Primary outcomes by 1q21+ status for isatuximab-treated patients with relapsed/refractory multiple myeloma: subgroup analyses from ICARIA-MM and IKEMA
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064165%3A_____%2F22%3A10456134" target="_blank" >RIV/00064165:_____/22:10456134 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11110/22:10456134
Výsledek na webu
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=eEcG.QFRcw" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=eEcG.QFRcw</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3324/haematol.2022.280660" target="_blank" >10.3324/haematol.2022.280660</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Primary outcomes by 1q21+ status for isatuximab-treated patients with relapsed/refractory multiple myeloma: subgroup analyses from ICARIA-MM and IKEMA
Popis výsledku v původním jazyce
Gain/amplification of 1q21, referred to as 1q21+ in this letter, is one of the most common chromosomal abnormalities in multiple myeloma (MM), being detected in approximately 40% of patients at diagnosis. The number of MM cells with 1q21+ and the number of copies of 1q21+ increases as the disease progresses. Furthermore, its negative impact on prognosis suggests that 1q21+ is involved in the pathophysiology of disease progression and resistance to MM treatment. The 1q21+ abnormality is defined as gain of 1q21 (gain[1q21], 3 copies) and amplification of 1q21 (amp[1q21], >=4 copies). Co-existence of certain high-risk chromosomal abnormalities is common and further worsens the prognosis for patients with 1q21+. In the phase III studies ICARIA-MM and IKEMA, the addition of the anti-CD38 monoclonal antibody isatuximab (Isa) to the backbone of pomalidomide-dexamethasone (Pd) or carfilzomib-dexamethasone (Kd), respectively, improved progression-free survival (PFS) among patients with relapsed/refractory MM, and subgroup analyses suggested benefit among patients with 1q21+. The current analyses examine four subgroups of patients from ICARIA-MM and IKEMA: 1q21+ (>=3 copies with or without high-risk chromosomal abnormalities), isolated 1q21+ (>=3 copies without high-risk chromosomal abnormalities), gain(1q21) (3 copies with or without high-risk chromosomal abnormalities), and amp(1q21) (>=4 copies with or without high-risk chromosomal abnormalities). The analyses show a clear benefit of Isa-based combinations in 1q21+ disease.
Název v anglickém jazyce
Primary outcomes by 1q21+ status for isatuximab-treated patients with relapsed/refractory multiple myeloma: subgroup analyses from ICARIA-MM and IKEMA
Popis výsledku anglicky
Gain/amplification of 1q21, referred to as 1q21+ in this letter, is one of the most common chromosomal abnormalities in multiple myeloma (MM), being detected in approximately 40% of patients at diagnosis. The number of MM cells with 1q21+ and the number of copies of 1q21+ increases as the disease progresses. Furthermore, its negative impact on prognosis suggests that 1q21+ is involved in the pathophysiology of disease progression and resistance to MM treatment. The 1q21+ abnormality is defined as gain of 1q21 (gain[1q21], 3 copies) and amplification of 1q21 (amp[1q21], >=4 copies). Co-existence of certain high-risk chromosomal abnormalities is common and further worsens the prognosis for patients with 1q21+. In the phase III studies ICARIA-MM and IKEMA, the addition of the anti-CD38 monoclonal antibody isatuximab (Isa) to the backbone of pomalidomide-dexamethasone (Pd) or carfilzomib-dexamethasone (Kd), respectively, improved progression-free survival (PFS) among patients with relapsed/refractory MM, and subgroup analyses suggested benefit among patients with 1q21+. The current analyses examine four subgroups of patients from ICARIA-MM and IKEMA: 1q21+ (>=3 copies with or without high-risk chromosomal abnormalities), isolated 1q21+ (>=3 copies without high-risk chromosomal abnormalities), gain(1q21) (3 copies with or without high-risk chromosomal abnormalities), and amp(1q21) (>=4 copies with or without high-risk chromosomal abnormalities). The analyses show a clear benefit of Isa-based combinations in 1q21+ disease.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30205 - Hematology
Návaznosti výsledku
Projekt
—
Návaznosti
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Ostatní
Rok uplatnění
2022
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Haematologica
ISSN
0390-6078
e-ISSN
1592-8721
Svazek periodika
107
Číslo periodika v rámci svazku
10
Stát vydavatele periodika
IT - Italská republika
Počet stran výsledku
7
Strana od-do
2485-2491
Kód UT WoS článku
000870533100022
EID výsledku v databázi Scopus
2-s2.0-85139536296