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1.
J Pediatr Hematol Oncol ; 43(1): 12-17, 2021 01.
Article in English | MEDLINE | ID: mdl-32675554

ABSTRACT

Body size influences bone mineral density (BMD) in health. Relationships of BMD with body mass index, fat mass (FM), fat-free mass, and appendicular lean mass were explored in acute lymphoblastic leukemia (ALL) survivors (n=75; 41 males; 45 standard risk ALL) >10 years from diagnosis. Dual energy radiograph absorptiometry performed body composition analysis. Relationships were assessed by regression analyses and Pearson correlation coefficients (r). Twenty subjects (26.3%) were osteopenic; lumbar spine (LS) BMD Z score <-1.00. Age at diagnosis, sex, ALL risk-category, type of post-induction steroid or cranial radiation did not correlate with LS or whole body (WB) BMD. Body mass index correlated significantly with LS BMD (r=0.333, P=0.004) and WB BMD (r=0.271, P=0.033). FM index (FM/height²) Z score showed no significant correlation with LS or WB BMD. Fat-free mass index Z score correlated strongly with LS BMD (r=0.386, P=0.013) and WB BMD (r=0.605, P<0.001) in males but not in females. The appendicular lean mass index, a surrogate for skeletal muscle mass, correlated significantly with LS BMD (r=0.367, P=0.018) and WB BMD (r=0.604, P<0.001) in males but not in females. Future studies to evaluate interventions to enhance BMD focused on improving body composition particularly skeletal muscle mass are warranted.


Subject(s)
Adiposity , Body Composition , Body Mass Index , Bone Density , Cancer Survivors/statistics & numerical data , Precursor Cell Lymphoblastic Leukemia-Lymphoma/rehabilitation , Survivors/statistics & numerical data , Adolescent , Adult , Cross-Sectional Studies , Female , Follow-Up Studies , Humans , Male , Precursor Cell Lymphoblastic Leukemia-Lymphoma/therapy , Prognosis , Young Adult
2.
Cancer ; 124(6): 1225-1231, 2018 03 15.
Article in English | MEDLINE | ID: mdl-29231963

ABSTRACT

BACKGROUND: The late effects of treatment for acute lymphoblastic leukemia (ALL) include disordered body composition, especially obesity. Less attention has been focused on the loss of skeletal muscle mass (SMM) and the combined morbidity of sarcopenic obesity. METHODS: A cross-sectional study of body composition was undertaken via dual-energy x-ray absorptiometry in 75 long-term survivors of ALL (more than 10 years after the diagnosis). Measures were obtained of the fat mass (FM), fat-free mass (equivalent to the lean body mass [LBM]), and whole-body bone mineral content. Health-related quality of life (HRQL) was measured with the Health Utilities Index. RESULTS: The sum of the FM, LBM, and whole-body bone mineral content matched the total body weight measured directly (r = 0.998). The appendicular lean mass (ALM) was derived from the LBM in all 4 limbs and accounted for approximately 75% of the SMM. According to the fat mass index (FMI; ie, FM/height2 ), 12% of females and 18% of males were frankly obese by World Health Organization criteria. The median FMI z score was + 0.40, whereas the median z score for the appendicular lean mass index (ALMI; ie, ALM/height2 ) was -0.40. Sarcopenic obesity, defined as a positive FMI z score with a negative ALMI z score, was present in 32 subjects (43%). There were statistically significant and clinically important differences in overall HRQL between subjects with and without sarcopenic obesity. CONCLUSIONS: Sarcopenic obesity is prevalent in long-term survivors of ALL, and this places them in double jeopardy from excess body fat and inadequate SMM (eg, a combination of metabolic and frailty syndromes). It is associated with an adverse impact on overall HRQL. Cancer 2018;124:1225-31. © 2017 American Cancer Society.


Subject(s)
Antineoplastic Agents/adverse effects , Body Composition/drug effects , Obesity/epidemiology , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Sarcopenia/epidemiology , Absorptiometry, Photon , Adolescent , Adult , Bone Density/drug effects , Cancer Survivors , Child , Child, Preschool , Cross-Sectional Studies , Female , Humans , Infant , Male , Muscle, Skeletal/diagnostic imaging , Obesity/diagnosis , Obesity/etiology , Precursor Cell Lymphoblastic Leukemia-Lymphoma/complications , Precursor Cell Lymphoblastic Leukemia-Lymphoma/mortality , Prevalence , Quality of Life , Sarcopenia/diagnosis , Sarcopenia/etiology , Time Factors , Young Adult
3.
J Nucl Med ; 49(4): 573-86, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18344441

ABSTRACT

In recent years, 6-l-18F-fluorodihydroxyphenylalanine (18F-DOPA) PET has emerged as a new diagnostic tool for the imaging of neuroendocrine tumors. This application is based on the unique property of neuroendocrine tumors to produce and secrete various substances, a process that requires the uptake of metabolic precursors, which leads to the uptake of 18F-DOPA. This nonsystematic review first describes basic aspects of 18F-DOPA imaging, including radiosynthesis, factors involved in tracer uptake, and various aspects of metabolism and imaging. Subsequently, this review provides an overview of current clinical applications in neuroendocrine tumors, including carcinoid tumors, pancreatic islet cell tumors, pheochromocytoma, paraganglioma, medullary thyroid cancer, hyperinsulinism, and various other clinical entities. The application of PET/CT in carcinoid tumors has unsurpassed sensitivity. In medullary thyroid cancer, pheochromocytoma, and hyperinsulinism, results are also excellent and contribute significantly to clinical management. In the remaining conditions, the initial experience with 18F-DOPA PET indicates that it seems to be less valuable, but further study is required.


Subject(s)
Dihydroxyphenylalanine/analogs & derivatives , Neuroendocrine Tumors/diagnostic imaging , Positron-Emission Tomography , Adenoma, Islet Cell/diagnostic imaging , Humans , Hyperinsulinism/diagnostic imaging , Pancreatic Neoplasms/diagnostic imaging , Pheochromocytoma/diagnostic imaging , Thyroid Neoplasms/diagnostic imaging
4.
Radiat Prot Dosimetry ; 123(1): 62-7, 2007.
Article in English | MEDLINE | ID: mdl-16825250

ABSTRACT

On 27 occasions, radiation doses were measured for a family member designated as the 'caregiver' for a patient receiving high-dose radioiodine outpatient therapy for differentiated thyroid carcinoma. For 25 of the administrations, patients received 3.7 GBq of (131)I. Radiation doses for the designated caregivers were monitored on an hourly basis for 1 week using electronic personal dosemeters. The average penetrating dose was 98 +/- 64 microSv. The maximum penetrating dose was 283 microSv. Measured dose rate profiles showed that, on average, one-third of the caregiver dose was received during the journey home from hospital. The mean dose rate profile showed rapid clearance of (131)I with three distinct phases. The corresponding clearance half-times were <1 h, 21 h and approximately 8 d. These components were associated, respectively, with the drive home, the clearance of radioiodine from an athyreotic patient and small quantities of (131)I contaminating the home.


Subject(s)
Caregivers , Iodine Radioisotopes/therapeutic use , Outpatients , Radiation Dosage , Radiation Injuries , Radiation Protection , Thyroid Neoplasms/radiotherapy , Environmental Exposure , Humans , Maximum Allowable Concentration , Radiation Monitoring
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