Health-related Quality of Life, Symptom Severity, and Pain Among Patients Treated With Alpelisib for PIK3CA-related Overgrowth Spectrum: A Mixed-methods Observational Study
Health-related Quality of Life, Symptom Severity, and Pain Among Patients Treated With Alpelisib for PIK3CA-related Overgrowth Spectrum: A Mixed-methods Observational Study
This was a mixed-methods observational study that incorporated both qualitative interviews and longitudinal quantitative data collection through an online survey (initial, 2 months, and 4 months).
This study collected qualitative data through interviews with patients and caregivers and qualitative data through a web-based longitudinal survey.
Both parts of the study were designed to collect information on HRQoL, symptom severity, and pain among patients with PROS who were receiving treatment with alpelisib in the US. In addition, patients who had not been treated with alpelisib also participated in the quantitative part of the study by providing data on HRQoL, symptom severity, and pain, collected from a single administration of the web-based survey.
Inclusion Criteria:
Adult patients:
At least 18 years of age
Self-reports having been diagnosed with 1 of the following syndromes:
Able to converse and read/answer survey questions in English
Willing and able to provide informed consent
Adolescent patients
Between the ages of 12 and 17 years
Self-reports having been diagnosed with one of the following syndromes:
Able to converse and read/answer survey questions in English independently, as assessed by guardian
Willing and able to provide assent
Has a parent/legal guardian who is able and willing to provide permission for the adolescent to participate
Caregivers
At least 18 years of age
Is the parent/legal guardian of a child/adolescent who has been diagnosed with one of the following syndromes:
Child is either between the ages of 5 and 11 (inclusive), or between the ages of 12 and 17 years (inclusive) but is unable to self-report due to cognitive difficulties
Able to converse and read/answer survey questions in English
Willing and able to provide informed consent
Exclusion Criteria:
There are no specific exclusion criteria. However, participants may be excluded if the quota related to alpelisib treatment (60 treated with alpelisib; 40 not treated with alpelisib) has been achieved. For example, if 40 participants not treated with alpelisib have been recruited into the study, any additional participants not treated with alpelisib will be excluded. Patients treated with alpelisib may be similarly excluded if the quota of 60 patients has already been achieved.