Literature DB >> 27060472

Single-centre study reports a 84% five-year overall survival rate for paediatric solid tumours.

Eero Teppo1, Jarkko Penttinen2, Outi Myöhänen1, Kim Vettenranta3, Olli Lohi1.   

Abstract

AIM: We investigated the characteristics and outcome of paediatric patients with solid tumours diagnosed and treated at the Tampere University Hospital, one of the five tertiary referral centres in Finland, for children and adolescents with malignancies.
METHODS: This retrospective cohort study collected data from hospital medical records on survival, diagnosis, age, sex, tumour size and stage at diagnosis. We also observed the disease recurrence and use of autologous haematopoietic stem cell transplantation. Data analyses were carried out with the Kaplan-Meier method, various nonparametric and parametric tests, and Cox regression modelling.
RESULTS: Between 1987 and May 2015, 424 children (59% boys), with a median age of 6.4 (IQR 2.5-11.8) years at diagnosis, were diagnosed and followed up for a median of 7.5 (range 0-27.9) years. Central nervous system (CNS) tumours were the most common (38%), followed by lymphomas (19%), soft tissue sarcomas (10%), renal tumours (9%) and neuroblastomas (9%). The five-year overall survival rate of all solid tumour patients was 84% (95% CI, 81-88%), 82% (95% CI, 76-89%) for CNS and 85% (95% CI, 80-90%) for non-CNS tumours. Advanced tumour stage at diagnosis predicted a poor prognosis.
CONCLUSION: The treatment results in our study are comparable with those previously published. A comprehensive local database allows for a timely follow-up of the characteristics and quality of treatment of childhood malignancies. ©2016 Foundation Acta Paediatrica. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Paediatric; Prognosis; Solid tumours

Mesh:

Year:  2016        PMID: 27060472     DOI: 10.1111/apa.13425

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  2 in total

Review 1.  Autologous hematopoietic stem cell transplantation following high-dose chemotherapy for nonrhabdomyosarcoma soft tissue sarcomas.

Authors:  Frank Peinemann; Heike Enk; Lesley A Smith
Journal:  Cochrane Database Syst Rev       Date:  2017-04-13

2.  Incidence and outcomes of cancer in 16- to 17-year-old adolescents.

Authors:  Julia Ventelä; Atte Nikkilä; Arja Jukkola; Olli Lohi
Journal:  Acta Paediatr       Date:  2021-11-11       Impact factor: 4.056

  2 in total

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