Recent advances in the understanding and treatment of acute myeloid leukemia

TET2

TET2 is a dioxygenase enzyme using alpha-ketoglutarate (αKG), Fe²⁺, and O₂ for hydroxylation of DNA methylcytosine (5mC), converting it into 5-hydroxymethylcytosine (5hmC), which can be converted into other derivatives, including ultimately demethylated DNA. TET2 is one of the most commonly mutated genes in myeloid malignancies, and TET2 mutations are also found in apparently hematologically normal individuals with clonal hematopoiesis^13,14. TET2 mutations are commonly an ancestral mutational event and, as such, constitute a suitable target for intervention in the early stages of hematopoietic stem cell/hematopoietic progenitor cell (HSC/HPC) expansion. Tet2 loss/haploinsufficiency in HSCs/HPCs leads to MDS/MPN development in mice and cooperates with other disease alleles (for example, AML1-ETO or FLT3-ITD) to induce AML^15–18. Specifically, Tet2 loss leads to increased HSC self-renewal and skewed differentiation toward the monocytic lineage^14,15. TET2 catalytic activity is required for its function as a myeloid leukemia tumor suppressor in HSCs/HPCs¹⁷.

TET2 mutations are mostly heterozygous, resulting in enzymatic haploinsufficiency, leading to decreased 5hmC and concomitantly increased 5mC. Therefore, a compelling therapeutic strategy is to augment TET2 function by increasing the enzymatic activity of the remaining wild-type allele. To split O₂ for dioxygenation, TET2 requires three electrons: two from αKG and one from vitamin C¹⁵. Agents such as dimethyl 2-oxoglutarate (DMKG) and vitamin C augment TET2 enzymatic activity in vitro and in mouse models and hold the potential to restore TET2 activity¹⁹. The phenotype of Tet2 restoration, which is mimicked by vitamin C treatment, includes reversal of aberrant hematopoietic stem and progenitor cell (HSPC) self-renewal and restoration of hypomethylation, differentiation, and cell death¹⁹. Activators of TET2 catalytic activity, such as vitamin C, are capable of reversing the leukemic-transforming ability of TET2 haploinsufficiency and thus represent promising combination partners with other therapies, such as DNA hypomethylating agents (HMAs) and p300 inhibitors¹⁹. Cimmino et al. have also shown that TET-mediated DNA oxidation induced by vitamin C treatment in leukemia cells may enhance their sensitivity to poly (ADP-ribose) polymerase (PARP) inhibitors¹⁹. Combining vitamin C with HMAs in TET2-mutant (TET2m) MDS to augment their therapeutic potential is now being studied in the clinic. Clinical trials using high-dose intravenous vitamin C in TET2m MDS, with or without concomitant HMA therapy, are now available (ClinicalTrials.gov Identifier: NCT03433781) and this represents an exciting new therapeutic strategy given that TET2m patients already have increased sensitivity to HMAs²⁰. Given that TET2 clonal hematopoiesis of indeterminate potential (CHIP) mutations affect older adults (~5%)¹³, the importance of developing TET2-targeted therapies will only become more relevant as the population ages and the incidence of both de novo and therapy-related MDS continues to rise.

ASXL1

The Drosophila additional sex-combs (ASX) gene is a chromatin-binding polycomb protein required for embryogenesis. Genomic studies have highlighted that the ASXL (additional sex combs-like) family members ASXL1 and ASXL2 are recurrently mutated in human AML. ASXL1 is mutated (deleted or truncated) at high frequencies in all forms of myeloid malignancy^21,22; it is associated with poor prognosis in patients with chronic myelomonocytic leukemia (CMML), MDS, myelofibrosis, and AML^23,24. Thus, therapies targeting mutant ASXL1-bearing cells are sorely needed. In contrast, ASXL2 is specifically mutated in t(8;21) AML²⁵. Importantly, ASXL1 and ASXL2 mutations occur in a mutually exclusive fashion in t(8;21) AML and, owing to their similarities, it has been hypothesized that there is a shared mechanism of leukemogenesis arising from these two mutations. However, it is still not clear whether mutations in ASXL1/2 confer loss-of-function, dominant-negative activity or generate a novel or altered function. Thus, their shared or unique mechanisms in leukemogenesis remain unclear. The majority of the ASXL1 mutations are nonsense/frameshift and heterozygous and expected to be loss of function. However, a truncated ASXL1 protein (C-terminus) has been shown to be expressed in cells harboring homozygous mutations of ASXL1, suggesting dominant-negative or even gain-of-function activity²⁶. Whether mutations in ASXL1 generate haploinsufficiency or dominant-negative or gain-of-function proteins (or combinations thereof) is a question with great clinical implications given the highly recurrent and adverse nature of ASXL1 mutations in MDS/AML.

To this end, various groups have generated model systems to dissect the possible roles of ASXL1/2 alterations in leukemogenesis and identify therapeutic vulnerabilities they may create^27,28. Avenues for identifying drug candidates for ASXL1/2-mutated myeloid malignancies include studying the biological effects of ASXL1 versus ASXL2 loss in the presence of cooperating mutations such as AML1-ETO.

Lysine acetyltransferases

The CBP/p300 coactivator family of histone lysine acetyltransferases (KATs) is another emerging and promising target in myeloid malignances. KATs—and, in particular, CBP/p300—have been shown to play important tumor suppressor and oncogenic roles in cancer^29,30. Whereas histone deacetylases have been targeted therapeutically in patients with myeloid neoplasms (with modest success), the KAT enzymes have been largely ignored. Since the first nuclear KAT enzyme was isolated 20 years ago³¹, exciting data have emerged implicating histone (and non-histone) protein acetylation in regulating gene expression and the pathways that control normal and neoplastic cell growth. CBP and p300 are two related, broadly expressed KAT proteins that have been shown to affect normal HSC self-renewal and differentiation²⁹. Mutations in the EP300 (KAT3B) and CBP (KAT3A) genes have been found in lymphoma, small cell lung cancer, and other solid tumors, identifying their tumor suppressor function³². p300 can also function as an oncogene in AML³³, melanoma³⁴, and prostate cancer³⁵. In fact, there appear to be distinct roles for p300 in mouse models of myeloid malignancies: an oncogenic role in AML1-ETO-driven AML³³ and a tumor suppressor role in MDS driven by the NUP98-HOXD13 (NHD13) fusion protein³⁶. Consequently, p300 may display variable activity, depending on the disease that it initiated. The cell context-specific functions of p300 suggest that developing both agonist and antagonist drugs may be therapeutically relevant.

CBP/p300 inhibitors. In 2011, we identified the critical role of p300 in binding to AML1-ETO and the subsequent acetylation of AML1-ETO on K43, which regulates the ability of AML1-ETO to activate gene expression, promote self-renewal, and trigger AML³³. We showed that both pharmacologic inhibition and genetic knockdown of p300 improve the survival of AML1-ETO-bearing mice and that CBP/p300 inhibitors impair the growth of AML1-ETO-expressing (and several other) human leukemia cell lines³³. This suggests that p300/CBP may be critical for leukemia cell self-renewal and that targeting its catalytic activity may have broad therapeutic potential in AML1-ETO-positive AML. The first selective CBP/p300 inhibitor (Lys-CoA) was developed in the 1990s³¹, and newer-generation, more potent CBP/p300 inhibitors are in active development and are being studied in pre-clinical cancer models³⁷. Salicylate derivatives and related anti-inflammatory drugs such as diflunisal have also been demonstrated to inhibit both CBP and p300 and shown anti-leukemic activity in pre-clinical AML models³⁸.

CBP/p300 activators. Despite the rarity of the t(2;11)(q31;p15) in MDS, NUP98-HOXD13-driven MDS mice have been studied since 2005 because they accurately reflect the clinical behavior of human MDS^39,40. This model has been used by us and others to study the role of p53⁴⁰, Msi2⁴¹, and p300^33,36 in MDS. Notably, deletion of p300 (but not CBP) markedly accelerated leukemogenesis in the setting of NHD13-driven MDS, as 100% of the NHD13⁺, p300 null mice died from AML within 20 weeks³⁶. Although NHD13⁺ bone marrow (BM) cells demonstrated defective in vitro growth, which is characteristic of MDS, the absence of p300 promoted the growth and self-renewal of these cells despite having little or no effect on normal mouse BM cells. The underlying mechanisms are being actively pursued using this and other mouse models of MDS/AML. Additionally, p300 activators are being investigated in these models. One candidate compound is I-CBP112, a selective and potent p300/CBP bromodomain inhibitor⁴² that unexpectedly stimulates the acetylation of nucleosomes by both p300 and CBP. Therefore, exposure to I-CBP112 increases H3K18Ac in multiple cancer cell lines⁴³. I-CBP112 is being assessed for anti-growth properties in myeloid malignancies with subnormal p300/CBP function. Ongoing studies will assess whether restoring p300/CBP function in neoplastic cells will trigger growth arrest or apoptosis.

Protein arginine methyltransferases

To date, cancer therapies targeting histone modifications have been directed primarily toward lysine methyltransferases, such as DOT1L and EZH2⁴⁴. More recently, the PRMTs have emerged as promising drug targets as well. PRMTs are ubiquitous enzymes and include PRMT1, PRMT4, PRMT5, and PRMT6. Type I PRMTs result in asymmetric arginine dimethylation, whereas type II enzymes catalyze symmetric arginine dimethylation. Most pre-clinical work at this time is focused on PRMT1 (type I), PRMT4 (type I), and PRMT5 (type II). PRMT4, also known as coactivator-associated arginine methyltransferase 1 (CARM1), is a transcriptional regulator with unique histone (H3R17 and H3R26) and non-histone (MLL, splicing factors, SWI/SNF, p300, and RUNX1) targets⁴⁵. PRMT4 has been shown to be overexpressed in AML cell lines and patient samples and to block myeloid differentiation, possibly through its effects on RUNX1⁴⁶. In pre-clinical models, PRMT4 short hairpin RNA (shRNA) knockdown has been shown to induce apoptosis and differentiation of AML cells. Further studies, with small-molecule PRMT4 inhibitors, are ongoing in AML cell lines and murine models. PRMT5 inhibitors are also under development for potential use in lymphoma, solid tumors, and AML^45,47,48. The PRMTs, particularly PRMT4 (but also PRMT1 and PRMT5), represent an exciting new epigenetic drug target class with the potential to help overcome the myeloid differentiation block and inhibit the aberrant self-renewal seen in AML cells.

CPX-351

CPX-351 is a dual drug liposomal encapsulation containing a 1:5 molar ratio of daunorubicin/cytarabine, which appears to optimize synergy between the two drugs and promote leukemia cell killing in pre-clinical models⁵¹. Phase I–III trials in AML have demonstrated that the pharmacokinetics of CPX-351 are dramatically different from conventional bolus dose anthracycline and infusional cytarabine (3+7) and that prolonged drug exposure is demonstrable in patient plasma for 24 hours^52,53. For induction, CPX-351 is given over 90 minutes for three doses on days 1, 3, and 5 (each dose contains 44 mg/m² of daunorubicin and 100 mg/m² of cytarabine) and this approach confers more prolonged and continuous exposure to daunorubicin than traditional 3+7. CPX-351 liposomes also appear to accumulate preferentially in the marrow relative to other tissues^54–56.

In a randomized phase III study of 309 patients, Lancet et al. showed that CPX-351 conferred a superior overall survival (OS) advantage compared with traditional 3+7 in older patients (60–75 years old) with newly diagnosed secondary AML (defined as t-AML or evolved from a prior hematologic disorder or the presence of MDS-related cytogenetic abnormalities)⁵⁷. Median OS was superior for CPX-351 versus 3+7 (9.6 versus 5.9 months; p = 0.005). CPX-351-treated patients had higher complete remission (CR) rates (38% versus 26%), and more patients in the CPX-351 arm were transplanted in CR1. Patients treated with CPX-351 had increased BM toxicity (delayed count recovery) and increased bleeding events compared with those receiving 3+7, including more fatal central nervous system hemorrhage (2% versus 0.7%). Whether the length of aplasia was the cause of the bleeding risk is not yet fully understood. In contrast, there was less colitis and diarrhea and, anecdotally, less hair loss in the CPX-351 arm, possibly reflecting less extramedullary exposure and toxicity-related CPX-351. It is important to realize that the FDA-approved label for CPX-351 includes all adults (≥18 years old) with t-AML or AML with myelodysplasia-related changes (AML-MRC) and is not limited to older patients. AML-MRC includes patients with a prior diagnosis of MDS or CMML, MDS-related cytogenetic changes, and (while not included in the phase III trial) significant morphologic dysplasia (≥50%) in at least two cell lineages. The optimal clinical role of CPX-351 in the treatment of patients with AML remains to be determined, but, given the CR and OS data, CPX-351 may become the new standard of care for older patients with t-AML/AML-MRC.

Enasidenib (IDH2 inhibitor)

Enasidenib (AG-221) is a selective, oral inhibitor of the mIDH2 enzyme. Approximately 12% of patients with AML have these mutations⁵⁸. In the setting of mIDH2, the oncometabolite D-2-hydroxyglutarate (2-HG) is generated rather than αKG. 2-HG inhibits TET protein activity, resulting in downstream DNA hypermethylation and a block in myeloid differentiation similar to the MDS phenotype of TET2 loss of function. The neomorphic mIDH2 enzyme is a promising drug target, and after much pre-clinical work^59,60, the first-in-human phase I/II study of an IDH2 inhibitor (enasidenib), conducted by Stein et al. (including our center), showed an overall response rate (ORR) of 40.3% and a CR rate of about 20% (24.4% for IDH2-R172 and 17.7% for IDH2-R140 isoforms) in relapsed/refractory AML patients (176 patients, many heavily pre-treated)⁶¹. The results of this dose escalation/expansion study led to the recent FDA approval of enasidenib for relapsed/refractory AML with mIDH2. The primary mechanism of response has been confirmed to be through myeloid differentiation⁶², and a clinically significant but manageable differentiation syndrome can occur in these patients (7%)⁶¹, similar to what has been more frequently observed in APL. Otherwise, the drug is generally well tolerated and grade 1–2 nausea/anorexia and indirect hyperbilirubinemia (grade 3–4 in 12%) are the most frequent side effects. The drug is approved at 100 mg orally daily. The dose was allowed to be increased to 150 or 200 mg daily for lack of response in the phase II portion of the study, but this would currently be off-label usage (of note, the maximum tolerated dose was not reached in the phase I portion at doses beyond 200 mg daily). The average duration of response is about 6 months, but there are some excellent responders with continuous remissions for more than 2 years. Interestingly, in most patients achieving CR, the IDH2 mutant clone persists in functioning neutrophils⁶². While mIDH2 variant allele frequency (VAF) and the extent of 2-HG suppression do not appear to impact response rates, total mutational burden and the co-occurrence of RAS mutations have been associated with a decreased response to IDH2 inhibition⁶². Combinations of enasidenib with induction chemotherapy in newly diagnosed mIDH2 AML patients⁶³ and with HMAs in older/unfit newly diagnosed or relapsed/refractory mIDH2 AML patients are ongoing⁶⁴ (ClinicalTrials.gov Identifier: NCT02719574).

Midostaurin (FLT3 inhibitor)

Midostaurin is a multi-targeted kinase inhibitor active in AML patients with an FLT3 mutation. The drug was recently approved by the FDA on the basis of the randomized, placebo-controlled phase III RATIFY trial (Randomized AML Trial In FLT3 in patients less than 60 Years old) conducted in younger (18–59 years old) newly diagnosed AML patients with an FLT3-ITD or FLT3-tyrosine kinase domain (FLT3-TKD) mutation^65,66. Patients (n = 717) were randomly assigned (1:1) to receive midostaurin 50 mg orally twice daily or placebo on days 8–21 of standard induction (3+7 with 60 mg/m² daunorubicin) and consolidation (high-dose cytarabine). This was a large study and cooperative effort that screened over 3,000 patients, and patients were stratified according to FLT3 mutation subtype (ITD versus TKD) and ITD-to-wild-type allele ratio (high versus low). Patients were allowed to receive allogeneic HSCT, and those who did not receive an allotransplant received maintenance midostaurin. There was improved OS and event-free survival (EFS) in the midostaurin-treated patients. The difference in median OS (74.7 versus 25.6 months; one-sided p = 0.009) appears quite large in favor of the midostaurin group; however, owing to the inflection points on the Kaplan-Meier curves, the authors acknowledged that the hazard ratio (HR) for death likely more accurately reflects the true clinical benefit (HR = 0.78, one-sided p = 0.009) (that is, a 22% reduction in death for the midostaurin-treated patients). This survival benefit persisted in patients censored for allogeneic HSCT, reminding us that some FLT3 patients, especially in the midostaurin era, can be cured without transplant. The adverse events occurring in both groups were expected and consistent with those patients receiving intensive chemotherapy experience. The only significant differences in grade 3 or higher toxicity between groups were anemia and rash, which were more common with midostaurin, and nausea, which was less common with midostaurin. Hematologic recovery of neutrophils and platelets were the same between groups. Lastly, it is important to note that patients did well in this study overall; 359 (50.1%) of 717 patients with FLT3 mutations survived at a median follow-up of 59 months. Whether this was due to better supportive care, improvements in transplantation, or patient selection bias on clinical trials remains to be seen.

Gemtuzumab ozogamicin

GO is an antibody–drug conjugate that targets CD33, a cell surface antigen that is expressed on the blast cells in 90% or more of patients with AML⁶⁷. The antibody is covalently linked to calicheamicin, a potent DNA-damaging agent. Most of the cytotoxic payload remains conjugated to the antibody until it is internalized and cleaved by hydrolytic enzymes, but circulating free drug does pose a risk of extramedullary toxicity. GO was initially licensed by the FDA in 2000 for relapsed AML at a dose of 9 mg/m² for two doses on days 1 and 14 (single agent) but was withdrawn from the market in 2010 because of the risk of hepatic veno-occlusive disease (VOD), particularly in patients who previously had or went on to receive allogeneic HSCT⁶⁸. The risk of VOD was related to the time elapsed between GO and transplantation or vice versa⁶⁹. Since then, however, the drug has been further studied, primarily in Europe, at reduced, fractionated doses. With these modifications, several groups have now demonstrated satisfactory safety and efficacy data, leading to the drug’s re-approval in the US in 2017. Adverse side effects include myelosuppression, hepatotoxicity, tumor lysis syndrome (TLS), and infusion reactions. The drug now has three approved indications for AML on the basis of the following three studies:

1. ALFA-0701 study: this 271-patient randomized phase III study examined the addition of GO to standard induction and consolidation chemotherapy (3+7) in patients with newly diagnosed de novo AML⁷⁰. The primary endpoint of median EFS was significantly longer in the GO versus the no GO arm: 17.3 versus 9.5 months (p ≤0.001). VOD occurred in 3% of patients in the GO arm and in none receiving standard of care.

2. AML-19 study: this was a randomized phase III study examining single-agent GO induction (and maintenance) in 237 previously untreated AML patients not candidates for intensive chemotherapy (median age of 77 years)⁷¹. Patients treated with GO had improved OS, and the HR for death was 0.69 (p = 0.005). The CR + complete response with incomplete blood recovery (CRi) rate with GO was 27%, and the clinical benefit rate—including partial remission (PR) and stable disease of more than 30 days—was 56.7%. Patients treated with GO experienced myelosuppression, but there was no excess non-hematologic toxicity—including febrile neutropenia, VOD, infection, and bleeding—making this a viable treatment option for older patients.

3. MyloFrance-1 study: this non-randomized 57-patient phase II study evaluated single-agent GO re-induction in de novo AML patients with intermediate-risk (78%) or poor-risk (22%) cytogenetics in first relapse (prior HSCT excluded)⁷². Patients received one course of GO 3.5 mg/m² on days 1, 4, and 7 (fractionated and lower cumulative dosing compared with prior studies in this population, which used 9 mg/m² on days 1 and 14). The CR rate in this study was 26%, and median relapse-free survival in these (CR2) patients was 11.6 months. Hematologic toxicity was expected and tolerable, and there was no grade 3 or greater liver toxicity and no VOD, including in patients who went on to receive HSCT.

The FDA has re-approved GO for three indications on the basis of the three studies above, which as a whole used fractionated and lower doses of GO than did the trials that led to its initial approval in 2001. However, GO may add to myelotoxicity during induction, and there is still a risk of VOD, particularly peri-transplant, so caution should be taken with its use. The optimal dose and schedule of GO are still being assessed, particularly in combination with induction chemotherapy, and less may be better, particularly in patients with core-binding factor (CBF) abnormalities^73,74.

Venetoclax

Venetoclax (ABT-199) is a highly selective oral inhibitor of the anti-apoptotic protein BCL2 and is approved for treatment-resistant 17p-deleted chronic lymphocytic leukemia. AML stem and progenitor cells depend on BCL2 for survival, and pre-clinical studies have demonstrated significant activity in AML models⁷⁵. Clinically, venetoclax was first examined as a single agent in a phase II study of 32 patients with AML (relapsed/refractory or unfit for conventional chemotherapy)⁷⁶. The venetoclax dose was increased in a stepwise fashion to mitigate the risk of TLS (20 mg on day 1, 50 mg on day 2, 100 mg on day 3, 200 mg on day 4, 400 mg on day 5, and 800 mg on day 6 and thereafter), and TLS did not occur in this study. The ORR in this study was 19% (two CRs and four patients with CRi), all occurring in previously treated patients. Another six (19%) patients had a significant (≥50%) reduction in BM blast percentage. More recently, venetoclax has been combined with HMA therapy⁷⁷ and low-dose ara-C (LDAC)⁷⁸ in treatment-naïve older patients (not candidates for induction) with high response rates and apparent safety, although data are still emerging. A recent phase Ib study of 57 patients treated with venetoclax HMA combination showed a 61% combined CR/CRi rate⁷⁷. Given the impressive response rates of about 60 to 70% observed with both HMA and LDAC combinations, venetoclax has received breakthrough therapy designation by the FDA to accelerate its development as a frontline combination partner for older/unfit AML patients (both HMA and LDAC combinations).

Other FLT3 inhibitors

The FLT3 receptor tyrosine kinase drives cellular proliferation and survival through the JAK-STAT, MEK/MAPK, and PI3K signaling pathways. Both ITD and point mutations in the TKD occur in AML, resulting in constitutive activity of the enzyme. FLT3-ITD is one of the most common mutations in AML (~30%) and is associated in general with a poor prognosis^79–81. Typically, patients have a high white blood cell count at presentation and are chemo-sensitive, usually achieving CR. However, relapse usually occurs without allogeneic HSCT, and patients rapidly become chemo-refractory. Co-occurring NPM1 mutations somewhat ameliorate the prognosis of FLT3-ITD AML⁸², placing patients in a more intermediate-risk category, whereas co-occurring DNMT3A mutations or trisomy 8 worsen the prognosis, as does a high FLT3-ITD allele burden, particularly in the absence of mutated NPM1^9,82. FLT3-TKD mutations (usually D835) occur in an additional 10% of patients (approximately), and the prognostic impact is less clear and is likely not as unfavorable as the ITD. Given the rapidly fatal nature of relapsed FLT3-mutant AML, FLT3 inhibitors have been in development for almost two decades. While FLT3 inhibitors have been shown to have clinical activity in AML and can serve as a bridge to allo-HSCT, there are still no approved FLT3 inhibitors for relapsed/refractory FLT3-AML. Sorafenib is a multi-kinase inhibitor that inhibits FLT3 along with vascular endothelial growth factor receptor and other kinases, and it is approved for hepatic, thyroid, and kidney cancer. Sorafenib is often used off-label in combination with azacitidine for relapsed/refractory or older/unfit FLT3-AML, given the lack of other good options for these patients outside of a clinical trial, and this use is supported by National Comprehensive Cancer Network guidelines based on a phase II trial of 37 evaluable patients with FLT3-AML showing an ORR of 46% with 10 CRi, six CR, and one PR⁸³. Median duration of response in this study was 2.3 months (range of 1–14.3 months), underscoring the fact that the emergence of treatment resistance to FLT3 inhibition is a frequent problem. Sorafenib has also shown promise as a maintenance therapy for FLT3-ITD-mutant AML post-transplant, and retrospective data show that it improves OS (HR 0.26, p = 0.021)⁸⁴. Other studies of newer-generation FLT3 inhibitors such as quizartinib, crenolanib, and gilteritinib are ongoing or completed. A problem with most FLT3 inhibitors is that, while they may be transiently effective against the FLT3-ITD and may serve as a bridge to allo-HSCT in some patients, acquired resistance-conferring point mutations at D835 (or other activation loop substitutions) or gatekeeper (F691) mutations commonly occur over a period of months, resulting in loss of response. Gilteritinib, an oral FLT3 and AXL inhibitor, was recently reported to have activity against some of these mutations. A phase I/II study in relapsed/refractory FLT3-mutated AML showed a 57.5% overall response rate and 47.2% composite CR rate—CR, CRi, and CR with incomplete platelet recovery (CRp)—in 106 patients receiving doses of 80 mg daily or higher⁸⁵. A phase III registration trial with gilteritinib is ongoing in relapsed/refractory FLT3-AML.

IDH1 inhibitors

Like the IDH2 gene, the IDH1 gene is mutated in AML. IDH1 resides primarily in the cytosol, whereas IDH2 is primarily mitochondrial. The phenotype of IDH1 or IDH2 mutant AML is similar, characterized by the gain-of-function, neomorphic mutant IDH activity producing 2-HG, which in turn impairs cellular differentiation. IDH1 mutations (IDH1m) are slightly less common than IDH2 mutations in AML; the former are seen in about 8 to 10% of patients, mostly those with normal karyotype AML, and the most commonly co-occurring mutations are in the NPM1, DNMT3A, and FLT3 genes⁸⁶. IDH1 and IDH2 mutations are mutually exclusive to each other and to TET2 and WT1 mutations. The first study using an IDH1 inhibitor (AG-120), a large phase I/II study, has now completed enrollment; response rates to AG-120 appear to be similar to those to enasidenib (AG-221). In the first 78 evaluable MDS/AML patients (most relapsed/refractory), the overall response rate was 38.5% with 14 CRs (17.9% of patients)⁸⁷. The side effect profile of AG-120 is similar to that of enasidenib (that is, it too is well tolerated). As with the IDH2 inhibitor, most patients achieving CR with AG-120 did not achieve IDH1 mutation clearance by next-generation sequencing (VAF ≥1%, median coverage 500×). As with IDH2 inhibitor therapy, differentiation-like syndrome can occur with IDH1 inhibitors, and it may be more common in patients receiving concomitant HMA therapy. Multiple studies of different IDH1 inhibitors are ongoing, including newer-generation IDH1 inhibitors and combinations of these agents (or AG-120) with HMAs and induction chemotherapy.

LSD1 inhibitors

In addition to IDH inhibitors, other new drugs targeting epigenetic modifications have strong therapeutic potential. Epigenetic enzymes such as DNMTs, histone deacetylases (HDACs), and histone methyltransferases/demethylases all represent bona fide targets for anti-cancer drug development and several have been discussed herein^40,88. It is important to remember that epigenetic events play an essential role in promoting myeloid leukemogenesis and that epigenetic alterations occur far more frequently than genetic mutations in AML blasts. Treatment with DNA demethylating agents leads to clinical responses in about 20 to 30% of cases⁸⁹. Two HMAs (azacitidine and decitabine) are well known and approved for MDS, CMML, and low-blast AML in the US and Europe (and are also approved for older adults with more than 30% blasts in Europe). However, histone methylation and DNA methylation both play critical roles in transcriptional regulation. Notably, specific histone methyl marks coordinately regulate chromatin structure to activate (for example, H3K4me2) or inactivate (for example, H3K27me2) myeloid differentiation programs. Specifically, the removal of H3K4me2 is catalyzed by lysine-specific demethylase 1 (LSD1), which removes mono- and di-methyl marks on H3K4. LSD1 is highly expressed in patients with AML. Removal of these marks by LSD1 generally interferes with myeloid differentiation; therefore, inhibiting LSD1 may result in the restoration of myeloid gene expression, although this may be cell context dependent. LSD1 is being actively investigated as a drug target; LSD1 inhibitors have shown anti-leukemic activity (generally cytostatic) in pre-clinical models and may function as differentiating agents^90,91. Early phase single-agent LSD1 inhibitor clinical trials are ongoing, and further studies combining LSD1 inhibitors with HMAs are being designed.

In addition, LSD1 inhibitors have promising therapeutic potential when given in combination with ATRA. ATRA has revolutionized the treatment of APL, a subtype of AML (about 5–10% of all AML) characterized by the PML-RARα (PML-RARA) fusion protein, arising from a balanced translocation involving the RARA gene on chromosome 17 and the PML gene on chromosome 15. When given in combination with chemotherapy or arsenic trioxide, ATRA induces differentiation and ultimately cure in virtually all APL patients who do not die from early bleeding events⁹². However, ATRA has little, if any, effect on differentiation or anti-leukemic activity in patients with non-APL AML. One of the underlying reasons for this lack of response to ATRA in non-APL AML is the failure to induce transcriptional activation of target genes such as RARA. However, LSD1 inhibition in combination with ATRA appears to unlock these transcriptional programs⁹³. Therefore, several LSD1 inhibitors are currently being studied with ATRA, including tranylcypromine (TCP) (Parnate^®), an irreversible monoamine oxidase (MAO) inhibitor that is FDA approved as an antidepressant and anxiolytic agent. TCP has more recently been shown to inhibit LSD1, decreasing H3K4 methylation⁹⁴, and Schenk et al. have demonstrated that, when added to ATRA, TCP greatly potentiates the differentiation response in non-APL AML cell lines and primary patient samples, leading to decreased leukemia burden and elimination of leukemia-initiating cells⁹³. Given the availability of TCP, it has already been re-purposed in combination with ATRA for phase I clinical trials in both the US and Europe, which are currently accruing. More potent LSD1 inhibitors than TCP are being studied pre-clinically and have demonstrated greater differentiative effect in combination with ATRA⁹⁵.

BET bromodomain inhibitors

Bromodomain (BRD) and extra terminal (BET) family proteins are epigenetic readers that bind acetylated histones and facilitate the transcription of various oncogenes, such as c-Myc, primarily by regulating their super-enhancers. BRD4 inhibitors are being studied in different clinical trials in a variety of solid-organ and hematologic malignancies, including AML (ClinicalTrials.gov Identifier: NCT02711137). MYC is overexpressed in most AML samples (~70%), as are other BRD-regulated pathways such as Ras and Hedgehog⁹⁶. Pre-clinically, BRD inhibition has activity in AML cell lines, including FLT-ITD-mutated and MLL-rearranged cells, as well as in mouse xenograft models⁹⁷. Several clinical trials are ongoing in myeloid neoplasms, including combinations with HMAs⁹⁸.

Targeting mutant TP53

The TP53/chromosomal aneuploidy subtype of AML represents about 10 to 20% of AML⁸ and is enriched in older patients, many of whom have antecedent MDS or t-AML¹⁰. TP53 alterations are common but not always present in complex karyotype AML (60%) and predict for even worse prognosis within this subgroup⁹⁹. Although CPX-351 has been approved for secondary-type AML (p53 status not known on the phase III trial) as previously discussed and may affect outcomes in this subgroup going forward, patients with TP53/aneuploidy historically fare extremely poorly even with allogeneic HSCT⁹⁹. Decitabine has shown some promise to bridge these patients to allo-HSCT, particularly the 10-day regimen, with high rates of blast clearance, but long-term outcomes with decitabine remain to be seen, and it has not been compared head-to-head with standard induction chemotherapy^49,100.

New agents are being developed for this very poor-risk subtype of AML. The neddylation (Nedd8) inhibitor pevonedistat has shown recent promise in this subgroup⁵⁰. Neddylation is a process similar to ubiquitination, is catalyzed by Nedd8-activating enzyme (NAE), and is required for cullin-ring ligase (CRL)-mediated degradation of various protein substrates. Inhibiting the polymerization of Nedd8 breaks down this process, resulting in the accumulation of cytotoxic substrates within the cell and apoptosis. In a phase I dose-escalation study of pevonedistat plus azacitidine in treatment-naïve older AML patients, the combination was well tolerated, ORR was 50% (20 CR, five CRi, and seven PR), and 63% of responders (20/32) responded during the first two cycles¹⁰¹. In addition, four out of five patients with TP53 mutations responded (CR/PR) with two maintaining response for more than 10 cycles. A randomized phase II study of pevonedistat (at the RP2D of 20 mg/m² intravenously on days 1, 3, and 5 of a 28-day cycle) with or without azacitidine (standard dose and schedule) in the same patient population has completed enrollment (ClinicalTrials.gov Identifier: NCT02610777), and a phase III study is ongoing (ClinicalTrials.gov Identifier: NCT03268954). In addition, for myeloid neoplasms with TP53 point mutations, refolding agents (for example, APR-246) to restore the wild-type conformation of the TP53 protein are being studied in clinical trials (ClinicalTrials.gov Identifier: NCT03072043).