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Serum B-Cell Maturation Antigen as a Biomarker for Predicting Outcomes and Monitoring Patients With Waldenström Macroglobulinemia.

1/5 보강
European journal of haematology 2026 Vol.116(1) p. 31-36
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
추출되지 않음
I · Intervention 중재 / 시술
prior therapy, while 34 were treatment-naïve (TN), 19 of whom never went on to require therapy (smoldering [S]WM)
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Baseline sBCMA levels positively correlated with β2 microglobulin (p = 0.0193) and M-protein (p = 0.0450), and negatively with hemoglobin (p = 0.0090) and albumin (p = 0.0016). Overall, these findings suggest sBCMA may serve as a biomarker for prognosis and monitoring for WM patients.

Goldwater MS, Moore J, Bujarski S, Danis R, Khan Z, Li M, Behare S, Swift R, Emamy-Sadr M, Eades B, Berenson JR

📝 환자 설명용 한 줄

Waldenström macroglobulinemia (WM) is an uncommon indolent B-cell lymphoma driven by MYD88 and CXCR4 mutations.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • p-value p < 0.0001
  • p-value p = 0.0002

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BibTeX ↓ RIS ↓
APA Goldwater MS, Moore J, et al. (2026). Serum B-Cell Maturation Antigen as a Biomarker for Predicting Outcomes and Monitoring Patients With Waldenström Macroglobulinemia.. European journal of haematology, 116(1), 31-36. https://doi.org/10.1111/ejh.70029
MLA Goldwater MS, et al.. "Serum B-Cell Maturation Antigen as a Biomarker for Predicting Outcomes and Monitoring Patients With Waldenström Macroglobulinemia.." European journal of haematology, vol. 116, no. 1, 2026, pp. 31-36.
PMID 40958369
DOI 10.1111/ejh.70029

Abstract

Waldenström macroglobulinemia (WM) is an uncommon indolent B-cell lymphoma driven by MYD88 and CXCR4 mutations. Although serum B-cell maturation antigen (sBCMA) has been shown to be a prognostic and monitoring tool for multiple myeloma patients, it has not been evaluated among those with WM. We assessed sBCMA levels among 50 WM patients: 16 had received prior therapy, while 34 were treatment-naïve (TN), 19 of whom never went on to require therapy (smoldering [S]WM). Levels were higher among WM patients (median, 63.76 ng/mL) than healthy subjects (median, 35.24 ng/mL; p < 0.0001). TNWM patients who required therapy showed higher initial levels (median, 137.71 ng/mL) than those with SWM (median, 50.19 ng/mL; p = 0.0002). sBCMA also correlated with disease status: levels decreased at best response (≥ minimal response; median, 38.36 ng/mL) compared to baseline (median, 117.00 ng/mL; p = 0.0078) and increased among patients who developed progressive disease (median, 79.42 ng/mL; p = 0.0625). Baseline sBCMA levels positively correlated with β2 microglobulin (p = 0.0193) and M-protein (p = 0.0450), and negatively with hemoglobin (p = 0.0090) and albumin (p = 0.0016). Overall, these findings suggest sBCMA may serve as a biomarker for prognosis and monitoring for WM patients.

MeSH Terms

Humans; Waldenstrom Macroglobulinemia; Male; Female; Aged; Prognosis; Middle Aged; Biomarkers, Tumor; B-Cell Maturation Antigen; Aged, 80 and over; Adult; Biomarkers; Treatment Outcome