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在接受基于伊沙佐米治疗的复发/难治性多发性骨髓瘤患者中(AGMT MM 1,II期试验),口腔微生物群的α多样性降低与无进展生存期缩短相关。

Reduced alpha diversity of the oral microbiome correlates with short progression-free survival in patients with relapsed/refractory multiple myeloma treated with ixazomib-based therapy (AGMT MM 1, phase II trial).

作者信息

Ludwig Heinz, Hausmann Bela, Schreder Martin, Pönisch Wolfram, Zojer Niklas, Knop Stefan, Gunsilius Eberhard, Egle Alexander, Petzer Andreas, Einsele Hermann, Hajek Roman, Weisel Katja, Krenosz Karl Jochen, Lang Alois, Lechner Daniel, Greil Richard, Berry David

机构信息

Wilhelminen Cancer Research Institute Vienna Austria.

Joint Microbiome Facility (JMF) Medical University of Vienna & University of Vienna Vienna Austria.

出版信息

EJHaem. 2020 Nov 8;2(1):99-103. doi: 10.1002/jha2.130. eCollection 2021 Feb.

Abstract

Alterations in the human microbiome have been linked to several malignant diseases. Here, we investigated the oral microbiome of 79 patients with relapsed/refractory multiple myeloma (MM) treated with ixazomib-thalidomide-dexamethasone. Increased alpha diversity (Shannon index) at the phylum level was associated with longer progression-free survival (PFS) (10.2 vs 8.5 months,  = .04), particularly in patients with very long (>75% quartile) PFS . Additionally, alpha diversity was lower in patients with progressive disease ( < .05). These findings suggest an interrelationship between the oral microbiome and outcome in patients with MM and encourage a novel direction for diagnostic and/or therapeutic strategies.

摘要

人类微生物组的改变已与多种恶性疾病相关联。在此,我们调查了79例接受伊沙佐米-沙利度胺-地塞米松治疗的复发/难治性多发性骨髓瘤(MM)患者的口腔微生物组。门水平上α多样性(香农指数)增加与更长的无进展生存期(PFS)相关(10.2个月对8.5个月,P = 0.04),特别是在PFS非常长(>四分位数75%)的患者中。此外,疾病进展患者的α多样性较低(P < 0.05)。这些发现表明MM患者口腔微生物组与预后之间存在相互关系,并为诊断和/或治疗策略开辟了新方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9a/9176146/59125be92231/JHA2-2-99-g001.jpg

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