Significance of spread through air spaces in small cell lung cancer

Purpose Tumor spread through air space (STAS) is a novel pattern of invasion related to poor prognosis in non-small cell cancer (NSCLC). Nevertheless, little is known about the role of STAS in small cell lung cancer (SCLC). We sought to determine whether STAS has a significant effect on recurrence a...

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Veröffentlicht in:Journal of cancer research and clinical oncology 2023-07, Vol.149 (8), p.5301-5308
Hauptverfasser: Han, Lu, Huang, Zhida, Zhang, Jing, Chen, Yan, Wang, Jue, Xiong, Yicheng, Yao, Wangchao, Hou, Likun, Zhang, Liping, Yu, Huansha, Song, Nan, Zhang, Zhonghong, Zhu, Yuming
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container_end_page 5308
container_issue 8
container_start_page 5301
container_title Journal of cancer research and clinical oncology
container_volume 149
creator Han, Lu
Huang, Zhida
Zhang, Jing
Chen, Yan
Wang, Jue
Xiong, Yicheng
Yao, Wangchao
Hou, Likun
Zhang, Liping
Yu, Huansha
Song, Nan
Zhang, Zhonghong
Zhu, Yuming
description Purpose Tumor spread through air space (STAS) is a novel pattern of invasion related to poor prognosis in non-small cell cancer (NSCLC). Nevertheless, little is known about the role of STAS in small cell lung cancer (SCLC). We sought to determine whether STAS has a significant effect on recurrence among SCLC patients. Methods We collected clinical and follow-up information from 181 resected stage I–III SCLC patients and compared overall survival (OS) and disease-free survival (DFS) between the patients with or without STAS using the Kaplan‒Meier method. To explore the effect of STAS on recurrence, a competing-risk analysis was conducted. Results Among 181 SCLC patients, STAS was observed in 56 (30.94%) patients, and 125 (69.06%) patients did not have STAS. Furthermore, 33 (18.23%) patients had recurrence, including 12 patients with brain metastases. Patients with STAS had worse DFS. The cumulative incidence of any recurrence was higher in patients with STAS than in those without STAS. Univariate and multivariate competing-risk regression analyses revealed that sublobar resection and STAS were independent risk factors for SCLC recurrence ( p  = 0.009 and p  = 0.029 for multivariate analysis, respectively). Conclusion SCLC patients with STAS have worse DFS than SCLC patients without STAS. STAS is an independent prognostic factor in SCLC patients.
doi_str_mv 10.1007/s00432-022-04462-8
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Nevertheless, little is known about the role of STAS in small cell lung cancer (SCLC). We sought to determine whether STAS has a significant effect on recurrence among SCLC patients. Methods We collected clinical and follow-up information from 181 resected stage I–III SCLC patients and compared overall survival (OS) and disease-free survival (DFS) between the patients with or without STAS using the Kaplan‒Meier method. To explore the effect of STAS on recurrence, a competing-risk analysis was conducted. Results Among 181 SCLC patients, STAS was observed in 56 (30.94%) patients, and 125 (69.06%) patients did not have STAS. Furthermore, 33 (18.23%) patients had recurrence, including 12 patients with brain metastases. Patients with STAS had worse DFS. The cumulative incidence of any recurrence was higher in patients with STAS than in those without STAS. Univariate and multivariate competing-risk regression analyses revealed that sublobar resection and STAS were independent risk factors for SCLC recurrence ( p  = 0.009 and p  = 0.029 for multivariate analysis, respectively). Conclusion SCLC patients with STAS have worse DFS than SCLC patients without STAS. STAS is an independent prognostic factor in SCLC patients.</description><identifier>ISSN: 0171-5216</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/s00432-022-04462-8</identifier><identifier>PMID: 36416957</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Cancer Research ; Hematology ; Internal Medicine ; Lung cancer ; Medical prognosis ; Medicine ; Medicine &amp; Public Health ; Metastases ; Multivariate analysis ; Non-small cell lung carcinoma ; Oncology ; Risk factors ; Small cell lung carcinoma</subject><ispartof>Journal of cancer research and clinical oncology, 2023-07, Vol.149 (8), p.5301-5308</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-a7a61a59df7be33fd8bd5c0d8553df89cd835087cbf59063b85bac4db43a3aed3</citedby><cites>FETCH-LOGICAL-c375t-a7a61a59df7be33fd8bd5c0d8553df89cd835087cbf59063b85bac4db43a3aed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00432-022-04462-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00432-022-04462-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,781,785,27929,27930,41493,42562,51324</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36416957$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Han, Lu</creatorcontrib><creatorcontrib>Huang, Zhida</creatorcontrib><creatorcontrib>Zhang, Jing</creatorcontrib><creatorcontrib>Chen, Yan</creatorcontrib><creatorcontrib>Wang, Jue</creatorcontrib><creatorcontrib>Xiong, Yicheng</creatorcontrib><creatorcontrib>Yao, Wangchao</creatorcontrib><creatorcontrib>Hou, Likun</creatorcontrib><creatorcontrib>Zhang, Liping</creatorcontrib><creatorcontrib>Yu, Huansha</creatorcontrib><creatorcontrib>Song, Nan</creatorcontrib><creatorcontrib>Zhang, Zhonghong</creatorcontrib><creatorcontrib>Zhu, Yuming</creatorcontrib><title>Significance of spread through air spaces in small cell lung cancer</title><title>Journal of cancer research and clinical oncology</title><addtitle>J Cancer Res Clin Oncol</addtitle><addtitle>J Cancer Res Clin Oncol</addtitle><description>Purpose Tumor spread through air space (STAS) is a novel pattern of invasion related to poor prognosis in non-small cell cancer (NSCLC). Nevertheless, little is known about the role of STAS in small cell lung cancer (SCLC). We sought to determine whether STAS has a significant effect on recurrence among SCLC patients. Methods We collected clinical and follow-up information from 181 resected stage I–III SCLC patients and compared overall survival (OS) and disease-free survival (DFS) between the patients with or without STAS using the Kaplan‒Meier method. To explore the effect of STAS on recurrence, a competing-risk analysis was conducted. Results Among 181 SCLC patients, STAS was observed in 56 (30.94%) patients, and 125 (69.06%) patients did not have STAS. Furthermore, 33 (18.23%) patients had recurrence, including 12 patients with brain metastases. Patients with STAS had worse DFS. The cumulative incidence of any recurrence was higher in patients with STAS than in those without STAS. Univariate and multivariate competing-risk regression analyses revealed that sublobar resection and STAS were independent risk factors for SCLC recurrence ( p  = 0.009 and p  = 0.029 for multivariate analysis, respectively). Conclusion SCLC patients with STAS have worse DFS than SCLC patients without STAS. 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Nevertheless, little is known about the role of STAS in small cell lung cancer (SCLC). We sought to determine whether STAS has a significant effect on recurrence among SCLC patients. Methods We collected clinical and follow-up information from 181 resected stage I–III SCLC patients and compared overall survival (OS) and disease-free survival (DFS) between the patients with or without STAS using the Kaplan‒Meier method. To explore the effect of STAS on recurrence, a competing-risk analysis was conducted. Results Among 181 SCLC patients, STAS was observed in 56 (30.94%) patients, and 125 (69.06%) patients did not have STAS. Furthermore, 33 (18.23%) patients had recurrence, including 12 patients with brain metastases. Patients with STAS had worse DFS. The cumulative incidence of any recurrence was higher in patients with STAS than in those without STAS. Univariate and multivariate competing-risk regression analyses revealed that sublobar resection and STAS were independent risk factors for SCLC recurrence ( p  = 0.009 and p  = 0.029 for multivariate analysis, respectively). Conclusion SCLC patients with STAS have worse DFS than SCLC patients without STAS. STAS is an independent prognostic factor in SCLC patients.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>36416957</pmid><doi>10.1007/s00432-022-04462-8</doi><tpages>8</tpages></addata></record>
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subjects Cancer Research
Hematology
Internal Medicine
Lung cancer
Medical prognosis
Medicine
Medicine & Public Health
Metastases
Multivariate analysis
Non-small cell lung carcinoma
Oncology
Risk factors
Small cell lung carcinoma
title Significance of spread through air spaces in small cell lung cancer
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