Literature DB >> 30289970

Low clinical trial accrual of patients with myelodysplastic syndromes: Causes and potential solutions.

David P Steensma1, Andrew M Brunner2, Amy E DeZern3, Guillermo Garcia-Manero4, Rami S Komrokji5, Olatoyosi S Odenike6, Gail J Roboz7, Michael R Savona8, Richard M Stone1, Mikkael A Sekeres9.   

Abstract

Despite few effective therapies, only a small percentage of patients diagnosed with myelodysplastic syndromes (MDS) in the United States are enrolled in prospective, interventional clinical trials. MDS-specific barriers to trial accrual include a high frequency of elderly patients with comorbid conditions, atypical disease features and uncertainty regarding the diagnosis (because other nonclonal processes also can cause dysplasia and cytopenias), a history of another nonmyeloid neoplasm resulting in therapy-related MDS, rapid disease recurrence after allogeneic stem cell transplantation, and an arbitrary division between MDS and acute myeloid leukemia. In addition, barriers to accrual that are common to other oncology populations, such as difficulty traveling to clinical trial enrollment sites and narrow trial eligibility criteria, also prevent patients with MDS from enrolling in studies. Collectively these barriers must be assessed systematically, and creative solutions are needed to improve outcomes for this needy patient population.
© 2018 American Cancer Society.

Entities:  

Keywords:  adverse events; barriers to clinical trials; clinical trial enrollment; drug development; myelodysplastic syndromes; referral patterns

Mesh:

Year:  2018        PMID: 30289970     DOI: 10.1002/cncr.31769

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  5 in total

1.  Representation of therapy-related myelodysplastic syndrome in clinical trials over the past 20 years.

Authors:  Uma Borate; Brianna A Norris; Abby Statler; Rongwei Fu; Taylor Bucy; Mikkael A Sekeres
Journal:  Blood Adv       Date:  2019-09-24

2.  Outcomes of patients with hematologic malignancies and COVID-19: a report from the ASH Research Collaborative Data Hub.

Authors:  William A Wood; Donna S Neuberg; J Colton Thompson; Martin S Tallman; Mikkael A Sekeres; Laurie H Sehn; Kenneth C Anderson; Aaron D Goldberg; Nathan A Pennell; Charlotte M Niemeyer; Emily Tucker; Kathleen Hewitt; Robert M Plovnick; Lisa K Hicks
Journal:  Blood Adv       Date:  2020-12-08

3.  Historical expectations with DNA methyltransferase inhibitor monotherapy in MDS: when is combination therapy truly "promising"?

Authors:  Andrew M Brunner; Geoffrey Fell; David P Steensma
Journal:  Blood Adv       Date:  2022-05-10

Review 4.  Treatment of myelodysplastic syndromes in the era of precision medicine and immunomodulatory drugs: a focus on higher-risk disease.

Authors:  Razan Mohty; Rama Al Hamed; Ali Bazarbachi; Eolia Brissot; Arnon Nagler; Amer Zeidan; Mohamad Mohty
Journal:  J Hematol Oncol       Date:  2022-08-31       Impact factor: 23.168

5.  Genomic Biomarkers to Predict Resistance to Hypomethylating Agents in Patients With Myelodysplastic Syndromes Using Artificial Intelligence.

Authors:  Aziz Nazha; Mikkael A Sekeres; Rafael Bejar; Michael J Rauh; Megan Othus; Rami S Komrokji; John Barnard; Cameron B Hilton; Cassandra M Kerr; David P Steensma; Amy DeZern; Gail Roboz; Guillermo Garcia-Manero; Harry Erba; Benjamin L Ebert; Jaroslaw P Maciejewski
Journal:  JCO Precis Oncol       Date:  2019-09-20
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.