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Erschienen in: Journal of Cancer Research and Clinical Oncology 2/2017

16.09.2016 | Original Article – Cancer Research

Cancer incidence in patients with hereditary hemorrhagic telangiectasia

verfasst von: Christine W. Duarte, Adam W. Black, F. Lee Lucas, Calvin P. H. Vary

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 2/2017

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Abstract

Purpose

Hereditary hemorrhagic telangiectasia (HHT) is a genetic disorder characterized by deficiency in endoglin, an angiogenic protein. We previously showed that HHT, in which systemic endoglin expression is reduced, was associated with better survival outcomes in cancer patients (Duarte et al. in Cancer Epidemiol Biomarkers Prev 23:117–125, 2014). Here, we evaluated whether HHT was associated with reduced cancer incidence.

Methods

A matched case–control analysis using SEER Medicare was conducted to evaluate the effect of HHT on diagnosis with breast, colorectal, lung, or prostate cancer between 2000 and 2007 (n = 633,162). Cancer and non-cancer patients were matched on age, sex, SEER registry region, and length of the ascertainment period for HHT. We assessed crude association using a McNemar’s test and then adjusted for demographic variables, cancer type, cancer stage, comorbidities, and ascertainment period with a conditional logistic regression model for cancer incidence.

Results

The McNemar’s test showed no significant association between HHT and cancer incidence (p = 0.74). Adjusting for covariates with the conditional logistic regression model did not change the result [HHT odds ratio 0.978; 95 % CI (0.795, 1.204)]. The lack of association between HHT and cancer incidence is unexpected given the previously discovered significant association between HHT and improved survival outcomes (Duarte et al. in Cancer Epidemiol Biomarkers Prev 23:117–125, 2014).

Conclusions

We conclude that the protective effect of reduced systemic endoglin expression in cancer is specific to cancer progression through its effect on vascularization and other stromal effects but does not extend to cancer initiation.
Literatur
Zurück zum Zitat Breen MJ, Moran DM, Liu W, Huang X, Vary CPH, Bergan RC (2013) Endoglin-mediated suppression of prostate cancer invasion is regulated by activin and bone morphogenetic protein type II receptors. Plos One 8:e72407CrossRefPubMedPubMedCentral Breen MJ, Moran DM, Liu W, Huang X, Vary CPH, Bergan RC (2013) Endoglin-mediated suppression of prostate cancer invasion is regulated by activin and bone morphogenetic protein type II receptors. Plos One 8:e72407CrossRefPubMedPubMedCentral
Zurück zum Zitat Charlson ME, Pompei P, Ales KL, Mackenzie CR (1987) A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis 40:373–383CrossRefPubMed Charlson ME, Pompei P, Ales KL, Mackenzie CR (1987) A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis 40:373–383CrossRefPubMed
Zurück zum Zitat Duarte CW, Murray K, Lucas FL, Fairfield K, Miller H, Brooks P, Vary CP (2014) Improved survival outcomes in cancer patients with hereditary hemorrhagic telangiectasia. Cancer Epidemiol Biomarkers Prev 23:117–125CrossRefPubMed Duarte CW, Murray K, Lucas FL, Fairfield K, Miller H, Brooks P, Vary CP (2014) Improved survival outcomes in cancer patients with hereditary hemorrhagic telangiectasia. Cancer Epidemiol Biomarkers Prev 23:117–125CrossRefPubMed
Zurück zum Zitat Fisher KJ, Lee JH, Ferrante JM, McCarthy EP, Gonzalez EC, Chen R, Love-Jackson K, Roetzheim RG (2013) The effects of primary care on breast cancer mortality and incidence among medicare beneficiaries. Cancer 119:2964–2972CrossRefPubMedPubMedCentral Fisher KJ, Lee JH, Ferrante JM, McCarthy EP, Gonzalez EC, Chen R, Love-Jackson K, Roetzheim RG (2013) The effects of primary care on breast cancer mortality and incidence among medicare beneficiaries. Cancer 119:2964–2972CrossRefPubMedPubMedCentral
Zurück zum Zitat Lakshman M, Huang X, Ananthanarayanan V, Jovanovic B, Liu Y, Craft CS, Romero D, Vary CP, Bergan RC (2011) Endoglin suppresses human prostate cancer metastasis. Clin Exp Metastasis 28:39–53CrossRefPubMed Lakshman M, Huang X, Ananthanarayanan V, Jovanovic B, Liu Y, Craft CS, Romero D, Vary CP, Bergan RC (2011) Endoglin suppresses human prostate cancer metastasis. Clin Exp Metastasis 28:39–53CrossRefPubMed
Zurück zum Zitat McAllister KA, Grogg KM, Johnson DW, Gallione CJ, Baldwin MA, Jackson CE, Helmbold EA, Markel DS, McKinnon WC, Murrell J et al (1994) Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nat Genet 8:345–351CrossRefPubMed McAllister KA, Grogg KM, Johnson DW, Gallione CJ, Baldwin MA, Jackson CE, Helmbold EA, Markel DS, McKinnon WC, Murrell J et al (1994) Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nat Genet 8:345–351CrossRefPubMed
Zurück zum Zitat Romero D, O’Neill C, Terzic A, Contois L, Young K, Conley BA, Bergan RC, Brooks PC, Vary CPH (2011) Endoglin regulates cancer-stromal cell interactions in prostate tumors. Cancer Res 71:3482–3493CrossRefPubMedPubMedCentral Romero D, O’Neill C, Terzic A, Contois L, Young K, Conley BA, Bergan RC, Brooks PC, Vary CPH (2011) Endoglin regulates cancer-stromal cell interactions in prostate tumors. Cancer Res 71:3482–3493CrossRefPubMedPubMedCentral
Zurück zum Zitat Rosen LS, Hurwitz HI, Wong MK, Goldman J, Mendelson DS, Figg WD, Spencer S, Adams BJ, Alvarez D, Seon BK, Theuer CP, Leigh BR, Gordon MS (2012) A phase I first-in-human study of TRC105 (anti-endoglin antibody) in patients with advanced cancer. Clin Cancer Res 18:4820–4829CrossRefPubMedPubMedCentral Rosen LS, Hurwitz HI, Wong MK, Goldman J, Mendelson DS, Figg WD, Spencer S, Adams BJ, Alvarez D, Seon BK, Theuer CP, Leigh BR, Gordon MS (2012) A phase I first-in-human study of TRC105 (anti-endoglin antibody) in patients with advanced cancer. Clin Cancer Res 18:4820–4829CrossRefPubMedPubMedCentral
Zurück zum Zitat Sabba C, Gallitelli M, Pasculli G, Suppressa P, Resta F, Tafaro GE (2006) HHT: a rare disease with a broad spectrum of clinical aspects. Curr Pharm Des 12:1217–1220CrossRefPubMed Sabba C, Gallitelli M, Pasculli G, Suppressa P, Resta F, Tafaro GE (2006) HHT: a rare disease with a broad spectrum of clinical aspects. Curr Pharm Des 12:1217–1220CrossRefPubMed
Zurück zum Zitat Sabba C, Pasculli G, Lenato GM, Suppressa P, Lastella P, Memeo M, Dicuonzo F, Guant G (2007) Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers. J Thromb Haemost 5:1149–1157CrossRefPubMed Sabba C, Pasculli G, Lenato GM, Suppressa P, Lastella P, Memeo M, Dicuonzo F, Guant G (2007) Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers. J Thromb Haemost 5:1149–1157CrossRefPubMed
Zurück zum Zitat Saluja S, White RI (2004) Hereditary hemorrhagic telangiectasia of the liver: hyperperfusion with relative ischemia–poverty amidst plenty. Radiology 230:25–27CrossRefPubMed Saluja S, White RI (2004) Hereditary hemorrhagic telangiectasia of the liver: hyperperfusion with relative ischemia–poverty amidst plenty. Radiology 230:25–27CrossRefPubMed
Zurück zum Zitat Shovlin CL, Guttmacher AE, Buscarini E, Faughnan ME, Hyland RH, Westermann CJ, Kjeldsen AD, Plauchu H (2000) Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu–Osler–Weber syndrome). Am J Med Genet 91:66–67CrossRefPubMed Shovlin CL, Guttmacher AE, Buscarini E, Faughnan ME, Hyland RH, Westermann CJ, Kjeldsen AD, Plauchu H (2000) Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu–Osler–Weber syndrome). Am J Med Genet 91:66–67CrossRefPubMed
Zurück zum Zitat Trabert B, Wentzensen N, Felix AS, Yang HP, Sherman ME, Brinton LA (2015) Metabolic syndrome and risk of endometrial cancer in the United States: a study in the SEER-medicare linked database. Cancer Epidemiol Biomarkers Prev 24:261–267CrossRefPubMedPubMedCentral Trabert B, Wentzensen N, Felix AS, Yang HP, Sherman ME, Brinton LA (2015) Metabolic syndrome and risk of endometrial cancer in the United States: a study in the SEER-medicare linked database. Cancer Epidemiol Biomarkers Prev 24:261–267CrossRefPubMedPubMedCentral
Metadaten
Titel
Cancer incidence in patients with hereditary hemorrhagic telangiectasia
verfasst von
Christine W. Duarte
Adam W. Black
F. Lee Lucas
Calvin P. H. Vary
Publikationsdatum
16.09.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 2/2017
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-016-2272-7

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