scholarly journals Publication Rate and Characteristics of Lung Cancer Clinical Trials

2019 ◽  
Vol 2 (11) ◽  
pp. e1914531
Author(s):  
Ghassan Al-Shbool ◽  
Hira Latif ◽  
Saira Farid ◽  
Shuqi Wang ◽  
Jaeil Ahn ◽  
...  
2019 ◽  
Vol 37 (15_suppl) ◽  
pp. e18211-e18211
Author(s):  
Ghassan Al-shbool ◽  
Hira Latif ◽  
Saira Farid ◽  
Anqi Yin ◽  
Jaeil Ahn ◽  
...  

e18211 Background: Clinical trials play a crucial role in shaping oncology practice. Publishing results of clinical trials is key to reducing publication bias. Lung cancer is the leading cause of cancer-related mortality in the U.S. We assessed the publication rate of registered lung cancer clinical trials. Methods: ClinicalTrials.gov was searched to identify registered lung cancer clinical trials with study completion date between 1/1/2000 and 8/7/2016. Interventional phase II and III clinical trials involving patients ³ 18 years old with a recruitment status of completed or terminated were included. Using National Clinical Trial identifier and keywords including the clinical trial name, three databases (PubMed, Google Scholar, EMBASE) were queried to assess the publication status of each trial. We analyzed the publication rate among the identified clinical trials and predictors of publication. Results: A total of 1293 clinical trials were identified. Among 1037 completed clinical trials, 690 (66.5%; 193,587 patients) were published in peer-reviewed journal, while 347 (33.5%; 51,505 patients) were unpublished. Industry sponsored, non-randomized, and single-center studies were less likely to be published with odds ratio 0.52 (95% CI: 0.28-0.97), 0.67 (0.45-1.00), and 0.36 (0.25-0.51), respectively. Among the 347 unpublished completed trials, 75 (21.6%) trials reported the results as meeting presentation and 63 (18.2%) trials posted the results only on ClinicalTrials.gov. Among 256 terminated clinical trials, 72 (28.1%; 19,858 patients) were published in peer-reviewed journal, while 184 (71.9%; 10,259 patients) were unpublished. Among the 184 unpublished terminated trials, 19 (10.3%) trials reported the results as meeting presentation and 70 (38.0%) trials posted the study results only on ClinicalTrials.gov; reporting of primary outcome was incomplete in 50 (71.4%) of 70 studies whose results were only available on ClinicalTrials.gov. Conclusions: A significant proportion of registered lung cancer clinical trials remain unpublished, raising the concern of publication bias in the field of thoracic oncology.


2018 ◽  
Vol 48 (11) ◽  
pp. 995-1000 ◽  
Author(s):  
Nobuaki Ochi ◽  
Tatsuyuki Kawahara ◽  
Yasunari Nagasaki ◽  
Nozomu Nakagawa ◽  
Tomoko Yamagishi ◽  
...  

2012 ◽  
Vol 30 (15_suppl) ◽  
pp. e19583-e19583
Author(s):  
Terufumi Kato ◽  
Ou Yamaguchi ◽  
Masahiro Yoshida ◽  
Hiroki Fukushima ◽  
Ryo Ogata ◽  
...  

e19583 Background: PF is commonly concomitant disorder with lung cancer. Because PF sometimes deteriorates and results unfavorable clinical course, patients with PF are excluded from most cancer clinical trials. S-1 is a novel active oral fluoropyrimidine anticancer agent consisting of tegafur, gimeracil and oteracil potassium. Although most anti-cancer agent have pulmonary toxicity, post marketing surveillance reported S-1 has lower pulmonary toxicity incidence. We have conducted feasibility study of S-1 and carboplatin combination for patients with advanced or ineligible for other treatment modality of NSCLC patients. Methods: Patients with histologically or cytologically confirmed NSCLC, clinically diagnosed pulmonary fibrosis, aged 80 years old or younger, performance status 0-2 and chemo naive were eligible for the study. Carboplatin (AUC 5) was administered on day 1 and S-1 (80mg/m2/day) on day 1 to 14 for four to six cycles. Endpoints were response rate, common safety profiles and effect to PF. Results: From March 2009 to December 2011, 21 pts (19 males/ 2 females, median age 67 years old, ranged 55 to 77, 10 adenocarcinoma, 10 squamous, 1 adenosquamous, stage IIA: 1, IIIA: 3, IIIB: 9, IV: 4, recurrence: 4) were enrolled. All patients had moderate or severe PF. Treatment delivery; 1 cycle: 3pts, 2: 3pts, 3: 3pts, 4: 10pts, 5; 1pts, 6: 1pts. Partial responses were observed in 7 patients (RR; 33%). The median progression free survival duration was 4.0 months and the median overall survival duration in 10.4 months. During the treatment, 2 patient experienced moderate deterioration of pulmonary fibrosis, 1 experienced infectious pneumonia, all three patients recovered from the event. There was no treatment related death. Besides pulmonary toxicity, most common adverse events were myelotoxicities. Conclusions: This is the first trial of S-1 and carboplatin combination for patients with PF and NSCLC. The study revealed S-1 and carboplatin combination was feasible and active even in patients with PF and NSCLC who are usually excluded from cancer clinical trials.


2019 ◽  
Vol 14 (10) ◽  
pp. S224
Author(s):  
S. Rashdan ◽  
S. Dahlberg ◽  
D. Gerber ◽  
A. Sandler ◽  
J. Schiller ◽  
...  

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