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David A. Sallman

h lee moffitt cancer center
H指数:46
被引数:9,121

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Oral Azacitidine Maintenance After CPX-351 in Transplant-Ineligible Patients With Therapy-Related or Myelodysplasia-Related Acute Myeloid Leukemia

在移植不适宜的继发性或骨髓增生异常综合征相关急性髓系白血病患者中,CPX-351治疗后口服阿扎胞苷维持治疗

2026-10-120
OAAI
Correction: spatial remodeling of bone marrow architecture defines tissue-state signatures of disease activity and therapeutic response in myelodysplastic neoplasms

更正:骨髓空间结构的重塑定义了骨髓增生异常性肿瘤中疾病活动性和治疗反应的组织状态特征

Leukemia
IF13.4
2026-10-070
OAAI
Phase 1 dose escalation and expansion trial of the bispecific CD47 inhibitor and CD40 agonist Fc-fusion protein SL-172154 (SIRPα-Fc-CD40L) in patients with higher-risk myelodysplastic syndrome or acute myeloid leukemia

I期剂量递增和扩展试验:双特异性CD47抑制剂和CD40激动剂Fc融合蛋白SL-172154(SIRPα-Fc-CD40L)在具有高风险骨髓增生异常综合征或急性髓系白血病患者中的应用

Cancer
IF5.1
2026-10-050
OAAI
Impact of Response to Hypomethylating Agent-Based Therapy on Survival Outcomes in the Context of Baseline Clinical-Molecular Risk and Transplant Status in Patients With Higher-Risk Myelodysplastic Syndromes/Neoplasms: An analysis From the International Consortium for MDS (icMDS)

基于低甲基化制剂治疗的反应对高风险骨髓增生异常综合征/肿瘤患者生存结局的影响:考虑基线临床-分子风险和移植状态的国际骨髓增生异常综合征联盟(icMDS)分析

2026-08-280
PRE
Spatial remodeling of bone marrow architecture defines tissue-state signatures of disease activity and therapeutic response in myelodysplastic neoplasms

骨髓空间结构重塑定义了骨髓增生异常综合征中疾病活动度和治疗反应的组织状态特征

Leukemia
IF13.4
2026-06-300
OA
Outcomes of patients with higher-risk myelodysplastic syndromes/neoplasms treated with hypomethylating agents + venetoclax—an analysis from the International Consortium for MDS (icMDS) VALIDATE database

高风险骨髓增生异常综合征/新生物患者接受去甲基化药物+维奈克拉治疗后的结局分析——国际骨髓增生异常综合征(icMDS)VALIDATE数据库分析

2026-06-290
OAAI
Prognostic Score for Myelodysplastic Syndromes Based on Molecular Evolution

基于分子演化的骨髓增生异常综合征预后评分

2026-05-262
PRE
Characterization of chromosome 5 aberrations in TP53 mutated myeloid neoplasms with ≥5% blasts: An International TP53 Investigators Network (iTiN) study

TP53突变髓系肿瘤中≥5%原始细胞染色体5异常的表征:一项国际TP53研究者网络(iTiN)研究

Cancer
IF5.1
2026-01-010
OAAI
Post-transplant MRD Monitoring by TP53 Duplex Sequencing with APR-246 + Azacitidine Maintenance Predicts Outcomes

移植后微小残留病(MRD)通过TP53双测序结合APR-246 + 去氧氟尿苷维持治疗预测预后

2025-11-270
OAAI
Downregulation of MICA/MICB improves cell persistence and clinical activity of NKG2DL CAR T-cells in patients with relapsed or refractory acute myeloid leukemia or myelodysplastic neoplasia

MICA/MICB的下调增强了NKG2DL CAR T细胞在复发或难治性急性髓系白血病或骨髓异常增生性肿瘤患者中的细胞持久性和临床活性。

Leukemia
IF13.4
2025-09-150
PRE
Hypomethylating Agent and Venetoclax Combination Is a Safe and Effective Alternative to Intensive Chemotherapy in Older (≥ 70 Years) Patients With Newly Diagnosed Favorable Risk Acute Myeloid Leukemia

去甲基化药物与Venetoclax联合方案是老年(≥70岁)新诊断低危急性髓系白血病患者接受强化化疗的安全有效替代方案。

2025-08-070
PREAI
XPO1 Drives Resistance to Eprenetapopt and Azacitidine and Can Be Targeted in TP53 Mutated Myeloid Malignancies

XPO1驱动对Eprenetapopt和Azacitidine的抵抗,并且可以在TP53突变的髓系恶性疾病中作为靶点

Blood
IF23.1
2025-08-050
PRE
Multiple TET2 mutations confer additional survival benefit in both myelodysplastic and myeloproliferative chronic myelomonocytic leukemia subtypes

多个TET2突变在骨髓增生异常和骨髓增生性慢性粒单核细胞白血病亚型中均带来额外的生存益处

Leukemia
IF13.4
2025-06-240
PRE
Pivotal results of SELECT-MDS-1 phase 3 study of tamibarotene with azacitidine in newly diagnosed higher-risk MDS

他米巴罗替与阿扎胞苷联合治疗新诊断高危骨髓增生异常综合征(MDS)的SELECT-MDS-1三期研究的关键结果

2025-05-090
OAAI