International Journal of Chemotherapy Research and Practice

International Journal of Chemotherapy Research and Practice

International Journal of Chemotherapy Research and Practice – Data Archiving Permissions

Open Access & Peer-Reviewed

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Data Stewardship

Data Archiving Permissions

Responsible data sharing for oncology research

IJCP supports open science and encourages authors to share data that improve reproducibility and enable secondary analyses in chemotherapy research.

We recognize that clinical and genetic datasets may be sensitive. Our policies balance accessibility with privacy, consent, and legal requirements.

Clear data archiving strengthens the evidence base for oncology care and enables validation of key findings.

Data Availability Requirements

All submissions must include a Data Availability Statement describing where underlying data can be accessed and any restrictions that apply. Statements should be specific enough for readers to understand the access process.

Acceptable options include public repository deposit, controlled access repositories, availability upon reasonable request, or restricted availability due to consent or legal limitations.

Authors are encouraged to share code, protocols, and analysis scripts when possible. Clear documentation improves reproducibility and supports reanalysis by other investigators.

When data are sensitive, consider sharing de identified or aggregated datasets that preserve privacy while still supporting validation of results.

Where possible, assign DOIs to datasets so they can be cited and tracked alongside the article.

Include repository access instructions and any data use agreements in the availability statement.

If embargoes apply, specify the timeline and rationale. Data statements should clarify licensing terms and any restrictions on reuse.

For proprietary datasets, describe the rationale for restrictions and provide a clear process for qualified researchers to request access under appropriate agreements.

Data availability statements should align with funder requirements and institutional policies when applicable.

When controlled access is required, provide the name of the repository, access criteria, and expected response timelines for requests.

Public Repositories

For non sensitive datasets, deposit in established repositories such as Dryad, Figshare, Zenodo, or relevant domain databases. These provide DOIs, version control, and preservation.

Controlled Access

Sensitive data should be placed in managed repositories with access review processes that protect participants while enabling qualified research use.

Available Upon Request

When deposit is not feasible, authors may provide data to qualified researchers upon reasonable request with clear conditions.

Restricted Data

If data cannot be shared, explain why and consider whether anonymized or aggregated data can be provided.

Self Archiving

Authors may share accepted and published versions in institutional repositories and on personal websites with proper citation.

Data Citation

Cite datasets in the reference list when possible to give credit and improve transparency.

Study Type Expectations

01

Clinical Trials

Follow ICMJE requirements and share datasets in line with consent and regulatory rules. Include trial registration details in the manuscript.

02

Omics and Genomics

Deposit sequence data in appropriate archives with accession numbers and metadata for reuse.

03

Epidemiology

Share de identified datasets or aggregated data where possible to support replication and modeling.

04

Qualitative Studies

Explain restrictions and provide supporting materials when full data cannot be shared, such as interview guides.

05

Preclinical Studies

Share protocols, code, and key datasets that enable replication across laboratories.

06

Imaging Data

Share imaging protocols and metadata when feasible to enable comparison across studies and platforms.

Archiving and Preservation

Long term accessibility depends on repository quality and documentation.

Controlled
Managed Access
Secure
Qualified use
Protected
Limited
Upon Request
Restricted
By approval
Case by case

Data Integrity Notes

🔐

De Identification

Remove direct identifiers and reduce indirect identifiers to protect participants and comply with regulations.

Consent

Ensure data sharing aligns with participant consent and ethics approvals across sites.

📄

Documentation

Provide codebooks, variable definitions, and processing notes for transparency.

📦

Preservation

Use repositories that commit to long term access and version control for reuse.

Transparent Data Builds Trust

Clear data policies improve reproducibility and strengthen the clinical impact of chemotherapy research. Responsible sharing enables secondary analyses that can improve care and inform policy while protecting patient privacy. Data citation also increases recognition for shared resources and supports reuse tracking across platforms. Transparent archiving supports funder compliance and long term access, and improves trust in results and synthesis. Clear archiving shortens reviewer questions and improves reuse.

Questions About Data Sharing?

We can advise on repository selection and data availability statements.

[email protected]

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Publish with transparent data policies and open access visibility.