Literature DB >> 24782093

Azithromycin enhances the favorable results of paclitaxel and cisplatin in patients with advanced non-small cell lung cancer.

D J Chu1, D E Yao2, Y F Zhuang2, Y Hong2, X C Zhu2, Z R Fang2, J Yu2, Z Y Yu2.   

Abstract

Although new chemotherapeutic drugs have been applied constantly, their efficacy for non-small cell lung cancer (NSCLC) is still not satisfactory. In recent years, epidemiological investigations have shown that lung cancer may be induced by chronic Chlamydia pneumoniae (Cpn) infection, since stable high titers of Cpn antibodies, especially IgA, are a hallmark of chronic infections. Azithromycin is commonly used for the treatment of Cpn infections; however, there are only few reports regarding the application of azithromycin (A) combined with paclitaxel and cisplatin (TP) for advanced NSCLC. Considering that patients with NSCLC have a higher rate of Cpn infection, we proposed to employ azithromycin for Cpn infection in chemotherapy for advanced NSCLC. The aim of this study was to explore the effects of azithromycin on chemotherapy for NSCLC. A total of 86 patients with stage III-IV NSCLC were randomly divided into TP and ATP groups; the characteristics of patients in the two groups showed no significant differences. The TP group was treated with paclitaxel and cisplatin, and the ATP group was treated with azithromycin combined with TP for at least 4 weeks, followed by evaluation and comparison of efficacy, side effects and patients' quality of life before and after chemotherapy between the two groups. Testing for Cpn infection revealed a significant difference in the case number before and after therapy in the ATP group (P < 0.01) compared with the TP group (P > 0.05), and a statistical difference was observed (P < 0.01) between the ATP and TP groups after treatment. The changes in quality of life of patients after two different chemotherapy regimens were statistically significant (P < 0.05), but there was a significant difference in only cognitive function after treatment. The changes in symptom scores of patients after the two different chemotherapy regimens were statistically significant (P < 0.05), but there was a significant difference in only shortness of breath and cough after treatment. Kaplan-Meier estimate was utilized to describe the survival function of patients in the two groups. The median survival time was 12.0 months for the TP group and 13.0 months for the ATP group. One-year survival rates of the TP and ATP groups were 45.0 and 75.0%, respectively, which were significantly different (P < 0.05). Our study of azithromycin+paclitaxe l+cisplatin on stage III-IV NSCLC patients achieved favorable results in terms of side effects and overall survival.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24782093     DOI: 10.4238/2014.April.14.8

Source DB:  PubMed          Journal:  Genet Mol Res        ISSN: 1676-5680


  13 in total

Review 1.  Plasticity of Cancer Stem Cell: Origin and Role in Disease Progression and Therapy Resistance.

Authors:  Plabon Kumar Das; Suja Pillai; Md Abdur Rakib; Jahan Ara Khanam; Vinod Gopalan; Alfred K Y Lam; Farhadul Islam
Journal:  Stem Cell Rev Rep       Date:  2020-04       Impact factor: 5.739

2.  Antibiotics that target mitochondria effectively eradicate cancer stem cells, across multiple tumor types: treating cancer like an infectious disease.

Authors:  Rebecca Lamb; Bela Ozsvari; Camilla L Lisanti; Herbert B Tanowitz; Anthony Howell; Ubaldo E Martinez-Outschoorn; Federica Sotgia; Michael P Lisanti
Journal:  Oncotarget       Date:  2015-03-10

3.  High mitochondrial mass identifies a sub-population of stem-like cancer cells that are chemo-resistant.

Authors:  Gillian Farnie; Federica Sotgia; Michael P Lisanti
Journal:  Oncotarget       Date:  2015-10-13

4.  Azithromycin effectively inhibits tumor angiogenesis by suppressing vascular endothelial growth factor receptor 2-mediated signaling pathways in lung cancer.

Authors:  Fajiu Li; Jie Huang; Dongyuan Ji; Qinghua Meng; Chuanhai Wang; Shi Chen; Xiaojiang Wang; Zhiyang Zhu; Cheng Jiang; Yi Shi; Shuang Liu; Chenghong Li
Journal:  Oncol Lett       Date:  2017-04-28       Impact factor: 2.967

Review 5.  Cancer Stem Cell Metabolism and Potential Therapeutic Targets.

Authors:  Vusala Snyder; Tamika C Reed-Newman; Levi Arnold; Sufi Mary Thomas; Shrikant Anant
Journal:  Front Oncol       Date:  2018-06-05       Impact factor: 6.244

Review 6.  Repurposing Established Compounds to Target Pancreatic Cancer Stem Cells (CSCs).

Authors:  Bernhard W Renz; Jan G D'Haese; Jens Werner; C Benedikt Westphalen; Matthias Ilmer
Journal:  Med Sci (Basel)       Date:  2017-06-19

Review 7.  OPALS: A New Osimertinib Adjunctive Treatment of Lung Adenocarcinoma or Glioblastoma Using Five Repurposed Drugs.

Authors:  Richard E Kast; Marc-Eric Halatsch; Rafael Rosell
Journal:  Cells       Date:  2021-05-10       Impact factor: 6.600

8.  Dihydromyricetin Enhances the Chemo-Sensitivity of Nedaplatin via Regulation of the p53/Bcl-2 Pathway in Hepatocellular Carcinoma Cells.

Authors:  Lianggui Jiang; Qingyu Zhang; Hao Ren; Sheng Ma; CaiJie Lu; Bin Liu; Jie Liu; Jian Liang; Mingyi Li; Runzhi Zhu
Journal:  PLoS One       Date:  2015-04-27       Impact factor: 3.240

Review 9.  Cancer stem cell metabolism.

Authors:  Maria Peiris-Pagès; Ubaldo E Martinez-Outschoorn; Richard G Pestell; Federica Sotgia; Michael P Lisanti
Journal:  Breast Cancer Res       Date:  2016-05-24       Impact factor: 6.466

Review 10.  Role of Mitochondria in Cancer Stem Cell Resistance.

Authors:  José Manuel García-Heredia; Amancio Carnero
Journal:  Cells       Date:  2020-07-15       Impact factor: 6.600

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.