Over the past decades, advances in treatment have led to an increasing number of children who survive cancer, resulting in a growing population of childhood cancer survivors. After end of cancer treatment on common protocols survivors are enrolled in non-harmonized follow-up programs with frequent visits and blood samples. However, the evidence for the value of these follow-up programs with respect to the effect on detecting relapse and the effects on overall survival is scarce. The aim of the study is to give a comprehensive description of the detection mode of relapsed acute lymphoblastic leukaemia (ALL), including symptoms and blood test results. Further, we aim to evaluate if the mode of detection affects survival.
Investigators have identified a cohort of children with B-precursor ALL and T-ALL enrolled in the Nordic Society of Paediatric Haematology and Oncology (NOPHO) ALL-92, ALL-2000 and ALL-2008 trials and experienced a relapse or an SMN as the first event after cessation of maintenance therapy (368 patients). From medical charts and blood test results it will be decided whether the relapse/SMN was diagnosed at a routine visit (including routine blood tests) or if the relapse was diagnosed because of symptoms at a non-scheduled visit or blood test. As the NOPHO database probably is one of the most complete databases globally, it is an advantage to perform this study as a NOPHO study. Results of this population based relapse study will provide an evidence-based background for planning optimal and relevant follow-up programs for children after therapy of ALL treated according to contemporary Nordic ALL protocols. The study is important and relevant in the light of today's high ALL cure rates and a need for optimal follow-up programs after cessation of ALL treatment and possible prediction of relapse. The timing of the project is an increased focus on the clinical relevance of routine clinical follow-up of patients treated for cancer.
Study Type
OBSERVATIONAL
Enrollment
277
Mode of relapse/SMN detection: whether the relapse/SMN was diagnosed because of symptoms of leukaemia or diagnosed at a routine visit in the outpatient clinic.
Department of Paediatrics and Adolescent Medicine, Aarhus University Hospital
Aarhus N, Denmark
Department of Paediatrics and Adolescent Medicine, Turku University Hospital
Turku, Finland
The National University Hospital of Iceland
Reykjavik, Iceland
Department of Childhood Oncology, University Hospital Tromsø
Tromsø, Norway
Department of Paediatric Oncology, Karolinska University Hospital
Stockholm, Sweden
Detection mode
The proportion of relapses diagnosed at a routine visit vs. relapses diagnosed at an extra scheduled visit.
Time frame: Investigators will review medical charts up to three months before the diagnosis of a relapse. Relapses will be categorized to be diagnosed by either a routine visit or an extra scheduled visit.
Survival
Survival, by detection mode (routine or extra visit)
Time frame: Time-to-Event measures (up to 23 years from date of relapse until censoring)
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