Postižení jater u nemocných s ne-Hodgkinovým lymfomem
[Hepatic involvement in patients with non-Hodgkins lymphoma]
Jazyk čeština Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
23909267
PII: 41156
- MeSH
- difúzní velkobuněčný B-lymfom farmakoterapie imunologie MeSH
- hepatitida B - antigeny povrchové imunologie MeSH
- kohortové studie MeSH
- lidé MeSH
- lymfom T-buněčný farmakoterapie imunologie MeSH
- myší monoklonální protilátky terapeutické užití MeSH
- nádory jater farmakoterapie MeSH
- nehodgkinský lymfom farmakoterapie imunologie MeSH
- přežití bez známek nemoci MeSH
- prognóza MeSH
- protinádorové látky terapeutické užití MeSH
- rituximab MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- hepatitida B - antigeny povrchové MeSH
- myší monoklonální protilátky MeSH
- protinádorové látky MeSH
- rituximab MeSH
Non-Hodgkins lymphoma (NHL) represent the most frequent hematological malignancy with frequent extranodal involvement. We have identified 79 pts (4.6%) out of 1,712 patients with NHL, who were diagnosed in our center between 1999-2010. Five cases were primary extranodal lymphomas and we have observed one primary hepatic lymphoma (0.015%). The most frequent (61.3%) NHL subtype in our cohort was diffuse large B-cell lymphoma. B-NHL formed 92.4% of all lymphomas. We have observed high number of HBsAg positive patients (10%). The whole group have poor prognostic features with high number of patients (85%) with intermediate-high and high risk according to international prognostic index. The patients were treated with chemotherapy in 95%, B-NHL patients recieved immunochemotherapy with rituximab in 77%. The median progression free survival, resp. overall survival 4.6, resp. 8.4 years in the whole group and 1.4, resp. 8.4 years in diffuse large B-cell lymphoma were observed with median follow-up 4.5 years. The outcome of T-NHL patients was significantly worse with overall survival median 1.2 vs 8.4 years (p < 0.033). The patients with B-NHL treated by immunochemoterapy with rituximab had significant death risk reduction (HR 0.44, p = 0.03) compared to the patients treated with chemotherapy.