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Burden of hospitalization in acute lymphoblastic leukemia patients treated with Inotuzumab Ozogamicin versus standard chemotherapy treatment

Authors :
Yun Su
Matthias Stelljes
Verna L Welch
David I. Marks
Fausto R. Loberiza
Ilse van Oostrum
Sabrina Mueller
Sarah Böhme
Erik Vandendries
Hagop M. Kantarjian
Source :
Cancer Medicine, Vol 8, Iss 13, Pp 5959-5968 (2019), Cancer Medicine
Publication Year :
2019
Publisher :
Wiley, 2019.

Abstract

Background Inotuzumab Ozogamicin (INO), has demonstrated an improvement in overall survival, high rate of complete remission, favorable patient‐reported outcomes, and manageable safety profile vs standard of care (SoC; intensive chemotherapy) for relapsed/refractory (R/R) acute lymphoblastic leukemia (ALL) in the phase 3 INO‐VATE trial. With a one‐hour weekly dosing schedule, INO might be associated with lower healthcare system burden. This study analyses hospitalizations for INO vs SoC. Methods All patients receiving study treatment in the INO‐VATE trial were included. The days hospitalized during study treatment was calculated. Due to different treatment durations for INO and SoC (median of 3 vs 1 cycles), number of hospital days was mainly reported per observed patient month. Hospital days per patient month were analyzed for different treatment cycles, subgroups, and main reasons for hospitalization. Differences between treatments were analyzed by the incidence rate ratio (IRR). Results Overall, 82.9% and 94.4% INO and SoC patients experienced at least one hospitalization. The mean hospitalization days per patient month was 7.6 and 18.4 days for INO and SoC (IRR = 0.413, P<br />Compared to current standard of care (intensive chemotherapy), Inotuzumab Ozogamicin reduces the hospitalization burden in relapsed/refractory acute lymphoblastic leukemia patients. It is likely this lower burden has a favorable impact on the quality of life of patients, healthcare budgets, and cost‐effectiveness considerations.

Details

ISSN :
20457634
Volume :
8
Database :
OpenAIRE
Journal :
Cancer Medicine
Accession number :
edsair.doi.dedup.....ddee571e623e6a72887ef1351df4f2ee