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Br J Cancer. 2016 Feb 16;114(4):463-8. doi: 10.1038/bjc.2016.11. Epub 2016 Feb 4.

High level of interleukin-10 in serum predicts poor prognosis in multiple myeloma.

Wang H1,2, Wang L1,2, Chi PD1,3, Wang WD1,2, Chen XQ1,2, Geng QR1,2, Xia ZJ1,2, Lu Y1,2.

Author information

1
State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, Guangdong 510060, People's Republic of China.
2
Department of Hematologic Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong 510060, People's Republic of China.
3
Department of Clinical Laboratory, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong 510060, People's Republic of China.

Abstract

BACKGROUND:

Interleukin-10 (IL-10) is a inhibiting inflammatory cytokine that plays an important role in immune suppressive microenvironment in multiple myeloma (MM). Whether the level of serum IL-10 could predict treatment response and survival outcomes or not needs to be investigated in MM patients.

METHODS:

The level of IL-10 in serum was measured using enzyme-linked immunosorbent assay in 188 patients with newly diagnosed MM.

RESULTS:

The best cutoff value for IL-10 in predicting survival is 169.69 pg ml(-1) with an area under the curve (AUC) value of 0.747 (P<0.001). In all, 92 patients (48.9%) were classified as high-IL-10 group (>169.96 pg ml(-1)) and 96 patients (51.1%) as low-IL-10 group (⩽169.96 pg ml(-1)). The overall response rate (ORR) was 79.2% in low-IL-10 group, significantly higher than that in high-IL-10 group (53.3%, P<0.001). Patients in low-IL-10 group had significantly better survival compared with those in high-IL-10 group (3-year PFS rate: 69.3% vs 13.3%, P<0.001; 3-year OS rate: 93.6% vs 51.9%, P<0.001). Multivariate analysis revealed that serum IL-10 level >169.96 pg ml(-1) at diagnosis and certain cytogenetic abnormalities were two adverse factors for PFS and OS.

CONCLUSIONS:

Our data suggest that serum IL-10 at diagnosis is a novel, powerful predictor of prognosis for MM.

PMID:
26882069
PMCID:
PMC4815778
DOI:
10.1038/bjc.2016.11
[Indexed for MEDLINE]
Free PMC Article

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