Clinical Trial Participants Call for More Inclusive, Patient-Centered Cancer Research
Nov 17, 2025
Three cancer trial participants share their transformative journeys, illuminating the importance of patient-centered approaches in clinical research. They discuss the shift towards offering early-phase trials alongside biomarker therapies and spotlight the benefits, like access to novel treatments and emotional support. However, they also highlight barriers like restrictive eligibility and financial challenges that limit participation. Encouraging broader access, improved communication, and enhanced patient advocacy are key recommendations to foster a more inclusive trial environment.
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insights INSIGHT
Early Trials Are Changing Role
Early-phase trials are shifting from a last-resort option to earlier treatment due to biomarker-guided therapies.
This change makes patient experience and trial design increasingly critical for outcomes and ethics.
insights INSIGHT
Trials Offer Big Benefits And Big Barriers
Trials offer access to novel therapies, close monitoring, emotional support, and purpose from contributing to research.
Significant barriers like restrictive eligibility, financial strain, and communication gaps limit patient participation.
question_answer ANECDOTE
Genomic Testing Led To Targeted Therapy
Another participant shared that genomic testing identified a targeted treatment after standard options failed.
Their experience highlights the value of molecular profiling in finding effective experimental therapies.
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BUFFALO, NY – November 17, 2025 – A new #research perspective was #published in Oncotarget (Volume 16) on November 14, 2025, titled “A personal perspective of patient-centred clinical trials.”
In this perspective, led by corresponding author Jia Liu of The Kinghorn Cancer Centre, St Vincent’s Hospital, the University of New South Wales, and the Garvan Institute of Medical Research, three early-phase clinical trial participants — Trevor Tyne, Elizabeth Ivimey, and Leanne Duggan — reflect on their personal experiences with experimental cancer treatments. Their stories offer a unique perspective on the patient journey through early-phase trials and emphasize the need to design clinical research that prioritizes patients’ needs, dignity, and lived realities. The authors highlight both the life-changing opportunities that trials can provide and the systemic barriers that still prevent many patients from participating.
This perspective captures a turning point in how early-phase trials are viewed. Once considered a last resort, these trials are now increasingly offered earlier in treatment, especially with the rise of biomarker-guided therapies. In this context, the patient experience has become critical. The authors outline key benefits of participation, including access to novel therapies, ongoing medical monitoring, emotional support, and a strong sense of purpose in contributing to future medical advancements. However, they also point out significant challenges, such as restrictive eligibility criteria, high financial and logistical burdens, and communication gaps between patients and trial staff.
“While no trial guarantees success, the level of support, access to innovative therapies, and sense of contribution to medical progress can be profoundly meaningful.”
Each narrative provides insight into the clinical trial experience. One patient explains how living with a visual impairment required tailored accessibility support throughout the trial process Another shares how genomic testing led to targeted treatment after standard options failed. Despite their different diagnoses and circumstances, all three stories reflect resilience, hope, and a shared call for trial designs that better reflect the realities of diverse patients.
To address these issues, the authors propose a number of improvements to trial design and delivery. These include expanding eligibility criteria, offering financial and logistical assistance, improving communication training for research staff, and introducing dedicated trial navigators to help guide patients through complex processes. They also focus on the importance of involving patient advocates in trial design and ensuring smoother transitions for patients moving between treatment centers.
While early-phase trials focus on safety and effectiveness, the authors argue they must also be guided by core values like ethics and patient empowerment. This perspective serves as a reminder that the future of cancer research depends not only on scientific innovation, but on an honest partnership between patients and the research community.
By sharing these real-world experiences, the article encourages a broader conversation about how to make clinical trials more responsive to the people they are designed to serve.
DOI - https://doi.org/10.18632/oncotarget.28776
Correspondence to - Jia Liu - jia.liu@svha.org.au
Abstract video - https://www.youtube.com/watch?v=2CCGN78n8ug
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