Defining Priorities in Value-Based Cancer Care: Insights From the Alliance for Clinical Trials in Oncology National Cooperative Group Survey

Author:

Allen Casey J.1ORCID,Snyder Rebecca A.2ORCID,Horn Danea Marie3ORCID,Hudson Matthew F.4ORCID,Barber Anne5,Smieliauskas Fabrice6ORCID,Spears Patty A.7,Edge Stephen8ORCID,Greenup Rachel A.9

Affiliation:

1. Division of Surgical Oncology, Institute of Surgery, Allegheny Health Network Cancer, Pittsburgh, PA

2. Departments of Surgical Oncology and Health Services Research, The University of Texas MD Anderson Cancer Center, Houston, TX

3. Department of Economics, Stanford University, Stanford, CA

4. Prisma Health Cancer Institute and University of South Carolina School of Medicine Greenville, Greenville, SC

5. Cancer Control Program of the Alliance for Clinical Trials in Oncology and Cancer Programs of the American College of Surgeons, Chicago, IL

6. Department of Economics and Department of Pharmacy Practice, Wayne State University, Detroit, MI

7. Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC

8. Roswell Park Comprehensive Cancer Center and Jacobs School of Medicine, University at Buffalo, Buffalo, NY

9. Department of Surgery and Smilow Cancer Hospital, Yale School of Medicine, New Haven, CT

Abstract

PURPOSE We determine how stakeholders prioritize the importance of oncologic outcomes, patient-reported outcomes (PROs), and cancer-related health care costs. METHODS A survey was distributed to the National Clinical Trials Network Alliance for Clinical Trials in Oncology cooperative group membership from May 14 to June 30, 2022. Respondents were asked to rate (5-point Likert scale) and rank (1-9) evidence-based value domains: overall survival, treatment toxicities/complications, quality of life (QOL), financial toxicity, access to care, compliance with evidence-based care, health system performance, scientific discovery and innovation, and cost to the health care system. RESULTS A total of 514 members responded, including researchers (24.7%), nurses (19.5%), medical oncologists (17.9%), administrators (9.3%), surgical and radiation oncologists (9.1%), patient advocates (3.1%), and nonphysician providers (16.4%). Participants represented various practice settings including National Cancer Institute–designated cancer centers (29.8%), university-affiliated academic cancer centers (21%), hospital-owned oncology practices (21.8%), and others (27.4%). There was agreement in how respondents prioritized value domains (W = 0.39, P < .001). Respondents ranked patient QOL (mean rank: 2.6 ± 1.9) as most important above all other metrics including survival (mean rank: 3.5 ± 0.3) and access to care (mean rank: 3.5 ± 2.1; P < .001). Members engaged in direct patient care also ranked access to care of higher importance than nonclinicians ( P = .026). Cost to the health care system (mean rank: 7.5 ± 2.1) and health system performance (mean rank: 7 ± 2) were ranked as least important ( P < .001). Inclusion of PROs into therapeutic assessment (59.3%) was the most frequently selected priority of future cooperative group initiatives. CONCLUSION Oncology community stakeholders deemed patient-centered value domains as most important and considered patient QOL the highest priority. Inclusion of PROs into clinical trials was endorsed as an important component of therapeutic assessment. These findings can be taken into consideration when creating a value framework for inclusion in cancer clinical trials.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Oncology (nursing),Health Policy,Oncology

Reference24 articles.

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