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Objective: To investigate survival differences based on MRD status at different landmarks and tumor staging in patients with early-stage non-small cell lung cancer (NSCLC) following surgical resection.
Methods: Data from six studies including 867 early-stage NSCLC patients who underwent surgery were summarized. Patients were grouped according to MRD status at different detection time points and tumor staging. Survival differences among subgroups were evaluated using the Kaplan-Meier method, and statistical significance was determined through the log-rank test.
Result: MRD-negative patients exhibit significantly better RFS and OS compared to MRD-positive patients. Based on MRD status at 3-7 days and 30 days post-surgery, combined with TNM staging, we propose a novel four-category prognostic stratification system centered on post-surgery dual-detection timepoints. This stratification system outperforms the traditional TNM staging and is divided into four groups: Group A: Post-surgery dual-negative with Stage I disease; Group B: Post-surgery dual-negative with Stage II disease; Group C: Post-surgery dual-negative with Stage III disease or MRD-positive at 3-7 days but negative at 30 days post-surgery (positive-to-negative conversion);Group D: Post-surgery dual-positive or MRD-negative at 3-7 days but positive at 30 days post-surgery (negative-to-positive conversion).The RFS outcomes are ranked as Group A > Group B > Group C > Group D. Notably, Group D has worse RFS than Stage III patients.
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http://dx.doi.org/10.1016/j.lungcan.2025.108634 | DOI Listing |
Drugs
September 2025
Section of Hematology/Oncology, University of Chicago, 5841 S. Maryland Ave, MC 2115, Chicago, IL, 60637, USA.
Measurable (or minimal) residual disease (MRD) testing offers critical prognostic insight in multiple myeloma (MM), surpassing conventional response criteria. While bone-marrow-based assays are most commonly performed, MRD assessment in peripheral blood and advanced imaging may add complementary value. A comprehensive approach, integrating serial MRD testing across compartments, may offer the most accurate appraisal of disease burden.
View Article and Find Full Text PDFHaematologica
September 2025
Hematology Department, Hospital Universitari i Politècnic La Fe, València, Spain; Instituto de Investigación Sanitaria La Fe, València, Spain; Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Instituto Carlos III, Madrid, Spain; Department of Medicine, University of Valencia, Va
We analyzed outcomes of 217 AML patients in complete remission who underwent allogeneic HCT with myeloablative conditioning and post-transplant cyclophosphamide-based GVHD prophylaxis, aiming to assess the prognostic significance of genetic risk categories. In the overall cohort, the 2-year overall survival (OS) and event-free survival (EFS) were 77% (95% CI, 71-83) and 72% (95% CI, 66- 78), respectively. ELN2022 risk stratification lacked prognostic value in HCT.
View Article and Find Full Text PDFBlood Adv
September 2025
Regeneron Pharmaceuticals, Inc., Tarrytown, New York, United States.
Odronextamab, a CD20×CD3 bispecific antibody, demonstrated robust efficacy and durable responses, with a generally manageable safety profile, in patients with relapsed/refractory follicular lymphoma (FL) and diffuse large B-cell lymphoma (DLBCL) in the Phase 2 ELM-2 study. This exploratory analysis evaluated the prognostic value of minimal residual disease (MRD) status and tumor molecular profiles, based on circulating tumor DNA (ctDNA) analysis, for determining patient outcomes in ELM-2. Baseline and on-treatment ctDNA samples were used for MRD evaluation (AVENIO Oncology Assay Non-Hodgkin Lymphoma Test); baseline ctDNA samples were also used for molecular profiling.
View Article and Find Full Text PDFFront Immunol
September 2025
School of Medicine, Nankai University, Tianjin, China.
Purpose: Relapse remains the leading cause of treatment failure in high-risk acute myeloid leukemia (AML) or myelodysplastic syndrome-IB (MDS-IB) patients after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Ruxolitinib has demonstrated antileukemic activity , and decitabine has been found to be tolerable when combined with modified busulfan-cyclophosphamide (mBu/Cy) conditioning regimen. Here, we investigated the efficacy of ruxolitinib and decitabine plus a mBu/Cy conditioning regimen (Rux-Dec-mBu/Cy) in reducing relapse in high-risk AML/MDS patients ().
View Article and Find Full Text PDFInvest New Drugs
September 2025
Department of Hematology, the Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, 310009, Zhejiang, China.
Acute myeloid leukemia (AML) carries a poor prognosis in elderly or medically unfit patients, with median overall survival (OS) of only 7-8 months for those ineligible for intensive chemotherapy. While venetoclax (VEN) combined with azacitidine (AZA) has become a standard therapy, real-world evidence indicates that Asian patients experience higher VEN exposure and toxicity with the standard 400 mg/day dose. This retrospective study aimed to evaluate the efficacy and safety of a reduced-dose regimen (VEN 200 mg/day + AZA) in frail/elderly Chinese AML patients deemed unfit for intensive therapy.
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