2022
DOI: 10.3324/haematol.2022.281398
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Daratumumab for treatment-refractory acquired idiopathic pure red cell aplasia

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Cited by 13 publications
(6 citation statements)
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References 9 publications
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“…11 Daratumumab demonstrated rapid and sustained response in treatment-refractory acquired idiopathic PRCA in a 74-year-old patient. 12 Daratumumab also successfully managed a patient of post-transplant PRCA with responses observed within 3 weeks. 13 Rituximab successfully managed two patients with PRCA secondary to CLL, and the patients became transfusion independent.…”
Section: Discussionmentioning
confidence: 97%
“…11 Daratumumab demonstrated rapid and sustained response in treatment-refractory acquired idiopathic PRCA in a 74-year-old patient. 12 Daratumumab also successfully managed a patient of post-transplant PRCA with responses observed within 3 weeks. 13 Rituximab successfully managed two patients with PRCA secondary to CLL, and the patients became transfusion independent.…”
Section: Discussionmentioning
confidence: 97%
“…In as many as 75% of CCS cases, the cytogenetic analysis revealed the reciprocal translocation t(12;22)(q13;q12) involving the EWSR1 gene and the ATF1 gene. 15,16 Four types of EWSR1/ ATF1 chimeric transcripts have been noted in CCS. 1,17 This translocation has not been described in malignant melanoma and, therefore, can help distinguish between the 2 diagnoses.…”
Section: Discussionmentioning
confidence: 99%
“…Daratumumab-mediated positive indirect antiglobulin test may persist for up to 6 months after the last daratumumab administration. Daratumumab bound to RBCs masks detection of antibodies to minor antigens in the patient's serum [see References (15)…”
Section: Interference With Serological Testingmentioning
confidence: 99%
“…З А К Л Ю Ч Е Н И Е Полученные данные, а также отдельные публи кации по данному вопросу дают основание судить о потенциальной безопасности и эф ф екти в ности даратумумаба в качестве терапии ПККА как у взрослых реципиентов ТГСК, так и у детей [2][3][4][5][14][15][16][17][18]. Предположения о механизме патоге неза ПККА у данной группы пациентов дают осно вания рассматривать возможность применения 112 КЛИНИЧЕСКИЕ НАБЛЮДЕНИЯ даратумумаба в первой линии терапии, что, безус ловно, заслуживает более предметного анализа [3,12].…”
Section: периферическая кровьunclassified
“…Возможные механизмы клеточного лизиса включают комплемент-и антителозависимую клеточно-опосре дованную цитотоксичность [16]. В профильных высо корейтинговых изданиях все чаще можно встретить описания клинических случаев эффективного приме нения даратумумаба в лечении ПККА у больных после ТГСК [2][3][4][5][15][16][17][18].…”
unclassified