Evaluating the impact of eligibility criteria in first-line clinical trials for follicular lymphoma: a MER/LEO cohort analysis

Author:

Luan Danny1,Fatola Tolulope1,Toure Ahmed1,Flowers Christopher R.2,Link Brian3ORCID,Friedberg Jonathan W.4,Cohen Jonathon B.5ORCID,Kahl Brad6ORCID,Lossos Izidore S.7ORCID,Nastoupil Loretta2,Maurer Matthew J.8ORCID,Cerhan James R.8ORCID,Martin Peter1

Affiliation:

1. 1Department of Hematology and Oncology, NewYork-Presbyterian Hospital/Weill Cornell Medical College, New York, NY;

2. 2Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX;

3. 3Department of Internal Medicine, University of Iowa Hospitals & Clinics, Iowa City, IA;

4. 4Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY;

5. 5Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA;

6. 6Department of Medicine, Washington University School of Medicine in St. Louis, St. Louis, MO;

7. 7Department of Medicine, University of Miami Health System, Miami, FL; and

8. 8Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN

Abstract

Abstract Cancer clinical trial eligibility criteria may create patient populations studied in trials that do not reflect the patient populations treated in the real-world setting. Follicular lymphoma (FL) is an indolent lymphoma with heterogeneous presentations across a broad range of individuals, resulting in many acceptable management strategies. We evaluated how first-line clinical trial eligibility criteria impacted the demographic makeup and outcomes of patients with FL for whom systemic therapy might be considered. We compared the characteristics of 196 patients with FL from a single institution to eligibility criteria from 10 first-line FL trials on clinicaltrials.gov. Next, we tabulated eligibility criteria from 24 first-line FL protocols and evaluated their impact on 1198 patients with FL with stages II to IV disease from the prospective Molecular Epidemiology Resource (MER) and Lymphoma Epidemiology of Outcomes (LEO) cohort studies. We found that 39.8% and 52.7% of patients with FL might be excluded from clinical trials based on eligibility criteria derived from clinicaltrials.gov and protocol documents, respectively. Patients excluded because of renal function, prior malignancy, and self-reported serious health conditions tended to be older. Expanding stage requirement from III-IV to II-IV, and platelet requirement from ≥150 000 to ≥75 000 increased population size by 21% and 8%, respectively, in MER and by 16% and 13%, respectively, in LEO, without impacting patient demographics or outcomes. These data suggest that management of older individuals with FL may not be fully informed by recent clinical trials. Moreover, liberalizing stage and platelet criteria might expand the eligible population and allow for quicker trial accrual without impacting outcomes.

Publisher

American Society of Hematology

Subject

Hematology

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