CAnadian CAncers With Rare Molecular Alterations (CARMA) - Basket Real-world Observational Study (BROS)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Cancer treatment with tyrosine kinase inhibitors (TKIs) or other molecularly targeted therapeutic agents., Patient-reported outcomes (PROs).
- Who it may be relevant to
- Registry conditions: Cancer, Malignancies Multiple, Malignant Solid Tumor, Cancer, Therapy-Related. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Canada
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
This study will collect data on Canadian cancer patients that have uncommon/rare changes in their tumours, such as alterations/rearrangements in the genetic material inside cells - known as deoxyribonucleic acid, or DNA, which acts as a map and gives directions to the cells on how to make other substances the body needs - because some of these changes have been found to respond to different drugs that help to stop the cancer. These rare changes occur in genes such as but not limited to ALK, EGFR, ROS1, BRAF, and NTRK which have targeted drugs in a family known as tyrosine kinase inhibitors (TKIs), and KRAS G12C mutation, which now has a targeted inhibitor drug therapy for patients with non small cell lung cancer (NSCLC). The goals for the study are to compare the natural history of such cancers and the treatment outcomes, including toxicities and patient-reported outcomes, for the different therapies.
Detailed description
Molecular heterogeneity in cancer tumours make it a complex disease to manage and treat. However, there have been significant advancements made in the detection of molecular alterations and we are able to now define distinct disease subtypes which permit targeted selection of therapies, thus optimizing treatment responses for patients and improving their survival.
With CARMA-BROS we will address the objectives that follow.
Primary Objectives:
1. To create a cohort of patients through which to better understand the natural history of disease in Canadian cancer patients with tumours that have been molecularly subtyped and identified to have rare molecular alterations. 2. To compare the natural history, stage distribution, treatment outcomes such as treatment effectiveness (composite of disease progression or death) and treatment toxicities across different patients with different molecular alterations, receiving different lines and types of therapy.
Secondary Objectives: 3. To determine the incidence, time to development, prevalence, and outcomes of patients with specific patterns of spread, such as brain metastases compared to those without, by different therapies and by molecular alterations. 4. To better understand real-world treatment patterns of rare molecular alterations in the Canadian context, across geographic or other factors, and how treatment patterns evolve over time and as new therapies become available, how patients are investigated and how targeted and other biomarkers are used as part of clinical practice in these patients. 5. To assess quality of life in patients with rare molecular alterations across different stages, lines and types of therapy. 6. To perform exploratory health economic evaluations focused on the costs and benefits of managing patients with rare molecular alterations. 7. To perform biomarker analyses, where appropriate, to improve our understanding of these rare molecular alterations.
Interventions
- Drug Cancer treatment with tyrosine kinase inhibitors (TKIs) or other molecularly targeted therapeutic agents.
Observing cancer patients who have received or are currently receiving tyrosine kinase inhibitors (TKIs) or other molecularly targeted therapies for their cancer treatment. - Other Patient-reported outcomes (PROs)
Prospectively enrolled participants will be provided with survey packets comprised of different PRO instruments at the initial/baseline visit, at 3 month follow up intervals and at the time when treatment/therapy is changed.
Primary outcome measures
- Composite of Progression Free Survival [PFS] or Overall Survival [OS] [Time frame: From the start date of cancer therapy until the date of first documented progression or date of death (any cause), assessed up to 120 months]
Secondary outcome measures (4)
- Brain metastasis/other metastatic tumours [Time frame: From the start date of cancer therapy until the date of first documented brain/other metastasis, assessed up to 120 months]
- EORTC quality of life questionnaires (QLQ) - cancer patient-reported health related quality of life [Time frame: Baseline and serial changes every 3 months, including whenever there is a change in treatment, up to 120 months (the duration of this study)]
- EQ-5D-5L - patient-reported health related quality of life measure [Time frame: Baseline and serial changes every 3 months, including whenever there is a change in treatment, up to 120 months (the duration of this study)]
- Patient-reported economic impact [Time frame: Baseline and serial changes every 3 months, including whenever there is a change in treatment, up to 120 months (the duration of this study)]
Eligibility criteria
Inclusion criteria
- Patients ≥ 18 years at cancer diagnosis
- Diagnosed with malignant tumour(s) with molecular testing completed that identified rare molecular alterations
- Accessible/available molecular testing reports/documentation to confirm type(s) of molecular alteration(s) (resulting from the conduct of polymerase chain reaction \[PCR\] based next generation sequencing \[NGS\], immunohistochemistry \[IHC\], fluorescence in situ hybridization \[FISH\], liquid biopsy)
- Canadian resident received follow-up for cancer care in Canada or is currently receiving/planning follow-up for cancer care to occur in Canada at time of enrollment
Exclusion criteria
- Previous refusal of the deceased patient, when living, to enroll in this study or patient approached for this study is unable to provide informed consent
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Canada · 27 centers
- Tom Baker Cancer Centre - University of Calgary - Alberta Health Services — Calgary
- Cross Cancer Institute, University of Alberta - Alberta Health Services — Edmonton
- BC Cancer — Vancouver
- CancerCare Manitoba/University of Manitoba — Winnipeg
- Dr. Everett Chalmers Regional Hospital — Fredericton
- Dr. H. Bliss Murphy Cancer Centre — St. John's
- Queen Elizabeth II (QEII) Health Sciences Centre — Halifax
- William Osler Health System - Brampton Civic Hospital — Brampton
- … and 19 more centers
Identifiers
NCT: NCT04151342 · CARMA-BROS · 18-5902 · 1632