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Availability and Accessibility of Biomolecular Technologies in Oncology

ESMO-Surevy-Availability-Accessibility-Biomolecular-technologies-1000x250

ESMO is committed to ensuring the timely and optimal treatment of cancer patients, which includes the usage of biomolecular technologies.

These technologies, which include biomarkers, are extremely important in the treatment of patients with cancer, but there is very little data regarding their availability, use or costs and reimbursement, so ESMO has decided to conduct a study on this important topic, first in Europe and subsequently globally.

Study objectives

The ESMO Study on Availability and Accessibility to Biomolecular Technologies in Oncology seeks to provide a comprehensive overview of availability of biomolecular technologies to patients, the status of their use and prescription, barriers to access, and potential economic issues related to cost and reimbursement.

The questions draw upon, among others, the Recommendations for the use of next-generation sequencing (NGS) for patients with metastatic cancers presented in a report from the ESMO Translational Research and Precision Medicine Working Group.

Open Peer Review

The preliminary survey data for Europe is open for peer review, after which feedback will be incorporated into the final manuscript for publication.

To participate click here. The deadline to submit your review is 20 June 2022.        

Methodology

The data was reported by oncologists, biologists and pathologists working in the field, and not from state authorities or statutory bodies. Reporters were asked to consult with health economists and/or regulatory authorities in circumstances in which they are unsure of an issue, for example, the cost of the testing to patients, barriers to access, or national regulations on biomolecular testing. The accuracy of the data depends on the reporting accuracy of country reporters and their due diligence in the verification of facts. Country reporters were nominated based on their recognised involvement in oncology practice, their involvement in their national professional society, and, in many cases, their leadership positions in their country.

The methodology used in this study incorporates measures to minimise error through the use of multiple reporters, cross-checks between reporter data, and a process of open peer review of the data collected.

Coordinating partners

This ESMO study was conducted under the auspices of the ESMO Global Policy Committee in collaboration with the Cancer Medicines Committee and the National Societies Committee with the following collaborating partners:

National Societies

Albanian Oncology Association Logo

Albanian Oncology Association

Croatia, Hrvatsko Društvo za internističku onkologiju (Croatian Society of Medical Oncology)

Deutsche Gesellschaft für Hämatologie und Medizinische Onkologie e. V. (German Society for Haematology and Medical Oncology)

Hellenic Society of Medical Oncology

Lithuania, Lietuvos Chemoterapeutᶙ draugija (Lithuanian Society for Medical Oncology)

Société Luxembourgeoise d'Oncologie (Luxembourg Society of Oncology)

Poland, Polskie Towarzystwo Onkologii Klinicznej, (Polish Society of Clinical Oncology)

Sociedade Portuguesa De Oncologia (Portuguese Society of Oncology)

Russian Society of Clinical Oncology (RUSSCO)

Udruzenje medikalnih onkologa Srbije (Serbian Society of Medical Oncology)

Slovenská onkologická spoločnosť (Slovak Oncology Society)

Medical Oncology Section within Slovenian Medical Association

Sociedad Española de Oncología Médica (Spanish Society of Medical Oncology)

Svensk Onkologisk Förening (Swedish Society of Oncology)

Association of Cancer Physicians (ACP)

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