Immune regulatory effects of panobinostat in patients with Hodgkin lymphoma through modulation of serum cytokine levels and T-cell PD1 expression

The Hodgkin Reed–Sternberg (HRS) cells of classical Hodgkin lymphoma (cHL) are surrounded by a number of reactive and inflammatory cells. The ability of HRS cells to evade immune surveillance is linked to a network of cytokines and chemokines that are produced by HRS and the surrounding cells, in addition to the occasional aberrant expression of programmed death ligand-1 (PDL-1) by HRS that inhibits the activation of PD1-expressing T lymphocytes. Histone deacetylase (HDAC) inhibitors can alter the levels of cytokines and chemokines in vitro, favoring a TH1-type immune response. HDAC inhibitors also enhance antitumor immunity by HDAC11-mediated upregulation of OX40L. Panobinostat is a potent oral pan-HDAC inhibitor, which induces cell death, autophagy and increase the expression of natural killer cell receptors in cHL cell lines. It triggers an enhanced lymphocyte-dependent lyses of cHL cells, suppresses the IFN-gamma release and increases TNF-alpha secretion. A recent phase II study of panobinostat in 129 patients with relapsed or refractory cHL showed overall response rate of 27% including complete response in 4%. Tumor size reduction was observed in 74% of patients, and the median progression-free survival duration was 6.1 months. In a subset of patients in this study, several serum cytokine and chemokine levels were analyzed, and the decrease of TARC levels were found associated with clinical responses. The present study shows the in vivo effect of the pan-HDAC inhibitor panobinostat on an expanded panel of 52 serum cytokines and chemokines from the phase II study. In addition, a pilot study of peripheral blood lymphocytes for PD1 expression before and after panobinostat treatment was conducted. The phase II clinical trial of single-agent panobinostat (clinicaltrials.gov NCT00742027) with exploratory correlative study was approved by the institutional review board at each center. All patients provided written informed consent. To be eligible for this clinical trial, patients were required to have age ⩾ 18 years, histopathologically confirmed cHL that had relapsed or were refractory to autologous stem cell transplant, and had ⩽ 5 prior systemic treatment regimens. The treatment consisted of oral panobinostat (40 mg) three times per week every week in 3-week cycles. Response assessment was based on Cheson Criteria, performed at the end of every two cycles. Serial serum samples were collected from 65 consenting patients with relapsed or refractory cHL treated in this study before (day 0) and during (days 8 and 21) therapy. Serum was prepared at each study site, and the samples were frozen, de-identified and shipped to UT MD Anderson Cancer Center. We analyzed serum levels of 52 cytokines (Figure 1a) and the levels were analyzed for their association with the eventual response. Serum cytokines and chemokine were measured using the Human Cytokine/Chemokine Magnetic Beads Panel kits (Millipore, Billerica, MA, USA, Cat. Nos HCYTMAG-60K-PX29 and MPXCHCYP2MK23) on Luminex-100 ELISA System (Luminex Corporation, Austin, TX, USA). Cytokine levels were plotted relative to the median value of healthy controls in box-and-whisker plots. Levels of IL2 and IL4 were plotted for their measured values because those cytokines were not detectable in healthy controls. Comparison of the levels in two groups or different time points were conducted by analysis of variance test. For a pilot analysis of peripheral blood lymphocytes for PD1 expression using a flow cytometry, blood samples were collected with EDTA and mononuclear cells were extracted and analyzed within 24 h. The expression levels were marked by the relative value (delta) to the immunoglobulin isotype expression in peripheral blood mononuclear cells with CD4 or CD8 expression. Serial serum samples (pretreatment, days 8 and 21) were available from 65 patients. In this group, median age was 32 years (range 18–70), 55% were male, complete response rate was 2%, overall response rate was 31%. The waterfall chart of the changes in the sum of the product of the diameters was similar to that of the entire population in the clinical trial. Thus, our population is generally considered representing the entire population treated with panobinostat in this study. Changes in the level of each cytokine are summarized in Figure 1a. Baseline values of 21 cytokines (EGF, Eotaxin2, IL6, IL16, MCP1, MCP2, MCP4, TARC, TPO, VEGF, 6Ckine, BCA1, cutaneous T-cell-attracting chemokine (CTACK), Eotaxin3, I309, MIP1 delta, Il20, SCT, SDF1alpha-beta, IL2 and IL4) were higher than the maximum value of normal controls in majority (475%) of patients. We have identified 14 cytokines whose serum levels significantly decreased after treatment with panobinostat (Figure 1a), and 11 of them were still considered significant after multiple testing adjustment with a method controlling falsediscovery rate (Figure 1a, EGF, VEGF, Eotaxin, GM-CSF, IL6, IL12p40, Eotaxin2, MCP2, MCP4, TARC, TPO and IL28A). IL8 levels were found to increase after treatment (P= 0.008) but the actual changes of the levels were small. We compared the levels of cytokines in responders (patients achieving complete or partial response) and nonresponders (patients without response). Cytokines whose levels were significantly different between responders and nonresponders on at least one of the days (day 0, 8 or 21) are shown in Figure 1b. Most notably, IL3 levels were consistently lower in responders than in nonresponders throughout the course of treatment. In addition, posttreatment levels of IL1-alpha (day 8), IL2 (day 8) and IL21 (day 21) were lower in responders than in nonresponders. Posttreatment levels of tumor necrosis factor-related apoptosisinducing ligand (TRAIL) (days 8 and 21) and CTACK (day 8) were higher in responders than in nonresponders. However, none of the changes from baseline was significantly related to response after multiple testing adjustment with a method controlling falsediscovery rate. We next analyzed the absolute (day 8− day 0) or relative ((day 8−day 0)/day 0) changes in the cytokine levels for their association with response (data not shown). Responders showed greater absolute decrease in the IL20 levels from day 0 to 8 Citation: Blood Cancer Journal (2014) 4, e236; doi:10.1038/bcj.2014.58 © 2014 Macmillan Publishers Limited All rights reserved 2044-5385/14