Personalized Reimbursement Model (PRM) program: A real-world data platform of cancer drugs use to improve and personalize drug pricing and reimbursement in France

PLoS One. 2022 Apr 19;17(4):e0267242. doi: 10.1371/journal.pone.0267242. eCollection 2022.

Abstract

Objective: This article describes the Personalized Reimbursement Model (PRM) program methodology, limitations, achievement and perspectives in using real-world data of cancer drugs use to improve and personalize drug pricing and reimbursement in France.

Materials and methods: PRM platform aggregates Electronic Pharmacy Records (EPR) data from French medical centers (PRM centers) to build retrospective cohorts of patients treated with injectable cancer drugs in a hospital setting. Data extracted on January 1st, 2020, from breast cancer (BC) patients who received trastuzumab, trastuzumab emtansin or pertuzumab since January 1st, 2011, and from lung cancer (LC) patients who received bevacizumab or atezolizumab since January 1st, 2015, enabled recovering their injectable cancer drugs history from diagnosis date until December 30th, 2019, and served as dataset for assessment.

Results: 123 PRM centers provided data from 30,730 patients (25,660 BC and 5,070 LC patients respectively). Overall, 20,942 (82%) of BC and 4,716 (93%) of LC patients were analyzed. Completion rate was above 98% for patients characteristics, diagnostic and treatment related data. PRM centers cover 48% and 33% of BC and LC patients in-hospital therapeutic management in France, respectively. Distribution of BC and LC patients therapeutic management, by medical center category and geographic location, was similar in PRM centers to all French medical centers, ensuring the representativeness of the PRM platform.

Conclusion: PRM Platform enabled building a national database generating on demand Real-World Evidence based on EPR. This enabled the first performance-based risk-sharing arrangements based on PRM data, between the CEPS and Roche, for atezolizumab cancer immunotherapy in metastatic non-small cell lung cancer indication.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents* / therapeutic use
  • Breast Neoplasms* / drug therapy
  • Breast Neoplasms* / pathology
  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • Drug Costs
  • Female
  • France
  • Humans
  • Lung Neoplasms* / drug therapy
  • Retrospective Studies
  • Trastuzumab / therapeutic use

Substances

  • Antineoplastic Agents
  • Trastuzumab

Grants and funding

PA. Squara was employed by Roche France SAS. VP. Luu is employed by Roche France SAS. D. Pérol received grants and non-financial support from Roche France SAS during the conduct of the study; personal fees from Roche France SAS, Pierre Fabre, Novartis, Bristol-Myers Squibb Co., Eli-Lilly, Ipsen, Takeda and MSD outside the submitted work; personal fees and non-financial support from AstraZeneca; and grants from MSD Avenir and Roche France SAS outside the submitted work. B. Coudert received fees from Roche France SAS during the conduct of the study and personal fees from Roche France SAS, Bristol-Myers Squibb Co. and AstraZeneca outside the submitted work. V. Machuron is employed by Roche France SAS. C. Bachot is employed by Roche France SAS. L. Samelson is employed by Roche France SAS. V. Florentin is employed by Roche France SAS. JM. Pinguet is employed by Roche France SAS. B. Ben Hadj Yahia is employed by Roche France SAS. This study was designed and conducted by Roche France SAS in collaboration with the French oncology healthcare ecosystem. This does not alter our adherence to PLOS ONE policies.