Interview
Jan 8

Revolutionizing Patient‑Centric Sampling: An Interview with Neil Spooner, Co‑Founder of PCSIG

BMC

The Biospecimen Management Consortium (BMC) recently had the privilege of sitting down with Neil Spooner, Co-Founder of the Patient-Centric Sampling Interest Group (PCSIG), to discuss the evolution of patient-centric sampling and its impact on clinical trials and healthcare. This insightful conversation sheds light on the innovative approaches that are reshaping how we collect biological samples from patients.

The Genesis of PCSIG

Neil Spooner's journey into patient-centric sampling began during his tenure at GSK, where he led a group focused on introducing new technologies for bioanalysis in clinical trials. The need for smaller blood volumes, particularly in pediatric studies, sparked interest in microsampling techniques such as heel pricks and dry blood spot sampling.

As the field evolved, Spooner and his colleagues realized the limitations of traditional sampling and the microsampling approaches available at that time, and began exploring alternative technologies that could provide the same benefits: small samples, dried samples, room temperature shipments, sub-sampling, and home sampling.

Defining Patient-Centric Sampling

For PCSIG, patient-centric sampling means putting the patient's needs at the forefront of the sampling process. Spooner explains, "The traditional way of collecting biological samples doesn't pay heed to the needs of the patient. It prioritizes the study, the healthcare provider, and the laboratory - the patient comes last".

PCSIG aims to change this paradigm by:

  1. Reducing the need for patients to travel long distances for sample collection
  2. Minimizing discomfort and invasiveness of sampling procedures
  3. Engaging underserved populations who may be deterred by traditional sampling methods
  4. Enabling sample collection during specific medical events or at the patient's convenience

PCSIG's Achievements and Impact

Since its inception, PCSIG has made significant strides in advancing patient-centric sampling:

  1. Raising Awareness: The group has successfully increased awareness of patient-centric technologies among healthcare professionals and researchers, through various workshops and webinars.
  2. Developing Resources: PCSIG is creating materials to help stakeholders understand and adopt patient-centric sampling in clinical trials, including decision trees and protocol templates.
  3. Addressing Barriers: By actively engaging with stakeholders, PCSIG identifies and works to overcome barriers to adoption.
  4. Facilitating Collaboration: The organization has brought together diverse groups, including device manufacturers, pharmaceutical companies, CROs, central labs, clinicians, academics, and patients, to share best practices and ideas.

Challenges and Future Directions

Despite the progress, challenges remain in the widespread adoption of patient-centric sampling. These include:

  1. Cost Perceptions: The perceived higher cost of patient-centric devices compared to standard blood tubes.
  2. Resistance to Change: Overcoming the inertia in adopting new technologies within established systems.
  3. Logistical Complexities: Managing the logistics of sample collection, transportation, and analysis when dealing with decentralized sampling locations.

To address these challenges, PCSIG is undertaking several initiatives, including:

  1. Conducting cost-benefit analyses to demonstrate the overall value of patient-centric sampling
  2. Collaborating with regulators to ensure compliance and address potential inspection concerns
  3. Working on improving the integration of patient-centric samples into existing laboratory automation systems

The Future of Patient-Centric Sampling

Neil Spooner envisions a future where traditional blood sampling coexists with patient-centric methods, each applied where most appropriate. He emphasizes the potential for patient-centric sampling to:

  • Improve access to healthcare for underserved populations
  • Enable more frequent and convenient sampling in clinical trials
  • Facilitate the collection of samples during specific medical events
  • Generate richer, longitudinal data for better patient understanding

As the Biospecimen Management Consortium, we are excited about the potential collaboration opportunities with PCSIG. Together, we can work towards optimizing sample management processes, addressing logistical challenges, and ultimately improving patient care and clinical research outcomes.

The future of patient-centric sampling is bright, and with organizations like PCSIG leading the charge, we can look forward to more innovative, patient-friendly approaches to biological sample collection in the years to come.

To learn more about PCSIG, visit https://www.pcsig.org/.