메뉴 건너뛰기




Volumn 17, Issue 4, 2008, Pages 365-372

Family history of pancreatic cancer in a high-risk cancer clinic: Implications for risk assessment

Author keywords

BRCA1 2; HBOS; Pancreatic cancer; Risk assessment

Indexed keywords

ADULT; AGED; ARTICLE; BRCA2 ONCOGENE; BREAST CANCER; CANCER RISK; CONTROLLED STUDY; FAMILIAL CANCER; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC COUNSELING; HEREDITARY BREAST OVARIAN SYNDROME; HIGH RISK POPULATION; HUMAN; JEW; MAJOR CLINICAL STUDY; MALE; ONCOGENE; OVARY CANCER; PANCREAS CANCER; PEDIGREE; RELATIVE; RISK ASSESSMENT;

EID: 48449083823     PISSN: 10597700     EISSN: 15733599     Source Type: Journal    
DOI: 10.1007/s10897-008-9154-3     Document Type: Article
Times cited : (6)

References (38)
  • 2
    • 0033523268 scopus 로고    scopus 로고
    • Cancer risks in BRCA2 mutation carriers. the Breast Cancer Linkage Consortium
    • anonymous
    • anonymous 1999 Cancer risks in BRCA2 mutation carriers. The Breast Cancer Linkage Consortium Journal of the National Cancer Institute 91 1310 1316
    • (1999) Journal of the National Cancer Institute , vol.91 , pp. 1310-1316
  • 4
    • 0030893779 scopus 로고    scopus 로고
    • Recommendations for follow-up care of individuals with an inherited predisposition to cancer. II. BRCA1 and BRCA2. Cancer genetics studies consortium
    • W. Burke M. Daly J. Garber J. Botkin M. J. Khan P. Lynch 1997 Recommendations for follow-up care of individuals with an inherited predisposition to cancer. II. BRCA1 and BRCA2. Cancer genetics studies consortium JAMA 277 997 1003
    • (1997) JAMA , vol.277 , pp. 997-1003
    • Burke, W.1    Daly, M.2    Garber, J.3    Botkin, J.4    Khan, M.J.5    Lynch, P.6
  • 7
    • 23044452932 scopus 로고    scopus 로고
    • Genetic services for familial cancer patients: A follow-up survey of National Cancer Institute Cancer Centers
    • M. Epplein K. P. Koon S. D. Ramsey J. D. Potter 2005 Genetic services for familial cancer patients: A follow-up survey of National Cancer Institute Cancer Centers Journal of Clinical Oncology 23 4713 4718
    • (2005) Journal of Clinical Oncology , vol.23 , pp. 4713-4718
    • Epplein, M.1    Koon, K.P.2    Ramsey, S.D.3    Potter, J.D.4
  • 8
    • 2942726188 scopus 로고    scopus 로고
    • A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO
    • D. G. Evans D. M. Eccles N. Rahman K. Young M. Bulman E. Amir 2004 A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO Journal of Medical Genetics 41 474 480
    • (2004) Journal of Medical Genetics , vol.41 , pp. 474-480
    • Evans, D.G.1    Eccles, D.M.2    Rahman, N.3    Young, K.4    Bulman, M.5    Amir, E.6
  • 10
    • 0023924052 scopus 로고
    • Upper gastrointestinal cancer in familial adenomatous polyposis
    • D. G. Jagelman J. J. DeCosse H. J. Bussey 1988 Upper gastrointestinal cancer in familial adenomatous polyposis Lancet 1 1149 1151
    • (1988) Lancet , vol.1 , pp. 1149-1151
    • Jagelman, D.G.1    Decosse, J.J.2    Bussey, H.J.3
  • 14
    • 0034650411 scopus 로고    scopus 로고
    • Inherited predisposition to pancreatic adenocarcinoma: Role of family history and germ-line p16, BRCA1, and BRCA2 mutations
    • G. Lal G. Liu B. Schmocker P. Kaurah H. Ozcelik S. A. Narod 2000 Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations Cancer Research 60 409 416
    • (2000) Cancer Research , vol.60 , pp. 409-416
    • Lal, G.1    Liu, G.2    Schmocker, B.3    Kaurah, P.4    Ozcelik, H.5    Narod, S.A.6
  • 15
    • 33749067855 scopus 로고    scopus 로고
    • Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: A systematic review
    • N. M. Lindor G. M. Petersen D. W. Hadley A. Y. Kinney S. Miesfeldt K. H. Lu 2005 Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review JAMA 27 1507 1517
    • (2005) JAMA , vol.27 , pp. 1507-1517
    • Lindor, N.M.1    Petersen, G.M.2    Hadley, D.W.3    Kinney, A.Y.4    Miesfeldt, S.5    Lu, K.H.6
  • 18
    • 0036143702 scopus 로고    scopus 로고
    • Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: The familial atypical multiple mole melanoma-pancreatic carcinoma syndrome
    • H. T. Lynch R. E. Brand D. Hogg C. A. Deters R. M. Fusaro J. F. Lynch 2002 Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: The familial atypical multiple mole melanoma-pancreatic carcinoma syndrome Cancer 94 84 96
    • (2002) Cancer , vol.94 , pp. 84-96
    • Lynch, H.T.1    Brand, R.E.2    Hogg, D.3    Deters, C.A.4    Fusaro, R.M.5    Lynch, J.F.6
  • 19
    • 4544308586 scopus 로고    scopus 로고
    • Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history
    • H. J. Murff D. R. Spigel S. Syngal 2004 Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history JAMA 292 1480 1489
    • (2004) JAMA , vol.292 , pp. 1480-1489
    • Murff, H.J.1    Spigel, D.R.2    Syngal, S.3
  • 20
    • 0036644884 scopus 로고    scopus 로고
    • Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer: Deleterious BRCA2 mutations in 17%
    • K. M. Murphy K. A. Brune C. Griffin J. E. Sollenberger G. M. Petersen R. Bansal 2002 Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer: Deleterious BRCA2 mutations in 17% Cancer Research 62 3789 3793
    • (2002) Cancer Research , vol.62 , pp. 3789-3793
    • Murphy, K.M.1    Brune, K.A.2    Griffin, C.3    Sollenberger, J.E.4    Petersen, G.M.5    Bansal, R.6
  • 21
    • 24644490720 scopus 로고    scopus 로고
    • Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: Systematic evidence review for the U.S. Preventive Services Task Force
    • H. D. Nelson L. H. Huffman R. Fu E. L. Harris 2005 Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: Systematic evidence review for the U.S. Preventive Services Task Force Annals of Internal Medicine 143 355 379
    • (2005) Annals of Internal Medicine , vol.143 , pp. 355-379
    • Nelson, H.D.1    Huffman, L.H.2    Fu, R.3    Harris, E.L.4
  • 23
    • 19444369006 scopus 로고    scopus 로고
    • Genetic cancer risk assessment in the newly diagnosed breast cancer patient is useful and possible in practice
    • M. R. Palomares B. Paz J. N. Weitzel 2005 Genetic cancer risk assessment in the newly diagnosed breast cancer patient is useful and possible in practice Journal of Clinical Oncology 23 3165 3166
    • (2005) Journal of Clinical Oncology , vol.23 , pp. 3165-3166
    • Palomares, M.R.1    Paz, B.2    Weitzel, J.N.3
  • 26
  • 28
    • 0035552404 scopus 로고    scopus 로고
    • Inherited pancreatic cancer: Surveillance and treatment strategies for affected families
    • S. J. Rulyak T. A. Brentnall 2001 Inherited pancreatic cancer: Surveillance and treatment strategies for affected families Pancreatology 1 477 485
    • (2001) Pancreatology , vol.1 , pp. 477-485
    • Rulyak, S.J.1    Brentnall, T.A.2
  • 29
    • 0038297512 scopus 로고    scopus 로고
    • Risk factors for the development of pancreatic cancer in familial pancreatic cancer kindreds
    • S. J. Rulyak A. B. Lowenfels P. Maisonneuve T. A. Brentnall 2003 Risk factors for the development of pancreatic cancer in familial pancreatic cancer kindreds Gastroenterology 124 1292 1299
    • (2003) Gastroenterology , vol.124 , pp. 1292-1299
    • Rulyak, S.J.1    Lowenfels, A.B.2    Maisonneuve, P.3    Brentnall, T.A.4
  • 31
    • 0037130887 scopus 로고    scopus 로고
    • Cancer incidence in BRCA1 mutation carriers
    • Breast Cancer Linkage Consortium
    • D. Thompson D. F. Easton Breast Cancer Linkage Consortium 2002 Cancer incidence in BRCA1 mutation carriers Journal of the National Cancer Institute 94 1358 1365
    • (2002) Journal of the National Cancer Institute , vol.94 , pp. 1358-1365
    • Thompson, D.1    Easton, D.F.2
  • 34
    • 0033063711 scopus 로고    scopus 로고
    • New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC
    • H. F. Vasen P. Watson J. P. Mecklin H. T. Lynch 1999 New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC Gastroenterology 116 1453 1456
    • (1999) Gastroenterology , vol.116 , pp. 1453-1456
    • Vasen, H.F.1    Watson, P.2    Mecklin, J.P.3    Lynch, H.T.4
  • 35
    • 4344600626 scopus 로고    scopus 로고
    • Bias in intervention studies that enroll patients from high-risk clinics
    • S. Wacholder 2004 Bias in intervention studies that enroll patients from high-risk clinics Journal of the National Cancer Institute 96 1204 1207
    • (2004) Journal of the National Cancer Institute , vol.96 , pp. 1204-1207
    • Wacholder, S.1
  • 36
    • 34250631251 scopus 로고    scopus 로고
    • Limited family structure and BRCA gene mutation status in single cases of breast cancer
    • J. N. Weitzel V. I. Lagos C. A. Cullinane P. J. Gambol J. O. Culver K. R. Blazer 2007 Limited family structure and BRCA gene mutation status in single cases of breast cancer JAMA 297 2587 2595
    • (2007) JAMA , vol.297 , pp. 2587-2595
    • Weitzel, J.N.1    Lagos, V.I.2    Cullinane, C.A.3    Gambol, P.J.4    Culver, J.O.5    Blazer, K.R.6
  • 37
    • 48449102495 scopus 로고    scopus 로고
    • Cancer risk assessment: Toward a primary prevention of breast and ovarian cancer
    • M. White O. I. Olopade 2000 Cancer risk assessment: Toward a primary prevention of breast and ovarian cancer Oncol Econ 1 40 45
    • (2000) Oncol Econ , vol.1 , pp. 40-45
    • White, M.1    Olopade, O.I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.