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Soluble interleukin-2 receptor retains prognostic value in patients with diffuse large B-cell lymphoma receiving rituximab plus CHOP (RCHOP) therapy

  • D. Ennishi
  • , M. Yokoyama
  • , Y. Terui
  • , H. Asai
  • , S. Sakajiri
  • , Y. Mishima
  • , S. Takahashi
  • , H. Komatsu
  • , K. Ikeda
  • , K. Takeuchi
  • , M. Tanimoto
  • , Kiyohiko Hatake

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Soluble interleukin-2 receptor (SIL-2R) is known to be a prognostic parameter in patients with diffuse large B-cell lymphoma (DLBCL) receiving cyclophosphamide, doxorubicin, vincristine and prednisone (CHOP) therapy. However, its prognostic value has not been well known since the introduction of rituximab. Patients and methods: We retrospectively evaluated the prognostic impact of SIL-2R in 228 DLBCL patients, comparing 141 rituximab-combined CHOP (RCHOP)-treated patients with 87 CHOP-treated patients as a historical control. Results: Patients with high serum SIL-2R showed significantly poorer event-free survival (EFS) and overall survival (OS) than patients with low SIL-2R in both the RCHOP group (2-year EFS, 66% versus 92%, P < 0.001; OS, 82% versus 95%, P = 0.005) and the CHOP group (2-year EFS, 40% versus 82%; OS, 61% versus 90%, both P < 0.001). Multivariate analysis including the five parameters of International Prognostic Index (IPI) and two-categorized IPI revealed that SIL-2R was an independent prognostic factor for EFS and OS in the RCHOP group as well as in the CHOP group. Conclusions: Our results demonstrate that SIL-2R retains its prognostic value in the rituximab era. The prognostic value of SIL-2R in DLBCL patients receiving rituximab-combined chemotherapy should be reassessed on a larger scale and by long-term follow-up.

Original languageEnglish
Pages (from-to)526-533
Number of pages8
JournalAnnals of Oncology
Volume20
Issue number3
DOIs
Publication statusPublished - 2009

Keywords

  • Diffuse large B-cell lymphoma
  • Rituximab
  • Soluble interleukin-2 receptor

ASJC Scopus subject areas

  • Hematology
  • Oncology

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