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The investigators aim to study the pattern and frequency of pathogenic variants among ALL newly diagnosed cancer patients in a genetically distinct population.
Additionally, the investigators will study the uptake rate of "cascade family screening", frequency of pathogenic variants and barriers against testing.
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| Measure | Description | Time Frame |
|---|---|---|
| Prevalence of pathogenic or likely pathogenic germline variants among newly diagnosed cancer patients tested by universal multigene panel testing | 2021-2023 | |
| Number of participants with variants of uncertain significance (VUS) as assessed by universal multigene panel testing | 2021-2023 | |
| To determine the reasons/ Barriers for refusal of genetic cascade testing among newly diagnosed cancer patients. | 2021-2023 |
| Measure | Description | Time Frame |
|---|---|---|
| Rate of cascade of family member testing of the participants with positive pathogenic mutation | The family of tested patients with pathogenic mutations will be offered the genetic testing | 2021-2023 |
| Prevalence of pathogenic or likely pathogenic mutations among tested family members of the participants with pathogenic mutations using the universal multigene panel |
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Inclusion Criteria:
Exclusion Criteria:
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All consecutive patients who fulfill the inclusion/exclusion criteria and are diagnosedat KHCC will be invited.
A total of 3000 patients are estimated to participate
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| Name | Affiliation | Role |
|---|---|---|
| Hikmat Abdel-Razeq | King Hussein Cancer Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| King Hussein Cancer Center | Amman | Amman Governorate | 11941 | Jordan |
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Peripheral Blood sample
| 2021-2023 |
| Prevalence of variants of uncertain significance (VUS) among tested family members of participants with pathogenic mutations as assessed by universal multigene panel testing | 2021-2023 |
| To determine the reasons/ Barriers for refusal of genetic cascade testing among family members of tested patients with pathogenic mutation | 2021-2023 |
| ID | Term |
|---|---|
| D020022 | Genetic Predisposition to Disease |
| ID | Term |
|---|---|
| D004198 | Disease Susceptibility |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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