Improved efficiency of daratumumab treatment of multiple myeloma adopting the subcutaneous route: A micro‐costing analysis in three Italian hematology centers

Author:

Pradelli Lorenzo1ORCID,Massaia Massimo2,Todisco Elisabetta3,Gherlinzoni Filippo4,Furlan Anna4ORCID,La Targia Maria3,Grande Elisabetta2,Tripoli Ignazio Ezio2,Occhipinti Francesca3,Comello Francesco4,Iannello Fabrizio5,Bellucci Stefania5

Affiliation:

1. AdRes HE&OR Torino Italy

2. S.C. Ematologia A.O. Santa Croce e Carle Cuneo Italy

3. U.O. Ematologia ASST Valle Olona Busto Arsizio Busto Arsizio Italy

4. Divisione di Ematologia Ospedale Cà Foncello di Treviso–ASL 2 Treviso Italy

5. Janssen‐Cilag SpA Cologno Monzese Italy

Abstract

AbstractBackgroundDaratumumab is a humanized monoclonal antibody approved for the treatment of adult patients with newly diagnosed or relapsed/refractory multiple myeloma (RRMM). Subcutaneous (SC) formulation proved to be non‐inferior in comparison with intravenous (IV) administration route. This study aimed at assessing the economic and time impact associated with the use of SC versus IV daratumumab in patients with RRMM from the perspective of the hematology center.MethodsThis was a 5‐month multicenter time‐and‐motion cross‐sectional micro‐costing study conducted in three Italian hematology centers among adult patients diagnosed with RRMM with ongoing treatment with IV or SC daratumumab. Measurements were performed by an ad hoc App.ResultsNineteen (20%) IV and 76 (80%) SC administration procedures were measured. Patients spent a mean of 4.85 ± 0.91 or 1.08 ± 0.56 h in the hematology center to receive IV or SC daratumumab, respectively. Healthcare professionals (HCPs) spent a mean of 49.38 ± 16.13 and 20.37 ± 7.88 min of active working time to manage IV and SC administrations, respectively. The infusion chair was occupied for a mean of 4.85 ± 0.91 and 0.99 ± 0.55 h during IV or SC administration, respectively. On average, considering the costs due to HCP and chair time, materials, and overhead costs, every IV and SC administration costed €80.33 and 34.90, respectively.ConclusionsIn conclusion, as compared with IV administration, SC daratumumab was associated with 78%, 59%, 80% savings in terms of patient time, HCP active working time, and infusion chair, respectively, and 56.6% budget savings.

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

Reference32 articles.

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2. European Medicines Agency.Darzalex. Summary of product characteristics.2022. Accessed March 14 2023https://www.ema.europa.eu/en/documents/product‐information/darzalex‐epar‐product‐information_en.pdf

3. Final analysis of the phase III non-inferiority COLUMBA study of subcutaneous versus intravenous daratumumab in patients with relapsed or refractory multiple myeloma

4. Subcutaneous versus intravenous daratumumab in patients with relapsed or refractory multiple myeloma (COLUMBA): a multicentre, open-label, non-inferiority, randomised, phase 3 trial

5. Humanistic and economic impact of subcutaneous versus intravenous administration of oncology biologics

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