TY - JOUR
T1 - Familial risk in patients with carcinoma of unknown primary
AU - Samadder, N. Jewel
AU - Smith, Ken Robert
AU - Hanson, Heidi
AU - Pimentel, Richard
AU - Wong, Jathine
AU - Boucher, Kenneth
AU - Akerley, Wallace
AU - Gilcrease, Glynn
AU - Ulrich, Cornelia M.
AU - Burt, Randall W.
AU - Curtin, Karen
N1 - Funding Information:
Support for this projectwas provided by National Cancer Institute grants P01- CA073992 (Dr Burt), R01-CA040641 (Dr Burt), an Endoscopic Research Award from the American Society for Gastrointestinal Endoscopy (Dr Samadder), and a Junior Faculty Career Development Award from the American College of Gastroenterology (Dr Samadder). Partial support for the Utah Population Database and this projectwas provided by the Huntsman Cancer Institute Cancer Center Support Grant P30CA042014 from the National Cancer Institute and the Huntsman Cancer Foundation. Support for the Utah Cancer Registry is provided by contract HHSN 261201000026C from theNational Cancer Institute with additional support from the Utah Department of Health and the University of Utah.
Publisher Copyright:
© 2016 American Medical Association. All rights reserved.
PY - 2016/3
Y1 - 2016/3
N2 - IMPORTANCE Carcinoma of unknown primary (CUP) accounts for 3%to 5%of all cancers and is associated with poor prognosis. Familial clustering of different cancer sites with CUP is unknown and may provide information regarding etiology, as well as elevated cancer risks in relatives. OBJECTIVE To quantify the risk of cancer by site in first- and second-degree relatives and first cousins of individuals with CUP. DESIGN, SETTING, AND PARTICIPANTS Nested case-control study of patients who received a diagnosis of CUP between 1980 and 2010 identified from the Utah Cancer Registry. Population controls with no CUP diagnosis were sex and age matched 10:1 to patients with CUP. Data about relatives were drawn from the Utah Population Database. MAIN OUTCOMES AND MEASURES Familial aggregation of cancer risk in relatives of cases compared with controls using Cox regression analysis. RESULTS For the 4160 index patients (median [interquartile range] age, 72 [62-81] years; 47.6%male) who had received a diagnosis of CUP, first-degree relatives were at an elevated risk of CUP themselves (hazard ratio [HR], 1.35 [95%CI, 1.07-1.70]), as well as lung (HR, 1.37 [95%CI, 1.22-1.54]), pancreatic (HR, 1.28 [95%CI, 1.06-1.54]),myeloma (HR, 1.28 [95%CI, 1.01-1.62]), and non-Hodgkin lymphoma (HR, 1.16 [95%CI, >1.00-1.35]) cancers compared with controls without CUP. When the analysis was restricted to relatives of cancer-free controls, additional increased risks for colon (HR, 1.19 [95%CI, 1.06-1.33]) and bladder (HR, 1.18 [95%CI, >1.00-1.38]) cancers were observed. Second-degree relatives of patients with CUP were at a slight increased risk of lung (HR, 1.14 [95%CI, 1.03-1.26]), pancreatic (HR, 1.17 [95%CI, 1.01-1.37]), breast (HR, 1.09 [95%CI, 1.02-1.16]), melanoma (HR, 1.09 [95%CI, >1.00-1.19]), and ovarian (HR, 1.19 [95%CI, 1.02-1.39]) cancers. CONCLUSIONS AND RELEVANCE Relatives of patients with CUP are at increased risk of CUP and several other malignant neoplasms, including lung, pancreatic, and colon cancer. The present data may suggest sites of origin for CUP and provide cancer risk information for relatives of patients with CUP that can lead to effective intervention. Relatives of patients with CUP should be aware of the elevated risks for lung, pancreatic, and colon cancer and encouraged to modify risk factors and adhere to site-specific population cancer screening.
AB - IMPORTANCE Carcinoma of unknown primary (CUP) accounts for 3%to 5%of all cancers and is associated with poor prognosis. Familial clustering of different cancer sites with CUP is unknown and may provide information regarding etiology, as well as elevated cancer risks in relatives. OBJECTIVE To quantify the risk of cancer by site in first- and second-degree relatives and first cousins of individuals with CUP. DESIGN, SETTING, AND PARTICIPANTS Nested case-control study of patients who received a diagnosis of CUP between 1980 and 2010 identified from the Utah Cancer Registry. Population controls with no CUP diagnosis were sex and age matched 10:1 to patients with CUP. Data about relatives were drawn from the Utah Population Database. MAIN OUTCOMES AND MEASURES Familial aggregation of cancer risk in relatives of cases compared with controls using Cox regression analysis. RESULTS For the 4160 index patients (median [interquartile range] age, 72 [62-81] years; 47.6%male) who had received a diagnosis of CUP, first-degree relatives were at an elevated risk of CUP themselves (hazard ratio [HR], 1.35 [95%CI, 1.07-1.70]), as well as lung (HR, 1.37 [95%CI, 1.22-1.54]), pancreatic (HR, 1.28 [95%CI, 1.06-1.54]),myeloma (HR, 1.28 [95%CI, 1.01-1.62]), and non-Hodgkin lymphoma (HR, 1.16 [95%CI, >1.00-1.35]) cancers compared with controls without CUP. When the analysis was restricted to relatives of cancer-free controls, additional increased risks for colon (HR, 1.19 [95%CI, 1.06-1.33]) and bladder (HR, 1.18 [95%CI, >1.00-1.38]) cancers were observed. Second-degree relatives of patients with CUP were at a slight increased risk of lung (HR, 1.14 [95%CI, 1.03-1.26]), pancreatic (HR, 1.17 [95%CI, 1.01-1.37]), breast (HR, 1.09 [95%CI, 1.02-1.16]), melanoma (HR, 1.09 [95%CI, >1.00-1.19]), and ovarian (HR, 1.19 [95%CI, 1.02-1.39]) cancers. CONCLUSIONS AND RELEVANCE Relatives of patients with CUP are at increased risk of CUP and several other malignant neoplasms, including lung, pancreatic, and colon cancer. The present data may suggest sites of origin for CUP and provide cancer risk information for relatives of patients with CUP that can lead to effective intervention. Relatives of patients with CUP should be aware of the elevated risks for lung, pancreatic, and colon cancer and encouraged to modify risk factors and adhere to site-specific population cancer screening.
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U2 - 10.1001/jamaoncol.2015.4265
DO - 10.1001/jamaoncol.2015.4265
M3 - Article
C2 - 26863281
AN - SCOPUS:84979520740
SN - 2374-2437
VL - 2
SP - 340
EP - 345
JO - JAMA Oncology
JF - JAMA Oncology
IS - 3
ER -