Literature DB >> 26494971

Prognostic significance of plasma interleukin-6/-8 in pancreatic cancer patients receiving chemoimmunotherapy.

Shintaro Tsukinaga1, Mikio Kajihara1, Kazuki Takakura1, Zensho Ito1, Tomoya Kanai1, Keisuke Saito1, Shinichiro Takami1, Hiroko Kobayashi1, Yoshihiro Matsumoto1, Shunichi Odahara1, Kan Uchiyama1, Hiroshi Arakawa1, Masato Okamoto1, Haruo Sugiyama1, Kazuki Sumiyama1, Toshifumi Ohkusa1, Shigeo Koido1.   

Abstract

AIM: To investigate the association of plasma levels of interleukin (IL)-6 and -8 with Wilms' tumor 1 (WT1)-specific immune responses and clinical outcomes in patients with pancreatic ductal adenocarcinoma (PDA) treated with dendritic cells (DCs) pulsed with three types of major histocompatibility complex class I and II-restricted WT1 peptides combined with chemotherapy.
METHODS: During the entire treatment period, plasma levels of IL-6 and -8 were analyzed by ELISA. The induction of WT1-specific immune responses was assessed using the WT1 peptide-specific delayed-type hypersensitivity (DTH) test.
RESULTS: Three of 7 patients displayed strong WT1-DTH reactions throughout long-term vaccination with significantly decreased levels of IL-6/-8 after vaccinations compared with the levels prior to treatment. Moreover, overall survival (OS) was significantly longer in PDA patients with low plasma IL-6 levels (< 2 pg/mL) after 5 vaccinations than in patients with high plasma IL-6 levels (≥ 2 pg/mL) (P = 0.025). After disease progression, WT1-DTH reactions decreased severely and were ultimately negative at the terminal stage of cancer. The decreased levels of IL-6/-8 observed throughout long-term vaccination were associated with WT1-specific DTH reactions and long-term OS.
CONCLUSION: Prolonged low levels of plasma IL-6/-8 in PDA patients may be a prognostic marker for the clinical outcomes of chemoimmunotherapy.

Entities:  

Keywords:  Chemoimmunotherapy; Delayed-type hypersensitivity; Dendritic cell; Interleukin-6; Interleukin-8; Pancreatic cancer; Wilms’ tumor 1

Mesh:

Substances:

Year:  2015        PMID: 26494971      PMCID: PMC4607914          DOI: 10.3748/wjg.v21.i39.11168

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


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