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Remote oncology monitoring that connects clinicians and cancer patients between visits.

Carevive is an oncology health technology company that gives care teams a remote patient monitoring platform to track symptoms, collect patient-reported outcomes, and manage cancer patients between clinic visits. The system is designed to surface actionable data for clinicians while reducing the burden on patients managing complex treatment regimens. On MarketScale, Carevive publishes content for oncology administrators, clinicians, and health systems evaluating remote care management tools.

51 episodes
Channel Brief·Carevive · 51 episodes
Updated Jan 9, 2023

Patient data, not claims data, transforms oncology care delivery

Carevive argues that real-world patient-reported outcomes, collected continuously during treatment, reveal what traditional big data cannot: how cancer patients actually experience disease and therapy in real time.

Carevive's core argument is that oncology improvement requires shifting from discrete, retrospective claims and clinical data to continuous, patient-reported experience data captured at the point of care. The channel demonstrates this through longitudinal case studies, registry analysis across 26 cancer types, and specific clinical workflows showing how alert-triggered interventions on symptom reports change care team behavior and patient adherence.

Drawn from Improving the Patient Experience in Cancer and 2 more

Big data is limited because its datapoints are discrete, providing only sequential snapshots without continuous assessment of patient experience on treatment.

Carevive, Improving the Patient Experience in Cancer

By the numbers

600,000

unique data points from 19,000 surveys across 26 cancer types

1,700+

patients represented across Carevive's registry

26

cancer types covered in Carevive's longitudinal dataset

19,000

surveys completed over two years in registry

What the channel argues

DataCarevive's registry spans 1,700+ patients across 26 cancer types with 19,000 completed surveys yielding 600,000 data points.
InsightPatient compliance with survey follow-ups is high during critical first three months of treatment when interventions matter most.
InsightPRO integration into clinical workflows improves patient therapy adherence and reduces hospitalizations and ER visits.
InsightAlert triggers for moderate to severe symptoms enable care teams to reach out, manage symptoms, and document care in real time.
DataEOM replaces OCM starting July 1, 2023, supporting care for seven common cancer types with emphasis on health equity and affordable care.
InsightReal-world data from standard-of-care populations offers contemporary, FDA-relevant PRO measure insights unlike outdated historical trial data.

What you'll learn

Why patient-reported outcomes collected during treatment reveal treatment experience that claims data and clinical snapshots cannot capture.
How continuous symptom monitoring with alert workflows changes care team response rates and patient adherence measurably.
What the transition from OCM to EOM in July 2023 means for oncology practices seeking to improve reimbursement and care equity.
How real-world patient data from diverse settings informs clinical trial design better than historical trial cohorts alone.
Why integrating PROs into routine clinical workflows, not as research overlays, drives both compliance and quality improvement.

What to do about it

Audit your oncology workflow to identify where patient-reported outcomes can be captured at point of care with built-in alert triggers for severe symptoms.
Prepare for EOM implementation by July 2023: assess revenue opportunities in the new model and identify which of seven supported cancer types represent your highest-volume lines.
Commission or partner on a health services research study using your own PRO data to quantify the impact of alert-based interventions on adherence, hospitalizations, and care costs.

Who and what shows up

Dr. Aaron Galaznik

Chief Scientific Officer, Carevive

Led NSCLC webinar on smart data insights and hosted multiple discussions on PRO platform capabilities, alert systems, and longitudinal analysis in breast cancer and lung cancer populations.

John Elliot

VP of Sales, Carevive

Interviewed on OCM-to-EOM transition and revenue implications, representing commercial perspective on model shift.

Dr. Ethan Basch

Expert in electronic patient-reported outcomes (ePROs)

Led webinar discussion on digital remote monitoring challenges and best practices for implementing and optimizing ePRO data collection and engagement across cancer programs.

Tyler Kern

Host, Oncology and Technology

Conducted interviews with Carevive team on OCM-to-EOM transition and expectations for cancer care.

Michelle Dawn Mooney

Host, Technology and Oncology Podcast

Hosted discussion with John Elliot on revenue-enhancing opportunities and real-world impact of EOM transition.

Questions this channel answers

Q

What makes Carevive's data different from traditional big data in oncology?

Carevive captures continuous, patient-reported experience at the point of care, not discrete clinical snapshots. Traditional big data provides sequential datapoints without continuous assessment of how patients actually experience treatment day to day.

Improving the Patient Experience in Cancer
Q

How does PRO data improve clinical decision-making in real time?

The platform integrates patient-reported outcomes into care team workflows, uses alert triggers when patients report moderate to severe symptoms, and enables timely interventions on therapy adherence and symptom management, with studies showing reduced hospitalizations and ER visits.

Patient Engagement and Compliance
Q

What are the revenue implications of moving from OCM to EOM?

EOM, effective July 1, 2023, replaces OCM and supports care for seven common cancer types with focus on health equity and accountable, affordable care, creating new revenue-enhancing opportunities for oncology practices.

The New Oncology Model Created to Improve Cancer Care
Q

How can real-world oncology data inform drug development and clinical trials?

Carevive's real-time data from standard-of-care populations offers contemporary, FDA-relevant insights into patient-centered domains unlike historical trial data, which quickly becomes outdated. This bridges real-world outcomes with trial design and post-marketing assessment.

CV/COS Webinar: Applications and Future Directions
Q

How engaged are cancer patients with continuous survey monitoring?

Patient compliance and persistence with survey follow-ups is impressive during the critical initial three months of treatment, the phase when care teams most need to monitor treatment experiences and intervene on adherence challenges.

Patient Engagement and Compliance
Topics:Patient-reported outcomes (PROs) in oncologyLongitudinal real-world data collectionEnhanced Oncology Model (EOM) transitionSymptom monitoring and alert workflowsClinical trial design and real-world data
Themes:Patient voice as clinical data, not survey artifactReal-world longitudinal evidence versus trial populationsAlert-driven, workflow-embedded symptom monitoring

Industry context

Real-world evidence collection is expanding beyond post-approval studies into early-phase trial design. Continuous monitoring generates substantially more data points than traditional periodic assessments, reshaping how clinical evidence is gathered in drug development.

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