Revised MALT‐IPI : A new predictive model that identifies high‐risk patients with extranodal marginal zone lymphoma
Year: 2022
Type: article
Study design: Observational Study
Abstract: Extranodal marginal zone lymphoma (EMZL) is a heterogeneous disease with a subset of patients exhibiting a more aggressive course. We previously reported that EMZL with multiple mucosal sites (MMS) at diagnosis is characterized by shorter survival. To better recognize patients with different patterns of progression-free survival (PFS) we developed and validated a new prognostic index primarily based on patient's disease characteristics. We derived the "Revised mucosa-associated lymphoid tissue International Prognostic Index" (Revised MALT-IPI) in a large data set (n = 397) by identifying candidate variables that showed highest prognostic association with PFS. The revised MALT-IPI was validated in two independent cohorts, from the University of Iowa/Mayo Clinic (n = 297) and from IELSG-19 study (n = 400). A stepwise Cox regression analysis yielded a model including four independent predictors of shorter PFS. Revised MALT-IPI has scores ranging from 0 to 5, calculated as a sum of one point for each of the following- age >60 years, elevated LDH, and stage III-IV; and two points for MMS. In the training cohort, the Revised MALT-IPI defined four risk groups: low risk (score 0, reference group), low-medium risk (score 1, HR = 1.85, p = .008), medium-high risk (score 2, HR = 3.84, p < .0001), and high risk (score 3+, HR = 8.48, p < .0001). Performance of the Revised MALT-IPI was similar in external validation cohorts. Revised MALT-IPI is a new index centered on disease characteristics that provides robust risk-stratification identifying a group of patients characterized by earlier progression of disease. Revised MALT-IPI can allow a more disease-adjusted management of patients with EMZL in clinical trials and practice.
Source: American Journal of Hematology
DOI: 10.1002/ajh.26715
Institutions: Sylvester Comprehensive Cancer Center, University of Miami, Mayo Clinic, University of Iowa, University of Iowa Health Care, Université Paris Cité, Assistance Publique – Hôpitaux de Paris, Hôpital Saint-Louis, Ospedale degli Infermi, Ente Ospedaliero Cantonale, Istituto Oncologico della Svizzera Italiana, University of Bern, University Hospital of Bern, Institute of Oncology Research, Università della Svizzera italiana
Language: English
Subfield: Pathology and Forensic Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Awards: G2111860640, G2156476721, G2190235346, G2660289629, G3723508571, G427533880, Identify the Mechanisms of LMO2-Mediated Inhibition of Homologous Recombination and Establish PARP-Targeted Synthetic Lethality as a New Therapy for DLBCL, G7738754637, G9000038791, G9000128122, G9000193499, G9000209416, G9000232133, G9000297869, Mayo Clinic Comprehensive Cancer Center Support Grant
OpenAlex ID: W4294495302
