scholarly journals P2.01-15 A Radiologist-Led Training Workshop for MR Based Normal Tissue and Tumour Delineation for Lung Cancer Radiotherapy.

2018 ◽  
Vol 13 (10) ◽  
pp. S670
Author(s):  
S. Brown ◽  
M. Dubec ◽  
H. Bainbridge ◽  
D. Cobben ◽  
F. Lalezari ◽  
...  
2018 ◽  
Vol 19 (1) ◽  
pp. e123-e130
Author(s):  
Yazan Abuodeh ◽  
Arash O. Naghavi ◽  
Michelle Echevarria ◽  
MaryLou DeMarco ◽  
Brian Tonner ◽  
...  

2007 ◽  
Vol 2 (8) ◽  
pp. S471-S472
Author(s):  
Keith R. Britton ◽  
George Starkschall ◽  
Helen Liu ◽  
Joe Y. Chang ◽  
Michael Kantor ◽  
...  

2017 ◽  
Vol 35 (15) ◽  
pp. 1641-1649 ◽  
Author(s):  
Carolyn Taylor ◽  
Candace Correa ◽  
Frances K. Duane ◽  
Marianne C. Aznar ◽  
Stewart J. Anderson ◽  
...  

Purpose Radiotherapy reduces the absolute risk of breast cancer mortality by a few percentage points in suitable women but can cause a second cancer or heart disease decades later. We estimated the absolute long-term risks of modern breast cancer radiotherapy. Methods First, a systematic literature review was performed of lung and heart doses in breast cancer regimens published during 2010 to 2015. Second, individual patient data meta-analyses of 40,781 women randomly assigned to breast cancer radiotherapy versus no radiotherapy in 75 trials yielded rate ratios (RRs) for second primary cancers and cause-specific mortality and excess RRs (ERRs) per Gy for incident lung cancer and cardiac mortality. Smoking status was unavailable. Third, the lung or heart ERRs per Gy in the trials and the 2010 to 2015 doses were combined and applied to current smoker and nonsmoker lung cancer and cardiac mortality rates in population-based data. Results Average doses from 647 regimens published during 2010 to 2015 were 5.7 Gy for whole lung and 4.4 Gy for whole heart. The median year of irradiation was 2010 (interquartile range [IQR], 2008 to 2011). Meta-analyses yielded lung cancer incidence ≥ 10 years after radiotherapy RR of 2.10 (95% CI, 1.48 to 2.98; P < .001) on the basis of 134 cancers, indicating 0.11 (95% CI, 0.05 to 0.20) ERR per Gy whole-lung dose. For cardiac mortality, RR was 1.30 (95% CI, 1.15 to 1.46; P < .001) on the basis of 1,253 cardiac deaths. Detailed analyses indicated 0.04 (95% CI, 0.02 to 0.06) ERR per Gy whole-heart dose. Estimated absolute risks from modern radiotherapy were as follows: lung cancer, approximately 4% for long-term continuing smokers and 0.3% for nonsmokers; and cardiac mortality, approximately 1% for smokers and 0.3% for nonsmokers. Conclusion For long-term smokers, the absolute risks of modern radiotherapy may outweigh the benefits, yet for most nonsmokers (and ex-smokers), the benefits of radiotherapy far outweigh the risks. Hence, smoking can determine the net effect of radiotherapy on mortality, but smoking cessation substantially reduces radiotherapy risk.


2014 ◽  
Vol 30 ◽  
pp. e93-e94 ◽  
Author(s):  
Fatma Rahma ◽  
Wiviann Ottosson ◽  
Claus F. Behrens ◽  
David Sjöström ◽  
Patrik Sibolt

Biomedicines ◽  
2020 ◽  
Vol 8 (9) ◽  
pp. 349 ◽  
Author(s):  
Olga Kovaleva ◽  
Polina Podlesnaya ◽  
Madina Rashidova ◽  
Daria Samoilova ◽  
Anatoly Petrenko ◽  
...  

The link between a lung tumor and the lung microbiome is a largely unexplored issue. To investigate the relationship between a lung microbiome and the phenotype of an inflammatory stromal infiltrate, we studied a cohort of 89 patients with non-small cell lung cancer. The microbiome was analyzed in tumor and adjacent normal tissue by 16S rRNA amplicon sequencing. Characterization of the tumor stroma was done using immunohistochemistry. We demonstrated that the bacterial load was higher in adjacent normal tissue than in a tumor (p = 0.0325) with similar patterns of taxonomic structure and alpha diversity. Lung adenocarcinomas did not differ in their alpha diversity from squamous cell carcinomas, although the content of Gram-positive bacteria increased significantly in the adenocarcinoma group (p = 0.0419). An analysis of an inflammatory infiltrate of tumor stroma showed a correlation of CD68, iNOS and FOXP3 with a histological type of tumor. For the first time we showed that high bacterial load in the tumor combined with increased iNOS expression is a favorable prognostic factor (HR = 0.1824; p = 0.0123), while high bacterial load combined with the increased number of FOXP3+ cells is a marker of poor prognosis (HR = 4.651; p = 0.0116). Thus, we established that bacterial load of the tumor has an opposite prognostic value depending on the status of local antitumor immunity.


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