Publication Outcomes of Phase II Oncology Clinical Trials

2009 ◽  
Vol 32 (3) ◽  
pp. 253-257 ◽  
Author(s):  
Rasmus T. Hoeg ◽  
Jennifer A. Lee ◽  
Michelle A. Mathiason ◽  
Kristina Rokkones ◽  
Stephanie L. Serck ◽  
...  
2006 ◽  
Vol 24 (18_suppl) ◽  
pp. 6010-6010 ◽  
Author(s):  
R. T. Hoeg ◽  
J. A. Lee ◽  
M. A. Mathiason ◽  
K. Rokkones ◽  
S. L. Serck ◽  
...  

6010 Background: Translation of evidence-based medicine into clinical practice depends on timely and full publication of clinical trials. Previous studies have shown that a substantial number of phase I and III trials presented at the annual meetings of ASCO remain unpublished more than 5 years after presentation. We investigated the outcome of phase II trials presented at ASCO. Methods: We searched for phase II trials using the 1997 ASCO Annual Meeting Proceedings. We excluded trials reporting only preliminary data or interim analyses. The following information were extracted from each study: type of presentation, country of origin, sample size, sponsor, treatment modality, novelty of treatment, and efficacy. A literature search was performed using the Medline and EMBASE databases up until January 2006 for full publications in peer-reviewed journals. If a trial was not found, the authors were contacted by E-mail. Results: We identified 124 phase II trials with 13.7%, 30.6%, and 55.6% presented orally, in poster, and in print, respectively. Most trials were either submitted from countries in North America (50.8%) or Europe (34.7%). Funding came from the pharmaceutical companies (24.2%), governments (20.2%), study institutions (15.3%), private foundations (9.7%), or was not specified (30.6%). The top 5 cancers studied were lung, breast, ovarian, gastric, and sarcoma. Treatment included mostly chemotherapy, either alone (87.1%) or in combination with other modalities (3.2%). To date only 70.2% of the trials have been published. The median time to publication for all abstracts was 23 months. The cumulative rates of publication were 12.9%, 34.7%, 51.6%, 64.5%, and 68.5% at 1, 2, 3, 5, and 7 years, respectively. None of the factors we analyzed, including type of presentation, country of origin, sample size, sponsor, novelty of treatment, and efficacy, influenced the likelihood of or time to publication. Conclusions: About a third of phase II oncology clinical trials initially presented as abstracts at the 1997 ASCO annual meeting have not been published almost a decade later. Similar to phase I and III trials, underreporting of phase II trials is an important problem with serious implications for clinical practice that needs to be addressed. No significant financial relationships to disclose.


2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Fei Qin ◽  
Jingwei Wu ◽  
Feng Chen ◽  
Yongyue Wei ◽  
Yang Zhao ◽  
...  

2019 ◽  
Vol 24 (8) ◽  
Author(s):  
Laura Franshaw ◽  
Maria Tsoli ◽  
Jennifer Byrne ◽  
Chelsea Mayoh ◽  
Siva Sivarajasingam ◽  
...  

2013 ◽  
Vol 9 (4) ◽  
pp. e174-e181 ◽  
Author(s):  
Leo Chen ◽  
Janice Grant ◽  
Winson Y. Cheung ◽  
Hagen F. Kennecke

Manually screening patient records increased enrollment to specific clinical trials. A screening intervention process, involving a dedicated screening coordinator, should be considered to improve clinical trial accrual.


2013 ◽  
Vol 31 (15_suppl) ◽  
pp. e17568-e17568
Author(s):  
Yee Hong Chia

e17568 Background: Phase II clinical trials in oncology have previously been reported to differ significantly in design compared to trials in other subspecialties. The purpose of this study is to provide a summary description of Phase II oncology clinical trials published in 2011, and to identify persistent major cross-specialty differences in clinical trial design. Methods: Records identified through a computerized literature search on PUBMED were reviewed manually using pre-defined criteria to identify abstracts of Phase II clinical trials published in 2011. The abstracts were classified according to variables including subspecialty, use of control group (active and/or placebo), randomization, blinding, and study conclusions. Trials with positive outcomes were defined as those in which the conclusion indicated that the intervention was safe and effective/worthy of further investigation. Statistical analysis was performed using the chi-squared test. Results: A total of 1,500 abstracts of Phase II clinical trials were identified, of which the majority (75%) describe trials on interventions for neoplastic diseases. Among oncology trials, the largest proportion of abstracts described trials evaluating intervention for hematologic neoplasms (16%), followed by upper and lower gastrointestinal (15%), lung (13%) and breast (11%) cancers. Compared to trials in other subspecialties, oncology trials are significantly less likely to include the use of randomization (17% vs 66%, p < 0.0001), blinding (3% vs 44%, p < 0.0001), and control (13% vs 70%, p < 0.0001). The majority of the abstracts reported positive outcomes (66% for oncology; 74% for the other subspecialties). Among oncology trials, trials utilizing a control group are less likely to report positive outcomes than those without a control group (53% vs 67%, p = 0.002). Conclusions: Major differences in design still exist between Phase II trials in oncology and other subspecialties. Only a minority of oncology trials report the use of randomization, blinding, or control groups. Whether the growing interest in randomized Phase II oncology trials will translate into a larger proportion of such trials in the future remains to be seen.


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