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Economic Analysis of Early vs Delayed Therapy in Newly Diagnosed Asymptomatic High-Risk Patients With Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma:

Chronic Lymphocytic Leukemia | Small Lymphocytic Lymphoma

Utilization data will be collected from all patients entered on the trial at Canadian centres from the time of registration until death, removal from study, or completion of 10 years of follow-up.

Protocol-specified health care utilization will be collected within trial case report forms, and will include study visits, radiographic assessments, laboratory investigations, and treatment administration.

Resource utilization data collection will be supplemented by a self-administered resource utilization form (Stanford SMRC) to document non-protocol specified utilization. This will include hospitalizations (including days in hospital), emergency room visits, and non-protocol specified ambulatory visits.

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 and up

Critères de participation

Inclusion Criteria:

* Patient must be eligible for the core CLC3/S1925 protocol.
* Patient consent must be appropriately obtained in accordance with applicable local and regulatory requirements. Each patient must sign a consent form prior to enrollment in the trial to document their willingness to participate.
* Patient is able (i.e. sufficiently fluent) and willing to complete the quality of life and/or health utility questionnaires in either English or French. The baseline assessment must be completed within required timelines, prior to enrollment. Inability (lack of comprehension in English or French, or other equivalent reason such as cognitive issues or lack of competency) to complete the questionnaires will not make the patient ineligible for the study. However, ability but unwillingness to complete the questionnaires will make the patient ineligible.
* Patients must be accessible for treatment and follow-up. Investigators must assure themselves the patients enrolled on this trial will be available for complete documentation of the treatment, adverse events, and follow-up.

Lieu de l'étude

Regional Health Authority B, Zone 2
Regional Health Authority B, Zone 2
Saint John, New Brunswick
Canada

Contactez l'équipe d'étude

Primary Contact

Alfonso Rivera Duarte

506 648-7109
The Jewish General Hospital
The Jewish General Hospital
Montreal, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Tanya Skamene

514 340-8222
CancerCare Manitoba
CancerCare Manitoba
Winnipeg, Manitoba
Canada

Contactez l'équipe d'étude

Primary Contact

Versha Banerji

204 787-4904
Ottawa Hospital Research Institute
Ottawa Hospital Research Institute
Ottawa, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

David A. MacDonald

QEII Health Sciences Centre
QEII Health Sciences Centre
Halifax, Nova Scotia
Canada

Contactez l'équipe d'étude

Primary Contact

Katherine Sue Robinson

902 473-2394
Allan Blair Cancer Centre
Allan Blair Cancer Centre
Regina, Saskatchewan
Canada

Contactez l'équipe d'étude

Primary Contact

Abdulhakim Eswedi

306 766-2691
BCCA - Vancouver
BCCA - Vancouver
Vancouver, British Columbia
Canada

Contactez l'équipe d'étude

Primary Contact

Alina Gerrie

604 877-6000
Lakeridge Health Oshawa
Lakeridge Health Oshawa
Oshawa, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Lakshman Vasanthamohan

905 576-8711
Étude parrainée par
Canadian Cancer Trials Group
Participants recherchés
Plus d'informations
ID de l'étude: NCT05371808