Day 14 Bone Marrow Biopsy in Acute Myeloid Leukemia Induction: The End of Story or Not Yet?

IF 2.7 4区 医学 Q3 ONCOLOGY
Technology in Cancer Research & Treatment Pub Date : 2026-01-01 Epub Date: 2026-03-08 DOI:10.1177/15330338261429620
Mostafa F Mohammed Saleh, Abdulrahman Nasiri, Ahmed Abdrabou, Ali Alahmari, Syed O Ahmed, Ayman Saad, Mahmoud Aljurf
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引用次数: 0

Abstract

The Day 14 bone marrow biopsy (D14 BMB) has historically been a key tool for early treatment response assessment in acute myeloid leukemia (AML), particularly following intensive chemotherapy. Traditionally, a blast count of <5% at D14 is associated with higher complete remission (CR) rates and improved overall survival (OS), while persistent disease often prompts re-induction therapy. However, emerging evidence suggests that while re-induction may increase CR rates, it does not consistently improve OS and is associated with significant morbidity. With the emergence of venetoclax-based and other targeted therapies, the traditional role of D14 BMB is being reconsidered, as these agents exhibit slower response kinetics, making later assessments and measurable residual disease (MRD) monitoring more reliable for treatment adaptation. This review critically examines the prognostic utility of D14 BMB in AML, its relevance across different treatment modalities, and its correlation with long-term outcomes. By synthesizing current evidence, we explore whether D14 BMB remains a valuable clinical tool or if a paradigm shift toward later assessments and MRD-guided decision-making is warranted in modern AML therapy.

Abstract Image

急性髓系白血病诱导的第14天骨髓活检:故事还没有结束吗?
第14天骨髓活检(D14 BMB)历来是急性髓性白血病(AML)早期治疗反应评估的关键工具,特别是在强化化疗后。传统上,爆炸计数为
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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
202
审稿时长
2 months
期刊介绍: Technology in Cancer Research & Treatment (TCRT) is a JCR-ranked, broad-spectrum, open access, peer-reviewed publication whose aim is to provide researchers and clinicians with a platform to share and discuss developments in the prevention, diagnosis, treatment, and monitoring of cancer.
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