Publication: Validation of the NCCN-IPI for diffuse large B-cell lymphoma (DLBCL): the addition of β2 -microglobulin yields a more accurate GELTAMO-IPI.
dc.contributor.author | Montalbán, Carlos | |
dc.contributor.author | Díaz-López, Antonio | |
dc.contributor.author | Dlouhy, Ivan | |
dc.contributor.author | Rovira, Jordina | |
dc.contributor.author | Lopez-Guillermo, Armando | |
dc.contributor.author | Alonso, Sara | |
dc.contributor.author | Martín, Alejandro | |
dc.contributor.author | Sancho, Juan M | |
dc.contributor.author | García, Olga | |
dc.contributor.author | Sánchez, Jose M | |
dc.contributor.author | Rodríguez, Mario | |
dc.contributor.author | Novelli, Silvana | |
dc.contributor.author | Salar, Antonio | |
dc.contributor.author | Gutiérrez, Antonio | |
dc.contributor.author | Rodríguez-Salazar, Maria J | |
dc.contributor.author | Bastos, Mariana | |
dc.contributor.author | Domínguez, Juan F | |
dc.contributor.author | Fernández, Rubén | |
dc.contributor.author | Gonzalez de Villambrosia, Sonia | |
dc.contributor.author | Queizan, José A | |
dc.contributor.author | Córdoba, Raul | |
dc.contributor.author | de Oña, Raquel | |
dc.contributor.author | López-Hernandez, Andrés | |
dc.contributor.author | Freue, Julian M | |
dc.contributor.author | Garrote, Heidys | |
dc.contributor.author | López, Lourdes | |
dc.contributor.author | Martin-Moreno, Ana M | |
dc.contributor.author | Rodriguez, Jose | |
dc.contributor.author | Abraira, Víctor | |
dc.contributor.author | García, Juan F | |
dc.contributor.author | GELTAMO-IPI Project Investigators | |
dc.date.accessioned | 2023-01-25T09:43:05Z | |
dc.date.available | 2023-01-25T09:43:05Z | |
dc.date.issued | 2017-01-20 | |
dc.description.abstract | The study included 1848 diffuse large B-cell lymphoma (DLBCL)patients treated with chemotherapy/rituximab. The aims were to validate the National Comprehensive Cancer Network International Prognostic Index (NCCN-IPI) and explore the effect of adding high Beta-2 microglobulin (β2M), primary extranodal presentation and intense treatment to the NCCN-IPI variables in order to develop an improved index. Comparing survival curves, NCCN-IPI discriminated better than IPI, separating four risk groups with 5-year overall survival rates of 93%, 83%, 67% and 49%, but failing to identify a true high-risk population. For the second aim the series was split into training and validation cohorts: in the former the multivariate model identified age, lactate dehydrogenase, Eastern Cooperative Oncology Group performance status, Stage III-IV, and β2M as independently significant, whereas the NCCN-IPI-selected extranodal sites, primary extranodal presentation and intense treatments were not. These results were confirmed in the validation cohort. The Grupo Español de Linfomas/Trasplante de Médula ósea (GELTAMO)-IPI developed here, with 7 points, significantly separated four risk groups (0, 1-3, 4 or ≥5 points) with 11%, 58%, 17% and 14% of patients, and 5-year overall survival rates of 93%, 79%, 66% and 39%, respectively. In the comparison GELTAMO IPI discriminated better than the NCCN-IPI. In conclusion, GELTAMO-IPI is more accurate than the NCCN-IPI and has statistical and practical advantages in that the better discrimination identifies an authentic high-risk group and is not influenced by primary extranodal presentation or treatments of different intensity. | |
dc.identifier.doi | 10.1111/bjh.14489 | |
dc.identifier.essn | 1365-2141 | |
dc.identifier.pmid | 28106247 | |
dc.identifier.unpaywallURL | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/bjh.14489 | |
dc.identifier.uri | http://hdl.handle.net/10668/10794 | |
dc.issue.number | 6 | |
dc.journal.title | British journal of haematology | |
dc.journal.titleabbreviation | Br J Haematol | |
dc.language.iso | en | |
dc.organization | Hospital Universitario Virgen del Rocío | |
dc.page.number | 918-928 | |
dc.pubmedtype | Journal Article | |
dc.pubmedtype | Research Support, Non-U.S. Gov't | |
dc.rights.accessRights | open access | |
dc.subject | DLBCL | |
dc.subject | prognostic scores | |
dc.subject | risk assessment | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Aged, 80 and over | |
dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols | |
dc.subject.mesh | Biomarkers | |
dc.subject.mesh | Female | |
dc.subject.mesh | Follow-Up Studies | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Kaplan-Meier Estimate | |
dc.subject.mesh | Lymphoma, Large B-Cell, Diffuse | |
dc.subject.mesh | Male | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Neoplasm Staging | |
dc.subject.mesh | Prognosis | |
dc.subject.mesh | Remission Induction | |
dc.subject.mesh | Reproducibility of Results | |
dc.subject.mesh | Treatment Outcome | |
dc.subject.mesh | beta 2-Microglobulin | |
dc.title | Validation of the NCCN-IPI for diffuse large B-cell lymphoma (DLBCL): the addition of β2 -microglobulin yields a more accurate GELTAMO-IPI. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 176 | |
dspace.entity.type | Publication |