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Poster session 17

1338P - Cost-effectiveness and direct impact analysis of clinical research in the clinical approach of metastatic renal cell carcinoma and neuroendocrine tumors in a large public Spanish university hospital

Date

10 Sep 2022

Session

Poster session 17

Topics

Clinical Research;  Cancer Care Equity Principles and Health Economics

Tumour Site

Renal Cell Cancer;  Neuroendocrine Neoplasms

Presenters

Silvia García-Garro

Citation

Annals of Oncology (2022) 33 (suppl_7): S600-S615. 10.1016/annonc/annonc1069

Authors

S. García-Garro1, P. Gajate Borau1, E. Gómez de Salazar2, T. Alonso Gordoa3, M.Á. Rodriguez Sagrado2, J. Molina Cerrillo4, L. Manzano Espinosa5, T. Bermejo Vicedo2, A. Carrato Mena3, J.J. Díez Gómez6, E. Grande Pulido7

Author affiliations

  • 1 Dept. Medical Oncology, Hospital Universitario Ramon y Cajal, 28031 - Madrid/ES
  • 2 Pharmacy Department, Hospital Universitario Ramon y Cajal, 28031 - Madrid/ES
  • 3 Medical Oncology Dept., Hospital Universitario Ramon y Cajal, 28031 - Madrid/ES
  • 4 Medica Oncology Department, Hospital Universitario Ramon y Cajal, 28031 - Madrid/ES
  • 5 Internal Medicine Department, Hospital Universitario Ramon y Cajal, 28031 - Madrid/ES
  • 6 Endocrinology Department, University Hospital Puerta de Hierro Majadahonda, 28222 - Majadahonda/ES
  • 7 Medical Oncology Department, MD Anderson Cancer Center Madrid, 28033 - Madrid/ES

Resources

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Abstract 1338P

Background

Clinical research leverages cancer patient care outcomes. We analyzed the direct impact of clinical trials (CTs) in terms of clinical outcomes and costs related expenses in patients with metastatic renal cell carcinoma (mRCC) and G1-G2 neuroendocrine tumors (mNETs) in the real-life setting.

Methods

Retrospectively, clinical data of the patients related to their baseline characteristics and the efficacy of the different lines of treatment were collected, as well as the direct healthcare costs of all patients diagnosed with mRCC or mNET and clinically followed by the Ramón y Cajal University Hospital Medical Oncology Service, in Madrid, Spain, between Jan 2010-Feb 2017. Subsequently, a comparative statistical analysis was performed of the results obtained in patients included in a CT vs. standard of care (SOC) patients.

Results

Of the 104 patients (65 mRCC and 39 mNET) included, 39 participated in a CT. Overall, the CT patients presented a higher overall survival (OS) than SOC patients (52 vs. 15 months. HR: 0.41; 95% CI: [0.23; 0.71]; p < 0.01). This survival improvement was consistent through all subgroups analyzed, including age, sex and prognostic factors. Regarding healthcare costs, patients who participated in CT yielded a mean annual savings of €46,109.56 per patient (p < 0.01) compared to patients treated according to SOC, mainly due to pharmacological savings (€27,406.42). Furthermore, the savings were identified in all subgroups regardless of age, sex and prognostic factors. Additionally, CT patients required 75.81% fewer hospitalisations (p < 0.01) with a lower associated mean cost (p = 0.02), and the mean annual cost corresponding to the use of the Emergency Service was also lower (p < 0.01). Finally, the unadjusted incremental cost-effectiveness ratio (ICER) was -€14,970.64 per year of life gained (YLG) and the adjusted ICER was -€42,656.11 per life saved.

Conclusions

The participation of patients with mRCC and NET in CTs is related to an improvement in OS and cost- savings. In short, the participation of cancer patients in CTs represents a cost-efficient therapeutic option for the national health system.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

P. Gajate Borau: Financial Interests, Institutional, Advisory Board: Bayer, Roche, Ipsen, Janssen, Eisai, Sanofi, Pfizer, Merk, MSD, Adacap, Astellas; Financial Interests, Institutional, Invited Speaker: Pfizer, BMS, Roche, Novartis, Janssen, Eisai, MSD, Ipsen, Adacap; Financial Interests, Institutional, Other, Travel expenses: Ipsen, Pfizer, Sanofi, Astellas, Janssen, Roche. T. Alonso Gordoa: Financial Interests, Personal, Advisory Board: Ipsen, Sanofi, Bayer, Eisai, Novartis Advanced Accelerator Applications, Lilly; Financial Interests, Personal, Invited Speaker: Pfizer, Roche, Janssen-Cilag; Financial Interests, Institutional, Advisory Board: Bristol Myers Squibb; Non-Financial Interests, , Project Lead: Pfizer, Ipsen. J. Molina Cerrillo: Financial Interests, Personal, Advisory Board: Ipsen, Janssen, BMS, Eisai; Financial Interests, Personal, Invited Speaker: Pfizer, AAA, Roche, Janssen; Financial Interests, Personal, Expert Testimony: Astellas; Financial Interests, Personal, Research Grant: Ipsen, Pfizer. A. Carrato Mena: Financial Interests, Institutional, Advisory Board: Merk, Roche, MSD, Pfizer, Bayer, Servier, Celgene, Amgen, Baxter; Financial Interests, Institutional, Research Grant: Celgene, Amgen, BMS. E. Grande Pulido: Financial Interests, Personal, Invited Speaker: Adacap, AstraZeneca, Bristol Myers Squibb, Eisai, Eusa Pharma, IPSEN, Janssen, Lilly, Merck KGa, Pfizer, Roche; Financial Interests, Personal, Advisory Board: Astellas, Bayer, MSD, Novartis, Sanofi-Genzyme; Financial Interests, Institutional, Advisory Board: Caris Life Sciences, ONCODNA (Biosequence); Financial Interests, Institutional, Research Grant, Independent research grant: Astellas, AstraZeneca, Lexicon, MTEM/Threshold, Nanostring Technologies, Pfizer, Roche, Merck; Financial Interests, Institutional, Invited Speaker, Independent research grant: Ipsen; Non-Financial Interests, , Other, AD board member: ENETS. All other authors have declared no conflicts of interest.

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