scholarly journals PA04.02 The Global State of Lung Cancer Research – Communicating the Messages

2017 ◽  
Vol 12 (1) ◽  
pp. S220-S222
Author(s):  
Sarah Winstone
Lung Cancer ◽  
2021 ◽  
Vol 154 ◽  
pp. 44-50
Author(s):  
Elena Pallari ◽  
Magnus Eriksson ◽  
Annika Billhult ◽  
Tommy Billhult ◽  
Ajay Aggarwal ◽  
...  

2018 ◽  
Vol 119 (6) ◽  
pp. 674-684 ◽  
Author(s):  
Maya Schulpen ◽  
Piet A. van den Brandt

AbstractThe evidence on a cancer-protective effect of the Mediterranean diet (MD) is still limited. Therefore, we investigated the association between MD adherence and lung cancer risk. Data were used from 120 852 participants of the Netherlands Cohort Study (NLCS), aged 55–69 years. Dietary habits were assessed at baseline (1986) using a validated FFQ and alternate and modified Mediterranean diet scores (aMED and mMED, respectively), including and excluding alcohol, were calculated. After 20·3 years of follow-up, 2861 lung cancer cases and 3720 subcohort members (case-cohort design) could be included in multivariable Cox regression analyses. High (6–8) v. low (0–3) aMED excluding alcohol was associated with non-significantly reduced lung cancer risks in men and women with hazard ratios of 0·91 (95 % CI 0·72, 1·15) and 0·73 (95 % CI 0·49, 1·09), respectively. aMED-containing models generally fitted better than mMED-containing models. In never smokers, a borderline significant decreasing trend in lung cancer risk was observed with increasing aMED excluding alcohol. Analyses stratified by the histological lung cancer subtypes did not identify subtypes with a particularly strong inverse relation with MD adherence. Generally, the performance of aMED and World Cancer Research Fund/American Institute for Cancer Research dietary score variants without alcohol was comparable. In conclusion, MD adherence was non-significantly inversely associated with lung cancer risk in the NLCS. Future studies should focus on differences in associations across the sexes and histological subtypes. Furthermore, exclusion of alcohol from MD scores should be investigated more extensively, primarily with respect to a potential role of the MD in cancer prevention.


2017 ◽  
Vol 12 (8) ◽  
pp. S1546
Author(s):  
O.W. Lindwasser ◽  
P. Ujhazy ◽  
M.A. Antman ◽  
S.A. Prindiville

2021 ◽  
Vol 39 (15_suppl) ◽  
pp. TPS8583-TPS8583
Author(s):  
Greg Andrew Durm ◽  
Muhammad Furqan ◽  
Lawrence Eric Feldman ◽  
Malini Patel ◽  
Richard Delmar Hall ◽  
...  

TPS8583 Background: There are approximately 35,000 cases of stage I lung cancer in the United States each year. While these patients have better 5-year overall survival (OS) rates than their counterparts with locally advanced and metastatic disease, there is still considerable room for improvement. Based on a recent publication validating the 8th edition of the TNM classification, the 5-year OS for node-negative pathologically-staged NSCLC between 1-4cm ranges from 73-86%, and recurrence rates for resected stage I NSCLC can range from 18-38%. Previous studies looking at adjuvant chemotherapy in this setting have shown no benefit for stage IA tumors, and the current standard of care is observation alone. Checkpoint blockade with PD-1/PD-L1 inhibitors has shown considerable activity in NSCLC including in metastatic disease, as consolidation in stage III disease after chemoradiation, and in studies evaluating neoadjuvant immunotherapy. Given this activity and their favorable safety profile, we designed a study of adjuvant PD-1 inhibition following resection in stage I NSCLC. Methods: This study is a randomized phase II multicenter trial of adjuvant Pembrolizumab versus observation alone following complete resection of stage I NSCLC with tumors between 1-4cm. The trial will enroll 368 patients randomized 1:1 to either Pembrolizumab 400mg IV every 6 weeks for up to 9 cycles or observation alone with scheduled CT scans and routine clinical follow-up. Stratification factors include PD-L1 ≥50% vs. < 50% and tumor size of 1-2cm vs. > 2-4cm. The lead site is Indiana University, and the trial will be conducted through the Big Ten Cancer Research Consortium. The primary endpoint is disease free survival (DFS), and secondary endpoints include OS, DFS at 1-, 2-, and 3-year time points, and toxicity. The trial opened to accrual at the lead site in May 2020, and there are currently 6 patients enrolled. Clinical trial information: NCT04317534.


2018 ◽  
Vol 13 (10) ◽  
pp. S767-S768
Author(s):  
T. Boyle ◽  
G. Quinn ◽  
M. Schabath ◽  
T. Munoz-Antonia ◽  
L. Duarte ◽  
...  

2016 ◽  
Vol 38 (2) ◽  
pp. 1
Author(s):  
Tom Stinchcombe
Keyword(s):  

Medicine ◽  
2021 ◽  
Vol 100 (13) ◽  
pp. e25055
Author(s):  
Zhiyun Xu ◽  
Xiang Gao ◽  
Binhui Ren ◽  
Shuai Zhang ◽  
Lin Xu

2016 ◽  
Vol 3 (3) ◽  
pp. 172
Author(s):  
V. Paul Doria-Rose ◽  
Lori C Sadoka ◽  
Christine M Neslund-Dudas ◽  
Debra P Ritzwoller ◽  
Heather S Feigelson ◽  
...  

2021 ◽  
Vol Volume 14 ◽  
pp. 1895-1909
Author(s):  
Hao Wang ◽  
Die Meng ◽  
Haoyue Guo ◽  
Chenglong Sun ◽  
Peixin Chen ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document