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   <subfield code="a">Lymphatic Vessel Invasion is a Significant Prognostic Indicator in Stage IA Lung Adenocarcinoma</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Kazuhito Funai, Haruhiko Sugimura, Toyohiko Morita, Yasumasa Shundo, Kei Shimizu, Norihiko Shiiya]</subfield>
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   <subfield code="a">Background: A radical resection is considered to be the most effective treatment for resectable non-small cell lung cancer. However, even when resected in early stages (T1aN0, T1bN0) up to 20% of patients will experience recurrence. The aim of this retrospective study was to evaluate the prognostic influence of lymphatic vessel invasion (LVI) in stage IA adenocarcinoma patients. Methods: From January 1983 to June 2003, a total of 229 consecutive patients with pT1a or T1b N0 M0 lung adenocarcinoma who had undergone radical resection and lymph node dissection were retrospectively reviewed. Sections stained by the hematoxylin-eosin and the Elastica van Gieson method were examined for the presence of LVI. The overall survival was estimated using the Kaplan-Meier method, log-rank test, and the Cox proportional hazards analysis. Results: The median follow-up was 81months. A total of 143 patients (62%) were able to be diagnosed with regard to the presence of LVI, while information was not provided for 86 patients (38%), who were therefore excluded from the study. LVI was noted in 22 of the evaluable patients (15%) and was not seen in the other 121 patients (85%). The 5-year overall survival rate of the LVI-negative group and the LVI-positive group was 94.5 and 70.9%, respectively (P = .003). A multivariate analysis revealed LVI to be an independent predictive factor (hazard ratio: 0.202; P = .001). Conclusion: LVI is an independent poor prognostic factor in patients with pathologic stage IA adenocarcinoma. The T1a and T1b patients with LVI both might benefit from adjuvant chemotherapy.</subfield>
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   <subfield code="a">Society of Surgical Oncology, 2011</subfield>
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   <subfield code="u">First Department of Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan</subfield>
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   <subfield code="a">Morita</subfield>
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   <subfield code="u">First Department of Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan</subfield>
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   <subfield code="a">Shundo</subfield>
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   <subfield code="u">First Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan</subfield>
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   <subfield code="u">First Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan</subfield>
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   <subfield code="u">First Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan</subfield>
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   <subfield code="t">Annals of Surgical Oncology</subfield>
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   <subfield code="g">18/10(2011-10-01), 2968-2972</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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