EPID-based in vivo dosimetry for stereotactic body radiotherapy of non-small cell lung tumors: Initial clinical experience

2017 ◽  
Vol 42 ◽  
pp. 157-161 ◽  
Author(s):  
R. Consorti ◽  
A. Fidanzio ◽  
V. Brainovich ◽  
F. Mangiacotti ◽  
M. De Spirito ◽  
...  
2001 ◽  
Vol 72 (1) ◽  
pp. 234-242 ◽  
Author(s):  
Joseph B Zwischenberger ◽  
Roger A Vertrees ◽  
Lee C Woodson ◽  
Eric A Bedell ◽  
Scott K Alpard ◽  
...  

2015 ◽  
Vol 115 ◽  
pp. S852
Author(s):  
S. Cilla ◽  
D. Meluccio ◽  
A. Fidanzio ◽  
L. Azario ◽  
F. Greco ◽  
...  

2016 ◽  
Vol 32 ◽  
pp. 14
Author(s):  
S. Cilla ◽  
A. Ianiro ◽  
F. Deodato ◽  
G. Macchia ◽  
C. Digesu ◽  
...  

2016 ◽  
Vol 32 (1) ◽  
pp. 52-58 ◽  
Author(s):  
Savino Cilla ◽  
Daniela Meluccio ◽  
Andrea Fidanzio ◽  
Luigi Azario ◽  
Anna Ianiro ◽  
...  

Cancer ◽  
2016 ◽  
Vol 123 (4) ◽  
pp. 688-696 ◽  
Author(s):  
Vivek Verma ◽  
Valerie K. Shostrom ◽  
Sameera S. Kumar ◽  
Weining Zhen ◽  
Christopher L. Hallemeier ◽  
...  

Cancers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 176
Author(s):  
Yuhei Miyasaka ◽  
Shuichiro Komatsu ◽  
Takanori Abe ◽  
Nobuteru Kubo ◽  
Naoko Okano ◽  
...  

Lung cancer is a leading cause of cancer-related deaths worldwide. Radiotherapy is an essential treatment modality for inoperable non-small cell lung cancer (NSCLC). Stereotactic body radiotherapy (SBRT) is the standard treatment for early-stage NSCLC because of its favorable local control (LC) compared to conventional radiotherapy. Carbon ion radiotherapy (CIRT) is a kind of external beam radiotherapy characterized by a steeper dose distribution and higher biological effectiveness. Several prospective studies have shown favorable outcomes. However, there is no direct comparison study between CIRT and SBRT to determine their benefits in the management of early-stage NSCLC. Thus, we conducted a retrospective, single-institutional, and contemporaneous comparison study, including propensity score-adjusted analyses, to clarify the differences in oncologic outcomes. The 3-year overall survival (OS) was 80.1% in CIRT and 71.6% in SBRT (p = 0.0077). The 3-year LC was 87.7% in the CIRT group and 79.1% in the SBRT group (p = 0.037). Multivariable analyses showed favorable OS and LC in the CIRT group (hazard risk [HR] = 0.41, p = 0.047; HR = 0.30, p = 0.040, respectively). Log-rank tests after propensity score matching and Cox regression analyses using propensity score confirmed these results. These data provided a positive efficacy profile of CIRT for early-stage NSCLC.


2021 ◽  
Vol 12 (7) ◽  
Author(s):  
Jianjiao Ni ◽  
Xiaofei Zhang ◽  
Juan Li ◽  
Zhiqin Zheng ◽  
Junhua Zhang ◽  
...  

AbstractBone is a frequent metastatic site of non-small cell lung cancer (NSCLC), and bone metastasis (BoM) presents significant challenges for patient survival and quality of life. Osteolytic BoM is characterised by aberrant differentiation and malfunction of osteoclasts through modulation of the TGF-β/pTHrP/RANKL signalling pathway, but its upstream regulatory mechanism is unclear. In this study, we found that lncRNA-SOX2OT was highly accumulated in exosomes derived from the peripheral blood of NSCLC patients with BoM and that patients with higher expression of exosomal lncRNA-SOX2OT had significantly shorter overall survival. Additionally, exosomal lncRNA-SOX2OT derived from NSCLC cells promoted cell invasion and migration in vitro, as well as BoM in vivo. Mechanistically, we discovered that NSCLC cell-derived exosomal lncRNA-SOX2OT modulated osteoclast differentiation and stimulated BoM by targeting the miRNA-194-5p/RAC1 signalling axis and TGF-β/pTHrP/RANKL signalling pathway in osteoclasts. In conclusion, exosomal lncRNA-SOX2OT plays a crucial role in promoting BoM and may serve as a promising prognostic biomarker and treatment target in metastatic NSCLC.


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