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Journal ArticleDOI

Retinoblastoma: Problems and Perspectives from India

TLDR
The salient clinical and epidemiological characteristics of retinoblastoma (RB) in India is examined, thereby highlighting the problems encountered there and a possibility of difference in the biology of the tumor seen in these patients.
Abstract
This study examined the salient clinical and epidemiological characteristics of retinoblastoma (RB) in India, thereby highlighting the problems encountered there. The epidemiological characteristics of 296 patients with RB over 8 years were evaluated using hospital records and postal follow-ups. Unilateral disease was seen in 61.8% of patients. The overall median age at presentation was 3.5 years (3.5 years for unilateral RB and 1.0 years for bilateral RB). The male/female ratio was 1.4:1. The median duration of symptomatic disease was 8 months. Consanguineous marriage was seen in 17% and family history of RB was noted in 1.7% cases. Also, 2% had a history of other malignancy in the family. Associated congenital malformation was seen in 10.5% of cases. A second malignancy was seen in 0.67% of cases at a mean duration of 4.5 years after completion of therapy. A predominance of advanced-stage disease (74.5% had Reese-Ellsworth group IV and V disease) was seen in our series. Only 43.6% of patients had disease localized to the globe without any infiltration/invasion. The majority of cases had advanced-stage disease at presentation and came from the underprivileged class of society. Patients with bilateral RB presented much earlier than those with unilateral disease. In patients with unilateral RB, higher age at presentation as well as advanced disease may be related to much delay in seeking medical attention. In view of the advanced stage at presentation, there also exist a possibility of difference in the biology of the tumor seen in these patients.

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Journal ArticleDOI

Epidemiology of childhood cancer in India.

TL;DR: The considerable inter-regional variation in incidence and mortality rates across India suggests a possible deficiency in ascertainment of cases and death notification, particularly in rural areas.
Journal ArticleDOI

A multicentre report from the Mexican Retinoblastoma Group

TL;DR: Given the great number of patients in advanced stages and the variability on treatment schemes, it is evident that it is mandatory to work in a cooperative group and develop a national early detection programme as well as a treatment protocol which include all specialists involved in the care of patients with RB.
Journal ArticleDOI

Metastatic and nonmetastatic models of retinoblastoma.

TL;DR: Two reproducible animal models with contrasting biological behaviors analogous to human retinoblastoma have been developed and Y79 and WERI-Rb model demonstrated specific tumor evolution similar to that seen in human invasive and metastatic disease.
Journal ArticleDOI

Identification and Insilico Analysis of Retinoblastoma Serum microRNA Profile and Gene Targets Towards Prediction of Novel Serum Biomarkers

TL;DR: From miRNA gene target prediction, key regulatory genes of cell proliferation, apoptosis, and positive and negative regulatory networks involved in RB progression were identified in the gene expression profile of RB tumors.
Journal ArticleDOI

Retinoblastoma in Central America: report from the Central American Association of Pediatric Hematology Oncology (AHOPCA).

TL;DR: The Central American Association of Pediatric Hematology Oncology (AHOPCA) aimed to standardize the approach and to improve outcomes of patients with retinoblastoma.
References
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Journal ArticleDOI

Mutation and Cancer: Statistical Study of Retinoblastoma

TL;DR: The hypothesis is developed that retinoblastoma is a cancer caused by two mutational events, in the dominantly inherited form, one mutation is inherited via the germinal cells and the second occurs in somatic cells.
Journal ArticleDOI

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

TL;DR: The isolation of a complementary DNA segment that detects a chromosomal segment having the properties of the gene at this locus is described, which is expressed in many tumour types, but no RNA transcript has been found in retinoblastomas and osteosarcomas.
Journal ArticleDOI

Second primary neoplasms in patients with retinoblastoma.

TL;DR: Evidence from this and other papers strongly suggests an association between retinoblastoma and malignant melanoma and the use of cyclophosphamide may increase the risk of second primary neoplasms in patients with genetic retinOBlastoma.
Journal ArticleDOI

Retinoblastoma: clues to human oncogenesis.

TL;DR: The observation that extra nonrandom copies of specific chromosomal regions occur in some of these tumors provides circumstantial evidence that an "expressor" gene (possibly an oncogene) may be involved in retinoblastoma development.
Journal ArticleDOI

Genetics of retinoblastoma

TL;DR: It is postulated that the distribution of the malignant ocular neoplasm most commonly termed retinoblastoma is not at random in human populations, and a disproportionate frequency of both "horizontal" and "vertical" constellations is observed.
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