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Featured researches published by Donna M. Bryant.


Journal of Oncology Practice | 2014

Use of the National Cancer Institute Community Cancer Centers Program Screening and Accrual Log to Address Cancer Clinical Trial Accrual

Diane St Germain; Andrea M. Denicoff; Eileen P. Dimond; Angela Carrigan; Rebecca A. Enos; Maria M. Gonzalez; Kathy Wilkinson; Michelle A. Mathiason; Brenda Duggan; Shaun Einolf; Worta McCaskill-Stevens; Donna M. Bryant; Michael A. Thompson; Stephen S. Grubbs; Ronald S. Go

PURPOSE Screening logs have the potential to help oncology clinical trial programs at the site level, as well as trial leaders, address enrollment in real time. Such an approach could be especially helpful in improving representation of racial/ethnic minority and other underrepresented populations in clinical trials. METHODS The National Cancer Institute Community Cancer Centers Program (NCCCP) developed a screening log. Log data collected from March 2009 through May 2012 were analyzed for number of patients screened versus enrolled, including for demographic subgroups; screening methods; and enrollment barriers, including reasons for ineligibility and provider and patient reasons for declining to offer or participate in a trial. User feedback was obtained to better understand perceptions of log utility. RESULTS Of 4,483 patients screened, 18.4% enrolled onto NCCCP log trials. Reasons for nonenrollment were ineligibility (51.6%), patient declined (25.8%), physician declined (15.6%), urgent need for treatment (6.6%), and trial suspension (0.4%). Major reasons for patients declining were no desire to participate in trials (43.2%) and preference for standard of care (39%). Major reasons for physicians declining to offer trials were preference for standard of care (53%) and concerns about tolerability (29.3%). Enrollment rates onto log trials did not differ between white and black (P = .15) or between Hispanic and non-Hispanic patients (P = .73). Other races had lower enrollment rates than whites and blacks. Sites valued the ready access to log data on enrollment barriers, with some sites changing practices to address those barriers. CONCLUSION Use of screening logs to document enrollment barriers at the local level can facilitate development of strategies to enhance clinical trial accrual.


Journal of Oncology Practice | 2015

Quality Improvement in the National Cancer Institute Community Cancer Centers Program: The Quality Oncology Practice Initiative Experience

Robert D. Siegel; Kathleen Castro; Jana Eisenstein; Holley Stallings; Patricia D. Hegedus; Donna M. Bryant; Pam J. Kadlubek; Steven B. Clauser

PURPOSE The National Cancer Institute (NCI) Community Cancer Centers Program (NCCCP) began in 2007; it is a network of community-based hospitals funded by the NCI. Quality of care is an NCCCP priority, with participation in the American Society of Clinical Oncology Quality Oncology Practice Initiative (QOPI) playing a fundamental role in quality assessment and quality improvement (QI) projects. Using QOPI methodology, performance on quality measures was analyzed two times per year over a 3-year period to enhance our implementation of quality standards at NCCCP hospitals. METHODS A data-sharing agreement allowed individual-practice QOPI data to be electronically sent to the NCI. Aggregated data with the other NCCCP QOPI participants were presented to the network via Webinars. The NCCCP Quality of Care Subcommittee selected areas in which to focus subsequent QI efforts, and high-performing practices shared voluntarily their QI best practices with the network. RESULTS QOPI results were compiled semiannually between fall 2010 and fall 2013. The network concentrated on measures with a quality score of ≤ 0.75 and planned voluntary group-wide QI interventions. We identified 13 measures in which the NCCCP fell at or below the designated quality score in fall 2010. After implementing a variety of QI initiatives, the network registered improvements in all parameters except one (use of treatment summaries). CONCLUSION Using the NCCCP as a paradigm, QOPI metrics provide a useful platform for group-wide measurement of quality performance. In addition, these measurements can be used to assess the effectiveness of QI initiatives.


Oncology Issues | 2011

Using an Online Tool to Understand and Improve Clinical Trial Accruals

Maria Gonzalez; Mitchell Berger; Tammy Brown; Donna M. Bryant; Julie Hugg; Rita Kaul; Mark Krasna; Claudia Lord; Shelley Lowen; Stephanie Smith; Nancy Sprouse

Oncology Issues March/April 2011 The National Cancer Institute (NCI) launched the Community Cancer Centers Program (NCCCP) in 2007 as a three-year pilot, forming a public-private partnership with 16 community hospitals to explore the best methods to enhance access to care—especially for those with healthcare disparities—improve quality of care, and expand research within the community setting.1 At the conclusion of the pilot period, the network sites collaborated to produce White Paper reports to document their experiences, addressing program deliverables in specific focus areas. A series about the NCCCP White Papers was first introduced in the January/February 2011 edition of Oncology Issues.2 This month’s edition features the Clinical Trials White Paper, divided into the following sections: Using an Online Tool to Understand and Improve Clinical Trial Accruals, Developing the NCCCP Trials Portfolio, Using a Minority Matrix and Patient Navigation to Improve Accrual to Clinical Trials, and Developing the RECIST Criteria Toolkit.


Oncology Issues | 2011

Using a Minority Matrix and Patient Navigation to Improve Accrual to Clinical Trials

Maria Gonzalez; Mitchell Berger; Donna M. Bryant; Christie Ellison; Jay K. Harness; Mark Krasna; Rachel Oelmann; Kathy Wilkinson

(2011). Using a Minority Matrix and Patient Navigation to Improve Accrual to Clinical Trials. Oncology Issues: Vol. 26, No. 2, pp. 59-60.


Journal of Clinical Oncology | 2012

Utilizing QOPI in the quality improvement efforts of the NCI Community Cancer Centers Program (NCCCP).

Robert D. Siegel; Holley Stallings; Donna M. Bryant; Pamela Kadlubek; Laurel Borowski; Kathleen Castro; Steven B. Clauser

208 Background: The NCCCP is a network of community based institutions from New England to Hawaii funded by the NCI. Quality of care is a priority of the NCCCP with participation in ASCOs Quality Oncology Practice Initiative (QOPI) playing a fundamental role. QOPI provides a process for quality assessment but we have also used it as a measure of quality improvement (QI) network-wide. Using QOPI methodology, we have analyzed our performance twice a year in an effort to enhance our implementation of quality indicators relevant to program aims. METHODS A data sharing agreement allows individual practice QOPI data to be electronically sent to the NCI where it is aggregated with the other NCCCP QOPI participants. Data are presented via webinar within the network using a variety of QI strategies. For example, blinded site performance distributions are benchmarked against NCCCP national averages on specific indicators. High performing practices voluntarily present their QI initiatives and best practices to the network. The NCCCP Quality of Care Subcommittee then selects QI projects and areas to focus quality improvement efforts. RESULTS In Spring 2012, 44 practices affiliated with 25 NCCCP sites participated in QOPI, a consistent pattern since Fall 2010. The table below describes the percent compliance with certain QOPI measures for the NCCCP aggregate over time. Selected measures were perceived as having had suboptimal compliance in Fall 2010. CONCLUSIONS QOPI is an effective tool for assessing quality within a network and for measuring quality improvement efforts. Best practices from within the network can be leveraged and disseminated to enhance the quality of cancer care. This methodology facilitates quality initiatives despite the logistical challenges of working with practices across the country. [Table: see text].


JAMA Oncology | 2015

Validity and Reliability of the US National Cancer Institute's Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE).

Amylou C. Dueck; Tito R. Mendoza; Sandra A. Mitchell; Bryce B. Reeve; Kathleen Castro; Lauren J. Rogak; Thomas M. Atkinson; Antonia V. Bennett; Andrea Denicoff; Ann M. O'Mara; Yuelin Li; Steven B. Clauser; Donna M. Bryant; James D. Bearden; Theresa A. Gillis; Jay K. Harness; Robert D. Siegel; Diane Paul; Charles S. Cleeland; Deborah Schrag; Jeff A. Sloan; Amy P. Abernethy; Deborah Watkins Bruner; Lori M. Minasian; Ethan Basch


Health and Quality of Life Outcomes | 2016

Mode equivalence and acceptability of tablet computer-, interactive voice response system-, and paper-based administration of the U.S. National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

Antonia V. Bennett; Amylou C. Dueck; Sandra A. Mitchell; Tito R. Mendoza; Bryce B. Reeve; Thomas M. Atkinson; Kathleen Castro; Andrea Denicoff; Lauren J. Rogak; Jay K. Harness; James D. Bearden; Donna M. Bryant; Robert D. Siegel; Deborah Schrag; Ethan Basch


Journal of Oncology Practice | 2013

Early-Phase Clinical Trials In The Community: Results From the National Cancer Institute Community Cancer Centers Program Early-Phase Working Group Baseline Assessment

Howard Zaren; Suresh G. Nair Md; Ronald S. Go; Rebecca A. Enos; Keith S Lanier; Michael A. Thompson; Jinxiu Zhao; Deborah L. Fleming; John C Leighton; Thomas Edward Gribbin; Donna M. Bryant; Angela Carrigan; Jennifer C. Corpening; Kimberly A. Csapo; Eileen P. Dimond; Christie Ellison; Maria M. Gonzalez; Jodi L. Harr; Kathy Wilkinson; Andrea M. Denicoff


ASCO Meeting Abstracts | 2012

Validity and reliability of the patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE).

Amylou Dueck; Tito R. Mendoza; Sandra A. Mitchell; Bryce B. Reeve; Kathleen Castro; Andrea Denicoff; Ann M. O'Mara; Lauren J. Rogak; Steven B. Clauser; Donna M. Bryant; Theresa A. Gillis; James D. Bearden; Robert D. Siegel; Jay K. Harness; Diane Paul; Charles S. Cleeland; Jeff A. Sloan; Deborah Schrag; Lori M. Minasian; Ethan M. Basch


Journal of Clinical Oncology | 2017

The clinical trial assessment of infrastructure matrix tool (CT AIM) to improve the quality of research conduct in the community.

Eileen P. Dimond; Robin Zon; Diane St. Germain; Andrea Denicoff; Angela Carrigan; Kandie Dempsey; Worta McCaskill-Stevens; Maria Gonzalez; Mitchell Berger; Lucy Gansauer; James D. Bearden; Kathy Wilkinson; Donna M. Bryant; Maria C. Bell; Beth I. LaVasseur; Phil Stella; Marjorie J. Good; Kathleen Igo; Octavio Quiñones; Stephen S. Grubbs

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Andrea Denicoff

National Institutes of Health

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Kathleen Castro

National Institutes of Health

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Kathy Wilkinson

Science Applications International Corporation

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Angela Carrigan

Science Applications International Corporation

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Christie Ellison

Science Applications International Corporation

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Eileen P. Dimond

Science Applications International Corporation

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James D. Bearden

Spartanburg Regional Medical Center

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Steven B. Clauser

Patient-Centered Outcomes Research Institute

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