The landscape and effectiveness of patient retention strategies in cancer clinical trials.

L Lexi S. Weintraub (Mount Sinai Tisch Cancer Center, New York, NY) A Alexander B Karol (Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Hospital, New York, NY) R Rodrigo Paredes (Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai West/Morningside, New York, NY) A Anna Argulian (Icahn School of Medicine at Mount Sinai, New York, NY) K Kasopefoluwa Oguntuyo (Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Hospital, New York, NY) J Justin Miller Y Yu Fujiwara H Himanshu Joshi D Deborah Blythe Doroshow (Division of Hematology & Medical Oncology, The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY) M Matthew D. Galsky (Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai)

Abstract

e23005 Background: Withdrawal without a defined reason (WWDR) can introduce unintended bias and reduce generalizability in therapeutic cancer clinical trials. Changes in patients’ perceived risks versus benefits of participation in clinical trials are the main drivers for withdrawal. Commonly employed retention strategies include supportive care, telemedicine, and patient education materials. However, the frequency and effectiveness of trial-endorsed approaches to patient retention are not well defined. Methods: We extracted WWDR rates and protocol-stated retention strategies from all phase III therapeutic cancer clinical trials conducted between August 20th, 2014, and August 20th, 2024, in the ClinicalTrials.gov database. WWDR was defined as withdrawal initiated by either patients or investigators without a recorded cause. Supportive care trials and trials without a Consolidated Standards of Reporting Trials diagram or descriptive equivalent were excluded. All protocol documents and available primary publications were reviewed. Univariate linear regression was performed to identify associations between retention strategies and WWDR using rate ratios (RR) and 95% confidence intervals (CI). Results: 300 trials, enrolling 165,674 patients, met our inclusion criteria and were analyzed: 93.7% (281) studies were multi-site, 95% (285) were international, and 88.8% (264) were randomized controlled trials. An overview of the protocol-stated retention methods is shown in the Table. Univariate analysis indicated that a lack of protocol-specified strategies (RR = 1.00; 95% CI: 0.76–1.33, p = 0.98), non-specific investigator approaches (RR = 1.08; 95% CI: 0.77–1.51, p = 0.66), contacting patients lost to follow-up (RR = 0.75; 95% CI: 0.44–1.23, p = 0.29), and unblinding (RR = 1.11; 95% CI: 0.54–2.29, p = 0.77) were not associated with an increased likelihood of WWDR. Conclusions: Over two thirds of trials did not specify any retention strategy. Only 5% of oncology clinical protocols included personalized retention approaches, and none of these methods correlated with decreased WWDR. Standardized reporting of retention strategy use is needed to accurately assess the efficacy of current practices. The development and testing of novel patient retention strategies will be critical to limiting WWDR. Patient retention strategies in clinical trials. Patient retention strategies # of trials (%) No retention strategy 204 (68.0%) Non-specific effort 54 (18.0%) Contact patients lost to follow up 19 (6.3%) Personalized interventions (home nursing; telemedicine; supportive care; encouragement; patient education) 15 (5.0%) Unblinding or cross over 10 (3.3%)

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (10)

L

Lexi S. Weintraub

Mount Sinai Tisch Cancer Center, New York, NY

A

Alexander B Karol

Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Hospital, New York, NY

R

Rodrigo Paredes

Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai West/Morningside, New York, NY

A

Anna Argulian

Icahn School of Medicine at Mount Sinai, New York, NY

K

Kasopefoluwa Oguntuyo

Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Hospital, New York, NY

J

Justin Miller

Y

Yu Fujiwara

H

Himanshu Joshi

D

Deborah Blythe Doroshow

Division of Hematology & Medical Oncology, The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY

M

Matthew D. Galsky

Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai