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Dive into the research topics where Karina Braga Ribeiro is active.

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Featured researches published by Karina Braga Ribeiro.


Cancer | 2001

Human papillomavirus as a prognostic factor in carcinoma of the penis: Analysis of 82 patients treated with amputation and bilateral lymphadenectomy

Artur L. R. Bezerra; Ademar Lopes; Geraldo H. Santiago; Karina Braga Ribeiro; Maria R. D. O. Latorre; Luisa L. Villa

Many studies have tried to identify prognostic factors to guide the selection of patients at high risk for metastases in penile carcinoma. The authors evaluated human papillomavirus (HPV) status with respect to clinical features, incidence of metastases, and prognosis of penile carcinoma.


Pediatric Blood & Cancer | 2009

Familial retinoblastoma in developing countries.

Guillermo L. Chantada; Ira J. Dunkel; Ibrahim Qaddoumi; Célia Beatriz Gianotti Antoneli; Alegría Benguigui de Totah; Serife Canturk; Ibrahim Nawaiseh; Adriana Fandiño; Imelda de Pifano; Gonul Peksayar; Karina Braga Ribeiro; David H. Abramson

Although screening for familial retinoblastoma has been shown to be beneficial we suspected that such screening programs may be less than optimal in developing countries (DC).


BMC Cancer | 2008

Interaction between polymorphisms of the Human Leukocyte Antigen and HPV-16 Variants on the risk of invasive cervical cancer

Patricia Soares Souza; Paulo Cesar Maciag; Karina Braga Ribeiro; Maria Luiza Petzl-Erler; Eduardo L. Franco; Luisa L. Villa

BackgroundPersistent infection with oncogenic types of human papillomavirus (HPV) is the major risk factor for invasive cervical cancer (ICC), and non-European variants of HPV-16 are associated with an increased risk of persistence and ICC. HLA class II polymorphisms are also associated with genetic susceptibility to ICC. Our aim is to verify if these associations are influenced by HPV-16 variability.MethodsWe characterized HPV-16 variants by PCR in 107 ICC cases, which were typed for HLA-DQA1, DRB1 and DQB1 genes and compared to 257 controls. We measured the magnitude of associations by logistic regression analysis.ResultsEuropean (E), Asian-American (AA) and African (Af) variants were identified. Here we show that inverse association between DQB1*05 (adjusted odds ratio [OR] = 0.66; 95% confidence interval [CI]: 0.39–1.12]) and HPV-16 positive ICC in our previous report was mostly attributable to AA variant carriers (OR = 0.27; 95%CI: 0.10–0.75). We observed similar proportions of HLA DRB1*1302 carriers in E-P positive cases and controls, but interestingly, this allele was not found in AA cases (p = 0.03, Fisher exact test). A positive association with DRB1*15 was observed in both groups of women harboring either E (OR = 2.99; 95% CI: 1.13–7.86) or AA variants (OR = 2.34; 95% CI: 1.00–5.46). There was an inverse association between DRB1*04 and ICC among women with HPV-16 carrying the 350T [83L] single nucleotide polymorphism in the E6 gene (OR = 0.27; 95% CI: 0.08–0.96). An inverse association between DQB1*05 and cases carrying 350G (83V) variants was also found (OR = 0.37; 95% CI: 0.15–0.89).ConclusionOur results suggest that the association between HLA polymorphism and risk of ICC might be influenced by the distribution of HPV-16 variants.


Cancer | 2007

Trends in childhood leukemia mortality in Brazil and correlation with social inequalities.

Karina Braga Ribeiro; Luiz Fernando Lopes; Beatriz de Camargo

Mortality from childhood leukemia has declined substantially in developed countries but less markedly in the developing world. This study was designed to describe mortality trends in childhood leukemia and the impact of social inequalities on these trends in Brazil from 1980 to 2002.


Journal of Clinical Oncology | 2009

Cisplatin and Etoposide in Childhood Germ Cell Tumor: Brazilian Pediatric Oncology Society Protocol GCT-91

Luiz Fernando Lopes; Carla Renata Pacheco Macedo; Elitânia Marinho Pontes; Simone dos Santos Aguiar; Maria José Mastellaro; Renato Melaragno; Sonia Maria Rossi Vianna; Paula Maria Azevedo Allemand Lopes; Nubia Mendonça; Maria T. Almeida; Viviane Sonaglio; Karina Braga Ribeiro; Victor M. Santana; Dominik T. Schneider; Beatriz de Camargo

PURPOSEnIn 1988, we formed a consortium of Brazilian institutions to develop uniform standards for the diagnostic assessment and multidisciplinary treatment of children and adolescents with germ cell tumors. We also implemented the first childhood Brazilian germ cell tumor protocol, GCT-91, evaluating two-agent chemotherapy with cisplatin and etoposide (PE). We now report on the clinical characteristics and survival of children and adolescents with germ cell tumors treated on this protocol.nnnPATIENTS AND METHODSnFrom May 1991 to April 2000, 115 patients (106 assessable patients) were enrolled onto the Brazilian protocol with a diagnosis of germ cell tumor.nnnRESULTSnPatients were treated with surgery only (n = 35) and chemotherapy (n = 71). Important prognostic factors included stage (P = .025), surgical procedure at diagnosis according to resectability (P < .032), and abnormal lactate dehydrogenase value at diagnosis (P < .001).nnnCONCLUSIONnThe improvement in survival by the introduction of a standard protocol is an important achievement. This is of particular importance for smaller institutions with previous limited experience in the treatment of childhood germ cell tumors. In addition, the results of a two-agent regimen with PE were favorable (5-year overall survival rate is 83.3% for patients in the high-risk group [n = 36] who received PE v 58.8% for patients in the high-risk patients group who received PE plus ifosfamide, vinblastine, and bleomycin [n = 17; P = .017]). Thus for selected patients, complex three-agent regimens may not be necessary to achieve long-term survival, even for some patients with advanced disease.


Pediatric Blood & Cancer | 2015

Ethnicity, race, and socioeconomic status influence incidence of langerhans cell histiocytosis

Karina Braga Ribeiro; Barbara A. Degar; Célia Beatriz Gianotti Antoneli; Barrett J. Rollins; Carlos Rodriguez-Galindo

Langerhans cell histiocytosis (LCH) is a rare disease, and its etiology is not well understood. Population‐based studies may contribute to etiologic research by defining incidence patterns. This study was designed to evaluate the descriptive epidemiology of disseminated LCH in the United States, using data from population‐based cancer registries.


Journal of Medical Virology | 2011

Low prevalence of HPV in Brazilian children with retinoblastoma.

Célia Beatriz Gianotti Antoneli; Karina Braga Ribeiro; Simone Treiger Sredni; Victor Arias; Maria Antonieta Andreoli; Beatriz de Camargo; João Simão Sobrinho; José M. Prado; Fernando Augusto Soares; Luisa L. Villa

Retinoblastoma is the most frequent intra‐ocular malignant tumor of the childhood, occurring in 1 of 18,000–30,000 live births. Little is known about the causes of sporadic retinoblastoma and only a few authors have investigated the etiologic role of human papillomavirus (HPV), with controversial results. Formalin‐fixed, paraffin‐embedded tissue blocks containing retinoblastoma were retrieved from the archives of the Department of Pathology at Hospital A C Camargo, São Paulo, Brazil. All patients were treated with enucleation (21 children had both eyes enucleated). Retinoblastoma and, when possible, normal retina of each specimen, were micro‐dissected under direct light microscopic visualization by using a PixCell II Laser Capture Micro‐dissection System. The DNA quality was evaluated by polymerase chain reaction (PCR) amplification of 110 base pairs fragment of the human β‐globin gene using primers PCO3+/PCO4+. All globin positive specimens were analyzed by PCR for the presence of HPV DNA using consensus primers GP5+/GP6+. A total of 154 specimens were evaluated. Forty‐four patients also had normal retinal specimens available for analysis of DNA HPV. The DNA HPV prevalence among all tumor specimens was 4.6% (95% CI 2.0; 8.8) (7 positive specimens/153 adequate specimens). Among normal retinal specimens, the DNA HPV prevalence was 9.1% (95% CI 2.9; 20.5) (4 positive specimens/44 specimens). There was no statistically significant difference between these rates (Pu2009=u20090.318). Excluding any experimental failure, our results indicate a low prevalence of HPV DNA in retinoblastomas. We were therefore unable to conclude about the association between these oncogenic viruses and this rare pediatric neoplasm. J. Med. Virol. 83:115–118, 2011.


Sao Paulo Medical Journal | 2005

Histological classification of 1,025 cases of Hodgkin's lymphoma from the State of São Paulo, Brazil

José Vassallo; Roberto Pinto Paes; Fernando Augusto Soares; Yara Menezes; Vera Lucia Aldred; Karina Braga Ribeiro; Antonio Correa Alves

CONTEXT AND OBJECTIVEnIt is currently asserted that, in industrialized countries, nodular sclerosis is the most frequent type of Hodgkins lymphoma, in contrast to developing countries, where mixed cellularity and lymphocyte depletion are more frequently seen. The objective was to review histological data from cases of Hodgkins lymphoma from São Paulo and Campinas cities.nnnDESIGN AND SETTINGnCross-sectional histopathological analysis, in four university hospitals and one cancer care center.nnnMETHODSn1,025 cases diagnosed as Hodgkins lymphoma between 1990 and 2000 were collected from five institutions; 631 of them (61.5%) had been immunophenotyped using antibodies to CD20, CD3, CD15 and CD30. The relative frequencies of histological types (as informed by the contributing authors, who are hematopathologists in their institutions) were determined according to age and gender.nnnRESULTSnThe Hodgkins lymphoma types were distributed as follows: lymphocyte predominance 4.8%, nodular sclerosis 69.2%, mixed cellularity 21.1% and lymphocyte depletion 4.6%.nnnCONCLUSIONSnThe controversy regarding the frequencies of Hodgkins lymphoma types within the Brazilian setting seems to be due to the small number of cases in previous studies. The present data show a picture close to the situation in the industrialized countries.


Pediatric Blood & Cancer | 2016

An Increased Risk of Second Malignant Neoplasms After Rhabdomyosarcoma: Population-Based Evidence for a Cancer Predisposition Syndrome?

Natasha M. Archer; Renata Parada Amorim; Rafaela Naves; Simone Hettmer; Lisa Diller; Karina Braga Ribeiro; Carlos Rodriguez-Galindo

Rhabdomyosarcoma survivors have an increased risk of developing second malignant neoplasms (SMN); this risk is traditionally attributed to the effects of multidisciplinary management required for cure. However, the impact of constitutional predisposition has not been properly analyzed.


Pediatric Blood & Cancer | 2008

Improvement in the outcome of children with germ cell tumors

Luiz Fernando Lopes; Viviane Sonaglio; Karina Braga Ribeiro; Dominik T. Schneider; Beatriz de Camargo

To describe the clinical characteristics and estimate the survival of children and adolescents with germ cell tumors treated with cisplatin‐based combination chemotherapy according to three different protocols in Brazil.

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Luisa L. Villa

University of São Paulo

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Victor Arias

University of São Paulo

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Carlos Rodriguez-Galindo

St. Jude Children's Research Hospital

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Daniel Onofre Vidal

Ludwig Institute for Cancer Research

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José M. Prado

Ludwig Institute for Cancer Research

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