Webinar: 2020 pan-Canadian Oncology Drug Review (pCODR) Updates
By Innomar Strategies
Ferg Mills, Director of Strategic Consulting, and George Wyatt, Executive Senior Consultant at InnomarConsulting, dig into the pan-Canadian Oncology Drug Review (pCODR) initiatives introduced in the first half of 2020.
In fact, as is evident in Figure 1 below, which illustrates various data collection points across a patient journey for a specialty product, there are multiple opportunities to collect a variety of real-world data along the continuum.
Figure 1
Having such an expansive and diverse net of data collection
generates more meaningful insights.
The need for data linkage
Despite the promise of data diversity and robustness,
joining disparate sources into a unified aggregated data set can be
challenging.
Healthcare system fragmentation produces an incomplete
picture of the patient, but linking the various sources together provides a
more accurate characterization.
Unfortunately, the current health data landscape can make it
difficult to bring data sets together.
Solving these challenges requires a data enrichment strategy
that's able to aggregate the different types of RWE across the care ecosystem ¾for
example, the analysis of prescriptions along with reporting of adverse events,
or the analysis of adherence and its
impact on long-term patient health outcomes. Data linkage and aggregation can
help address the shortcomings of single-source data capture while also
bolstering the scientific quality and validity of research studies. Linking
together these sources helps manufacturers and providers alike to assemble a
more holistic view of the patient and expand the set of questions that can be
answered on the effectiveness and overall value of treatments.
Another opportunity in data linkage comes from public
sources, as the Canadian healthcare model itself creates new opportunities for
collaborative partnerships around analysis. Through this linkage of
governmental data with information on health service utilization (such as
hospital stay, ER use and outpatient and physician visits), manufacturers can
glean more comprehensive insights that are invaluable to understand the patient
journey and outcomes.
Manufacturer opportunities
While payers and regulators seek to facilitate the adoption
of RWE, manufacturers are taking a leadership position in finding, generating,
and contextualizing that evidence.
Simply put, the government and the payers are very open to
RWE, but they want manufacturers to drive RWE solutions (particularly for
adoption and continued use of the manufacturer's products).
As Figure 1 demonstrates, PSPs are an integral part of the
patient journey. They enrich existing information because of the large
enrollment/patient capture and multiple touchpoints with patients, which are
all opportunities to collect data. PSPs also have direct communication with
patients' healthcare team and physicians, payers, and caregivers ¾ representing even more opportunities for data collection.
Data that resides within the PSPs remain critical for fully
understanding RWE. One way to ensure the PSPs are structured to support RWE
collection is by creating a strategy that prioritizes patient-reported data.
One aspect of patient support programs that can be particularly useful is
contacting the patients directly to gather information. Additionally, as
digital health solutions such as app and wearables increase in utilization,
personal technologies represent another source of continuous data collection
that should be considered. When setting up PSPs, it is also important to ensure
the quality and accuracy of the data by investing in validated quality control
systems to provide confidence in the credibility of the data collected.
Successful commercialization strategies will utilize and
incorporate real-world evidence across the product life cycle, and the need to
link data to forecast and track outcomes over time. Especially in the new era
of COVID-19, RWE will be critical in measuring and understanding the long-term
impact of the disease, which in turn will help create a treatment roadmap and
allow us to expedite launching therapies across the world.
Working with an experienced vendor in the
nuances of data analysis and linkage can enable manufacturers to achieve their
commercial initiatives and improve patient and health outcomes.