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Annual Meeting Proceedings Part 1 - American Society of Clinical ...

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1571 General Poster Session (Board #5E), Sat, 1:15 PM-5:15 PM<br />

The effect <strong>of</strong> family history on adherence to breast cancer screening<br />

guidelines. Presenting Author: Lauren Marie Hibler, Yale University, New<br />

Haven, CT<br />

Background: A family history <strong>of</strong> breast cancer increases the risk <strong>of</strong><br />

developing this disease. We sought to determine the effect <strong>of</strong> a family<br />

history <strong>of</strong> a first degree relative with breast cancer (FDFHx) on adherence to<br />

mammography (MMG) and clinical breast examination (CBE) guidelines.<br />

Methods: The National Health Interview Survey (NHIS), conducted annually<br />

by the Centers for Disease Control, is designed to be representative <strong>of</strong> the<br />

US population. The 2010 NHIS data was used to evaluate the effect <strong>of</strong><br />

FDFHx on the likelihood that women aged � 30 had MMG and/or CBE<br />

within the past year. Results: Of the 12,320 women aged � 30, 1276<br />

(10.7%) had a FDFHx; 1263 (99.0%) <strong>of</strong> female breast cancer and 13<br />

(1.0%) <strong>of</strong> male breast cancer. Overall, 4573 (38.4%) <strong>of</strong> women reported<br />

having had MMG within the past year; 5377 (46.3%) had CBE within the<br />

past year. FDFHx was associated with use <strong>of</strong> MMG and CBE within the past<br />

year (58.0% vs. 36.0%, p�0.001, and 57.5% vs. 45.0%, p�0.001,<br />

respectively). Women with a FDFHx <strong>of</strong> male breast cancer were no more<br />

likely to have MMG (72.5% vs. 57.9%, p�0.313) nor CBE (66.8% vs.<br />

57.4%, p�0.518) within the past year than those with a FDFHx <strong>of</strong> female<br />

breast cancer. On multivariate analysis controlling for age, race, personal<br />

history <strong>of</strong> breast cancer (PHx), income, insurance, education and region,<br />

FDFHx was associated with a higher likelihood <strong>of</strong> having MMG (OR�1.75;<br />

95% CI: 1.48-2.06, p�0.001) and CBE (OR�1.48; 95% CI: 1.26-1.74,<br />

p�0.001) within the past year. Region was not associated with adherence<br />

to either MMG or CBE screening guidelines. Conclusions: FDFHx, along with<br />

age, race, PHx, income, insurance, and education, is an independent<br />

predictor <strong>of</strong> adherence to screening MMG and CBE guidelines. Still, only<br />

58% <strong>of</strong> women with a FDFHx had MMG and CBE in the past year. Further<br />

efforts are warranted to improve screening in this population at increased<br />

risk.<br />

Multivariate analysis.<br />

Factor<br />

MMG<br />

p value<br />

CBE<br />

p value<br />

FHx �0.001 �0.001<br />

Age �0.001 �0.001<br />

Race 0.018 �0.001<br />

PHx �0.001 �0.001<br />

Income �0.001 �0.001<br />

Insurance �0.001 �0.001<br />

Education 0.005 �0.001<br />

Region 0.700 0.196<br />

1573 General Poster Session (Board #5G), Sat, 1:15 PM-5:15 PM<br />

Esophageal cancer incidence gender disparity. Presenting Author: Luckson Noe<br />

Mathieu, Sidney Kimmel Comphrehensive Cancer Center at Johns Hopkins<br />

Hospital, Baltimore, MD<br />

Background: Over the past 30 years, esophageal cancer incidence has been<br />

increasing more rapidly than any other solid neoplasm in the Western world.<br />

Globally, there is a large male predominance in both esophageal squamous and<br />

adenocarcinoma. The reasons for this gender difference and the possible role <strong>of</strong><br />

estrogen are unclear. The objective <strong>of</strong> this study is to determine if estrogen<br />

exposure is consistent with the male predominance observed in esophageal<br />

cancer incidence. Methods: A database assessment <strong>of</strong> esophageal cancer<br />

incidence rates (age-adjusted) from 1975 to 2008 was conducted in the<br />

National SEER 9 Database and the Maryland Cancer Registry. Rates by gender<br />

and age were calculated. Gender-specific incidence rate ratios were compared<br />

across age groups. <strong>Annual</strong> percentage change (APC) was compared for each<br />

gender-age group. Results: In both national and state, male and female, adeno<br />

and squamous cell histologies, incidence rates increase with patient age. SEER<br />

data trends revealed the 50-64 aged female cohort as the only gender-age cohort<br />

APC decreasing between 1975-2008. Furthermore, a significant increase in<br />

incidence for females is observed in the 65� age groups; whereas among males,<br />

the rates are rising in all age groups. Conclusions: Using age as a proxy for<br />

estrogen exposure, our findings suggest a hormonal component in the declining<br />

male: female esophageal cancer incidence rate ratios with increasing age and<br />

confirm gender differences in incidence long observed in esophageal cancer.<br />

Histological features may be predictive <strong>of</strong> a lower rate ratio. (Bodelon et al.<br />

2011) Estrogen exposure may play a protective role in esophageal cancer which<br />

dissipates with time after age 60-69. Our data suggest possible future roles <strong>of</strong><br />

estrogen as a chemopreventive agent in esophageal cancer (Barone et al. 2011).<br />

Esophageal cancer annual percentage change, 1975-2008, SEER 9.<br />

Age 50-64 Age 65-74 Age 75�<br />

Males �1.2 �1.4 �1.9<br />

Females -1.5 �0.3 �0.7<br />

The M: F incidence ratio decreases with age in the nation (SEER) and in Maryland.<br />

Male to female incidence ratio, SEER, 1975-2008 and MD Registry 1992-<br />

2008.<br />

Age 40-49 Age 50-59 Age 60-69 Age 70-79 Age 80-89<br />

SEER 9.0 7.6 7.9 5.7 4.3<br />

MD 6.0 6.0 5.4 4.2 3.3<br />

Cancer Prevention/Epidemiology<br />

103s<br />

1572 General Poster Session (Board #5F), Sat, 1:15 PM-5:15 PM<br />

ABO blood group and the risk <strong>of</strong> breast cancer: Multicenter, case-control,<br />

observational study. Presenting Author: Yuksel Urun, Department <strong>of</strong><br />

Medical Oncology, Ankara University School <strong>of</strong> Medicine, Ankara, Turkey<br />

Background: The role <strong>of</strong> genetic factors in the development <strong>of</strong> cancer is<br />

widely accepted. ABO blood type is an inherited characteristic and previous<br />

studies have observed an association between ABO blood group and risk <strong>of</strong><br />

certain malignancies, including pancreatic and gastric cancer. The data on<br />

the role <strong>of</strong> ABO blood group and Rh factor in breast cancer is inconclusive.<br />

Methods: All patients who had breast cancer (BC) and treated between<br />

2000-2010 at the Departments <strong>of</strong> Medical Oncology <strong>of</strong> both Ankara and<br />

Hacettepe Universities (Ankara, Turkey) with defined ABO blood type and<br />

Rh factor were included in our retrospective reviews <strong>of</strong> tumor registry<br />

records. A group <strong>of</strong> volunteer healthy women donors <strong>of</strong> Turkish Red<br />

Crescent between 2004-2011 were identified as a control group, without<br />

any matching factors. The relationship <strong>of</strong> ABO blood types and Rh factor<br />

with various prognostic factors such as age at diagnosis, menopausal<br />

status, family history <strong>of</strong> breast cancer, and ER/PR/HER2 status were<br />

evaluated from 1740 BC patients. We compared the distributions <strong>of</strong> ABO<br />

blood types, Rh factors among 1740 patients and 204,553 healthy<br />

controls. Among BC patients, differences between each <strong>of</strong> aforementioned<br />

ABO blood groups and Rh factors with respect to various prognostic factors<br />

were explored, respectively. Results: Overall distributions <strong>of</strong> ABO blood<br />

groups as well as Rh factor were comparable between patients (44% A, 8%<br />

AB, 16% B, 32% O, 88% Rh�) and controls (41% A, 8% AB, 16% B, 35%<br />

O, 87% Rh�). However, there were statistically significant differences<br />

between patients and controls with respect to A vs. nonA (p�0.019) and<br />

marginal significance (p�0.051) for O vs. nonO. Among patients, there<br />

were statistically significant differences between A and nonA with respect<br />

to HER2 (p�0.0421), M stage (p�0.0447), T stage (p�0.0020). Only T<br />

stage (p�0.0337) were significantly different between O vs nonO. Grade<br />

(p�0.0227) and M stage (p�0.0107) were significantly different between<br />

Rh factors. Conclusions: In our study sample, ABO blood type was<br />

statistically significantly associated with breast cancer. Additional studies<br />

are necessary to determine the mechanisms by which ABO blood type may<br />

influence the risk <strong>of</strong> breast cancer.<br />

1574 General Poster Session (Board #5H), Sat, 1:15 PM-5:15 PM<br />

Study KBP-2010-CPHG: Characteristics and management <strong>of</strong> 7,051 new<br />

cases <strong>of</strong> lung cancer managed in French general hospitals in 2010.<br />

Presenting Author: Chrystele Locher, Saint-Faron Hospital, Meaux, France<br />

Background: An initial epidemiologic study was performed in 2000 by the<br />

French College <strong>of</strong> General Hospital Respiratory Physicians (Study KBP-<br />

2000-CPHG). Over the last 10 years, lung cancer management changed:<br />

new drugs such as targeted therapies appeared; new diagnostic techniques<br />

such as exploration for genetic mutations in the tumour have been<br />

developed; a new TNM classification has been drawn up. The aims <strong>of</strong> this<br />

study were to describe patient characteristics, first-line management, 1, 4<br />

and 5-year survival rates and to compare the results with those <strong>of</strong> Study<br />

KBP-2000-CPHG. Methods: A prospective multi-centre study included all<br />

patients �18 years presenting with a new case <strong>of</strong> primary lung cancer,<br />

histologically or cytologically diagnosed between 1 January and 31 December<br />

2010 and managed by one <strong>of</strong> the participating centers. A standardised<br />

form was completed for each patient. A steering committee checked the<br />

exhaustivity <strong>of</strong> data’s collection. Results: 7,610 patients from 119 general<br />

hospitals were included between 1 January and 31 December 2010. The<br />

main patient characteristics were: mean age 65.5 years (�/-11.3); 24.3%<br />

female; 10.9% non-smokers, 39.9% ex-smokers, 49.2% current smokers;<br />

68.9% performance status 0 and 1; 9.1% <strong>of</strong> patients had lost �10 kg<br />

within the previous 3 months. The main tumour characteristics were:<br />

13.7% small-cell lung cancer; 46.2% adenocarcinoma, 26.8% squamouscell<br />

carcinoma; EGFR mutation, explored in 30.5% <strong>of</strong> cases, were found in<br />

10.5% <strong>of</strong> cases; 16.4% stage IA to IIB, 13.4% stage IIIA, 10.2% stage<br />

IIIB and 60.0% stage IV. First-line treatments were: curative surgery,<br />

16.6%; chemotherapy, 63.4%; radiotherapy alone, 17.8%; combined<br />

radio-chemotherapy, 8.8%; and supportive care, 11.1%. Targeted therapy<br />

was used in 6.6% <strong>of</strong> patients treated by chemotherapy. Conclusions: In 10<br />

years, characteristics <strong>of</strong> lung cancer patients changed with an significantly<br />

increase <strong>of</strong> women, non-smokers, adenocarcinoma histology and stage IV at<br />

diagnosis.<br />

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