Chronic lymphocytic leukaemia: clinical-aetiological findings in 66 patients and their families

<p>Abstract</p> <p>Background</p> <p>Little is known about the aetiology of chronic lymphocytic leukaemia (CLL). The family medical history is a "genomic tool" capturing interactions of genetic susceptibility, shared environment and common behaviours.</p>...

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Main Authors: Weber Walter, Maurer Patrick F, Estoppey Jacqueline, Zwahlen Marcel
Format: Article
Language:English
Published: BMC 2007-12-01
Series:Hereditary Cancer in Clinical Practice
Subjects:
Online Access:http://www.hccpjournal.com/content/5/4/210
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author Weber Walter
Maurer Patrick F
Estoppey Jacqueline
Zwahlen Marcel
author_facet Weber Walter
Maurer Patrick F
Estoppey Jacqueline
Zwahlen Marcel
author_sort Weber Walter
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Little is known about the aetiology of chronic lymphocytic leukaemia (CLL). The family medical history is a "genomic tool" capturing interactions of genetic susceptibility, shared environment and common behaviours.</p> <p>Methods</p> <p>A cohort of 66 consecutives patients with CLL (probands) was studied in a medical oncology practice (W.W.) from 1981 until 2005. A German version of the NCI medical history questionnaire for cancer aetiology was used. Familial clustering analysis was done by comparing the proportion of specific tumours in the first degree relatives of the CLL practice cohort with corresponding proportions of population-based cancer registry data.</p> <p>Results</p> <p>18 (41%) male and 5 (23%) female CLL probands had multiple malignancies, e.g. 2 meningiomas, 7 and 19 years after diagnosis of CLL. 46 (12%) first degree relatives had malignancies with an excess of CLL. Other conspicuous familial associations are CLL with malignancies of the upper GI tract (oesophagus, stomach) and of the nervous system.</p> <p>Conclusion</p> <p>1. Chronic lymphocytic leukaemia clusters in some families like any other disease. Predisposition genes should be searched. 2. Cancer prevention and early detection should be continued in CLL patients because of their longevity and high risk for multiple malignancies. 3. The overrepresentation of upper GI malignancies in first degree relatives of CLL patients calls for targeted oesophago-gastroscopy screening studies.</p>
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spelling doaj.art-4abf7d33b9e04b8ba648f5c81f604e7e2022-12-22T00:14:54ZengBMCHereditary Cancer in Clinical Practice1897-42872007-12-015421021210.1186/1897-4287-5-4-210Chronic lymphocytic leukaemia: clinical-aetiological findings in 66 patients and their familiesWeber WalterMaurer Patrick FEstoppey JacquelineZwahlen Marcel<p>Abstract</p> <p>Background</p> <p>Little is known about the aetiology of chronic lymphocytic leukaemia (CLL). The family medical history is a "genomic tool" capturing interactions of genetic susceptibility, shared environment and common behaviours.</p> <p>Methods</p> <p>A cohort of 66 consecutives patients with CLL (probands) was studied in a medical oncology practice (W.W.) from 1981 until 2005. A German version of the NCI medical history questionnaire for cancer aetiology was used. Familial clustering analysis was done by comparing the proportion of specific tumours in the first degree relatives of the CLL practice cohort with corresponding proportions of population-based cancer registry data.</p> <p>Results</p> <p>18 (41%) male and 5 (23%) female CLL probands had multiple malignancies, e.g. 2 meningiomas, 7 and 19 years after diagnosis of CLL. 46 (12%) first degree relatives had malignancies with an excess of CLL. Other conspicuous familial associations are CLL with malignancies of the upper GI tract (oesophagus, stomach) and of the nervous system.</p> <p>Conclusion</p> <p>1. Chronic lymphocytic leukaemia clusters in some families like any other disease. Predisposition genes should be searched. 2. Cancer prevention and early detection should be continued in CLL patients because of their longevity and high risk for multiple malignancies. 3. The overrepresentation of upper GI malignancies in first degree relatives of CLL patients calls for targeted oesophago-gastroscopy screening studies.</p>http://www.hccpjournal.com/content/5/4/210CLLchronic lymphocytic leukaemiafamilial leukaemiafamilial cancer
spellingShingle Weber Walter
Maurer Patrick F
Estoppey Jacqueline
Zwahlen Marcel
Chronic lymphocytic leukaemia: clinical-aetiological findings in 66 patients and their families
Hereditary Cancer in Clinical Practice
CLL
chronic lymphocytic leukaemia
familial leukaemia
familial cancer
title Chronic lymphocytic leukaemia: clinical-aetiological findings in 66 patients and their families
title_full Chronic lymphocytic leukaemia: clinical-aetiological findings in 66 patients and their families
title_fullStr Chronic lymphocytic leukaemia: clinical-aetiological findings in 66 patients and their families
title_full_unstemmed Chronic lymphocytic leukaemia: clinical-aetiological findings in 66 patients and their families
title_short Chronic lymphocytic leukaemia: clinical-aetiological findings in 66 patients and their families
title_sort chronic lymphocytic leukaemia clinical aetiological findings in 66 patients and their families
topic CLL
chronic lymphocytic leukaemia
familial leukaemia
familial cancer
url http://www.hccpjournal.com/content/5/4/210
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AT maurerpatrickf chroniclymphocyticleukaemiaclinicalaetiologicalfindingsin66patientsandtheirfamilies
AT estoppeyjacqueline chroniclymphocyticleukaemiaclinicalaetiologicalfindingsin66patientsandtheirfamilies
AT zwahlenmarcel chroniclymphocyticleukaemiaclinicalaetiologicalfindingsin66patientsandtheirfamilies