Oncology Data

Custom Oncology Datasets
for AI Training

Hospital-sourced pathology images, medical imaging, clinical records, molecular data, treatment histories, and longitudinal outcomes — collected and prepared to your project specifications.

REMI Data helps AI developers and life sciences companies evaluate and organize custom oncology data sourcing through healthcare institutions and laboratories in Ukraine.

Custom Hospital Sourcing · Multimodal Data · Same-Patient Linkage · Retrospective & Prospective Collection

Oncology Data Modalities

Six core data modalities organized around buyer-defined oncology requirements. Actual fields, patient counts, linkage and source permissions depend on the specific project.

Digital Pathology

  • H&E whole-slide images
  • Immunohistochemistry (IHC)
  • Pathology reports
  • FFPE-associated data
  • Slide digitization
  • Histological grading and staging
  • Pathologist annotation where available
  • Scanner and image metadata

Medical Imaging

  • CT
  • MRI
  • Diagnostic imaging
  • Image acquisition metadata
  • Imaging-to-diagnosis linkage
  • Additional modalities subject to feasibility

Clinical & EHR Data

  • Diagnosis and medical history
  • Demographics
  • Cancer staging
  • Laboratory results
  • Clinical notes
  • Biomarker measurements
  • Longitudinal patient records

Molecular & Genomic Data

  • Molecular profiling
  • Genetic mutations
  • Biomarker results
  • Bulk RNA-seq
  • Single-cell RNA-seq
  • Other multi-omics data where available

Treatment Histories

  • Surgery
  • Radiotherapy
  • Chemotherapy
  • Immunotherapy
  • Hormonal therapy
  • Targeted therapies
  • Treatment dates and sequences
  • Response to treatment

Longitudinal Outcomes

  • Recurrence
  • Progression
  • Metastasis
  • Disease-free survival
  • Progression-free survival
  • Overall survival
  • Follow-up duration
  • Outcome events and censoring

Custom Datasets Across Oncology Indications

REMI Data evaluates buyer-defined data sourcing requirements across solid tumors, hematologic malignancies, and skin cancers. Potential sourcing configurations vary by diagnosis, required data modalities, available medical records, treatment histories, and clinical endpoints.

Bladder Cancer / NMIBC
Breast Cancer
Colorectal Cancer
Endometrial Cancer
Leukemia / AML
Liver Cancer / HCC
Lung Cancer / NSCLC
Melanoma & Skin Cancer
Pancreatic Cancer
Prostate Cancer
Other Solid Tumors
Rare Cancers

This list represents potential areas for feasibility evaluation, not a catalogue of confirmed datasets.

Multiple Data Modalities.
One Linked Patient Record.

De-Identified Patient Identifier
Pathology
Medical Imaging
Clinical Records
Molecular Data
Treatment Timeline
Longitudinal Outcomes

A useful oncology AI dataset often requires mapping images, diagnosis, treatments, and outcome events to the same patient, specimen, or clinical episode. Patient-level linkage enables multimodal model development, outcome prediction, and clinical validation.

Linkage feasibility, completeness, and missingness are assessed for each requested cohort. Complete multimodal linkage is not guaranteed for every case.

Datasets Structured Around
Your AI Requirements

Illustrative cancer-agnostic dataset schema. Actual content is defined by your project specifications.

CategoryExample Fields
Identifierspatient_id, specimen_id, slide_id
PathologyWSI file, histology, tumor grade
Clinicaldiagnosis, TNM stage, laboratory values
Imagingmodality, image_id, acquisition metadata
Molecularbiomarkers, mutations, expression data
Treatmenttreatment_type, treatment_start_date
Outcomesrecurrence, progression, survival
Follow-uplast_follow_up, censoring_status

Illustrative data structure only. Actual dataset content, eligible patient counts, completeness, and commercial licensing are determined through feasibility assessment.

Retrospective & Prospective
Data Collection

Two sourcing models for custom oncology datasets.

Retrospective Collection

Potential assessment of existing hospital archives and records:

  • Archived pathology material
  • Existing hospital records
  • Historical diagnostic imaging
  • Treatment histories
  • Recorded follow-up
  • Available outcome data
  • Digitization and abstraction requirements

Prospective Collection

Potential organization of buyer-defined protocols:

  • Inclusion/exclusion criteria
  • Clinical data collection
  • Pathology and image acquisition
  • Structured metadata
  • Medical specialist involvement
  • Quality assurance
  • Follow-up procedures

Long-term survival data generally require existing longitudinal records or future follow-up periods. Immediate delivery of outcomes requiring years of observation should not be assumed.

Custom Sourcing Process

From requirements to delivery in five steps.

01

Define

Cancer indication, cohort size, data modalities, clinical endpoints, inclusion criteria, delivery format, geography, and intended AI use.

02

Feasibility

Evaluate potential Ukrainian hospital and laboratory sources, case availability, completeness, technical specifications, and timelines.

03

Governance

Review data permissions, legal requirements, de-identification, privacy, commercial AI training rights, and contractual restrictions.

04

Collection

Where feasible and authorized, coordinate collection, digitization, clinical abstraction, linkage, normalization, annotation, and quality control.

05

Delivery

Validate accepted data against agreed specifications and coordinate secure delivery and documentation.

Clinical Data Governance

Data governance and licensing requirements are evaluated and documented for each specific project. De-identification alone does not establish commercial licensing rights.

Legal Basis & Consent

Applicable consent, legal basis and healthcare source permissions verified for each data source and intended use.

Privacy & Regulation

Ukrainian privacy and health-data regulations, HIPAA and GDPR considerations where applicable.

De-Identification

De-identification and privacy safeguards applied according to project requirements and regulatory standards.

Commercial AI Rights

Commercial AI-training rights assessed and documented per project. Access to data does not automatically create usage rights.

Secure Transfer

Secure data transfer methods and data-use agreements structured for each delivery.

Quality & Traceability

Quality assurance, source verification and dataset traceability documented throughout the sourcing process.

Frequently Asked Questions

Can REMI Data source oncology datasets across different cancer indications?
REMI Data evaluates buyer-defined sourcing requirements across solid tumors, hematologic malignancies, and skin cancers. Potential sourcing configurations vary by diagnosis, required data modalities, available medical records, and clinical endpoints. Each project begins with a feasibility assessment through our Ukrainian institutional network.
Can pathology images be linked to clinical records and treatment outcomes?
Patient-level linkage of pathology, clinical records, treatment and outcomes is a core capability we evaluate for each project. Linkage feasibility, completeness and data availability depend on the specific institutions, cancer type and requested clinical endpoints.
Can datasets include molecular, imaging, and clinical modalities?
Multimodal datasets combining pathology, medical imaging, clinical records, molecular data, treatment histories and outcomes can be explored. Actual availability of each modality depends on the specific institutions, patient populations and data systems involved.
Does REMI support retrospective and prospective collection?
Both models are supported. Retrospective collection draws on archived hospital records, pathology materials and imaging. Prospective collection organizes new data capture under buyer-defined protocols. Long-term survival data generally require existing longitudinal records or future follow-up periods.
How is patient-level data linkage evaluated?
Linkage feasibility is assessed for each requested cohort based on the institution's record systems, patient identifiers, data completeness and available modalities. Complete multimodal linkage is not guaranteed for every case — missingness and completeness are reported as part of the feasibility assessment.
How is eligible cohort availability established?
After receiving buyer specifications, REMI evaluates potential Ukrainian hospital and laboratory sources against the requested cancer indication, cohort size, data modalities, clinical endpoints and inclusion criteria. Feasibility findings are reported before any collection commitment.
Can the data be used for commercial AI training?
Commercial AI-training rights are assessed and documented for each specific project. REMI does not assume that access to clinical data or de-identification alone establishes commercial licensing rights. Rights, consent and legal basis are verified with each data source.
How does a custom oncology sourcing project begin?
Contact REMI Data with your cancer indication, required data modalities, target cohort size, clinical endpoints and intended AI application. We evaluate source feasibility, provide a structured assessment, and proceed to collection only after agreement on scope, governance and commercial terms.

Tell Us About Your Oncology
Dataset Requirements

Whether you're developing a digital pathology model, multimodal oncology AI system, diagnostic algorithm, or clinical outcome prediction model, REMI Data can review your requirements and evaluate potential sourcing options through Ukrainian medical providers.

Request a Dataset Feasibility Assessment