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Higher than reported adolescent and young adult clinical trial enrollment during the “Golden Age” of melanoma clinical trials

Clinical trial enrollments in adolescents and young adults (AYA) with cancer have historically been lower than those in pediatric and older adult populations. We sought to examine therapeutic trial enrollment rates at our cancer center. We performed a retrospective evaluation of AYA patients treated...

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Autores principales: Sreeraman Kumar, Radhika, Thapa, Ram, Kim, Youngchul, Khushalani, Nikhil I., Sondak, Vernon K., Reed, Damon R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911596/
https://www.ncbi.nlm.nih.gov/pubmed/29478277
http://dx.doi.org/10.1002/cam4.1307
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author Sreeraman Kumar, Radhika
Thapa, Ram
Kim, Youngchul
Khushalani, Nikhil I.
Sondak, Vernon K.
Reed, Damon R.
author_facet Sreeraman Kumar, Radhika
Thapa, Ram
Kim, Youngchul
Khushalani, Nikhil I.
Sondak, Vernon K.
Reed, Damon R.
author_sort Sreeraman Kumar, Radhika
collection PubMed
description Clinical trial enrollments in adolescents and young adults (AYA) with cancer have historically been lower than those in pediatric and older adult populations. We sought to examine therapeutic trial enrollment rates at our cancer center. We performed a retrospective evaluation of AYA patients treated before and after the first checkpoint inhibitor trial opened at our cancer center in 2007. We examined gender, stage at presentation and insurance status in terms of trial enrollment. We compared the trial participation rate of AYA patients with that of older adults. In this adult facility, 12.7% (1,831) of total patients were between age 15 and 39. Overall therapeutic clinical trial rate was 17.6% which increased to 19.8% since 2007. Both nodal disease or metastatic disease at presentation was associated with increasing odds of trial enrollment (OR = 5.36 and P < 0.001 for nodal disease and OR = 7.96 and P < 0.001 for metastatic disease). There was a nonstatistically significant trend toward improved 3‐year overall survival in the AYA patients with advanced presentation that enrolled on clinical trials compared with those not enrolled on trials since 2007. AYA clinical trial enrollment at a comprehensive care center melanoma program was higher than reported in the literature overall for AYA patients. This 1,831 patient cohort may provide a foundation for more detailed investigation toward quantifying the effects of clinical trial enrollment in terms of age‐specific benefits and toxicities for AYA patients with malignancies that have their peak incidence in older adults.
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spelling pubmed-59115962018-04-30 Higher than reported adolescent and young adult clinical trial enrollment during the “Golden Age” of melanoma clinical trials Sreeraman Kumar, Radhika Thapa, Ram Kim, Youngchul Khushalani, Nikhil I. Sondak, Vernon K. Reed, Damon R. Cancer Med Clinical Cancer Research Clinical trial enrollments in adolescents and young adults (AYA) with cancer have historically been lower than those in pediatric and older adult populations. We sought to examine therapeutic trial enrollment rates at our cancer center. We performed a retrospective evaluation of AYA patients treated before and after the first checkpoint inhibitor trial opened at our cancer center in 2007. We examined gender, stage at presentation and insurance status in terms of trial enrollment. We compared the trial participation rate of AYA patients with that of older adults. In this adult facility, 12.7% (1,831) of total patients were between age 15 and 39. Overall therapeutic clinical trial rate was 17.6% which increased to 19.8% since 2007. Both nodal disease or metastatic disease at presentation was associated with increasing odds of trial enrollment (OR = 5.36 and P < 0.001 for nodal disease and OR = 7.96 and P < 0.001 for metastatic disease). There was a nonstatistically significant trend toward improved 3‐year overall survival in the AYA patients with advanced presentation that enrolled on clinical trials compared with those not enrolled on trials since 2007. AYA clinical trial enrollment at a comprehensive care center melanoma program was higher than reported in the literature overall for AYA patients. This 1,831 patient cohort may provide a foundation for more detailed investigation toward quantifying the effects of clinical trial enrollment in terms of age‐specific benefits and toxicities for AYA patients with malignancies that have their peak incidence in older adults. John Wiley and Sons Inc. 2018-02-25 /pmc/articles/PMC5911596/ /pubmed/29478277 http://dx.doi.org/10.1002/cam4.1307 Text en © 2018 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Sreeraman Kumar, Radhika
Thapa, Ram
Kim, Youngchul
Khushalani, Nikhil I.
Sondak, Vernon K.
Reed, Damon R.
Higher than reported adolescent and young adult clinical trial enrollment during the “Golden Age” of melanoma clinical trials
title Higher than reported adolescent and young adult clinical trial enrollment during the “Golden Age” of melanoma clinical trials
title_full Higher than reported adolescent and young adult clinical trial enrollment during the “Golden Age” of melanoma clinical trials
title_fullStr Higher than reported adolescent and young adult clinical trial enrollment during the “Golden Age” of melanoma clinical trials
title_full_unstemmed Higher than reported adolescent and young adult clinical trial enrollment during the “Golden Age” of melanoma clinical trials
title_short Higher than reported adolescent and young adult clinical trial enrollment during the “Golden Age” of melanoma clinical trials
title_sort higher than reported adolescent and young adult clinical trial enrollment during the “golden age” of melanoma clinical trials
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911596/
https://www.ncbi.nlm.nih.gov/pubmed/29478277
http://dx.doi.org/10.1002/cam4.1307
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