Evidence map›Paper›PMID 41677892›Full record

ArticleCancer immunology, immunotherapy : CII2026

Predictive value of natural killer (NK) cells in bone marrow for relapse in diffuse large B cell lymphoma: integrating antibody-dependent cell-mediated cytotoxicity (ADCC)-based immunotherapy.

Sofía Rincón-López, Johelys Atencio-Matos, Olalla Pereda-Sainz, Javier Larreina-Pérez, Andrea Campeny-Najara, Ada Esteban-Figuerola, Montserrat Hernandez-Perez, Puy Garrastachu-Zumaran, María Velasco-Ruiz, Isabel García-Bosque and 6 more

Abstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Sofía Rincón-LópezDepartment of Hematology, Hospital Universitario San Pedro, 26006, Logroño, La Rioja, Spain.ORCID https://orcid.org/0009-0009-8972-7006
Johelys Atencio-MatosDepartment of Hematology, Hospital Universitario San Pedro, 26006, Logroño, La Rioja, Spain.ORCID https://orcid.org/0009-0009-5217-6319
Olalla Pereda-SainzDepartment of Hematology, Hospital Universitario San Pedro, 26006, Logroño, La Rioja, Spain.ORCID https://orcid.org/0009-0007-0871-8198
Javier Larreina-PérezDepartment of Hematology, Hospital Universitario San Pedro, 26006, Logroño, La Rioja, Spain.ORCID https://orcid.org/0009-0005-1660-5228
Andrea Campeny-NajaraDepartment of Hematology, Hospital Universitario San Pedro, 26006, Logroño, La Rioja, Spain.
Ada Esteban-FiguerolaDepartment of Hematology, Hospital Universitario San Pedro, 26006, Logroño, La Rioja, Spain.ORCID https://orcid.org/0000-0002-4590-0999
Montserrat Hernandez-PerezDepartment of Hematology, Hospital Universitario San Pedro, 26006, Logroño, La Rioja, Spain.
Puy Garrastachu-ZumaranDepartment of Diagnostic Imaging (Radiology) and Nuclear Medicine, University Hospital San Pedro and Centre for Biomedical Research of La Rioja (CIBIR), Logroño, La Rioja, Spain.ORCID https://orcid.org/0000-0001-5344-0737
María Velasco-RuizDepartment of Diagnostic Imaging (Radiology) and Nuclear Medicine, University Hospital San Pedro and Centre for Biomedical Research of La Rioja (CIBIR), Logroño, La Rioja, Spain.
Isabel García-BosqueHematology and Hemotherapy Service, Fundación Hospital Calahorra, Calahorra, La Rioja, Spain.ORCID https://orcid.org/0000-0001-9483-2606
Carmen Rodriguez-LeflerHematology and Hemotherapy Service, Fundación Hospital Calahorra, Calahorra, La Rioja, Spain.ORCID https://orcid.org/0009-0006-5781-9780
Estefanía Ruiz de GaonaHematology and Hemotherapy Service, Fundación Hospital Calahorra, Calahorra, La Rioja, Spain.
Jesús FeliuDepartment of Hematology, Hospital Universitario San Pedro, 26006, Logroño, La Rioja, Spain.ORCID https://orcid.org/0000-0002-9630-8813
Juan CabelloCell Proliferation and Differentiation Group Oncology Area, CIBIR (Center for Biomedical Research of La Rioja) La Rioja, Logroño, Spain.ORCID https://orcid.org/0000-0002-3835-0116
Alfonso Martín-CarniceroMedical Oncology Department, Hospital Universitario San Pedro, Logroño, Spain.ORCID https://orcid.org/0000-0002-8564-2875
Ricardo García-MuñozDepartment of Hematology, Hospital Universitario San Pedro, 26006, Logroño, La Rioja, Spain. rgmunoz@riojasalud.es.ORCID https://orcid.org/0000-0003-3201-3909

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDiffuse large B cell lymphoma (DLBCL) is characterized by high relapse rates and immunobiological complexity. The therapeutic efficacy of CD20-targeting monoclonal antibodies depends largely on antibody-dependent cellular cytotoxicity (ADCC), mediated by natural killer (NK) cells.

methodsWe evaluated the percentage of bone marrow NK cells in 47 newly diagnosed DLBCL patients by flow cytometry prior to first-line chemoimmunotherapy. ADCC potential was assessed using immunological parameters.

resultsPatients with ≥ 14% bone marrow NK cells had significantly better event-free survival (EFS), with median EFS nearly doubled compared with those below this threshold (HR = 0.24, p < 0.05). Logistic regression predicted a 77% probability of remaining relapse-free at NK percentages > 14%. In multivariable Cox regression, bone marrow NK percentage remained independently predictive of EFS after adjustment for International Prognostic Index (IPI), age, and treatment regimen. Although overall survival did not differ significantly, higher NK levels were associated with improved clinical response.

conclusionPatients with higher NK cell percentages may better tolerate chemotherapy-induced depletion, thereby preserving or restoring their effector pool more efficiently. Elevated bone marrow NK cell percentages predict favorable outcomes in DLBCL and support their potential role as translational biomarkers. Incorporating NK cell monitoring into clinical protocols could improve risk stratification and guide immunotherapeutic strategies for personalized patient management.

Indexed as

Antibody-Dependent Cell CytotoxicityBone MarrowImmunotherapyKiller Cells, NaturalLymphoma, Large B-Cell, DiffuseNeoplasm Recurrence, LocalAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansMaleMiddle AgedPrognosisAggressive lymphomaAntibody-dependent cellular cytotoxicity (ADCC)BiomarkerBone marrowDiffuse large B cell lymphoma (DLBCL)Natural killer (NK)

Identifiers

PMID41677892
PMCPMC12900990

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.