Nutritional status is a measurable and modifiable factor that is often not considered during treatment and its clinical impact undervalued due in part to the heavy demands on clinicians in low and middle income countries to deliver therapy to large numbers of patients. The proposed study will create a biobank of clinical data and biological specimens which will foster future studies on cancer progression and prognosis as well as toxicities during treatment which may impact survivorship and late-effects. Eligible patients must be between 3 years and 18 years of age at time of assent/consent, have newly diagnosed B- or T-cell acute lymphoblastic leukemia or mixed phenotype acute leukemia confirmed by pathology report, and must be receiving treatment at one of the participating centers. Patients receiving hematopoietic cell transplant will be excluded. Institutions were selected to ensure representation of several global health indicators related to nutritional status and wealth classification according to the World Bank. Data related to demographic variables (socioeconomic status, food security), lifestyle habits (diet, physical activity), nutritional anthropometrics (height, weight and arm anthropometry), and nutritional biological indices (stool and blood) will be collected at designated timepoints throughout treatment and one year after the end of treatment.
Study Type
OBSERVATIONAL
Enrollment
4,900
No intervention
Columbia University Irving Medical Center
New York, New York, United States
ACTIVE_NOT_RECRUITINGHospital de Cancer Infanto Juvenil de Barretos
Barretos, Brazil
RECRUITINGInstituto de Medicina Integral Prof. Fernando Figueira (IMIP)
Recife, Brazil
RECRUITINGInstituto de Tratamento do Câncer Infantil (ITACI)
São Paulo, Brazil
RECRUITINGUnidad Nacional De Oncologia Pediatrica
Guatemala City, Guatemala
RECRUITINGHospital Escuela
Tegucigalpa, Honduras
RECRUITINGPost-Graduate Institute of Medical Education and Research (PGIMER)
Chandigarh, India
RECRUITINGMuhumbili Hospital
Dar es Salaam, Dar es Salaam Region, Tanzania
RECRUITINGCreate a prospective multinational biorepository of pediatric specimens (stool, blood) obtained at diagnosis, end of induction, beginning of maintenance, end of treatment, and 1-year after treatment among children/adolescents with ALL.
Time frame: 7 years
Collect sociodemographic data at sequential timepoints during treatment for ALL.
Time frame: 7 years
Collect dietary data at sequential timepoints during treatment for ALL.
Time frame: 7 years
Collect physical activity data at sequential timepoints during treatment for ALL.
Time frame: 7 years
Collect clinical information (disease characteristics, treatment-related toxicities, survival) at sequential timepoints during treatment for ALL to accompany the biorepository of blood and stool specimens.
Time frame: 7 years
Collect nutritional anthropometrics at sequential timepoints during treatment for ALL to accompany the biorepository of blood and stool specimens.
Time frame: 7 years
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