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Primary adenoid cystic carcinoma of the lung: Clinicopathological features, treatment and results

Adenoid cystic carcinoma of the lung (ACCL) is a rare salivary gland-type malignant neoplasm that occurs infrequently as a primary tumor of the airway. Owing to its low incidence, the clinicopathological features, immunohistochemical expression spectrum, treatment and long-term survival have not bee...

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Autores principales: HU, MING-MING, HU, YING, HE, JIA-BEI, LI, BAO-LAN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314995/
https://www.ncbi.nlm.nih.gov/pubmed/25663934
http://dx.doi.org/10.3892/ol.2015.2859
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author HU, MING-MING
HU, YING
HE, JIA-BEI
LI, BAO-LAN
author_facet HU, MING-MING
HU, YING
HE, JIA-BEI
LI, BAO-LAN
author_sort HU, MING-MING
collection PubMed
description Adenoid cystic carcinoma of the lung (ACCL) is a rare salivary gland-type malignant neoplasm that occurs infrequently as a primary tumor of the airway. Owing to its low incidence, the clinicopathological features, immunohistochemical expression spectrum, treatment and long-term survival have not been fully elucidated. The present study retrospectively assessed the clinical features, immunohistochemical characters, treatment strategy and long-term survival of 34 patients diagnosed with ACCL at the Beijing Chest Hospital, Capital Medical University (Beijing, China) between January 1993 and June 2014. ACCL tended to occur in younger patients, with an approximate male/female ratio of 1:1. The majority of ACCL arose from the central airway. Positive immunochemical staining was found in wide-spectrum keratin (n=17), cytokeratin (CK)7 (n=11), p63 (11/12), S-100 (7/8), vimentin (10/12) and smooth muscle actin (6/9). No staining of thyroid transcription factor-1 (0/14), synaptophysin (0/7), cluster of differentiation 56 (0/7), CK20 (0/4) or chromogranin A (0/4) was observed. In the operable group (n=26), the addition of adjuvant radiotherapy to a positive margin resection (R1 resection) obtained long-term survival times equivalent to that found in patients with a negative margin resection (R0 resection). No significant survival benefit from post-operative radiotherapy was observed in the R0 resection group. For advanced cases, palliative radiotherapy and chemotherapy did not work efficiently. In addition, epidermal growth factor receptor mutation was a rare event in the ACCL patients. The results indicated that surgical resection is the optimal management for ACCL whenever feasible. Adjuvant radiotherapy with R1 resection is able to obtain long-term survival times comparable with those found using an R0 resection. The recommendation of post-operative radiotherapy for all patients with ACCL undergoing resection appears controversial. Owing to a poor response to radiotherapy and chemotherapy, more focus should be placed on the study of advanced ACCL in order to improve overall survival.
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spelling pubmed-43149952015-02-06 Primary adenoid cystic carcinoma of the lung: Clinicopathological features, treatment and results HU, MING-MING HU, YING HE, JIA-BEI LI, BAO-LAN Oncol Lett Articles Adenoid cystic carcinoma of the lung (ACCL) is a rare salivary gland-type malignant neoplasm that occurs infrequently as a primary tumor of the airway. Owing to its low incidence, the clinicopathological features, immunohistochemical expression spectrum, treatment and long-term survival have not been fully elucidated. The present study retrospectively assessed the clinical features, immunohistochemical characters, treatment strategy and long-term survival of 34 patients diagnosed with ACCL at the Beijing Chest Hospital, Capital Medical University (Beijing, China) between January 1993 and June 2014. ACCL tended to occur in younger patients, with an approximate male/female ratio of 1:1. The majority of ACCL arose from the central airway. Positive immunochemical staining was found in wide-spectrum keratin (n=17), cytokeratin (CK)7 (n=11), p63 (11/12), S-100 (7/8), vimentin (10/12) and smooth muscle actin (6/9). No staining of thyroid transcription factor-1 (0/14), synaptophysin (0/7), cluster of differentiation 56 (0/7), CK20 (0/4) or chromogranin A (0/4) was observed. In the operable group (n=26), the addition of adjuvant radiotherapy to a positive margin resection (R1 resection) obtained long-term survival times equivalent to that found in patients with a negative margin resection (R0 resection). No significant survival benefit from post-operative radiotherapy was observed in the R0 resection group. For advanced cases, palliative radiotherapy and chemotherapy did not work efficiently. In addition, epidermal growth factor receptor mutation was a rare event in the ACCL patients. The results indicated that surgical resection is the optimal management for ACCL whenever feasible. Adjuvant radiotherapy with R1 resection is able to obtain long-term survival times comparable with those found using an R0 resection. The recommendation of post-operative radiotherapy for all patients with ACCL undergoing resection appears controversial. Owing to a poor response to radiotherapy and chemotherapy, more focus should be placed on the study of advanced ACCL in order to improve overall survival. D.A. Spandidos 2015-03 2015-01-08 /pmc/articles/PMC4314995/ /pubmed/25663934 http://dx.doi.org/10.3892/ol.2015.2859 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
HU, MING-MING
HU, YING
HE, JIA-BEI
LI, BAO-LAN
Primary adenoid cystic carcinoma of the lung: Clinicopathological features, treatment and results
title Primary adenoid cystic carcinoma of the lung: Clinicopathological features, treatment and results
title_full Primary adenoid cystic carcinoma of the lung: Clinicopathological features, treatment and results
title_fullStr Primary adenoid cystic carcinoma of the lung: Clinicopathological features, treatment and results
title_full_unstemmed Primary adenoid cystic carcinoma of the lung: Clinicopathological features, treatment and results
title_short Primary adenoid cystic carcinoma of the lung: Clinicopathological features, treatment and results
title_sort primary adenoid cystic carcinoma of the lung: clinicopathological features, treatment and results
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314995/
https://www.ncbi.nlm.nih.gov/pubmed/25663934
http://dx.doi.org/10.3892/ol.2015.2859
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