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Year Number of Results
1979 1
1980 1
1990 1
1991 1
1992 1
1996 1
1998 1
2001 1
2003 2
2006 2
2007 5
2008 2
2009 2
2012 1
2013 4
2014 4
2015 1
2016 2
2017 1
2018 2
2019 2
2020 1
2024 0

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34 results

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Page 1
Trilateral retinoblastoma.
Antoneli CB, Ribeiro Kde C, Sakamoto LH, Chojniak MM, Novaes PE, Arias VE. Antoneli CB, et al. Pediatr Blood Cancer. 2007 Mar;48(3):306-10. doi: 10.1002/pbc.20793. Pediatr Blood Cancer. 2007. PMID: 16572402 Review.
BACKGROUND: Trilateral retinoblastoma (TRB) is a syndrome consisting of unilateral or bilateral hereditary retinoblastoma (Rb) associated with an intracranial neuroblastic tumor. ...
BACKGROUND: Trilateral retinoblastoma (TRB) is a syndrome consisting of unilateral or bilateral hereditary retinoblastoma (Rb) …
The Incidence of Trilateral Retinoblastoma: A Systematic Review and Meta-Analysis.
de Jong MC, Kors WA, de Graaf P, Castelijns JA, Moll AC, Kivelä T. de Jong MC, et al. Am J Ophthalmol. 2015 Dec;160(6):1116-1126.e5. doi: 10.1016/j.ajo.2015.09.009. Epub 2015 Sep 12. Am J Ophthalmol. 2015. PMID: 26374932 Free article. Review.
For patients with bilateral retinoblastoma the unadjusted chance of developing trilateral retinoblastoma across all cohorts was 5.3% (95% confidence interval [CI]: 3.3%-7.7%); the chance of pineal trilateral retinoblastoma was 4.2% (95% CI: 2.6%-6.2%) and the chance of nonpineal …
For patients with bilateral retinoblastoma the unadjusted chance of developing trilateral retinoblastoma across all cohorts was 5.3% (95% co …
The etiology of osteosarcoma.
Ottaviani G, Jaffe N. Ottaviani G, et al. Cancer Treat Res. 2009;152:15-32. doi: 10.1007/978-1-4419-0284-9_2. Cancer Treat Res. 2009. PMID: 20213384 Review.
Although extremely rare, osteosarcoma has occasionally been observed in several members of the same family. No other clinical abnormalities in the proband or the affected members were reported. ...A genetic predisposition to osteosarcoma is found in patients with heredi …
Although extremely rare, osteosarcoma has occasionally been observed in several members of the same family. No other clinical abnorma …
Bone and Soft-Tissue Sarcoma Risk in Long-Term Survivors of Hereditary Retinoblastoma Treated With Radiation.
Kleinerman RA, Schonfeld SJ, Sigel BS, Wong-Siegel JR, Gilbert ES, Abramson DH, Seddon JM, Tucker MA, Morton LM. Kleinerman RA, et al. J Clin Oncol. 2019 Dec 10;37(35):3436-3445. doi: 10.1200/JCO.19.01096. Epub 2019 Oct 17. J Clin Oncol. 2019. PMID: 31622129 Free PMC article.
PURPOSE: Survivors of hereditary retinoblastoma have excellent survival but substantially increased risks of subsequent bone and soft-tissue sarcomas, particularly after radiotherapy. Comprehensive investigation of sarcoma risk patterns would inform clinical …
PURPOSE: Survivors of hereditary retinoblastoma have excellent survival but substantially increased risks of subsequent bone a …
Correlation between RB1germline mutations and second primary malignancies in hereditary retinoblastoma patients treated with external beam radiotherapy.
Chaussade A, Millot G, Wells C, Brisse H, Laé M, Savignoni A, Desjardins L, Dendale R, Doz F, Aerts I, Jimenez I, Cassoux N, Stoppa Lyonnet D, Gauthier Villars M, Houdayer C. Chaussade A, et al. Eur J Med Genet. 2019 Mar;62(3):217-223. doi: 10.1016/j.ejmg.2018.07.017. Epub 2018 Jul 18. Eur J Med Genet. 2019. PMID: 30031154
Second cranio-facial malignancies in hereditary retinoblastoma survivors previously treated with radiation therapy: clinic and radiologic characteristics and survival outcomes.
Rodjan F, Graaf Pd, Brisse HJ, Verbeke JI, Sanchez E, Galluzzi P, Göricke S, Maeder P, Aerts I, Dendale R, Desjardins L, de Franscesco S, Bornfeld N, Sauerwein W, Popovic MB, Knol DL, Moll AC, Castelijns JA. Rodjan F, et al. Eur J Cancer. 2013 May;49(8):1939-47. doi: 10.1016/j.ejca.2013.01.010. Epub 2013 Feb 14. Eur J Cancer. 2013. PMID: 23415887 Free article.
INTRODUCTION: Hereditary retinoblastoma survivors have an increased risk for cranio-facial second primary tumours (SPT), especially after treatment with external beam radiotherapy (EBRT). ...PATIENTS AND METHODS: Clinical and radiological data of 42 heredi …
INTRODUCTION: Hereditary retinoblastoma survivors have an increased risk for cranio-facial second primary tumours (SPT), espec …
Subsequent malignancies and their effect on survival in patients with retinoblastoma.
Shinohara ET, DeWees T, Perkins SM. Shinohara ET, et al. Pediatr Blood Cancer. 2014 Jan;61(1):116-9. doi: 10.1002/pbc.24714. Epub 2013 Aug 5. Pediatr Blood Cancer. 2014. PMID: 23918737
BACKGROUND: As cure rates for retinoblastoma have improved, it is clear that patients with hereditary retinoblastoma experience increased risk of subsequent malignant neoplasms (SMNs). ...
BACKGROUND: As cure rates for retinoblastoma have improved, it is clear that patients with hereditary retinoblastoma experienc …
Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutation.
Brichard B, Heusterspreute M, De Potter P, Chantrain C, Vermylen C, Sibille C, Gala JL. Brichard B, et al. Eur J Cancer. 2006 Jan;42(1):65-72. doi: 10.1016/j.ejca.2005.07.027. Eur J Cancer. 2006. PMID: 16343894
Conclusive identification of RB1 mutations in retinoblastoma is predicted to improve the clinical management of affected children and relatives. However, despite clear clinical benefits, RB1 screening remains difficult, most of the alterations being unique and ra …
Conclusive identification of RB1 mutations in retinoblastoma is predicted to improve the clinical management of affected children and …
Risk of subsequent malignant neoplasms in long-term hereditary retinoblastoma survivors after chemotherapy and radiotherapy.
Wong JR, Morton LM, Tucker MA, Abramson DH, Seddon JM, Sampson JN, Kleinerman RA. Wong JR, et al. J Clin Oncol. 2014 Oct 10;32(29):3284-90. doi: 10.1200/JCO.2013.54.7844. Epub 2014 Sep 2. J Clin Oncol. 2014. PMID: 25185089 Free PMC article.
PURPOSE: Hereditary retinoblastoma (Rb) survivors have increased risk of subsequent malignant neoplasms (SMNs). ...
PURPOSE: Hereditary retinoblastoma (Rb) survivors have increased risk of subsequent malignant neoplasms (SMNs). ...
Craniofacial second primary tumors in patients with germline retinoblastoma previously treated with external beam radiotherapy: A retrospective institutional analysis.
Jiménez I, Laé M, Tanguy ML, Savignoni A, Gauthier-Villars M, Desjardins L, Cassoux N, Dendale R, Rodriguez J, Doz F, Brisse HJ, Aerts I. Jiménez I, et al. Pediatr Blood Cancer. 2020 Apr;67(4):e28158. doi: 10.1002/pbc.28158. Epub 2020 Jan 6. Pediatr Blood Cancer. 2020. PMID: 31904159
PROCEDURE: We studied the incidence, risk factors, and prognosis of specific craniofacial SPTs developed within the margins of radiation field in a cohort of 209 patients with germline retinoblastoma treated with EBRT at our institution between 1977 and 2010. Clinical char …
PROCEDURE: We studied the incidence, risk factors, and prognosis of specific craniofacial SPTs developed within the margins of radiation fie …
34 results