Acute myeloid leukemia (AML) is a sub-type of acute leukemia, with pathogenetic heterogeneity. It is typically driven by different genetic abnormalities, influencing hematopoietic stem or progenitor cells, and eventually causing the emergence of abnormal clones. Although researchers have explored the mechanisms of leukemogenesis, and have conducted clinical trials for many potential therapies, intensive chemotherapy (IC) remains the mainstay of induction chemotherapy regimen for fit AML patients, which combines anthracyclines and cytarabine (known as the “7 + 3” regimen), followed by several courses of consolidation chemotherapy and/or hematopoietic stem cell transplantation (HSCT).[2,3] Unfortunately, AML patients older than 65 years, with various complications, cannot tolerate IC, and have very limited survival rates of 10% or lower.[4–6]
Epigenetics encompass changes to chromatin structure occurring through histone modifications, DNA methylation, as well as abnormalities of the higher-order chromatin structures, affecting the level of gene expression.[7,8] Epigenetic regulators can be categorized as “writers,” “erasers,” and “readers,” and they include DNA and histone methyltransferases, histone deacetylases (HDACs), and bromodomain-containing proteins, respectively. Epigenetic dysregulation is essential for disease occurrence and progression of hematological malignancies.[10,11] This is especially true for AML, in which several epigenetic mutations have been discovered and shown to be critical drivers in leukemogenesis and disease development. Such mutations, causing epigenetic alterations, include those related to regulation of histone modification (eg, enhancer of zeste homolog 2) and DNA methylation (eg, DNA (cytosine-5-)-methyltransferase 3 alpha), as well as enzymes involved in metabolism (eg, isocitrate dehydrogenase) causing consequences of epigenetics.[2,9,12–14] A further exploration of epigenetic abnormality will illuminate the mechanisms of leukemogenesis, elucidate prognosis, and shed light on molecular biomarkers for response prediction.
Abnormal DNA methylation and DNA hydroxymethylation are critical steps towards silencing tumor suppressor genes and, eventually, fulfilling an essential role in the process of malignant transformation.[15,16] DNA methyltransferase (DNMT) inhibitors (eg, 5-azacytidine [5-AZA], and 5-aza-2′deoxycytidine [decitabine, DAC]), are known as hypomethylating agents (HMAs). They have been used for more than 10 years to treat AML patients who are either ineligible for IC or are at high-risk for myelodysplastic syndromes (MDS). A prolonged survival has been observed from clinical trials under the treatment of HMAs compared to supporting treatment in MDS patients, with a tendency for better prognosis in AML cohorts. In real-world settings, however, treatment failure is often found.[17–20]
Besides, gene transcription is modified during the dynamic process of histone acetylation, which is closely controlled by the competing effects of histone lysine acetyltransferases and HDACs with histone acetylation always causing a more accessible to be chromatin structure facilitating gene transcription. HDAC inhibitors include heterogenous structures that improve the level of histone acetylation, ultimately promoting transcription of different genes associated with cell differentiation, cell cycle modification, and cell apoptosis. Yet, low response rates have been shown in several clinical trials under the monotherapy of HDAC inhibitors in AML.
In the following sections, we present an overview of the mechanisms of action and relevant clinical trials, in which HMAs and HDAC inhibitors were used to treat AML patients. Due to the limited therapeutic effects of HDAC inhibitors and HMAs when used alone, combined strategies of HMAs and HDAC are explored currently in various phases of clinical trials, and will also be the emphasis of this review.
Mechanisms of DAC and 5-AZA treatment in AML
The HMAs, 5-AZA and DAC, are most commonly used DNMT inhibitors, and have been approved for clinical treatment of hematologic malignancies (specifically for AML and high-risk MDS). It has also been found that lower doses of the drugs could be clinically effective and tolerable.
The mechanisms of the two approved HMAs remain to be fully elucidated. DAC is phosphorylated by deoxycytidine kinase, and ultimately transforms into decitabine triphosphate, which can be incorporated into DNA and has no direct influence on RNA. 5-AZA is initially phosphorylated and activated by uridine-cytidine kinase that can be integrated into the RNA structure and significantly inhibit the formulation of proteins.[23–25] Azacitidine diphosphate is then converted by ribonucleotide reductase into decitabine diphosphate, which is further phosphorylated by nucleoside diphosphate kinases to become decitabine triphosphate. It then competitively replaces cytosine in the CpG islands occurring in clusters of promoter regions. Subsequently, decitabine triphosphate suppresses methylation level of the promoter, based on a covalent bond with the DNMT enzymes, resulting in their eventual degradation.[26,27] When compared with 5-AZA, DAC shows a more potent function in restraining the level of methylation at equimolar doses, probably because of more incorporation of 5-AZA into the structure of RNA than into DNA. High dose of active decitabine triphosphate can result in its incorporation into DNA, inhibiting DNA synthesis, and ultimately causing cytotoxic effect. At lower doses, it mainly depletes DNMT enzymes, followed by reduced DNA methylation level and methylation-induced gene silencing[24,25,29–32] [Figure 1]. Therefore, the use of low-dose DAC or 5-AZA in AML has been evaluated in various clinical trials.
In vitro studies have shown a synergistic influence of HDAC inhibitors and HMAs [Figure 1], which will be further discussed in the following sections. Additionally, several studies have shown that the combination of HMAs with cytarabine or anthracycline also has a synergistic anti-leukemic influence, probably because the active phosphorylated form of cytarabine can be phosphorylated by deoxycytidine kinase induced by 5-AZA.[33,34] HMAs can also work as chemosensitizers, restore expression level of tumor suppressor genes and eventually improve the susceptibility to chemotherapies. In more details, a recent study reported that DAC increased cytotoxicity in Kasumi-1 and HL60/ADR cells when combined with cytarabine, aclarubicin, and harringtonine. DAC-induced depletion of DNMT is S-phase-dependent and is more extensive in actively cycling cells. Leukemic cells at the G0/G1 phase could be induced into the S-phase by granulocyte colony-stimulating factor (G-CSF), making them more responsive to DAC. Based on these synergistic effects, several completed clinical trials combining HMAs and chemotherapy have been reported.
Selective clinical trials of HMAs in AML
In the early clinical trials of HMAs, DAC was used at a tolerated dose of 1500 to 2500 mg/m2 to induce DNA synthesis arrest and cytotoxicity. More recently, DAC at high-dose was stopped due to severe hematological toxicity and prolonged myelosuppression.
A phase I/II clinical trial was performed to explore the therapeutic effects of low-dose DAC. Elderly AML patients were given doses of 30 to 90 mg/m2 of DAC, three times per day for 3 days. These low doses resulted in an overall response rate (ORR) of 45% after about two intensive courses, including 15% complete remission (CR) rate and 30% partial remission rate. For these responders, the median survival duration was 19 weeks. A phase II multicenter study in older AML cohorts undergoing DAC treatment at a dose of 135 mg/m2 every 6 weeks demonstrated that DAC is tolerable and patients had a relatively interesting ORR of 26% and median overall survival (OS) of 5.5 months, free of adverse-risk karyotypes [Table 1]. A similar trial with DAC at a dose of 20 mg/m2 for five days within a 4-week cycle, obtained a CR of 24%. These results contributed to a randomized phase III multicenter trial for older AML cohorts (the DACO-016 trial), in which patients received DAC at a dose of 20 mg/m2 given daily for 5 days in a 4-week cycle vs. other therapies composed of the best supportive care (BSC) and low-dose cytarabine (LDAC). The findings demonstrated a remarkably improved response rate for DAC (18% vs. 8%; P = 0.001) and a tendency for improved OS (8 vs. 5 months, P = 0.108). And for 271 patients having white blood cells <15 × 109/L and bone marrow (BM) blasts >30% in this trial, a better response rate of 27% for DAC could be observed when compared to the other treatment regimens (11%), contributing to a remarkably improved OS for the DAC arm (8.6 vs. 4.7 months, P = 0.0033).
In a single-center study including 84 patients with AML or MDS and treated with 10-day DAC 20 mg/m2, the results illustrated patients with adverse-risk karyotypes had better DAC response rates than those with intermediate or low-risk cytogenetics (67% vs. 34%, P < 0.001). Furthermore, response rate in patients harboring TP53 mutation was significantly higher compared to all other patients (100% vs. 41%, P < 0.001). However, responses in patients with adverse-risk karyotypes remained to be limited and caused OS similar to those with intermediate-risk karyotypes. Based on these findings, it remains controversial whether the 5 or 10-day DAC regimen should be recommended. In a phase II trial containing a smaller cohort, 53 AML patients presented a better CR rate (47%) and ORR (64%) after a median of three 10-day therapy courses. Cases with adverse-risk karyotypes benefited particularly well, achieving CR rate of 52%. Based on results from the two studies, a phase III randomized clinical trial with the prolonged treatment of DAC vs. the 5-day application would be conducted to settle this question. Besides, it is still unknown about how DAC would function when used as the consolidation regimen. A hint in this direction comes from a retrospective study including 75 patients with AML. Patients received HMAs either as induction therapy (n = 34), consolidation (n = 13), or salvage (n = 28) regimens. Results showed that response rate in first-line treatment was obviously better than in the salvage course (26.5% vs. 3.6%). However, prolonged OS was actually observed during salvage treatment, thereby indicating that HMAs might be useful at all treatment stages [Table 1].
5-AZA (75 mg/m2 given for 7 days) is an approved therapeutic option for high-risk MDS and older AML patients unfit for IC. In the MDS cancer and leukemia group B (CALGB) trial, 103 patients reclassified into AML obtained a response rate of 35% to 48% and achieved the median survival duration of 19.3 months when given 5-AZA rather than BSC (12.9 months). Subsequently, results from the AZA-001 trial on 113 older AML patients indicated that 5-AZA also contributed to an increased OS (24.5 months) compared to conventional care regimens (CCR, including BSC, LDAC, or IC, 16 months). These studies illustrate that 5-AZA is superior to LDAC or BSC in AML patients with a low blast percentage (21%–30%). Besides, in older AML cases with BM blasts ≥30% the AML-001 trial, 488 patients were randomly given either 5-AZA or CCR. Although the CR rates for both arms were similar (5-AZA 28% vs. CCR 25%), AML patients receiving 5-AZA had a tendency of improved median OS (10.4 vs. 6.5 months, P = 0.100). Particularly, OS significantly increased after censoring AML patients that were treated with 5-AZA at the beginning of the second-line treatment (12.1 vs. 6.9 months, P = 0.019). For consolidation regimen after two or more courses of induction chemotherapies, 5-AZA might also be considered as a potential treatment option as was shown in a phase III clinical trial, demonstrating prolonged disease-free survival of 63% vs. 39% for 5-AZA vs. control, respectively (P = 0.005). In a retrospective study on relapsed or refractory AML (r/r AML), 5-AZA given for a median of four courses obtained an ORR of 17% and a median OS of 8.4 months [Table 1].
Due to the synergistic anti-leukemic effects in the combination of HMAs and anthracycline or cytarabine mentioned above, several clinical trials have been performed to explore the therapeutic effect of this combination. A regimen of HMAs plus cytarabine was proposed to be an interesting option for older AML patients unsuitable for IC, due to the moderate and transient response rates from both agents when used alone.[40,46] Initial phase I or II studies were performed in AML patients who received sequential treatment of HMAs followed by “7 + 3” regimens, showing CR rate of 83%, without increased toxicity.[35,50,51] However, a larger phase II clinical trial in older AML cohorts presented opposite results, showing that a combination of 5-AZA + “7 + 3” induction regimen not only failed to show any prolonged survival, but also caused more adverse events (AEs) when compared with intensive induction chemotherapy alone [Table 1]. Identifying molecular biomarkers as predictors for responses to HMAs, fine-tuning of the therapeutic schedules, and checking this combination in patients with intermediate- or favorable-risk cytogenetics might be a viable option to explore in the future.
Mechanisms of HDAC inhibitors in AML
Histones are critical for packaging the DNA into formulations such as nucleosomes and chromatin. Histone acetyltransferases and HDAC fulfil the functions of histone tails’ acetylation and deacetylation, respectively, playing a key role in epigenetic mechanisms that regulate genes transcription. Generally speaking, HDACs deacetylate lysine residue on proteins regulating cell apoptosis and proliferation, and are divided into four types according to their similarity to yeast HDACs. From structural aspect, HDAC inhibitors most commonly contain a hydroxamic acid or a benzamide zinc-binding cluster. However, several HDAC inhibitors can also attach to zinc in the absence of hydroxamic acid or benzamide. HDAC inhibitors are employed to treat malignancies because they inhibit excessive histone deacetylation [Figure 1] and modulate transcription factors, particularly those controlling expression level of tumor suppressor genes. A study on HDAC inhibitors showed that they could function in a number of ways: (i) inhibit the G1 phase of the cell cycle, (ii) promote cell apoptosis by inducing the mitochondria-driven apoptotic pathway or up-regulating death ligands and receptors, (iii) lead to DNA defects that cause cell death during mitosis, and (iv) contribute to autophagy through a number of pathways. Through these functions, HDAC inhibitors mainly mediate the death of cancerous cells and revealed less cellular cytotoxicity in healthy cells, thereby making these agents attractive for clinical treatment.
The drug panobinostat inhibits Class I of HDACs and degrades the oncoprotein AML1/ETO9a, a trigger of AML. Panobinostat contributed to a remarkable anti-leukemic effect without the requirement of functional p53 gene nor activation of conventional apoptotic pathways and could also affect cell cycle regulation. In a mouse model with t(8;21) AML, panobinostat achieved an obvious anti-leukemic effect and induced cell differentiation. Vorinostat is another HDAC inhibitor. It contains hydroxamic acid, and it binds to the zinc-containing pocket in the catalytic site of HDAC 1, 2, 3, and 6, leading to reversible inhibition of HDACs, promoting protein acetylation, regulating gene expression, and inducing differentiation, growth arrest, and apoptosis of cancer cells. Anti-tumor activity of vorinostat might arise from the oxidative stress it promotes, its modulation of gene expression, and its induction of DNA damage and genomic instability.[60,61] Valproic acid (VPA) is a short-chain fatty acid that also inhibits HDAC activity. It can induce differentiation by targeting the AML1/ETO-complex, and functions as AML cell proliferation inhibitor and apoptosis inducer, especially in t(8;21) AML. The susceptibility to natural killer (NK) cell-mediated lysis can also be improved by this drug. This is done through up-regulation of NK cell ligands on the leukemic cells,[63,64] and the result is that NK cells attack leukemic stem cells. The orally bioavailable benzamide HDAC inhibitor, entinostat, inhibits class I of HDAC enzymes, resulting in inhibition of cell growth and increased cytotoxicity to human cancer cells.[67–71] Entinostat is also shown to promote loss of leukemia maintenance and prolonged survival in murine model.[67,72] These growth inhibition and cytotoxicity might be due to transcript activation of anti-proliferation genes (eg, p21), transformation of growth factor-β type II receptor, and the induction of the maturation marker gelsolin.[67,71,73] Chidamide is a structural analog of entinostat that selectively inhibits HDAC1, 2, 3, 10. Through the function of reactive oxygen species, chidamide exhibited efficient anti-proliferative activity in AML cells, including stem cells, accompanied by the arrest at G0/G1 phase of the cell cycle and cell apoptosis. It controls anti-apoptotic- and pro-apoptotic-related proteins (PARP), including B-cell lymphoma 2, and activates caspase-3, causing the degradation of PARP. CD40 could also be activated by chidamide, and its downstream signaling pathways, c-Jun N-terminal kinase and nuclear factor kappa-light-chain-enhancer of activated B, were thus regulated. These results suggest that chidamide might be a novel medication targeting leukemia stem cells.[74,75]
Overall, HDAC inhibitors are a significant group of promising treatment agents for AML. However, the monotherapy of HDAC inhibitors has always presented moderate anti-leukemic effects, which will be discussed in the following sections. Therefore, it is necessary to explore special combination regimens, including HDAC inhibitors and other therapies. HDAC inhibitors have shown synergistic effect when combined with various IC [Figure 1], such as nucleoside analogs (eg, cytarabine), anthracyclines (eg, idarubicin), and topoisomerase inhibitors (eg, etoposide).[76–79] The mechanism of these synergistic effects has not been completely elucidated, but it is assumed that HDAC inhibitors help formulating a more open chromatin structure that probably allows for more extensive access of topoisomerase inhibitors to the DNA structure and thereby causing higher therapeutic effects of chemotherapies. Other studies, exploring this synergistic influence, for instance, between panobinostat and doxorubicin, implicated DNA double-strand breaks and activated the caspase-dependent apoptosis pathways, showing anti-leukemic efficacy. These results are the foundation of clinical trials combining HDAC inhibitors and IC.
Selected clinical trials of HDAC inhibitors in AML
A series of clinical trials have been performed with HDAC inhibitors in AML cohorts. Generally, HDAC inhibitor monotherapy achieved low response rates (10%–20%). In a phase II trial in 37 AML patients treated with vorinostat, only one case had hematologic improvement. In another phase I/II study, 42 patients with high-risk MDS (n = 5) or AML (n = 37) treated with panobinostat after allogenic-HSCT, received one of two schedules: schedule A of 10 mg weekly or schedule B of 20 mg every other week, using a “3 + 3” design. At least one G3/4 AE occurred in 35 out of the 42 cases, of which 22 cases were considered panobinostat-related. Incidence rates of G3/4 AEs were not different between the two schedules (A: n = 12, B: n = 10; A vs. B, 57% vs. 48%). After 2-year treatment with panobinostat, the relapse and non-relapse mortality across all doses was 20% and 5%, respectively, and survival probabilities of 2-year OS and relapse free survival (RFS) were 81% and 75%, respectively. In a phase II study of VPA alone or VPA combined with all-trans retinoic acid (ATRA), 75 cases with MDS or refractory and relapsed AML received either of the VPA regimens. 24% of the patients responded to the treatments [Table 2]. Other studies in adverse-risk AML and MDS, in which patients were treated with VPA, either as a monotherapy or combined with ATRA, have also revealed limited effects.[83–85] Due to these moderate or limited results of HDAC inhibitors monotherapy in AML, clinical trials have been designed to combine HDAC inhibitors with other therapies, such as IC or HMAs.
Phase I trial of vorinostat combined with cytarabine for r/r AML patients showed interesting outcomes: six of 17 (35%) cases had CR, although five of these patients later relapsed and died. In a larger phase II trial, testing a combination of vorinostat, cytarabine and idarubicin in 75 cases with AML or high-risk MDS, ORR was up to 85% and the addition of vorinostat did not cause increased toxicity. Interestingly, in this study, all patients with FLT3-ITD mutation responded positively, and NRF2 and CYBB mutations were considered as biomarkers related to higher survival rate. In a phase III trial (SWOG 1203), comparing between idarubicin plus high-dose cytarabine, IC, and vorinostat plus idarubicin, in 738 AML older patients (>60 years old), CR rates were similar across all groups (75%–79%), achieving clearly better outcomes for cases harboring favorable karyotypes in the “7 + 3” group. However, in another cohort that included r/r or secondary AML patients, the combination regimen of vorinostat, etoposide, and cytarabine, showed relatively lower response rate (33%) [Table 2].
In another clinical trial exploring panobinostat combined with cytarabine and idarubicin in older AML patients, the addition of panobinostat caused dose-limiting degree of toxicity but a longer RFS was also observed. In a phase II study evaluating the safety and efficacy of the same drug combination in 46 older AML patients with adverse-risk cytogenetics, the doses of panobinostat escalated at 15, 20, and 25 mg, given thrice weekly from the second week of a 4-week course. The ORR was 60.9%, including 43.5% of CR and 17.4% of Complete remission with incomplete blood count recovery (CRi). The event free survival (EFS) probability at 1-year was 78.3%. These results also revealed that a combination of panobinostat with IC demonstrated tolerable safety and efficacy in younger patients with high-risk AML. In another phase I study combining panobinostat and IC in older AML patients (60–85 years old), patients were treated daily with oral administration of 20 to 60 mg panobinostat, and on day 1, day 3, day 5, and day 8 patients also received fixed doses of daunorubicin and cytarabine. The CR/CRi was up to 32%, without dose-limited toxicity occurring in the dose escalation arms. The median OS was 10 months, which represents 23 months with CR/CRi vs. 7.8 months without CR/CRi (P = 0.02). Improved level of histone acetylation after the treatment with panobinostat was remarkably related to CR/CRi rates. These results illustrate that the combination of panobinostat with “7 + 3” for older AML patients was tolerable and that the improved level of histone acetylation induced by panobinostat was a predictor for CR/CRi [Table 2].
In a phase III randomized German-Austrian AML Study (Group 06-04), 186 AML patients randomly received two induction courses of a combination of idarubicin, cytarabine, and ATRA, either with VPA or without (regarded as the standard therapy). After induction chemotherapy, the VPA arm showed a tendency of lower CR rates when compared to the standard therapy (40% vs. 52%; P = 0.14), resulting from a tendency of higher early mortality in the VPA arm (26% vs. 14%; P = 0.06). As a result, VPA was restricted to the first induction course and the dose of idarubicin was reduced. Toxicities after this change dropped to rates comparable to those in the standard therapy. The two arms did not differ in EFS and OS (P = 0.95 and P = 0.57, respectively). However, RFS markedly increased in the VPA arm (5-year survival probability: 24.4% vs. 6.4%; P = 0.02). Subsequential analyses suggested that NPM1 mutation-positive AML patients might particularly benefit from the VPA regimen [Table 2].
Combination of HMAs and HDAC Inhibitors
Mechanisms of HMAs in combination with HDAC inhibitors in AML
Gene silencing is usually related to modification of histone tails and cytosine methylation in the gene promoter region. There might be a synergistic effect between HDAC inhibitors and HMAs to relieve transcriptional repression from tumor suppressor genes.In vitro studies have also demonstrated the presence of a synergistic influence between HMAs and HDAC inhibitors [Figure 1].
Transcriptome analyses in a reported study showed that a combination of DAC with panobinostat or VPA resulted in significantly higher transcripts than either treatment alone, illustrating a quantitative synergistic influence on genome-wide expression in U937 cells. This combined treatment particularly affected a mass of genes down-regulation, including epigenetic modifiers (eg, KDM2B) and oncogenes (eg, MYC) that are always overexpressed in solid and hematological malignancies. Gene body DNA demethylation and changes in acH3K9/27 could also be observed.
In another study, chidamide, combined with DAC, showed a noticeable synergistic anti-leukemic effect. Chidamide and this combination could both inhibit the proliferation of HL60 and NB4 cells. The G0/G1 phase could be blocked by chidamide alone, while the combination of chidamide and DAC mainly blocked the cycle at the G2/M phase, accompanied by higher p21 expression. In both chidamide monotherapy or the combination treatment, apoptosis of leukemic cells was induced through up-regulation of Bax and Caspase-3, and down-regulation of BCL-2, showing synergistic cytotoxicity.
Decitabine, combined with vorinostat, also showed a synergistic induction of cell apoptosis, inhibition of cell proliferation, promotion of histone acetylation, and further inhibition of the enzyme DNMT1 in HL60 cells. This combination therapy also caused reprogramming of unique biomarkers, including the receptor tyrosine kinase (AXL) gene that is known to be associated with cell survival and an adverse prognosis in AML. Based on this information, a combination of BGB324 (an AXL-specific inhibitor), DAC, and vorinostat increased the sensitivity of OCI-AML3 cells and significantly reduced disease burden and prolonged survival of murine models injected with pre-treated OCI-AML3 cells.
The combined influence of 5-AZA + HDAC1/2 inhibitors (ACY-1035, ACY-957) was also explored in HL60 and MV-4-11 cell lines. This combined treatment significantly reduced S phase cells, increased the number of CD11b-positive cells, and induced higher rate of cell apoptosis, when compared with 5-AZA or HDAC1/2 inhibitors alone. These results indicate the presence of a synergetic effect between 5-AZA and HDAC1/2 inhibitors in inhibiting primary AML blasts proliferation. More specifically, gene set enrichment analysis demonstrated that when compared to 5-AZA monotherapy, the combination of 5-AZA and HDAC1/2 inhibitors helped the enrichment of genes, including GATA binding sites within their promoter regions, showing GATA2 gene might be critical for the synergistic influence of HDAC1/2 inhibitors and 5-AZA.
Selected clinical trials of HMAs combined with HDAC inhibitors in AML
The combined effect of HDAC inhibitors and HMAs revealed in vitro studies contributed to a series of clinical trials in AML and MDS patients, in which the combined HMAs and HDAC inhibitors were tested.[66,99–106] Most studies showing a synergy were single-arm trials. Sequential multi-arm studies, comparing therapeutic effects between the combination of HMAs with HDAC inhibitors and monotherapy of HMA, yielded disappointing results. In a multi-center, open-label, prospective, randomized phase II trial, 259 patients with AML (n = 217) and MDS (n = 42) randomly received either 5-AZA alone (75 mg/m2 × 7 days, every 4 weeks) or 5-AZA in combination with vorinostat (300 mg orally, twice a day from day 3 to day 9). The combination regimen did not improve the ORR (P = 0.84) or OS (P = 0.32). Two larger phase II clinical trials that compared combined treatment with 5-AZA and HDAC inhibitors (entinostat or vorinostat) to 5-AZA monotherapy, also showed disappointing survival benefits for the combination therapy[66,105,107] [Table 3].
In addition, more hematologic side effects occurred in the combined regimen, leading to earlier termination of this treatment. A molecular basis for the lower response rate in the combination regimen showed lower reversal of methylation in promoter regions that were more prominent in the combined regimen than in the 5-AZA monotherapy. In addition, the therapeutic schedule of HDAC inhibitors in these trials was heterogenous in terms of the molecular targets. The pleotropic influence of these drugs might have cause the excessive cell toxicity, leading to reduced treatment duration and insufficient exposure time to drugs. Therefore, molecular biomarkers that can predict responses are highly desirable.[21,108] Future challenges for the combination regimen of HDAC inhibitors and HMAs are optimization of therapeutic schedules, including sequence of administration, dose of each drug, and drug administration time. Elucidating these aspects is important as pharmacodynamic antagonism between the drugs that were included in various regimens has been a critical problem, and must be settled in future clinical trials. Choosing more selective HDAC inhibitors is also of importance. Entinostat particularly targeting HDACs and vorinostat with less selection acting on other protein deacetylases have demonstrated similar results in MDS patients. But their utility in treating AML patients remains to be explored.[105,107] It is also important to explored whether novel HDAC inhibitors, such as belinostat, pracinostat, or panobinostat can show any additional therapeutic benefit.[108,109] To date, only one single-arm multicenter phase II study has evaluated the safety and efficacy of pracinostat in combination with 5-AZA in AML patients ≥65 years old who were ineligible for IC. The patients received pracinostat 60 mg/day, 3 days/week, for 3 consecutive weeks, plus 5-AZA at a daily dose of 75 mg/m2 for one week, in a 4-week course. Twenty-six of the fifty patients (52%) responded to the treatment, including 42% of CR, 4% of CRi, and 6% of morphologic leukemia-free state. These results are higher than historical data for 5-AZA alone. Median OS and PFS were 19.1 and 12.6 months, respectively, with a 1-year OS probability of 62%. When treated with the combined regimen, 43 cases (86%) had as least one grade 3 or worse therapy-related unfavorable events. Mortality rates in the 30 and 60-day treatments were 2% and 10%, respectively. It was concluded that pracinostat, combined with 5-AZA, was tolerable and active in the first-line treatment of older AML patients ineligible for IC,[110,111] which contributed to a phase III clinical trial of 5-AZA with/without pracinostat [Table 3].
Furthermore, due to the limited response to combination of HDAC inhibitors and HMAs, and the synergetic effects between ICs and either HDAC inhibitors or HMAs in experiments and clinical trials, a phase I/II multi-center clinical trial has been performed to investigate the safety and efficacy of epigenetic modifiers (chidamide and DAC) plus aclarubicin, cytarabine, and G-CSF, in 93 r/r AML patients. In total, 24 r/r AML patients achieved CR and 19 cases obtained CRi, with 46% of ORR. The OS of the 43 responders was remarkably prolonged. 55.6% of patients with mutations involved in transcription factors and epigenetics but without FLT3-ITD mutation had CR/Cri, whereas the ORR was 36.7% for the remaining patients. It was therefore clear that the combined CDCAG regimen was well-tolerated and effective in r/r AML patients. Patients with gene aberrations associated with epigenetics and transcription factors, but without FLT3-ITD, might benefit from this novel regimen [Table 3].
Epigenetic therapy in AML treatment is still in its infancy, but has developed quickly, holding great promise as a new therapeutic approach. In some early trials, treatment of AML patients with HMAs or HDAC inhibitors alone achieved modest or even disappointing therapeutic effects. Combination regimens, such as co-treatment with HMAs/HDAC inhibitors and IC, resulted in better response rates and prolonged survival, when compared to HMAs or HDAC inhibitors monotherapy. However, the therapeutic effects of combination of HMAs with HDAC inhibitors still need to be further explored from various aspects. Further research is also necessary to identify the therapeutic effect of the triple combination of HMAs, HDAC inhibitors, and IC.
This work was supported by grants from the National Natural Science Foundation of China (No. 81670162, No. 81970151, and No. 81470010).
Conflicts of interest
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