4.6 Article

Prospective longitudinal evaluation of treatment-related toxicity and health-related quality of life during the first year of treatment for pediatric acute lymphoblastic leukemia

期刊

BMC CANCER
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12885-022-10072-x

关键词

ALL; Health related quality of life; Treatment related toxicity; Quality of life; Psychosocial; Child; Registries

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资金

  1. Kids Cancer Alliance (a Translational Cancer Research Centre of Cancer Institute NSW)
  2. Cancer Institute NSW [ECF 181430]
  3. Royal Australasian College of Physicians -Kids Cancer Project Research Entry Scholarship
  4. Cancer Therapeutics CRC (CTx) PhD Clinician Researcher Top-Up Scholarship
  5. Anthony Rothe Memorial Trust
  6. Kids Cancer Project
  7. Australian Government
  8. Kids Cancer Alliance
  9. Kids to Adults (K2A) Clinical Academic Group
  10. Kids with Cancer Foundation
  11. Cancer Council New South Wales Program Grant [PG16-02]
  12. NHMRC Australia [APP1142627]
  13. Cancer Research Foundation (CLCRF, Australia)
  14. Estate of the Late Harry McPaul

向作者/读者索取更多资源

This study aims to investigate the treatment-related toxicities (TRTs) and impaired quality of life during pediatric acute lymphoblastic leukemia (ALL) therapy, compare the outcomes of different treatment methods, and evaluate their impacts on children and parents.
Background Pediatric acute lymphoblastic leukemia (ALL) therapy is accompanied by treatment-related toxicities (TRTs) and impaired quality of life. In Australia and New Zealand, children with ALL are treated with either Children's Oncology Group (COG) or international Berlin-Frankfurt-Munster (iBFM) Study Group-based therapy. We conducted a prospective registry study to document symptomatic TRTs (venous thrombosis, neurotoxicity, pancreatitis and bone toxicity), compare TRT outcomes to retrospective TRT data, and measure the impact of TRTs on children's general and cancer-related health-related quality of life (HRQoL) and parents' emotional well-being. Methods Parents of children with newly diagnosed ALL were invited to participate in the ASSET (Acute Lymphoblastic Leukaemia Subtypes and Side Effects from Treatment) study and a prospective, longitudinal HRQoL study. TRTs were reported prospectively and families completed questionnaires for general (Healthy Utility Index Mark 3) and cancer specific (Pediatric Quality of Life Inventory (PedsQL)-Cancer Module) health related quality of life as well the Emotion Thermometer to assess emotional well-being. Results Beginning in 2016, 260 pediatric patients with ALL were enrolled on the TRT registry with a median age at diagnosis of 59 months (range 1-213 months), 144 males (55.4%), majority with Pre-B cell immunophenotype, n = 226 (86.9%), 173 patients (66.5%) treated according to COG platform with relatively equal distribution across risk classification sub-groups. From 2018, 79 families participated in the HRQoL study through the first year of treatment. There were 74 TRT recorded, reflecting a 28.5% risk of developing a TRT. Individual TRT incidence was consistent with previous studies, being 7.7% for symptomatic VTE, 11.9% neurotoxicity, 5.4% bone toxicity and 5.0% pancreatitis. Children's HRQoL was significantly lower than population norms throughout the first year of treatment. An improvement in general HRQoL, measured by the HUI3, contrasted with the lack of improvement in cancer-related HRQoL measured by the PedsQL Cancer Module over the first 12 months. There were no persisting differences in the HRQoL impact of COG compared to iBFM therapy. Conclusions It is feasible to prospectively monitor TRT incidence and longitudinal HRQoL impacts during ALL therapy. Early phases of ALL therapy, regardless of treatment platform, result in prolonged reductions in cancer-related HRQoL.

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