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Adam D. Cohen

Abramson Cancer Center
H指数:63
被引数:1.8万

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Author Correction: FcRH5×CD3 bispecific antibody cevostamab in relapsed or refractory multiple myeloma: a phase 1 trial

作者更正:FcRH5×CD3 双特异性抗体 cevostamab 在复发或难治性多发性骨髓瘤中的研究:一项1期临床试验

2026-10-200
OAAI
FcRH5×CD3 bispecific antibody cevostamab in relapsed or refractory multiple myeloma: a phase 1 trial

FcRH5×CD3双特异性抗体塞沃司单抗在复发或难治性多发性骨髓瘤中的应用:一项I期临床试验

2026-07-220
OAAI
Investigating Associations Between Psychological Distress and Changes in Peripheral Blood Monocytes in Patients With CLL/SLL Managed With Active Surveillance

探究心理困扰与接受主动监测的CLL/SLL患者外周血单核细胞变化之间的关联

2026-05-150
OAAI
CD4+ T cells mediate CAR-T cell-associated immune-related adverse events after BCMA CAR-T cell therapy

CD4 T细胞介导BCMA car-t细胞治疗后car-t细胞相关的免疫相关不良事件

2026-01-150
PRE
Outcomes of relapse after teclistamab therapy in multiple myeloma

接受特昔利珠单抗治疗后多发性骨髓瘤复发的结局

2025-11-050
OAAI
Trial in Progress (TiP): Interim analysis of a Phase 2 study of BPM31510 (a lipid nanodispersion of oxidized CoQ10) with Vitamin K in combination with Standard of Care (SOC) RT and TMZ in Glioblastoma Multiforme (GBM) patients without prior therapy

进行中试验(TiP):一项关于BPM31510(氧化辅酶Q10的脂质纳米分散体)联合维生素K,与标准护理(SOC)放疗(RT)和替莫唑胺(TMZ)联用治疗未经前期治疗的胶质母细胞瘤(GBM)患者的II期研究的期中分析

2025-11-010
OAAI
Efficacy and Safety of Anti-CDI9 and Anti-BCMA Chimeric Antigen Receptor (CAR) T-Cell Therapies in Patients with Autoimmune Disease and Lymphoma or Myeloma

抗CDI9和抗BCMA嵌合抗原受体(CAR)T细胞疗法在自身免疫性疾病、淋巴瘤或骨髓瘤患者中的疗效与安全性

BLOOD
IF23.1
2024-11-050
PRE
Tasquinimod, an S100A9 Inhibitor, in Combination with Ixazomib, Lenalidomide, and Dexamethasone for Relapsed and Refractory Multiple Myeloma

Tasquinimod,一种S100A9抑制剂,与伊沙佐米、来那度胺和地塞米松联合用于复发性和难治性多发性骨髓瘤。

BLOOD
IF23.1
2024-11-050
PRE
T cell lymphoma and secondary primary malignancy risk after commercial CAR T cell therapy

商业CAR T细胞治疗后T细胞淋巴瘤和继发性原发性恶性肿瘤风险

2024-01-2481
PRE
Health-related quality of life in patients given ciltacabtagene autoleucel for relapsed or refractory multiple myeloma (CARTITUDE-1): a phase 1b-2, open-label study
2022-12-0121
PRE