The neoplastic impact of tobacco-free betel-quid on the histological type and the anatomical site of aerodigestive tract cancers

Little is known about any consequences of swallowing tobacco‐free betel‐quid (TF‐BQ) juice/remnants following chewing and its carcinogenic impact on the upper aerodigestive tract (UADT) to gastrointestinal tract (GIT). We investigated the neoplastic impact of TF‐BQ on different anatomical locations...

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Published inInternational journal of cancer Vol. 131; no. 5; pp. E733 - E743
Main Authors Lee, Chien-Hung, Lee, Ka-Wo, Fang, Fu-Min, Wu, Deng-Chyang, Tsai, Shih-Meng, Chen, Ping-Ho, Shieh, Tien-Yu, Chen, Chung-Ho, Wu, I-Chen, Huang, Hsiao-Ling, Chen, Bai-Hsiun, Chang, Cheng-Hsien, Chen, Mu-Kuan, Chou, Shah-Hwa, Tsai, Yi-Shan, Chiang, Shang-Lun, Ko, Ying-Chin
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.09.2012
Wiley Subscription Services, Inc
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Summary:Little is known about any consequences of swallowing tobacco‐free betel‐quid (TF‐BQ) juice/remnants following chewing and its carcinogenic impact on the upper aerodigestive tract (UADT) to gastrointestinal tract (GIT). We investigated the neoplastic impact of TF‐BQ on different anatomical locations along UADT and GIT, and differences according to their histological categories. We conducted a multicenter case–control study examining patients with 2,163 pathology‐proven UADT and GIT cancers, comparing them with 2,250 control subjects. Generalized additive models, piecewise regression and polytomous logistic models were applied to identify possible dose‐dependent structures and cancer risks. Contrary to nonsignificant GIT‐adenocarcinoma risk (aOR = 0.9), TF‐BQ users experienced a 1.7‐ to 16.2‐fold higher risk of UADT‐squamous cell carcinomas than nonusers, with the peak risk discovered in oral neoplasms. We separately observed a curvilinear and linear TF‐BQ dose‐risk relationship in oral/pharyngeal/esophageal and laryngeal cancers. Chewers of betel inflorescence were generally at a greater UADT cancer risk. A higher first‐piecewise increased risk of esophageal cancer was recognized among areca‐fluid swallowers than among nonswallowers (continuous aOR = 1.12 vs. 1.03). TF‐BQ use accounted for 66.1–78.7% and 17.8–33.2% of the cases of oral/pharyngeal and esophageal/laryngeal cancers, respectively. However, a reduction from heavy TF‐BQ consumption to low‐to‐moderate consumption only reduced 11.3–34.6% of etiologic fraction of oral/pharyngeal cancers. Alcohol supra‐additively modified the risk of TF‐BQ in determining the development of oral, pharyngeal and esophageal cancers. In conclusion, the interplay of TF‐BQ and alcohol/tobacco use, combined with how chewing habit is practiced, influences carcinogenic consequences on anatomically diverse sites of UADT and GIT cancers, and histologically different types.
Bibliography:Cancer Medical Treatment Foundation
Excellence for Cancer Research Center Grant - No. DOH100-TD-C-111-002
ArticleID:IJC27401
Taiwan National Health Research Institutes - No. NHRI-CN-IN-9006P; No. NHRI-97-A1-PDCO-03-0710-1
Research Center of Excellence for Environmental Medicine
Kaohsiung Medical University - No. KMU-OC097001
ark:/67375/WNG-QXDBCTD6-H
Kaohsiung Medical University - No. KMU-EM-97-1.2b; No. KMU-EM-98-1.2b; No. KMU-EM-99-1-6
istex:8F5255321E67B45192EA8438D8137666B471E8F4
Taiwan National Science Council - No. NSC 99-2314-B-037-057-MY3
Tel.: +886‐7‐311‐4418, Fax: +886‐7‐316‐2725
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ISSN:0020-7136
1097-0215
1097-0215
DOI:10.1002/ijc.27401