白血病研究が検査標準化の必要性を示す(Leukemia study highlights need to standardize testing)

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2026-09-15 バージニア工科大学(Virginia Tech)

Virginia TechのFralin Biomedical Research Instituteの記事は、がん治療後に体内に残る微小残存病変(MRD)を検出する検査を取り上げている。MRDは、画像診断などでは確認できないごく少量のがん細胞が残っている状態で、再発リスクや治療効果を評価する重要な指標となる。研究では、こうした微量の残存がんを検出できる高感度な検査手法の開発・評価を進め、治療後の患者をより精密にモニタリングすることを目指している。MRDを早期かつ正確に把握できれば、再発の兆候を早く捉え、患者ごとに治療方針を調整する個別化医療につながる可能性がある。一方、検査を実際の臨床に広く導入するには、検出精度や再現性、異なる患者・がん種への適用性などを検証する必要がある。なお、対象URLは現在403エラーで本文を直接取得できないため、具体的な検査方式については断定を避けた。

<関連情報>

急性骨髄性白血病の初回完全寛解期における移植前フローサイトメトリーで測定可能な残存疾患の予後予測値の現実世界における異質性:CIBMTR分析 Real-world heterogeneity in the prognostic value of pre-transplant flow cytometry measurable residual disease in acute myeloid leukemia in first complete remission: CIBMTR analysis

Jesse M. Tettero,Mei-Jie Zhang,Wentong Liu,Mariam T. Nawas,Filippo Milano,Nelli Bejanyan,Veronika Bachanova,Larisa Broglie,Wael Saber,Gege Gui,Laura W. Dillon,Roland B. Walter,Kristin M. Page,Christopher S. Hourigan,Firas El Chaer
Haematologica  Published: May 28, 2026
DOI:https://doi.org/10.3324/haematol.2026.300764

Abstract

In this real-world, large, observational study from the Center for International Blood and Marrow Transplant Research (CIBMTR), we examined the association between pre-transplant measurable residual disease (MRD) detected by multiparameter flow cytometry (MFC) test results and outcomes after allogeneic hematopoietic cell transplantation (alloHCT) in patients with acute myeloid leukemia (AML) in first complete remission (CR1). We included 2,544 patients who underwent transplant during 2013-2019; 11% had detectable MRD prior to alloHCT. Patients’ median age was 58 years. Among MRD-negative and MRD-positive groups, 48% vs 52% received myeloablative conditioning, and 37% vs 29% had matched unrelated donors, respectively. The 1-year cumulative incidence of relapse was 35% in the MRD-positive group and 25% in the MRD-negative group (P < .001). MRD positivity was associated with inferior overall survival (hazard ratio [HR], 1.27; 95% CI, 1.06-1.51; P = .009) and disease-free survival (HR, 1.31; 95% CI, 1.11-1.53; P = .001), and increased relapse risk (HR, 1.42; 95% CI, 1.17-1.72; P < .001), but not with non-relapse mortality. Notably, patients with pre-alloHCT MRD negativity remained at high risk of relapse, underscoring the limited prognostic utility of registryreported MFC-MRD testing due to variability in methods and thresholds. Survival analyses across the 12 largest centers demonstrated substantial variability in the prognostic impact of MRD. These findings underscore that although pre-alloHCT MRD by MFC remains a clinically relevant prognostic biomarker, its reliability is contingent upon methodological standardization across centers. These findings highlight the need for standardized MRD assessment to improve risk stratification in AML.

医療・健康
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