J 2022

Clinical value of ALK and CD30 expression in mature systemic T cell lymphomas: analysis from the Czech Lymphoma Study Group database (NIHIL)

JANÍKOVÁ, Andrea, Jozef MICHALKA, Renata CHLOUPKOVÁ, Natasa KOPALOVA, V. CAMPR et. al.

Základní údaje

Originální název

Clinical value of ALK and CD30 expression in mature systemic T cell lymphomas: analysis from the Czech Lymphoma Study Group database (NIHIL)

Autoři

JANÍKOVÁ, Andrea (203 Česká republika, garant, domácí), Jozef MICHALKA (703 Slovensko, domácí), Renata CHLOUPKOVÁ (203 Česká republika, domácí), Natasa KOPALOVA (203 Česká republika), V. CAMPR (203 Česká republika), K. KAMARADOVA (203 Česká republika), Leoš KŘEN (203 Česká republika, domácí), D. BELADA (203 Česká republika), K. BENESOVA (203 Česká republika), J. DLOUHA, P. KLENER, V. PROCHÁZKA, H. MOCIKOVA (203 Česká republika), J. DURAS (203 Česká republika) a M. TRNENY (203 Česká republika)

Vydání

Annals of hematology, New York, Springer Verlag, 2022, 0939-5555

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30205 Hematology

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 3.500

Kód RIV

RIV/00216224:14110/22:00126151

Organizační jednotka

Lékařská fakulta

UT WoS

000745380700001

Klíčová slova anglicky

Peripheral T cell lymphoma; CD30; ALK; Prognosis

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 28. 6. 2022 10:42, Mgr. Tereza Miškechová

Anotace

V originále

Mature T cell lymphomas (MTCLs) have worse prognosis, and in contrast to B cell lymphomas, there is no universal marker like CD20 with exception of ALK and CD30, which are present in proportion of MTCL only. Up to now, ALK is traditionally associated with good prognosis in ALCLs, and there are some evidences that CD30-positive T cell or B cell lymphomas have better prognosis. In our retrospective, population-based analysis, we analyzed the real clinical value of ALK and CD30 in the most frequent MTCL subtypes. Between 2000 and 2017, we identified 732 patients with newly diagnosed ALCL, AITL, or PTCL-NOS. Among them, 207 ALCL patients were with known ALK, whereas 61 AITL and 238 PTCL-NOS with known CD30 expression. There were 69/207 (33.3%) ALK + ALCLs, who displayed better 5-year PFS (65.6% vs. 36.2%) (p .001) and 5-year OS (71.5% vs. 45.9%) (p .002) compared to ALK -; ALK + patients were significantly younger (median 48 vs. 60 years; p < 0.001). For patients >= 60 years, 5-year PFS (38.5% vs. 31.2%) and 5-year OS (38.5% vs. 39.6%) were similar between ALK + vs. ALK - patients. For AITL and PTCL-NOS, there were 44/61 (72.1%) and 120/238 (50.4%) CD30 + samples, and difference in CD30 expression was significant (p .02). AITL patients had 5-year OS of 43.8% vs. 55.7% (p 0.848) and 5-year PFS of 36.7% vs. 29.4% (p .624) for CD30 + vs. CD30 - patients, whereas PTCL-NOS had 5-year OS of 35.7% vs. 34.3% (p .318) and 5-year PFS of 29.3% vs. 22.5% (p .114) for CD30 + vs. CD30 - cases. We conclude that ALK in ALCLs (>= 60 years) and CD30 expression in PCTL-NOS and AITL have only limited prognostic value.