable to give written consent - Non-Danish citizens Patients will be included by their treating physcian at their local department. All analyses are centralized. Blood samples for research puporses will be taken before, midway (tipically before 3rd / 4th series depending on regimen) and 4-8 weeks after treatment. Also QOL questionaires will be sent electronically to the patients. The results of the tests performed will blinded to the patient and the treating physician.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 300
• Est. completion date: January 1, 2035
• Est. primary completion date: December 31, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 60 Years and older

Eligibility

Inclusion Criteria:

• Diagnosis of r/r B-cell Non-Hodgkin lymphoma
• In need of systemic treatment with second (2.) or higher line of active therapy for lymphoma
• 60 years of age or older (no age maximum)

Exclusion Criteria:

• Unable to give written consent
• Non-Danish citizens

Related Conditions & MeSH terms

• Chemotherapeutic Toxicity
• Chemotherapy-induced Neutropenia
• Chemotherapy-Related Leukemia
• Lymphoma
• Neutropenia

Intervention

Diagnostic Test:
• DNA repair gene mutation analysis
Prospective monitoring of patients with next-generation sequencing for blood mutations

Locations

Country	Name	City	State
Denmark	Dept. of Hematology, Rigshospitalet	Copenhagen

Sponsors (9)

Lead Sponsor	Collaborator
Rigshospitalet, Denmark	Aalborg University Hospital, Aarhus University Hospital, Danish Cancer Society, Gødstrup Hospital, Odense University Hospital, Sonderborg Hospital, Vejle Hospital, Zealand University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Event-free survival (EFS)	EFS according to Revised Lugano Criteria	2 years
Secondary	Overall survival (OS)	OS	2 years