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Status: Bibliographieeintrag

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Verfasst von:Spencer, Andrew [VerfasserIn]   i
 Moreau, Philippe [VerfasserIn]   i
 Mateos, Maria-Victoria [VerfasserIn]   i
 Goldschmidt, Hartmut [VerfasserIn]   i
 Suzuki, Kenshi [VerfasserIn]   i
 Levin, Mark-David [VerfasserIn]   i
 Sonneveld, Pieter [VerfasserIn]   i
 Orlowski, Robert Z. [VerfasserIn]   i
 Yoon, Sung-Soo [VerfasserIn]   i
 Usmani, Saad Z. [VerfasserIn]   i
 Weisel, Katja [VerfasserIn]   i
 Reece, Donna [VerfasserIn]   i
 Ahmadi, Tahamtan [VerfasserIn]   i
 Pei, Huiling [VerfasserIn]   i
 Mayo, Wendy Garvin [VerfasserIn]   i
 Gai, Xue [VerfasserIn]   i
 Carey, Jodi [VerfasserIn]   i
 Bartlett, J. Blake [VerfasserIn]   i
 Carson, Robin [VerfasserIn]   i
 Dimopoulos, Meletios A. [VerfasserIn]   i
Titel:Daratumumab for patients with myeloma with early or late relapse after initial therapy
Titelzusatz:subgroup analysis of CASTOR and POLLUX
Verf.angabe:Andrew Spencer, Philippe Moreau, Maria-Victoria Mateos, Hartmut Goldschmidt, Kenshi Suzuki, Mark-David Levin, Pieter Sonneveld, Robert Z. Orlowski, Sung-Soo Yoon, Saad Z. Usmani, Katja Weisel, Donna Reece, Tahamtan Ahmadi, Huiling Pei, Wendy Garvin Mayo, Xue Gai, Jodi Carey, J. Blake Bartlett, Robin Carson, and Meletios A. Dimopoulos
E-Jahr:2024
Jahr:January 23 2024
Umfang:11 S.
Illustrationen:Illustrationen
Fussnoten:Vorab veröffentlicht: 4. Dezember 2023 ; Gesehen am 12.11.2024
Titel Quelle:Enthalten in: Blood advances
Ort Quelle:Washington, DC : American Society of Hematology, 2016
Jahr Quelle:2024
Band/Heft Quelle:8(2024), 2 vom: Jan., Seite 388-398
ISSN Quelle:2473-9537
Abstract:High-risk multiple myeloma (MM) is often defined based on cytogenetic abnormalities, but patients who relapse early after initial therapy are considered a functional high-risk group. In the phase 3 CASTOR and POLLUX studies, daratumumab plus bortezomib/dexamethasone (D-Vd) or lenalidomide/dexamethasone (D-Rd) improved progression-free survival (PFS) and overall survival (OS), regardless of cytogenetic risk, and achieved higher rates of complete response or better (≥CR) and minimal residual disease (MRD) negativity vs that with Vd/Rd alone in relapsed/refractory MM. Post hoc analyses of CASTOR and POLLUX evaluated patient subgroups with 1 prior line of therapy based on timing of progression/relapse (early or late) after initiation of first line of therapy. PFS consistently favored the daratumumab-containing regimens across subgroups using both a 24- and 18-month early-relapse cutoff. In the CASTOR/POLLUX pooled data set, daratumumab reduced the risk of disease progression or death by 65% (hazard ratio [HR], 0.35; 95% confidence interval [CI], 0.26-0.48; P < .0001) in the early-relapse (<24 months) subgroup and by 65% (HR, 0.35; 95% CI, 0.26-0.47; P < .0001) in the late-relapse (≥24 months) subgroup. OS also favored the daratumumab-containing regimens in both the early-relapse (HR, 0.62; 95% CI, 0.45-0.86; P = .0036) and late-relapse (HR, 0.67; 95% CI, 0.48-0.93; P = .0183) subgroups in the pooled population using a 24-month cutoff. Rates of ≥CR and MRD negativity (10−5) were higher with daratumumab vs control, regardless of progression/relapse timing. Although daratumumab is unable to fully overcome the adverse prognosis of early relapse, our results support the use of daratumumab for patients with 1 prior line of therapy, including for those who progress/relapse early after initial therapy and are considered to have functional high-risk MM. These trials were registered at www.clinicaltrials.gov as #NCT02136134 (CASTOR) and #NCT02076009 (POLLUX).
DOI:doi:10.1182/bloodadvances.2023010579
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1182/bloodadvances.2023010579
 DOI: https://doi.org/10.1182/bloodadvances.2023010579
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1908281707
Verknüpfungen:→ Zeitschrift

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