AI Article Synopsis

  • Clinical trials select patients based on specific eligibility criteria, while disease registries, like the Danish Metastatic Melanoma Database (DAMMED), gather real-world data to evaluate the effectiveness and safety of oncology medicines in broader patient groups.
  • The DAMMED database registered over 4,156 patients and 7,420 treatment regimens for advanced melanoma, enabling comparisons of patient response rates and survival data between clinical trials and real-world outcomes.
  • Overall, the findings emphasize that nationwide disease registries can enhance clinical practice and support health technology assessments, highlighting both the similarities and disparities with clinical trial data.

Article Abstract

Background: Clinical trials enroll patients with specific diseases based on certain pre-defined eligibility criteria. Disease registries are crucial to evaluate the efficacy and safety of new expensive oncology medicines in broad non-trial patient populations.

Methods: We provide detailed information on the structure, including variables, and the scientific results from a nation-wide Danish database covering advanced melanoma, illustrating the importance of continuous real-world data registration. Disease status and treatment-related information on all patients with American Joint Committee on Cancer (AJCC) 8th edition stage III or IV melanoma candidates to medical treatment in Denmark are prospectively registered in the Danish Metastatic Melanoma Database (DAMMED).

Results: By January 1st, 2021, DAMMED includes 4156 patients and 7420 treatment regimens. Response rates and survival data from published randomized clinical trial data are compared with real-world efficacy data from DAMMED and presented. Overall, nine independent manuscripts highlighting similarities and discrepancies between real-world and clinical trial results are already reported to date.

Conclusion: Nation-wide disease registries take into consideration the complexity of daily clinical practice. We show a concrete example of how disease registries can complement clinical trials' information, improving clinical practice, and support health-related technology assessment.

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Source
http://dx.doi.org/10.1016/j.canep.2021.101943DOI Listing

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