Evidence map›Paper›PMID 38469299›Full record

Trial reportFrontiers in immunology2024

CD8+ NKs as a potential biomarker of complete response and survival with lenalidomide plus R-GDP in the R2-GDP-GOTEL trial in recurrent/refractory diffuse large B cell lymphoma.

Lourdes Hontecillas-Prieto, Daniel J García-Domínguez, Natalia Palazón-Carrión, Alejandro Martín García-Sancho, Esteban Nogales-Fernández, Carlos Jiménez-Cortegana, María L Sánchez-León, Silvia Silva-Romeiro, Rocío Flores-Campos, Fernando Carnicero-González and 20 more

Open access · goldAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 20% of its field
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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
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

30 authors at 17 institutions in 1 country.

Lourdes Hontecillas-Prieto *Clinical Biochemistry Service, Virgen Macarena University Hospital, University of Seville, Seville, Spain.
Daniel J García-Domínguez *Department of Medical Biochemistry and Molecular Biology and Immunology, Medical School, Virgen Macarena University Hospital, University of Seville, Seville, Spain.
Natalia Palazón-CarriónClinical Oncology Service, Hospital Universitario Virgen Macarena, University of Seville, Seville, Spain.
Alejandro Martín García-SanchoDepartment of Hematology, Hospital Universitario de Salamanca, IBSAL, CIBERONC, University of Salamanca, Salamanca, Spain.
Esteban Nogales-FernándezClinical Oncology Service, Hospital Universitario Virgen Macarena, University of Seville, Seville, Spain.
Carlos Jiménez-CorteganaDepartment of Medical Biochemistry and Molecular Biology and Immunology, Medical School, Virgen Macarena University Hospital, University of Seville, Seville, Spain.
María L Sánchez-LeónClinical Oncology Service, Hospital Universitario Virgen Macarena, University of Seville, Seville, Spain.
Silvia Silva-RomeiroClinical Oncology Service, Hospital Universitario Virgen Macarena, University of Seville, Seville, Spain.
Rocío Flores-CamposClinical Oncology Service, Hospital Universitario Virgen Macarena, University of Seville, Seville, Spain.
Fernando Carnicero-GonzálezDepartment of Hematology, Hospital San Pedro de Alcántara de Cáceres, Cáceres, Spain.
Eduardo Ríos-HerranzDepartment of Hematology, Hospital Universitario de Valme, Seville, Spain.
Fátima de la Cruz-VicenteDepartment of Hematology, Hospital Universitario Virgen del Rocío, Seville, Spain.
Guillermo Rodríguez-GarcíaDepartment of Hematology, Hospital Universitario Virgen del Rocío, Seville, Spain.
Rubén Fernández-ÁlvarezDepartment of Hematology, Cabueñes Hospital, Gijón, Spain.
Natividad Martínez-BanaclochaOncology Dept., Dr. Balmis General University Hospital, Alicante Institute for Health and Biomedical Research (ISABIAL), Alicante, Spain.
Josep Gumà-PadròDepartment of Clinical Oncology, Hospital Universitari Sant Joan de Reus URV, IISPV, Reus, Spain.
José Gómez-CodinaDepartment of Clinical Oncology, Hospital Universitario La Fé, Valencia, Spain.
Antonio Salar-SilvestreDepartment of Hematology, Hospital del Mar, Barcelona, Spain.
Delvys Rodríguez-AbreuDepartment of Clinical Oncology, Hospital Universitario Insular, Las Palmas de Gran Canaria, Spain.
Laura Gálvez-CarvajalDepartment of Medical Oncology Intercenter Unit, Regional and Virgen de la Victoria University Hospitals, IBIMA, Málaga, Spain.
Jorge LabradorDepartment of Hematology, Research Unit, Hospital Universitario de Burgos, Burgos, Spain.
María Guirado-RisueñoDepartment of Clinical Oncology, Hospital General Universitario de Elche, Elche, Spain.
Mariano Provencio-PullaDepartment of Medical Oncology, Hospital Universitario Puerta de Hierro-Majadahonda, Facultad de Medicina, Universidad Autónoma de Madrid, IDIPHISA, Madrid, Spain.
Margarita Sánchez-BeatoDepartment of Medical Oncology, Lymphoma Research Group, Hospital Universitario Puerta de Hierro-Majadahonda, IDIPHISA, CIBERONC, Madrid, Spain.
Lejeune MaryleneDepartment of Pathology, Plataforma de Estudios Histológicos, Citológicos y de Digitalización, Hospital de Tortosa Verge de la Cinta, IISPV, URV, Tortosa, Tarragona, Spain.
Tomás Álvaro-NaranjoDepartment of Pathology, Hospital de Tortosa Verge de la Cinta, Catalan Institute of Health, Institut d'Investigació Sanitària Pere Virgili (IISPV), Tortosa, Tarragona, Spain.
María Casanova-EspinosaDepartment of Hematology/Clinical Oncology, Hospital Costa del Sol, Marbella, Spain.
Antonio Rueda-DomínguezDepartment of Hematology/Clinical Oncology, Hospital Costa del Sol, Marbella, Spain.
Víctor Sánchez-MargaletClinical Biochemistry Service, Virgen Macarena University Hospital, University of Seville, Seville, Spain.
Luis de la Cruz-MerinoInstitute of Biomedicine of Seville, Virgen Macarena University Hospital, CSIC, University of Seville, Seville, Spain.
Hospital Universitario Virgen Macarena · ESHospital Costa del Sol · ESHospital Universitario Puerta de Hierro Majadahonda · ESHospital Universitario Virgen del Rocío · ESInstitut de Recerca Biomèdica Catalunya Sud · ESHospital Del Mar · ESHospital General Universitario de Alicante Doctor Balmis · ESHospital General Universitario de Elche · ESHospital San Pedro de Alcántara · ESHospital Universitari de Tortosa Verge de la Cinta · ESHospital Universitari i Politècnic La Fe · ESHospital Universitario de Burgos · ESHospital Universitario De Cabueñes · ESHospital Universitario de Valme · ESHospital Universitario Insular de Gran Canaria · ESInstituto de Investigación Biomédica de Málaga · ESUniversidad de Salamanca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Diffuse large B cell lymphoma (DLBCL) is the most common non-Hodgkin lymphoma worldwide. DLBCL is an aggressive disease that can be cured with upfront standard chemoimmunotherapy schedules. However, in approximately 35-40% of the patients DLBCL relapses, and therefore, especially in this setting, the search for new prognostic and predictive biomarkers is an urgent need. Natural killer (NK) are effector cells characterized by playing an important role in antitumor immunity due to their cytotoxic capacity and a subset of circulating NK that express CD8 have a higher cytotoxic function. In this substudy of the R2-GDP-GOTEL trial, we have evaluated blood CD8+ NK cells as a predictor of treatment response and survival in relapsed/refractory (R/R) DLBCL patients. Methods: 78 patients received the R2-GDP schedule in the phase II trial. Blood samples were analyzed by flow cytometry. Statistical analyses were carried out in order to identify the prognostic potential of CD8+ NKs at baseline in R/R DLBCL patients. Results: Our results showed that the number of circulating CD8+ NKs in R/R DLBCL patients were lower than in healthy donors, and it did not change during and after treatment. Nevertheless, the level of blood CD8+ NKs at baseline was associated with complete responses in patients with R/R DLBCL. In addition, we also demonstrated that CD8+ NKs levels have potential prognostic value in terms of overall survival in R/R DLBCL patients. Conclusion: CD8+ NKs represent a new biomarker with prediction and prognosis potential to be considered in the clinical management of patients with R/R DLBCL. Clinical trial registration: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2014-001620-29 EudraCT, ID:2014-001620-29.

Indexed as

Lymphoma, Large B-Cell, DiffuseLymphoma, Non-HodgkinBiomarkersCD8-Positive T-LymphocytesHumansKiller Cells, NaturalLenalidomideNeoplasm Recurrence, LocalPathologic Complete ResponseBiomarkersLenalidomideB cell lymphomabiomarkerCD8+ NKDLBCLimmune systemnatural killerR2-GDP-GOTELrecurrent/refractory disease

Identifiers

PMID38469299
PMCPMC10926187
OpenAlexW4392157908

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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 OpenQuestion graph.