Literature DB >> 24369221

Prognostic importance of the soluble form of IL-2 receptorα (sIL-2Rα) and its relationship with surface expression of IL-2Rα (CD25) of lymphoma cells in diffuse large B-cell lymphoma treated with CHOP-like regimen with or without rituximab: a retrospective analysis of 338 cases.

Yoko Hashimoto1, Akihiko Yokohama, Akio Saitoh, Hirotaka Nakahashi, Kohtaro Toyama, Takeki Mitsui, Hiromi Koiso, Takayuki Saitoh, Hiroshi Handa, Hideki Uchiumi, Takahiro Jinbo, Kayoko Murayama, Morio Matsumoto, Morio Sawamura, Masamitsu Karasawa, Hirokazu Murakami, Junko Hirato, Yoshihisa Nojima, Masaru Kojima, Norifumi Tsukamoto.   

Abstract

We evaluated the prognostic significance of the serum level of the soluble form of interleukin-2 receptorα (sIL-2Rα) and investigated its association with CD25 expression on tumor cells in diffuse large B-cell lymphoma (DLBCL). Three hundred and thirty-eight adult patients with newly diagnosed DLBCL were eligible for this retrospective study. 32.2% of patients were treated with CHOP-like regimen and 67.8% with R-CHOP-like regimen. CD25 expression on the surface of tumor cells was evaluated in 143 cases and its relationship with sIL-2Rα level was also investigated. Both overall survival (OS) and progression-free survival (PFS) were poorer in patients with higher sIL-2Rα, in both R-CHOP and CHOP groups. sIL-2Rα > 1,000 U/mL and performance status (PS) ≥ 2 were independently associated with poorer OS, and sIL-2Rα > 1,000 U/mL, age > 60 years, and ≥ 2 extranodal sites were independently associated with poorer PFS in the R-CHOP group. The sIL-2Rα level was higher in the CD25-positive group than in the CD25-negative group in stage 3 or 4 disease (p = 0.010). Multiple linear regression analysis showed CD25 expression to be independently correlated with sIL-2Rα levels. High sIL-2Rα is an important risk factor for survival in DLBCL treated with not only CHOP-like, but also R-CHOP-like regimens, regardless of the tumor's expression of CD25.

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Year:  2013        PMID: 24369221     DOI: 10.3960/jslrt.53.197

Source DB:  PubMed          Journal:  J Clin Exp Hematop        ISSN: 1346-4280


  4 in total

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  4 in total

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