A model and nomogram to predict tumor site origin for squamous cell cancer confined to cervical lymph nodes. Issue 22 (24th July 2014)
- Record Type:
- Journal Article
- Title:
- A model and nomogram to predict tumor site origin for squamous cell cancer confined to cervical lymph nodes. Issue 22 (24th July 2014)
- Main Title:
- A model and nomogram to predict tumor site origin for squamous cell cancer confined to cervical lymph nodes
- Authors:
- Ali, Arif N.
Switchenko, Jeffrey M.
Kim, Sungjin
Kowalski, Jeanne
El‐Deiry, Mark W.
Beitler, Jonathan J. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="cncr28901-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>The current study was conducted to develop a multifactorial statistical model to predict the specific head and neck (H&amp;N) tumor site origin in cases of squamous cell carcinoma confined to the cervical lymph nodes ("unknown primaries").</p> </sec> <sec id="cncr28901-sec-0002" sec-type="section"> <title>METHODS</title> <p>The Surveillance, Epidemiology, and End Results (SEER) database was analyzed for patients with an H&amp;N tumor site who were diagnosed between 2004 and 2011. The SEER patients were identified according to their H&amp;N primary tumor site and clinically positive cervical lymph node levels at the time of presentation. The SEER patient data set was randomly divided into 2 data sets for the purposes of internal split‐sample validation. The effects of cervical lymph node levels, age, race, and sex on H&amp;N primary tumor site were examined using univariate and multivariate analyses. Multivariate logistic regression models and an associated set of nomograms were developed based on relevant factors to provide probabilities of tumor site origin.</p> </sec> <sec id="cncr28901-sec-0003" sec-type="section"> <title>RESULTS</title> <p>Analysis of the SEER database identified 20, 011 patients with H&amp;N disease with both site‐level and lymph node‐level data. Sex, race, age, and lymph node levels were<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="cncr28901-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>The current study was conducted to develop a multifactorial statistical model to predict the specific head and neck (H&amp;N) tumor site origin in cases of squamous cell carcinoma confined to the cervical lymph nodes ("unknown primaries").</p> </sec> <sec id="cncr28901-sec-0002" sec-type="section"> <title>METHODS</title> <p>The Surveillance, Epidemiology, and End Results (SEER) database was analyzed for patients with an H&amp;N tumor site who were diagnosed between 2004 and 2011. The SEER patients were identified according to their H&amp;N primary tumor site and clinically positive cervical lymph node levels at the time of presentation. The SEER patient data set was randomly divided into 2 data sets for the purposes of internal split‐sample validation. The effects of cervical lymph node levels, age, race, and sex on H&amp;N primary tumor site were examined using univariate and multivariate analyses. Multivariate logistic regression models and an associated set of nomograms were developed based on relevant factors to provide probabilities of tumor site origin.</p> </sec> <sec id="cncr28901-sec-0003" sec-type="section"> <title>RESULTS</title> <p>Analysis of the SEER database identified 20, 011 patients with H&amp;N disease with both site‐level and lymph node‐level data. Sex, race, age, and lymph node levels were associated with primary H&amp;N tumor site (nasopharynx, hypopharynx, oropharynx, and larynx) in the multivariate models. Internal validation techniques affirmed the accuracy of these models on separate data.</p> </sec> <sec id="cncr28901-sec-0004" sec-type="section"> <title>CONCLUSIONS</title> <p>The incorporation of epidemiologic and lymph node data into a predictive model has the potential to provide valuable guidance to clinicians in the treatment of patients with squamous cell carcinoma confined to the cervical lymph nodes. <bold><italic>Cancer</italic> 2014;120:3469–3476</bold>. © 2014 The Authors. <italic>Cancer</italic> published by Wiley Periodicals, Inc. on behalf of <italic>American Cancer Society</italic>. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.</p> </sec> </abstract> … (more)
- Is Part Of:
- Cancer. Volume 120:Issue 22(2014)
- Journal:
- Cancer
- Issue:
- Volume 120:Issue 22(2014)
- Issue Display:
- Volume 120, Issue 22 (2014)
- Year:
- 2014
- Volume:
- 120
- Issue:
- 22
- Issue Sort Value:
- 2014-0120-0022-0000
- Page Start:
- 3469
- Page End:
- 3476
- Publication Date:
- 2014-07-24
- Subjects:
- Cancer -- Periodicals
Cancer -- Cytopathology -- Periodicals
616.99405 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0142 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cncr.28901 ↗
- Languages:
- English
- ISSNs:
- 0008-543X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.450000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3310.xml