Abstract:Abstract. Neuroblastoma, an embryonal malignancy of the sympathetic nervous system, is the most frequent extracranial solid tumor The clinico-epidemiological features of neuroblastoma in infants and children were investigated between January 2005 and January 2010 at the Pediatric Oncology units of Mansoura, Zagazig, and Tanta University Children's Hospitals (Egypt). Of 142 cases of neuroblastoma, 10 were omitted from the study due to defective data. The median age of the patients was 30 months, with 75.8% aged… Show more
“…The overall AIR we calculated for SEE (10.1) is comparable to the respective rate (10.9) reported in another European study including 59 registries in 19 countries participating in the Automated Childhood Cancer Information System (1978–1997) and ranging from 9 in the British Isles to 12 in Western‐Southern Europe, but higher than those reported for the well‐controlled health care systems of the Nordic countries (Denmark: 8.6, 1981–2000; Sweden: 7, 1983–2010) . However, much lower rates are reported in the less affluent African, Southern‐Eastern Asian and Southern American countries …”
Section: Discussionsupporting
confidence: 74%
“…4,27 However, much lower rates are reported in the less affluent African, Southern-Eastern Asian and Southern American countries. 1,2,[28][29][30][31] The association of higher incidence rates of neuroblastoma with higher HDI in our study was restricted to cases diagnosed before the age of 5 years, when most of the cases are diagnosed. The differences by socioeconomic status have been traditionally attributed to the availability of modern imaging technology, provision of health care services and quality of cancer registration.…”
Neuroblastoma comprises the most common neoplasm during infancy (first year of life). Our study describes incidence of neuroblastoma in Southern-Eastern Europe (SEE), including - for the first time - the Nationwide Registry for Childhood Hematological Malignancies and Solid Tumors (NARECHEM-ST)/Greece, compared to the US population, while controlling for human development index (HDI). Age-adjusted incidence rates (AIR) were calculated for 1,859 childhood (0-14 years) neuroblastoma cases, retrieved from 13 collaborating SEE registries (1990-2016), and were compared to those of SEER/US (N = 3,166; 1990-2012); temporal trends were assessed using Poisson regression and Joinpoint analyses. The overall AIR was significantly lower in SEE (10.1/million) compared to SEER (11.7 per million); the difference was maximum during infancy (43.7 vs. 53.3 per million, respectively), when approximately one-third of cases were diagnosed. Incidence rates of neuroblastoma at ages <1 and 1-4 years were positively associated with HDI, whereas lower median age at diagnosis was correlated with higher overall AIR. Distribution of primary site and histology was similar in SEE and SEER. Neuroblastoma was slightly more common among males compared to females (male-to-female ratio: 1.1), mainly among SEE infants. Incidence trends decreased in infants in Slovenia, Cyprus and SEER and increased in Ukraine and Belarus. The lower incidence in SEE compared to SEER, especially in infants living in low HDI countries possibly indicates a lower level of overdiagnosis in SEE. Hence, increases in incidence rates in infancy noted in some subpopulations should be carefully monitored to avoid the unnecessary costs health impacts of tumors that could potentially spontaneously regress.
“…The overall AIR we calculated for SEE (10.1) is comparable to the respective rate (10.9) reported in another European study including 59 registries in 19 countries participating in the Automated Childhood Cancer Information System (1978–1997) and ranging from 9 in the British Isles to 12 in Western‐Southern Europe, but higher than those reported for the well‐controlled health care systems of the Nordic countries (Denmark: 8.6, 1981–2000; Sweden: 7, 1983–2010) . However, much lower rates are reported in the less affluent African, Southern‐Eastern Asian and Southern American countries …”
Section: Discussionsupporting
confidence: 74%
“…4,27 However, much lower rates are reported in the less affluent African, Southern-Eastern Asian and Southern American countries. 1,2,[28][29][30][31] The association of higher incidence rates of neuroblastoma with higher HDI in our study was restricted to cases diagnosed before the age of 5 years, when most of the cases are diagnosed. The differences by socioeconomic status have been traditionally attributed to the availability of modern imaging technology, provision of health care services and quality of cancer registration.…”
Neuroblastoma comprises the most common neoplasm during infancy (first year of life). Our study describes incidence of neuroblastoma in Southern-Eastern Europe (SEE), including - for the first time - the Nationwide Registry for Childhood Hematological Malignancies and Solid Tumors (NARECHEM-ST)/Greece, compared to the US population, while controlling for human development index (HDI). Age-adjusted incidence rates (AIR) were calculated for 1,859 childhood (0-14 years) neuroblastoma cases, retrieved from 13 collaborating SEE registries (1990-2016), and were compared to those of SEER/US (N = 3,166; 1990-2012); temporal trends were assessed using Poisson regression and Joinpoint analyses. The overall AIR was significantly lower in SEE (10.1/million) compared to SEER (11.7 per million); the difference was maximum during infancy (43.7 vs. 53.3 per million, respectively), when approximately one-third of cases were diagnosed. Incidence rates of neuroblastoma at ages <1 and 1-4 years were positively associated with HDI, whereas lower median age at diagnosis was correlated with higher overall AIR. Distribution of primary site and histology was similar in SEE and SEER. Neuroblastoma was slightly more common among males compared to females (male-to-female ratio: 1.1), mainly among SEE infants. Incidence trends decreased in infants in Slovenia, Cyprus and SEER and increased in Ukraine and Belarus. The lower incidence in SEE compared to SEER, especially in infants living in low HDI countries possibly indicates a lower level of overdiagnosis in SEE. Hence, increases in incidence rates in infancy noted in some subpopulations should be carefully monitored to avoid the unnecessary costs health impacts of tumors that could potentially spontaneously regress.
“…Recently, an Italian neuroblastoma cohort study reported that stage 4S NBL had a significant peak among July births; however no trend in the date of diagnosis was found [17]. In the present study, we could not classify the patients' stages; however, stage 4S NBL accounts for less than 5% of all NBL cases, so our seasonal NBL pattern is surely different from that reported in the Italian study [18]. With regards to AML, while ALL and AML are biologically different diseases with distinct etiologies [19], it is possible that different infectious agents play a role in the development of both.…”
This study tentatively suggests that the diagnosis of childhood malignancy follows a seasonal trend in Korea, and has a possible correlation with viral prevalence in several diseases. Further long-term analysis of epidemiological data is needed to explore possible causality.
“…This study represented the first documented multicenter retrospective cohort study of NB in sub‐Saharan Africa. Although the majority of cases were diagnosed in the 18‐ to 60‐month age group, similar to international trends, the median age was higher at 39.9 months compared with 19 months in the United States (HIC) or 33.2 months in Egypt (MIC) …”
Background: Outcome data for neuroblastoma in sub-Saharan Africa are minimal, whereas poor outcome is reported in low-and middle-income countries. A multi-institutional retrospective study across South Africa was undertaken to determine outcome. pediatric oncology units were included. Kaplan-Meier curves and Cox regression models were employed to determine two-year survival rates and to identify prognostic factors.Results: Data from 390 patients were analyzed. The median age was 39.9 months (range, 0-201 months). The majority presented with stage 4 disease (70%). The main chemotherapy regimens were OPEC/OJEC (44.8%), St Jude NB84 protocol (28.96%), and Rapid COJEC (22.17%).Only 44.4% had surgery across all risk groups, whereas only 16.5% of high-risk patients received radiotherapy. The two-year overall survival (OS) for the whole cohort was 37.6%: 94.1%, 81.6%, and 66.7%, respectively, for the very-low-risk, low-risk, and intermediate-risk groups and 27.6% for the high-risk group (P < 0.001, 95% CI). The median survival time for the whole group was
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