Pregled bibliografske jedinice broj: 1193970
Primary refractory follicular lymphoma: a poor outcome entity with high risk of transformation to aggressive B cell lymphoma
Primary refractory follicular lymphoma: a poor outcome entity with high risk of transformation to aggressive B cell lymphoma // European journal of cancer (1990), 157 (2021), 132-139 doi:10.1016/j.ejca.2021.08.005 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1193970 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Primary refractory follicular lymphoma: a poor
outcome entity with high risk of transformation to
aggressive B cell lymphoma
Autori
Alonso-Álvarez, Sara ; Manni, Martina ; Montoto, Silvia ; Sarkozy, Clémentine ; Morschhauser, Franck ; Wondergem, Marielle J. ; Guarini, Attilio ; Magnano, Laura ; Alcoceba, Miguel ; Chamuleau, Martine ; Galimberti, Sara ; Gomes da Silva, Maria ; Holte, Harald ; Zucca, Emanuele ; Lockmer, Sandra ; Aurer, Igor ; Marcheselli, Luigi ; Stepanishyna, Yana ; Caballero Barrigón, María Dólores ; Salles, Gilles ; Federico, Massimo
Izvornik
European journal of cancer (1990) (0959-8049) 157
(2021);
132-139
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
primary refractory follicular lymphoma ; histologic transformation ; rituximab era
Sažetak
Background: Primary refractory (PREF) follicular lymphoma (FL) has a completely different clinical course from that of FL that responds to front-line treatments. In addition to having poor responses to salvage therapies, it seems that patients with PREF are at increased risk of histological transformation (HT). The Aristotle consortium presented the opportunity of investigating the risk of HT in a very large series of cases. Thus, we investigated the risk of HT in patients with PREF FL compared with that of responding patients or in stable disease and ultimately their outcome. Methods: Six thousand three hundred thirty-nine patients from the Aristotle database were included in the analysis. These patients had a histologically confirmed grade 1, 2 or 3a FL diagnosed between 1997 and 2013. The primary end- points were the cumulative incidence (CI) of HT at the first progression or relapse and the survival after transformation. Findings.: The 5-year CI of HT among patients with PREF was 34% (95% confidence interval (CI): 27e43), whilst it was 7.1% (95% CI: 6.0e8.5) in the group of patients with partial response (PR) or stable disease (SD) (PR þ SD) and 3.5% (95% CI: 3.0e4.2) in the group of patients achieving complete response (CR). The 5-year survival after relapse (SAR) was 33% (95% CI: 28e39) for the PREF group, 57% (95% CI 54e61) in patients with PR, 51% (95% CI 43e58) in the SD group after first-line therapy and 63% (95% CI: 66e72) in patients with CR after initial treatment (p-value <0.001). The 5-year SAR for those patients with PREF who developed HT was 21% (95% CI: 12e31), clearly diminished when compared with those patients with PREF who did not experience HT (38% [95% CI: 31e44]) (pvalue Z 0.001). Interpretation.: Patients with PREF FL have a dismal outcome and an associated very high rate of HT that further worsens their poor prognosis.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb
Profili:
Igor Aurer
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE