Home > Haematology > ASH 2020 > Acute Lymphoblastic Leukaemia > Strong correlation between peripheral blood and bone marrow NGS MRD

Strong correlation between peripheral blood and bone marrow NGS MRD

Presented by
Dr Lori Muffly, Stanford University, California, USA
Conference
ASH 2020
A prospective observational study demonstrated a strong correlation between measurable residual disease (MRD) analysis by next-generation sequencing (NGS) using either peripheral blood or bone marrow in acute lymphoblastic leukaemia (ALL). These results show that non-invasive monitoring of peripheral blood MRD represents a viable alternative to serial bone marrow examinations.

The prognostic and predictive utility of MRD assessments using bone marrow aspirates is well-established in the management of ALL. However, frequent bone marrow MRD monitoring post-therapy is limited by the invasive, expensive, and at times impractical nature of numerous bone marrow examinations. Limited retrospective reports have suggested that NGS MRD using peripheral blood may provide a viable alternative to MRD monitoring of the bone marrow.

Dr Lori Muffly (Stanford University, California, USA) and colleagues conducted a prospective, multi-institutional observational study of NGS-based MRD of the peripheral blood among 62 adult ALL patients undergoing cellular therapies, namely haematopoietic cell transplantation (HCT) and chimaeric antigen receptor T cells (CAR T), to determine the correlation between peripheral blood and bone marrow MRD and to explore the clinical utility of monitoring MRD in the peripheral blood [1].

Median age of patients was 42 years, 36 (58%) were male, 54 (87%) had B-cell ALL, 16 (26%) were BCR-ABL+, and 28 (46%) had extramedullary involvement. Across all patients, peripheral blood MRD was highly correlated with bone marrow MRD (r=0.87; P<0.0001). Of the 129 paired samples, 15 (12%) had discordance with MRD identified in either the peripheral blood and not bone marrow (5%) or in the bone marrow and not peripheral blood (6%). Similarly, peripheral blood and bone marrow MRD were highly correlated in the HCT (r=0.86; P<0.0001) and CAR T cohorts (r=0.86; P<0.001) [1].

  1. Muffly L, et al. Monitoring Measurable Residual Disease Using Peripheral Blood in Acute Lymphoblastic Leukemia: Results of a Prospective, Observational Study. 62nd ASH Annual Meeting, 5-8 December 2020. Abstract 975.




Posted on