TY - JOUR
T1 - First report of screening an asymptomatic population for cancer
T2 - The yield of an integrated cancer prevention center
AU - Boursi, Ben
AU - Guzner-Gur, Hanan
AU - Mashich, Yaquv
AU - Miler, Udi
AU - Gur, Eyal
AU - Inbar, Roy
AU - Blachar, Arye
AU - Sperber, Fanny
AU - Kleiman, Shlomi
AU - Yafo, Ariel
AU - Elran, Hanoch
AU - Sella, Tal
AU - Naumov, Inna
AU - Kazanov, Diana
AU - Kraus, Sarah
AU - Galazan, Lior
AU - Reshef, Netta
AU - Sion-Tadmor, Tali
AU - Rozen, Miri
AU - Liberman, Eliezer
AU - Moshkowitz, Menachem
AU - Arber, Nadir
PY - 2010/1
Y1 - 2010/1
N2 - Background: Cancer is a leading cause of mortality worldwide. The most effective way to combat cancer is by prevention and early detection. Objectives: To evaluate the outcome of screening an asymptomatic population for the presence of benign and neoplastic lesions. Methods: Routine screening tests for prevention and/or early detection of 11 common cancers were conducted in 300 consecutive asymptomatic apparently healthy adults aged 25-77 years. Other tests were performed as indicated. Results: Malignant and benign lesions were found in 3.3% and 5% of the screenees, respectively, compared to 1.7% in the general population. The most common lesions were in the gastrointestinal tract followed by skin, urogenital tract and breast. Advanced age and a family history of a malignancy were associated with increased risk for cancer with an odds ratio of 9 and 3.5, respectively (95% confidence interval 1.1-71 and 0.9-13, respectively). Moreover, high serum C-reactive protein levels and polymorphisms in the APC and CD24 genes indicated high cancer risk. When two of the polymorphisms existed in an individual, the risk for a malignant lesion was extremely high (23.1%; OR 14, 95% CI 2.5-78). Conclusions: Screening asymptomatic subjects identifies a significant number of neoplastic lesions at an early stage. Incorporating data on genetic polymorphisms in the APC and CD24 genes can further identify individuals who are at increased risk for cancer. Cancer can be prevented and/or diagnosed at an early stage using the screening facilities of a multidisciplinary outpatient clinic.
AB - Background: Cancer is a leading cause of mortality worldwide. The most effective way to combat cancer is by prevention and early detection. Objectives: To evaluate the outcome of screening an asymptomatic population for the presence of benign and neoplastic lesions. Methods: Routine screening tests for prevention and/or early detection of 11 common cancers were conducted in 300 consecutive asymptomatic apparently healthy adults aged 25-77 years. Other tests were performed as indicated. Results: Malignant and benign lesions were found in 3.3% and 5% of the screenees, respectively, compared to 1.7% in the general population. The most common lesions were in the gastrointestinal tract followed by skin, urogenital tract and breast. Advanced age and a family history of a malignancy were associated with increased risk for cancer with an odds ratio of 9 and 3.5, respectively (95% confidence interval 1.1-71 and 0.9-13, respectively). Moreover, high serum C-reactive protein levels and polymorphisms in the APC and CD24 genes indicated high cancer risk. When two of the polymorphisms existed in an individual, the risk for a malignant lesion was extremely high (23.1%; OR 14, 95% CI 2.5-78). Conclusions: Screening asymptomatic subjects identifies a significant number of neoplastic lesions at an early stage. Incorporating data on genetic polymorphisms in the APC and CD24 genes can further identify individuals who are at increased risk for cancer. Cancer can be prevented and/or diagnosed at an early stage using the screening facilities of a multidisciplinary outpatient clinic.
KW - Cancer
KW - Early detection
KW - Genetic polymorphisms
KW - Prevention
KW - Screening
UR - http://www.scopus.com/inward/record.url?scp=76049096758&partnerID=8YFLogxK
M3 - מאמר
C2 - 20450124
AN - SCOPUS:76049096758
VL - 12
SP - 21
EP - 25
JO - Israel Medical Association Journal
JF - Israel Medical Association Journal
SN - 1565-1088
IS - 1
ER -