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- Publisher Website: 10.1111/resp.14508
- Scopus: eid_2-s2.0-85156220261
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Article: Prediction model on disease recurrence for low risk resected stage I lung adenocarcinoma
Title | Prediction model on disease recurrence for low risk resected stage I lung adenocarcinoma |
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Authors | |
Keywords | genetics low risk lung cancer NSCLC stage I non-small cell carcinoma of lung |
Issue Date | 27-Apr-2023 |
Publisher | Wiley |
Citation | Respirology, 2023, v. 28, n. 7, p. 669-676 How to Cite? |
Abstract | Background and ObjectiveAlthough stage I non-small cell lung carcinoma (NSCLC) typically carries a good prognosis following complete resection, early disease recurrence can occur. An accurate survival prediction model would help refine a follow-up strategy and personalize future adjuvant therapy. We developed a post-operative prediction model based on readily available clinical information for patients with stage I adenocarcinoma. MethodsWe retrospectively studied the disease-free survival (DFS) of 408 patients with pathologically confirmed low-risk stage I adenocarcinoma of lung who underwent curative resection from 2013 to 2017. A tree-based method was employed to partition the cohort into subgroups with distinct DFS outcome and stepwise risk ratio. These covariates were included in multivariate analysis to build a scoring system to predict disease recurrence. The model was subsequently validated using a 2011–2012 cohort. ResultsNon-smoker status, stage IA disease, epidermal-growth factor receptor mutants and female gender were associated with better DFS. Multivariate analysis identified smoking status, disease stage and gender as factors necessary for the scoring system and yielded 3 distinct risk groups for DFS [99.4 (95% CI 78.3–125.3), 62.9 (95% CI 48.2–82.0), 33.7 (95% CI 24.6–46.1) months, p < 0.005]. External validation yielded an area under the curve by receiver operating characteristic analysis of 0.863 (95% CI 0.755–0.972). ConclusionThe model could categorize post-operative patients using readily available clinical information, and may help personalize a follow-up strategy and future adjuvant therapy. |
Persistent Identifier | http://hdl.handle.net/10722/329009 |
ISSN | 2023 Impact Factor: 6.6 2023 SCImago Journal Rankings: 1.559 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Kwok, Wang Chun | - |
dc.contributor.author | Ma, Ting Fung | - |
dc.contributor.author | Ho, James Chung Man | - |
dc.contributor.author | Lam, David Chi Leung | - |
dc.contributor.author | Sit, Ko Yung | - |
dc.contributor.author | Ip, Mary Sau Man | - |
dc.contributor.author | Au, Timmy Wing Kuk | - |
dc.contributor.author | Tam, Terence Chi Chun | - |
dc.date.accessioned | 2023-08-05T07:54:35Z | - |
dc.date.available | 2023-08-05T07:54:35Z | - |
dc.date.issued | 2023-04-27 | - |
dc.identifier.citation | Respirology, 2023, v. 28, n. 7, p. 669-676 | - |
dc.identifier.issn | 1323-7799 | - |
dc.identifier.uri | http://hdl.handle.net/10722/329009 | - |
dc.description.abstract | <h3>Background and Objective</h3><p>Although stage I non-small cell lung carcinoma (NSCLC) typically carries a good prognosis following complete resection, early disease recurrence can occur. An accurate survival prediction model would help refine a follow-up strategy and personalize future adjuvant therapy. We developed a post-operative prediction model based on readily available clinical information for patients with stage I adenocarcinoma.</p><h3>Methods</h3><p>We retrospectively studied the disease-free survival (DFS) of 408 patients with pathologically confirmed low-risk stage I adenocarcinoma of lung who underwent curative resection from 2013 to 2017. A tree-based method was employed to partition the cohort into subgroups with distinct DFS outcome and stepwise risk ratio. These covariates were included in multivariate analysis to build a scoring system to predict disease recurrence. The model was subsequently validated using a 2011–2012 cohort.</p><h3>Results</h3><p>Non-smoker status, stage IA disease, epidermal-growth factor receptor mutants and female gender were associated with better DFS. Multivariate analysis identified smoking status, disease stage and gender as factors necessary for the scoring system and yielded 3 distinct risk groups for DFS [99.4 (95% CI 78.3–125.3), 62.9 (95% CI 48.2–82.0), 33.7 (95% CI 24.6–46.1) months, <em>p</em> < 0.005]. External validation yielded an area under the curve by receiver operating characteristic analysis of 0.863 (95% CI 0.755–0.972).</p><h3>Conclusion</h3><p>The model could categorize post-operative patients using readily available clinical information, and may help personalize a follow-up strategy and future adjuvant therapy.</p> | - |
dc.language | eng | - |
dc.publisher | Wiley | - |
dc.relation.ispartof | Respirology | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | genetics | - |
dc.subject | low risk | - |
dc.subject | lung cancer | - |
dc.subject | NSCLC | - |
dc.subject | stage I non-small cell carcinoma of lung | - |
dc.title | Prediction model on disease recurrence for low risk resected stage I lung adenocarcinoma | - |
dc.type | Article | - |
dc.identifier.doi | 10.1111/resp.14508 | - |
dc.identifier.scopus | eid_2-s2.0-85156220261 | - |
dc.identifier.volume | 28 | - |
dc.identifier.issue | 7 | - |
dc.identifier.spage | 669 | - |
dc.identifier.epage | 676 | - |
dc.identifier.eissn | 1440-1843 | - |
dc.identifier.isi | WOS:000975699200001 | - |
dc.identifier.issnl | 1323-7799 | - |