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DOI 10.1016/j.clinbiochem.2013.11.026

Медицинская библиотека · Clinical biochemistry · 2013

Elevated soluble IL-2 receptor levels correlate with tumor bulk of follicular lymphomas with intestinal involvement.

Iwamuro Masaya, Shinagawa Katsuji, Okada Hiroyuki, Takata Katsuyoshi, Yoshino Tadashi, Yamamoto Kazuhide

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Аннотация

OBJECTIVES

Establish a correlation between serum soluble interleukin 2 receptor (sIL-2R) levels and clinical characteristics of follicular lymphoma patients with gastrointestinal involvement.

DESIGN AND

METHODS

Patients (n=44) presenting with follicular lymphoma lesions in the gastrointestinal tract were enrolled into the study and divided into 2 groups based on sIL-2R levels (normal vs. elevated). Clinical characteristics were also analyzed between groups.

RESULTS

Patients with elevated sIL-2R levels likely had systemic follicular lymphoma involvement (Ann Arbor system staging IIIES/IV or Lugano system staging II-2/IV), involvement of 5 or more nodal areas, and presentation of bulky tumors in the gastrointestinal tract. These patients also presented a high Follicular Lymphoma International Prognostic Index (FLIPI) score, suggestive of poor prognosis. No differences were found among other clinical characteristics including sex, age at lymphoma diagnosis, histological grade, LDH levels, bone marrow involvement, hemoglobin levels, and identification of tracer accumulation in gastrointestinal lesions by positron-emission tomography scanning.

CONCLUSIONS

sIL-2R levels can be used as an independent prognostic index in follicular lymphoma patients based on the correlation with the FLIPI score. Moreover, since high sIL-2R levels were associated with a large tumor bulk, sIL-2R may serve as a good indicator for monitoring disease relapse or progression.

Для цитирования: Iwamuro Masaya, Shinagawa Katsuji, Okada Hiroyuki, Takata Katsuyoshi, Yoshino Tadashi, Yamamoto Kazuhide. Elevated soluble IL-2 receptor levels correlate with tumor bulk of follicular lymphomas with intestinal involvement.. Clinical biochemistry. 2013. DOI: 10.1016/j.clinbiochem.2013.11.026.

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