Risk of late effects of treatment in children newly diagnosed with standard-risk acute lymphoblastic leukaemia: a report from the Childhood Cancer Survivor Study cohort
- PMID: 24954778
- PMCID: PMC4142216
- DOI: 10.1016/S1470-2045(14)70265-7
Risk of late effects of treatment in children newly diagnosed with standard-risk acute lymphoblastic leukaemia: a report from the Childhood Cancer Survivor Study cohort
Abstract
Background: Treatment of patients with paediatric acute lymphoblastic leukaemia has evolved such that the risk of late effects in survivors treated in accordance with contemporary protocols could be different from that noted in those treated decades ago. We aimed to estimate the risk of late effects in children with standard-risk acute lymphoblastic leukaemia treated with contemporary protocols.
Methods: We used data from similarly treated members of the Childhood Cancer Survivor Study cohort. The Childhood Cancer Survivor Study is a multicentre, North American study of 5-year survivors of childhood cancer diagnosed between 1970 and 1986. We included cohort members if they were aged 1·0-9·9 years at the time of diagnosis of acute lymphoblastic leukaemia and had received treatment consistent with contemporary standard-risk protocols for acute lymphoblastic leukaemia. We calculated mortality rates and standardised mortality ratios, stratified by sex and survival time, after diagnosis of acute lymphoblastic leukaemia. We calculated standardised incidence ratios and absolute excess risk for subsequent neoplasms with age-specific, sex-specific, and calendar-year-specific rates from the Surveillance, Epidemiology and End Results Program. Outcomes were compared with a sibling cohort and the general US population.
Findings: We included 556 (13%) of 4329 cohort members treated for acute lymphoblastic leukaemia. Median follow-up of the survivors from 5 years after diagnosis was 18·4 years (range 0·0-33·0). 28 (5%) of 556 participants had died (standardised mortality ratio 3·5, 95% CI 2·3-5·0). 16 (57%) deaths were due to causes other than recurrence of acute lymphoblastic leukaemia. Six (1%) survivors developed a subsequent malignant neoplasm (standardised incidence ratio 2·6, 95% CI 1·0-5·7). 107 participants (95% CI 81-193) in each group would need to be followed-up for 1 year to observe one extra chronic health disorder in the survivor group compared with the sibling group. 415 participants (376-939) in each group would need to be followed-up for 1 year to observe one extra severe, life-threatening, or fatal disorder in the group of survivors. Survivors did not differ from siblings in their educational attainment, rate of marriage, or independent living.
Interpretation: The prevalence of adverse long-term outcomes in children treated for standard risk acute lymphoblastic leukaemia according to contemporary protocols is low, but regular care from a knowledgeable primary-care practitioner is warranted.
Funding: National Cancer Institute, American Lebanese-Syrian Associated Charities, Swiss Cancer Research.
Copyright © 2014 Elsevier Ltd. All rights reserved.
Conflict of interest statement
The authors declared no conflicts of interest.
Figures
Comment in
-
How safe is a standard-risk child with ALL?Lancet Oncol. 2014 Jul;15(8):782-3. doi: 10.1016/S1470-2045(14)70294-3. Epub 2014 Jun 19. Lancet Oncol. 2014. PMID: 24954780 No abstract available.
Similar articles
-
The changing burden of long-term health outcomes in survivors of childhood acute lymphoblastic leukaemia: a retrospective analysis of the St Jude Lifetime Cohort Study.Lancet Haematol. 2019 Jun;6(6):e306-e316. doi: 10.1016/S2352-3026(19)30050-X. Epub 2019 May 8. Lancet Haematol. 2019. PMID: 31078468 Free PMC article.
-
Temporal patterns in the risk of chronic health conditions in survivors of childhood cancer diagnosed 1970-99: a report from the Childhood Cancer Survivor Study cohort.Lancet Oncol. 2018 Dec;19(12):1590-1601. doi: 10.1016/S1470-2045(18)30537-0. Epub 2018 Nov 8. Lancet Oncol. 2018. PMID: 30416076 Free PMC article.
-
Pulse therapy with vincristine and dexamethasone for childhood acute lymphoblastic leukaemia (CCCG-ALL-2015): an open-label, multicentre, randomised, phase 3, non-inferiority trial.Lancet Oncol. 2021 Sep;22(9):1322-1332. doi: 10.1016/S1470-2045(21)00328-4. Epub 2021 Jul 27. Lancet Oncol. 2021. PMID: 34329606 Free PMC article. Clinical Trial.
-
Long-term outcome of treatment with protocols AL841, AL851, and ALHR88 in children with acute lymphoblastic leukemia: results obtained by the Kyushu-Yamaguchi Children's Cancer Study Group.Int J Hematol. 2001 Apr;73(3):369-77. doi: 10.1007/BF02981964. Int J Hematol. 2001. PMID: 11345205 Review.
-
[SENTIERI - Epidemiological Study of Residents in National Priority Contaminated Sites. Sixth Report].Epidemiol Prev. 2023 Jan-Apr;47(1-2 Suppl 1):1-286. doi: 10.19191/EP23.1-2-S1.003. Epidemiol Prev. 2023. PMID: 36825373 Italian.
Cited by
-
Late Effects in Survivors of Adolescent and Young Adult Acute Lymphoblastic Leukemia.JNCI Cancer Spectr. 2020 Apr 2;4(4):pkaa025. doi: 10.1093/jncics/pkaa025. eCollection 2020 Aug. JNCI Cancer Spectr. 2020. PMID: 32704618 Free PMC article.
-
Neurocognitive outcomes in long-term survivors of childhood acute lymphoblastic leukemia treated on contemporary treatment protocols: A systematic review.Neurosci Biobehav Rev. 2015 Jun;53:108-20. doi: 10.1016/j.neubiorev.2015.03.016. Epub 2015 Apr 7. Neurosci Biobehav Rev. 2015. PMID: 25857254 Free PMC article.
-
Review of a three-year study on the dental care of onco-hematological pediatric patients.Clinics (Sao Paulo). 2018 Dec 3;73:e721. doi: 10.6061/clinics/2017/e721. Clinics (Sao Paulo). 2018. PMID: 30517306 Free PMC article. Review.
-
Risk of hospitalization among survivors of childhood and adolescent acute lymphoblastic leukemia compared to siblings and a general population sample.Cancer Epidemiol. 2017 Aug;49:216-224. doi: 10.1016/j.canep.2017.06.005. Epub 2017 Jul 19. Cancer Epidemiol. 2017. PMID: 28734233 Free PMC article.
-
Parental decision making regarding consent to randomization on Children's Oncology Group AALL0932.Pediatr Blood Cancer. 2021 Apr;68(4):e28907. doi: 10.1002/pbc.28907. Epub 2021 Jan 26. Pediatr Blood Cancer. 2021. PMID: 33501773 Free PMC article.
References
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical