2014
Retrospective analysis of 235 unselected patients with mantle cell lymphoma confirms prognostic relevance of Mantle Cell Lymphoma International Prognostic Index and Ki-67 in the era of rituximab: long-term data from the Czech Lymphoma Project Database
ŠÁLEK, David; Pavla VESELÁ; Ludmila BOUDOVÁ; Andrea JANÍKOVÁ; Pavel KLENER et al.Základní údaje
Originální název
Retrospective analysis of 235 unselected patients with mantle cell lymphoma confirms prognostic relevance of Mantle Cell Lymphoma International Prognostic Index and Ki-67 in the era of rituximab: long-term data from the Czech Lymphoma Project Database
Autoři
ŠÁLEK, David; Pavla VESELÁ; Ludmila BOUDOVÁ; Andrea JANÍKOVÁ; Pavel KLENER; Samuel VOKURKA; Milada JANKOVSKA; Robert PYTLIK; David BELADA; Jan PIRNOS; Mojmír MOULIS; Roman KODET; Michal MICHAL; Eva JANOUŠOVÁ; Jan MUŽÍK; Jiří MAYER a Marek TRNĚNÝ
Vydání
Leukemia & lymphoma, London, Informa Healthcare, 2014, 1042-8194
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.891
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/14:00074886
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Mantle cell lymphoma; MIPI; Ki-67; proliferation; immunochemotherapy; prognosis
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 28. 5. 2014 15:06, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
Although a prognostic model (MIPI, Mantle Cell Lymphoma International Prognostic Index) for patients with mantle cell lymphoma (MCL) has been established, its clinical significance for daily practice in the rituximab era remains controversial. Data of 235 unselected patients with MCL from the Czech Lymphoma Project Database were analyzed. MIPI, simplified MIPI (s-MIPI) and Ki-67 proliferation index were assessed for all patients and for a subgroup of 155 rituximab-treated (RT) patients. MIPI divided all patients into subgroups of low-risk (22%), intermediate-risk (29%) and high-risk (49%), with median overall survival 105.8 vs. 54.1 vs. 24.6 months, respectively (p < 0.001). s-MIPI revealed similar results. The validity of both indexes was confirmed in RT patients. We confirmed the Ki-67 index to be a powerful single prognostic factor for overall survival (64.4 vs. 20.1 months, p < 0.001) for all patients and for the RT subset. Our results confirm the clinical relevance of MIPI, s-MIPI and Ki-67 for risk stratification in MCL also in the rituximab era.