Literature DB >> 31327681

Association of specific metastatic organs with the prognosis and chemotherapeutic response in patients with advanced lung cancer.

Nobuhiro Kanaji1, Akira Tadokoro2, Naoki Watanabe2, Takuya Inoue2, Norimitsu Kadowaki2, Tomoya Ishii2.   

Abstract

BACKGROUND: This study was performed to investigate the influence of specific metastatic organs on the prognosis and therapeutic effect in patients with advanced lung cancer.
METHODS: We retrospectively analyzed 400 patients with pathologically diagnosed advanced lung cancer to determine the association of the patients' metastatic status with their prognoses and responses to first-line therapy. Metastases within the chest cavity (pulmonary metastasis, pleural effusion, and pericardial effusion) were counted as one organ.
RESULTS: The numbers of metastatic organs in the patients were as follows: one (n=199 patients), two (n=99), three (n=61), and four or more (n=41). A multivariate analysis showed that liver and muscle metastases were independently associated with shorter overall survival (median of 207 and 120 days, respectively) and shorter progression-free survival (median of 125 and 53 days, respectively). Chest cavity, bone, brain, and lymph node metastases were not associated with survival. The presence of either muscle or skin metastasis was associated with a lower response rate to first-line therapy than was the absence of each metastasis (14.3% vs. 49.4% and 11.1% vs. 48.9% in patients with vs. without muscle or skin metastasis, respectively).
CONCLUSIONS: Muscle and liver metastases were associated with poor outcomes. Muscle and skin metastases were associated with a lower response rate to treatment. For patients with advanced lung cancer, oncologists should select treatment strategies considering the patients' metastatic statuses as well as other clinical characteristics.
Copyright © 2019 The Japanese Respiratory Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Lung cancer; Metastasis; Organ; Prognosis; Response rate

Mesh:

Year:  2019        PMID: 31327681     DOI: 10.1016/j.resinv.2019.06.004

Source DB:  PubMed          Journal:  Respir Investig        ISSN: 2212-5345


  3 in total

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  3 in total

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