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Marginal zone lymphoma international prognostic index: a unifying prognostic index for marginal zone lymphomas requiring systemic treatment.
Arcaini, Luca; Bommier, Côme; Alderuccio, Juan Pablo; Merli, Michele; Fabbri, Nicole; Nizzoli, Maria Elena; Maurer, Matthew J; Tarantino, Vittoria; Ferrero, Simone; Rattotti, Sara; Talami, Annalisa; Murru, Roberta; Khurana, Arushi; Mwangi, Raphael; Deodato, Marina; Cencini, Emanuele; Re, Francesca; Visco, Carlo; Feldman, Andrew L; Link, Brian K; Delamain, Marcia Torresan; Spina, Michele; Annibali, Ombretta; Pulsoni, Alessandro; Ferreri, Andrés J M; Stelitano, Caterina Cecilia; Pennese, Elsa; Habermann, Thomas M; Marcheselli, Luigi; Han, Sunwoo; Reis, Isildinha M; Paulli, Marco; Lossos, Izidore S; Cerhan, James R; Luminari, Stefano.
Afiliação
  • Arcaini L; Department of Molecular Medicine, University of Pavia, Pavia, Italy.
  • Bommier C; Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Alderuccio JP; Hemato-Oncology Department, DMU DHI, Hôpital Saint Louis, Paris, France.
  • Merli M; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
  • Fabbri N; Division of Hematology, Department of Medicine, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Nizzoli ME; Division of Hematology, University Hospital Ospedale di Circolo e Fondazione Macchi-ASST Sette Laghi, University of Insubria, Varese, Italy.
  • Maurer MJ; Department of Molecular Medicine, University of Pavia, Pavia, Italy.
  • Tarantino V; Division of Hematology, Azienda Unità Sanitaria Locale - IRCCS, Reggio Emilia, Italy.
  • Ferrero S; Clinical and Experimental Medicine Doctorate School, Università degli Studi di Modena e Reggio Emilia, Italy.
  • Rattotti S; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
  • Talami A; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Murru R; Division of Hematology, Azienda Ospedaliera Ospedali Riuniti Villa Sofia-Cervello, Palermo, Italy.
  • Khurana A; Division of Hematology, Department of Molecular Biotechnologies and Health Sciences, University of Torino, and AOU "Città della Salute e della Scienza di Torino", Torino, Italy.
  • Mwangi R; Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Deodato M; Clinical and Experimental Medicine Doctorate School, Università degli Studi di Modena e Reggio Emilia, Italy.
  • Cencini E; Hematology and Stem Cell Transplantation Unit, Ospedale Oncologico A. Businco, ARNAS G. Brotzu, Cagliari, Italy.
  • Re F; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Visco C; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
  • Feldman AL; Division of Hematology, Niguarda Cancer Center, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.
  • Link BK; Division of Hematology, Azienda Ospedaliera Universitaria Senese and University of Siena, Siena, Italy.
  • Delamain MT; Division of Hematology, Azienda Ospedaliero-Universitaria di Parma, Parma, Italy.
  • Spina M; Division of Hematology, San Bortolo Hospital, AULSS 8 Berica, Vicenza, Italy.
  • Annibali O; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Pulsoni A; Department of Internal Medicine, University of Iowa Hospitals, Iowa City, IA, USA.
  • Ferreri AJM; Faculty of Medical of Minas Gerais, Feluma, Brazil for Faculty of Medical of Minas Gerais, Belo Horizonte, Brazil.
  • Stelitano CC; Division of Medical Oncology and Immune-Related Tumors, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano, Italy.
  • Pennese E; Division of Hematology, Stem Cell Transplantation, University Campus Bio-Medico, Roma, Italy.
  • Habermann TM; Division of Hematology, Sapienza University - Polo Pontino, Department of Translational and Precision Medicine, S.M. Goretti Hospital, Latina, Italy.
  • Marcheselli L; Lymphoma Unit, IRCCS San Raffaele Scientific Institute, and University Vita-Salute San Raffaele, Milano, Italy.
  • Han S; Division of Hematology, Grande Ospedale Metropolitano, Bianchi Melacrino Morelli, Reggio Calabria, Reggio Calabria, Italy.
  • Reis IM; Division of Hematology, Ospedale Spirito Santo, Pescara, Italy.
  • Paulli M; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Lossos IS; Fondazione Italiana Linfomi ETS, Italy.
  • Cerhan JR; Biostatistics and Bioinformatics Shared Resource, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Luminari S; Biostatistics and Bioinformatics Shared Resource, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, USA.
EClinicalMedicine ; 72: 102592, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38633575
ABSTRACT

Background:

Marginal zone lymphomas (MZL), comprised of three unique but related subtypes, lack a unifying prognostic score applicable to all the patients in need for systemic chemotherapy and/or immunotherapy.

Methods:

Patients from the prospective NF10 study (NCT02904577) with newly diagnosed MZL and receiving frontline systemic therapy at diagnosis or after observation were used to train a prognostic model. The primary endpoint was progression-free survival (PFS) from start of treatment. The model was externally validated in a pooled analysis of two independent cohorts from the University of Iowa and Mayo Clinic Molecular Epidemiology Resource and the University of Miami.

Findings:

We identified 501 eligible patients. After multivariable modeling, lactate dehydrogenase (LDH) above upper normal limit, hemoglobin <12 g/dL, absolute lymphocyte count <1 × 109/L, platelets <100 × 109/L, and MZL subtype (nodal or disseminated) were independently associated with inferior PFS. The proposed MZL International Prognostic index (MZL-IPI) combined these 5 factors, and we defined low (LRG, 0 factors, 27%), intermediate (IRG, 1-2 factors, 57%) and high (HRG, 3+ factors, 16%) risk groups with 5-y PFS of 85%, 66%, and 37%, respectively (c-Harrell = 0.64). Compared to the LRG, the IRG (Hazard Ratio [HR] = 2.30, 95% CI 1.39-3.80) and HRG (HR = 5.41, 95% CI 3.12-9.38) had inferior PFS. Applying the MZL-IPI to the pooled US cohort (N = 353), 94 (27%), 192 (54%), and 67 (19%) patients were classified as LRG, IRG, and HRG, respectively, and the model was validated for PFS (log-rank test p = 0.0018; c-Harrell = 0.578, 95% CI 0.54-0.62). The MZL-IPI was also prognostic for OS in both the training and the external validation sets.

Interpretation:

MZL-IPI is a new prognostic score for use in all patients with MZL considered for systemic treatment.

Funding:

The MER was supported by P50 CA97274 and U01 CA195568.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: EClinicalMedicine Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: EClinicalMedicine Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália