Longitudinal Health-Related Quality of Life Among Patients With High-Risk Pediatric Hodgkin Lymphoma Treated on the Children's Oncology Group AHOD 1331 Study

Author:

Williams AnnaLynn M.1ORCID,Rodday Angie Mae2ORCID,Pei Qinglin3,Henderson Tara O.4ORCID,Keller Frank G.5ORCID,Punnett Angela6,Kelly Kara M.7ORCID,Castellino Sharon M.5,Parsons Susan K.2ORCID

Affiliation:

1. Department of Surgery, Division of Supportive Care in Cancer, University of Rochester Medical Center, Rochester, NY

2. Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA

3. Department of Biostatistics, University of Florida, Gainesville, FL

4. Department of Pediatrics, University of Chicago Pritzker School of Medicine, Comer Children's Hospital, Chicago, IL

5. Department of Pediatrics, Emory University School of Medicine, Atlanta, GA

6. Division of Hematology-Oncology, Hospital for Sick Children and University of Toronto, Toronto, ON, Canada

7. Department of Pediatrics, Roswell Park Comprehensive Cancer Center, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, NY

Abstract

PURPOSE There have been no previous longitudinal assessments of health-related quality of life (HRQoL) during treatment for pediatric Hodgkin lymphoma (HL). The addition of brentuximab vedotin (BV) to a multidrug chemotherapy backbone demonstrated superior efficacy to standard chemotherapy for patients with pediatric high-risk HL in the AHOD 1331 trial. However, the impact on HRQoL is unknown. PATIENTS AND METHODS After treatment random assignment, 268 participants older than 11 years were enrolled in a prespecified, longitudinal, patient-reported outcomes substudy. HRQoL was assessed using the seven-item Child Health Ratings Inventories (CHRIs)–Global scale before treatment (T1) and at cycle 2 (T2), cycle 5 (T3), and end of treatment (T4). A clinically meaningful increase in HRQoL was considered 7 points on the CHRIs-Global. Multivariable linear regression estimated associations between demographic/clinical variables and HRQoL at T1. Linear mixed models estimated changes in HRQoL across the treatment arm. RESULTS Participant characteristics were balanced by treatment arm. Ninety-three percent of participants completed the CHRIs at T1, 92% at T2, 89% at T3, and 77% at T4. At T1, female sex and fever ( P < .05) were each associated with worse HRQoL. By T2, participants in the BV arm experienced a statistically and clinically significant improvement in HRQoL (β = 7.3 [95% CI, 3.2 to 11.4]; P ≤ .001), which was greater than the change in the standard arm (difference in change β = 5.1 [95% CI, −0.2 to 10.3]; P = .057). The standard arm did not experience a statistically or clinically significant increase in HRQoL until T4 (β = 9.3 [95% CI, 4.7 to 11.5]; P < .001). CONCLUSION These data demonstrate successful collection of serial HRQoL from youth with high-risk pediatric HL and improvement in HRQoL over the course of initial therapy, sooner and to a greater extent in the group receiving the novel agent BV.

Publisher

American Society of Clinical Oncology (ASCO)

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