The nucleophosmin (NPM1) gene encodes for a multifunctional nucleolar protein with shuttling and chaperone properties [1, 2]. In 2005, we discovered that NPM1 was mutated (often in association with FLT3) in about one-third of AML (mostly with normal cytogenetics) and that the NPM1 mutant protein was delocalized in the cytoplasm of leukaemic cells [3]. We subsequently proposed that NPM1-mutated AML represented a disease with distinctive clinical, pathological and molecular features [4] and promoted this concept within the Clinical Advisory Committees of World Health Organization (WHO). This eventually led to include NPM1-mutated AML as a new entity in the 2017 WHO classification of lympho-haematopoietic tumors [1, 5].

Clinical management of AML patients, including those with NPM1-mutated AML, is based upon the European LeukemiaNet (ELN) genetic-based risk stratification [6, 7]. NPM1-mutated AML without FLT3-ITD or with FLT3-ITD low allelic ratio (<0.5; FLT3-ITDlow) belongs to the ELN favourable risk category whilst NPM1-mutated AML with FLT3-ITD high allelic ratio (≥0.5; FLT3-ITDhigh) falls into the intermediate risk group [6]. However, NPM1-mutated AML may carry a large variety of concomitant mutations that may influence its clinical course and prognosis [8, 9]. Thus, risk stratification of NPM1-mutated AML is an evolving area that in the future is expected to expand, including genotypes other than those currently recognized by the ELN. A recent study also points to the importance of race in risk stratification based on genomics [10].

Assessment of measurable residual disease (MRD) by real time quantitative polymerase chain reaction (RT-qPCR) for NPM1 mutant transcripts [11] can be combined with the ELN risk stratification to inform therapeutic decisions, e.g. helping to select patients who may benefit from allogeneic haematopoietic stem cell transplantation (allo-HSCT) [7]. NPM1 mutations are an ideal target for monitoring MRD since they are AML specific [12], common [3], stable and do not drive clonal haematopoiesis [13]. Moreover, NPM1 mutant transcripts are expressed at high levels, allowing sensitivity up to 1:105–1:106.

Despite most patients achieving MRD-negativity may still have up to 107 residual leukaemic cells, they do not relapse, suggesting that the host immune system may control or eradicate the residual disease. Interestingly, T lymphocytes reactive against HLA-presented NPM1 mutant neoantigens were demonstrated in patients [14]. Conversely, about 30% of MRD-negative cases relapse [9], probably because their immune system is unable to clear the residual leukaemic cells, especially when FLT3-ITD (imparting a high proliferative index) is present.

Whatever is the mechanism of MRD eradication, achieving MRD negativity in PB [9] or BM [15] or a marked drop of MRD in BM [16, 17] or in PB [18] is predictive of low risk of leukaemia relapse and good survival. Pre-allotransplant monitoring of MRD is also important for predicting outcome, since MRD-positivity in this setting is associated with poor outcome [19,20,21]. In fact, although allo-HSCT is effective in eradicating MRD, post-transplant MRD negativity is more durable in patients who are MRD-negative before allo-HSCT [22]. Nevertheless, myeloablative allo-HSCT [20] still performs better than standard CHT [18, 23].

Nearly 50% of MRD-positive patients with <1000–2000 NPM1 mutant transcripts copies/105 ABL [24] at the end of CHT achieve MRD negativity spontaneously or retain stable low-level expression without relapsing at a minimum follow-up of 8 months [25]. Patients with both FLT3-ITD and <4 log reduction in NPM1 transcript levels at the end of CHT are at high risk of disease progression and should be considered for pre-emptive treatment [25].

In the everyday clinical practice, haematologists involved in management of AML patients have sometimes to face with diagnostically complex cases and difficult therapeutic choices. Here, we present 6 challenging NPM1-mutated AML cases, in order to provide criteria for the appropriate diagnosis and therapy of this common leukaemia entity.

Case 1: adult young patient with NPM1-mutated AML, multilineage dysplasia and clonal evolution of FLT3-ITD

A 58-year-old woman presented with urinary tract infection. The complete blood count (CBC) showed: white blood cells (WBC) 12.8 × 109/L, haemoglobin (Hb) 9.5 g/dL and platelets 144 × 109/L. The bone marrow (BM) showed AML with multilineage dysplasia (MLD). NPM1 mutation A and FLT3 wild-type were detected. The BM karyotype was normal. She was treated with a ‘7 + 3’ regimen, achieving a complete remission (CR) and 2.7 log reduction of NPM1 mutant transcripts at RT-qPCR (Fig. 1). The patient then received two idarubicin/cytarabine-based consolidation cycles. In the following months, we observed a progressive increase of NPM1 MRD in the BM (Fig. 1) that was rapidly followed by haematological relapse (15% blasts). A small FLT3-ITD subclone (0.5%) had also appeared. She received a combination of fludarabine, cytarabine, idarubicin and etoposide that led to CR and 1.7-log reduction of NPM1 transcripts (Fig. 1). Allo-HSCT from an haploidentical donor was performed and she is now in molecular CR, almost 2 years after allotransplant (Fig. 1).

Fig. 1: NPM1 MRD monitoring by RT-qPCR in case 1.
figure 1

Monitoring of NPM1mut transcripts during therapy and follow-up (see text). 0.0001%NPM1mut/ABL is equivalent to MRD negativity. 1st CHT, first line chemotherapy; 2nd CHT, salvage chemotherapy; allo-HSCT, allogeneic haematopoietic stem cell transplant.

Questions and recommendations

Our patient showed AML with MLD (i.e. dysplasia in at least 50% of cells, in at least two BM cell lines [5]) and expression of cytoplasmic NPM1 in different haematopoietic cell lineages (Fig. 2A, B). MLD is one of the diagnostic criteria defining AML with myelodysplasia related changes (AML-MRC) but, according to WHO classification, when it coexists with NPM1 mutation, the genetic lesion supersedes morphology and the case should be diagnosed as NPM1-mutated AML [5, 7, 26]. Conversely, a previous history of myelodysplastic syndrome (MDS) or MRC-related cytogenetic abnormalities, even in the presence of NPM1 mutation, are diagnostic of AML-MRC [5]. Thus, our patient was diagnosed as NPM1-mutated AML since only MLD but no history of MDS or MRC-related cytogenetic abnormalities were documented.

Fig. 2: AML with multilineage dysplasia and cell of origin of NPM1-mutated AML.
figure 2

A Multilineage involvement is documented by the presence of myeloid blasts (single arrow) expressing cytoplasmic NPM1 (blue) and immature erythroid cells (double arrows) expressing cytoplasmic NPM1 (blue) and surface glycophorin (brown) (double staining for NPM1/immune-alkaline phosphatase APAAP technique and glycophorin/ immunoperoxidase, x400). B Another area of BM biopsy showing cytoplasmic NPM1 in dysplastic megakaryocytes (arrow) and myeloid cells (APAAP immunostaining; x400) C Cartoon depicting the putative cell of origin of NPM1-mutated AML. Lighting bolts indicate the suggested putative cells of origin.

MLD also helps defining the cell of origin of NPM1-mutated AML. Studies in mice suggest that NPM1-mutated AML may derive from a granulocytic-monocytic progenitor (GMP) [27]. We propose it may also originate from either a common myeloid progenitor (CMP) or a haematopoietic stem cell (HSC) (Fig. 2C), for the following reasons: (i) Erythroid and megakaryocytic cell lineages frequently show cytoplasmic NPM1 (Fig. 2A, B) or mutations in microdissected cells [28]; (ii) Precursors carrying NPM1 mutations with the immunophenotype of leukaemic stem cells (CD34 + /CD38-/CD123 + /CD33 + /CD90-) are present in BM of NPM1-mutated AML patients [29]; and (iii) Human NPM1-mutated CD34 + AML cells transplanted into NSG mice generate an AML recapitulating the original patient’s disease, with monocytic differentiation and loss of CD34 [29].

Because our patient belonged to the ELN favorable risk category (NPM1-mutated without FLT3-ITD) [6], she received induction plus consolidation without allo-HSCT. In fact, patients with this genotype have <40% cumulative risk of relapse and high probability to achieve a second CR and to be salvaged by allo-HSCT. Allo-HSCT in first CR (CR1) has been proposed for patients <50 years, with low transplant-related risk and HLA-identical donor [30], but this option remains investigational [7]. Thus, we only administered consolidation CHT.

MRD monitoring documented an early molecular relapse [24] shortly followed by haematological relapse. The molecular relapse may have been heralded by the MRD suboptimal reduction after two cycles of CHT [9]. This could serve as another reasonable criterion for favoring allo-HSCT in CR1 [9] in otherwise favorable risk NPM1-mutated AML according to ELN [6]. Currently, this issue is addressed in a multicenter, MRD-driven study on AML patients with favorable/intermediate-risk sponsored by Gruppo Italiano Malattie EMatologiche dell’Adulto, GIMEMA (NCT04168502). Sequential monitoring for MRD may allow pre-emptive intervention before haematological relapse [31,32,33].

The emergence of a small FLT3-ITD subclone (0.5%) at relapse suggests clonal evolution towards a more aggressive AML. FLT3-ITD is an unstable mutation that may be lost (if present at diagnosis) or acquired at relapse. Interestingly, 4/6 NPM1-mutated AML patients with FLT3 wild-type at diagnosis who relapsed with FLT3-ITD (according to conventional PCR), harbored very small FLT3-ITD subclones already at diagnosis, when analyzed by a highly sensitive patient-specific RT-qPCR for FLT3-ITD [34].

Therefore, the patient was treated with salvage CHT followed by allo-HSCT. She did not receive an FLT3 inhibitor since it was not approved at that time. Salvage CHT induced a new CR and about 2-log reduction in NPM1 transcripts. Although NPM1 MRD positivity before allo-HSCT has been associated with higher relapse rate [19,20,21], our patient is still in molecular CR almost 2 years after allotransplant.

Case 2. Older fit patient with NPM1/FLT3-TKD/DNMT3A triple mutated AML, trisomy 8 and extramedullary disease

A 72-year-old woman presented because routine examinations revealed WBC 35.8 × 109/L, Hb 12.6 g/dL and platelets 84 × 109/L. The BM was diffusely infiltrated by myelomonocytic leukaemic cells expressing cytoplasmic NPM1. Mutations of NPM1 (type A), FLT3-D835 and DNMT3A were detected. The BM karyotype revealed a trisomy 8 in about 20% of metaphases. Multiple light-purple skin nodules were found on clinical examination and a skin biopsy revealed dermal infiltration by leukaemic cells with cytoplasmic NPM1 (Fig. 3A, B). She received a ‘7 + 3’ regimen plus midostaurin, achieving haematological CR. Disappearance of FLT3-D835 mutation and a 3.8-log reduction of NPM1 mutant transcripts were observed (Fig. 3C). The patient received two cytarabine-based consolidation cycles plus a FLT3 inhibitor (midostaurin) achieving a maximum of 4.5-log reduction of NPM1 MRD (Fig. 3C); FLT3-D835 remained negative. In the following months, NPM1 MRD in the BM progressively increased (Fig. 3C), the patient remaining in haematological CR. No skin lesions were observed. She received pre-emptive therapy with venetoclax plus the hypomethylating agent (HMA) 5-azacytidine. She is now in molecular CR at the fifth cycle of this combo (Fig. 3C).

Fig. 3: NPM1/FLT3-D835/DNMT3A triple-mutated AML with skin involvement.
figure 3

A Skin biopsy showing marked dermal infiltration by leukaemic cells. E indicates the overlying epidermis (Haematoxylin-Eosin, x400). B Leukaemic cells express cytoplasmic NPM1 (single arrow) whilst the cells of the overlying epidermis show nucleus-restricted NPM1 positivity (double arrows) (APAAP immunostaining, x400). E indicates the overlying epidermis. C MRD monitoring by RT-qPCR. 0.0001%NPM1mut/ABL is equivalent to MRD negativity. CHT + FLT3i, chemotherapy plus midostaurin; AZA + VEN, azacytidine plus venetoclax. Arrows indicate the beginning of each cycle of azacytidine plus venetoclax.

Questions and recommendations

Our patient carried the D835 mutation involving the tyrosine kinase domain (TKD) of FLT3. Accordingly, we administered CHT plus midostaurin. The benefit of using this combo for the NPM1-mutated/FLT3-TKD genotype was shown in a recent study [35]. However, the best post-remission therapy for these patients (consolidation CHT vs allo-HSCT) remains controversial. In fact, FLT3-TKD mutations have been associated with favorable prognosis in some studies [36,37,38] but not in others [39, 40]. The NPM1-mutated/FLT3-TKD genotype in the RATIFY trial showed a 5-year OS rate of 70% [35]. Thus, patients receiving CHT plus midostaurin should be probably not allotransplanted in CR1 and we adopt this strategy.

Then, the question raises whether the early molecular relapse in our patient could have been related to the concomitant DNMT3A mutation. In fact, NPM1-mutated AML elderly patients co-mutated for DNMT3A seem to have high risk of relapse even though they achieve good molecular responses post-induction CHT. They should be considered for allo-HSCT or maintenance strategies, even if they belong to the favorable ELN risk group [41].

NPM1-mutated AML co-mutated for FLT3-ITD and DNMT3A was initially recognized to display distinctive microRNA and epigenetic features [42]. The triple-mutated AMLNPM1/FLT3-ITD/DNMT3A is clinically characterized by high WBC count, monocytic phenotype, absence of multilineage dysplasia, extramedullary involvement, normal karyotype and poor outcome [8, 43, 44]. Our triple-mutated patient carried FLT3-TKD instead of FLT3-ITD. Although it is difficult to make a comparison based upon only one case, she exhibited clinical and biological features similar to those of typical AMLNPM1/FLT3-ITD/DNMT3A and responded poorly to CHT plus midostaurin. The introduction of more powerful FLT3 inhibitors may increase the percentage of triple-mutated patients who may be bridged to allo-HSCT. Preclinical studies suggest that triple mutated AMLNPM1/FLT3-ITD/DNMT3A may be sensitive to venetoclax [45]. Our patient responded to pre-emptive therapy with venetoclax plus HMA, but this observation requires further clinical validation.

Did the trisomy 8 conditioned the suboptimal response to therapy in our case? About 15% of NPM1-mutated AML exhibit an abnormal karyotype [3], usually characterized by +8, +4, -Y, del(9q) and +21, monosomy of chromosomes 5 and 7 and complex karyotype being very rare [46]. These aberrations represent secondary late events during the clonal evolution of NPM1-mutated AML [46]. Thus, trisomy 8 (as in our case) has no prognostic impact in NPM1-mutated AML [46]. Adverse-risk aberrations in NPM1-mutated AML include monosomy 7 or 5 or TP53 deletion [47]. However, cases with these genetic abnormalities would fill in the WHO category of AML-MRC.

Skin lesions, as in our patient, have been described in association with NPM1-mutated AML showing monocytic features [48]. Whether skin involvement represents a poor prognostic factor in the context of our patient’s genotype remains unknown. In a study including >3,000 AML patients, extramedullary disease did not show an independent prognostic value [49] but mutational landscape was not investigated. Interestingly, our patient relapsed in the BM but not in the skin.

Case 3. Older unfit patient with NPM1-mutated AML without FLT3-ITD presenting during the COVID-19 pandemic

An asymptomatic 74-year-old woman presented during the COVID-19 pandemic with a routine CBC revealing WBC 2.1 × 109/L, Hb 7.6 g/dL and platelets 109 × 109/L. BM examination showed infiltration by myelomonocytic leukaemic cells that were negative for CD34, positive for myeloperoxidase and macrophage-restricted CD68, and expressed cytoplasmic NPM1. The NPM1 mutation A was detected whilst FLT3 was wild-type. The BM karyotype was normal. The patient, considered unfit for CHT, received venetoclax plus 5-azacytidine. She achieved MRD-positive CR after the first cycle and is now in CR MRD-negative after five cycles of this combo.

Questions and recommendations

What is the best treatment available for our patient? Venetoclax plus HMA or low dose cytarabine (LDAC), induced CR in 70–90% of NPM1-mutated AML patients [50, 51]. Similar dramatic responses have been also reported in NPM1-mutated myeloid sarcoma [52, 53]. Thus, the standard therapy for older unfit NPM1-mutated AML patients is now venetoclax plus HMA [7, 50]. CR is frequently achieved after one cycle and the regimen is usually well tolerated, with an early mortality of only 7% [51]. Nevertheless, patients experience a prolonged drug-related pancytopenia that should be differentiated from refractoriness to therapy by BM evaluation at appropriate time points. Persistent neutropenia may require prolonging intervals between cycles, reducing the duration of venetoclax administration per cycle or using granulocyte colony-stimulating factor.

Venetoclax-based regimens have been also recommended as temporary alternative to intensive CHT in older fit NPM1-mutated AML patients during COVID-19 pandemic [54, 55]. MRD assessment may be particularly helpful under these circumstances, although the optimal time points for monitoring need to be established for this combo [56].

Venetoclax plus HMA is also approved by the Italian Drug Agency as frontline therapy for fit AML patients ≥75 years old. In NPM1-mutated AML patients >65 years old, this combo compared favorably with intensive CHT [57]. However, these results need to be confirmed in randomized prospective studies. We currently treat fit NPM1-mutated AML patients >60 but <75 years old with standard CHT, although outcome remains poor, independently of FLT3 status (3-year overall survival of 35%) [58]. Older eligible patients, who achieve complete remission after one or two cycles of CHT, should be offered reduced-intensity conditioning [59] or non-myeloablative [60] allo-HSCT.

Case 4. Pediatric NPM1-mutated AML patient with unusual co-mutations

A 17-years-old girl presented with fever, cough and abdominal pain. The CBC showed WBC 1.3 × 109/L, Hb 8.0 g/dL and platelet 25 × 109/L. The BM was diffusely infiltrated by monoblasts positive for macrophage-restricted CD68 and negative for myeloperoxidase and CD34. Next generation sequencing (NGS) of 43 genes detected a previously unnoted NPM1 mutation (see below), a rare FLT3 N841H mutation and two TET2 mutations. The BM karyotype showed a trisomy 8 in 4/25 metaphases. She received a ‘7 + 3’ induction, achieving CR. NGS after the first consolidation cycle showed disappearance of NPM1 mutation but persistence of FLT3-N841H. Parents asked for a consultation since allo-HSCT from the HLA-identical sister was proposed at another Institution.

Questions and recommendations

NPM1 mutations are much less frequent in the childhood than in adults (about 7% vs 30%) [61]. Such a difference could be related to the fact that, in order to occur, NPM1 mutations require a background of clonal haematopoiesis (usually driven by DNMT3A and TET2 mutations) that is a very rare event in children but progressively increases with age [62]. NGS revealed a new NPM1 mutation (deletion of two nucleotides and an insertion of four nucleotides at position 864) leading to loss of tryptophans 288 and 290 and the creation of a putative nuclear export signal (NES) at the NPM1 C-terminus, both required for cytoplasmic dislocation of NPM1 [63]. Given the rarity of this NPM1 mutation, NGS and patient-specific RT-qPCR represent the best methods for MRD monitoring in this case.

What is the significance of the accompanying FLT3 and TET2 mutations in our patient? The FLT3-N841H mutation is located in the amino-terminal portion of TKD (activation loop of FLT3) and had previously reported only in one old patient with de novo AML FAB-M5 [64]. FLT3-N841H causes substitution of histidine for asparagine at codon 841 and leads to conformational changes of activation loop similar to substitutions of histidine for isoleucine (N841I) or tyrosine (N841Y) [65] that were previously shown to have transforming properties. Notably, NGS analysis of BM sample in CR after the first consolidation cycle showed disappearance of NPM1 mutation but persistence of FLT3-N841H at 49% VAF. This finding raised the question whether the mutation was germline or related to clonal haematopoiesis [66]. Presence of FLT3-N841H in patient’s hair demonstrated its germline origin. The two mutations of TET2 were missense and most likely not pathogenetically relevant. The lack of impact of trisomy 8 in risk stratification of NPM1-mutated AML patients has been already discussed in case 2.

What is the best post-remission treatment for this young girl? Although the ELN stratification model [6] mainly applies to adult patients age 18–60 years, NPM1 mutations appear to be a prognostic predictor even in children [67]. Because the FLT3-N841H mutation is germline and not functionally relevant, our patient should be assigned to the ELN favorable risk and receive only CHT without FLT3 inhibitors. No allo-HSCT in CR1 is recommended either.

Case 5: AML with NPM1 exon 11 mutation

A 64-year-old woman presented with fatigue, diarrhea, nausea, dyspnea and fever. CBC showed WBC 43.3 × 109/L, Hb 3.5 g/dL and platelets 67 × 109/L. The BM was diffusely infiltrated by leukaemic cells with myelomonocytic (FAB-M4) appearance expressing cytoplasmic NPM1 (Fig. 4A, B) with no mutations at NPM1 exon 12; FLT3 was wild-type and the BM karyotype was normal. She received a ‘7 + 3’ induction regimen, achieving CR. We then administered two consolidation cycles with intermediate dose cytarabine and daunorubicin. She is now in CR, 6 years after the initial diagnosis.

Fig. 4: AML with mutation of NPM1, exon 11.
figure 4

A Diffuse BM infiltration by leukaemic cells. Dysplastic megakaryocytes are also present (arrow). B Mononucleated blasts and dysplastic megakaryocytes (arrow) express cytoplasmic NPM1 (APAAP immunostaining, x400). C Sanger sequencing of exon 11 showing a heterozygous 8 nucleotides insertion leading to a stop codon at amino acid 275. D Schematic representation of the new mutant protein (Mut) compared with the wild-type (WT). Analysis of the new protein sequence predicted a truncated protein (274 aa length), with a newly acquired NES motif (VxxxFxxLxIx). Both proteins are recognized by the anti-NPM1, Clone 376 mAb: monoclonal antibody.

Questions and recommendations

NPM1 mutations almost exclusively affect exon 12 [68] and all of them cause changes at the C-terminus of NPM1 (mutation of tryptophans and creation of a NES motif) resulting in enhanced nuclear export of NPM1 mutants and their aberrant accumulation in the cytoplasm of AML cells [63]. Very rare mutations involving exons 9 [69], 11 [70] and 5 [71] also lead to cytoplasmic delocalization of mutant NPM1 through a similar molecular mechanism.

Cytoplasmic expression of NPM1 (a surrogate for NPM1 mutations) can be detected by IHC in BM biopsies [3]. In our patient, the discrepancy between IHC (cytoplasmic NPM1) and conventional molecular analysis of exon 12 (absence of NPM1 mutation) prompted us to study the entire NPM1 coding sequence, revealing a mutation at exon 11 (Fig. 4C), similar to the one we previously described [70]. As expected, this mutation caused the loss of the two C-terminal tryptophans and the creation of a NES (Fig. 4D), explaining the abnormal cytoplasmic localization of NPM1.

IHC represents a valuable tool for predicting all NPM1 mutations [72]. NGS can also identify all NPM1 mutations but the commercially available panels are designed to recognize mutations at exon 12 only. Thus, they must be adapted for this purpose. Without IHC or NGS, cases like ours would be wrongly assigned to the ELN intermediate risk category (NPM1 wild-type without FLT3-ITD) rather than to the favorable risk group (NPM1-mutated without FLT3-ITD). Our patient had good outcome after CHT alone, suggesting that cases with exon 11 mutations may behave similarly to those with exon 12 mutations, but confirmatory studies are needed. MRD monitoring of these very rare NPM1 mutations may require designing a patient-specific RT-qPCR assay [73].

Case 6: NPM1-mutated AML carrying BCR-ABL1

A 49-year-old man presented with fever, myalgia, haematuria, WBC 98.7 × 109/L, Hb 9.9 g/dL and platelets 14 × 109/L. BM evaluation performed at another Institution was diagnostic of AML with 46,XY,t(9;22)(q34;q11)[9]/47,idem,+8[7]/46,XY[4]; a BCR-ABL1 rearrangement (p210 fusion) (Fig. 5A) and NPM1 mutation type B were detected (Fig. 5B), whilst FLT3 was wild type. Dasatinib was started at a different institution but discontinued after 2 weeks due to pericardial effusion. He presented at our Institution with WBC 2.3 × 109/L, Hb 7.8 g/dl and platelets 19 × 109/L. BM biopsy was massively infiltrated by myeloid (FAB-M2) blasts (Fig. 5C) expressing cytoplasmic NPM1 (Fig. 5D), indicating no response to dasatinib. Sequencing ABL1 exons 4–10 showed no mutations. A ‘7 + 3’ regimen induced partial response (10% residual NPM1 cytoplasmic-positive AML cells) (Fig. 5E, F). He was re-induced with fludarabine, cytarabine and idarubicin, achieving CR whilst fluorescent in situ hybridization (FISH) revealed 0.5% of nuclei with BCR-ABL1. He underwent allo-HSCT from an HLA-identical sibling and is now in molecular CR for NPM1 and BCR-ABL1, 12 months after the allotransplant.

Fig. 5: AML with NPM1 mutation and BCR-ABL1 rearrangement.
figure 5

A G-banding showing a subclone with the following karyotype: 47,XY,t(9;22)(q34;q11),+8 (see the text for the full karyotype). B Sanger trace of NPM1 exon 12, demonstrating mutation B. C Massive BM infiltration by leukaemic cells. T indicates bone trabecula (BM biopsy, haematoxylin-eosin, x400). D Leukaemic cells exhibit aberrant cytoplasmic expression of NPM1 (BM biopsy, APAAP staining, x400). E BM re-evaluation after the first cycle of CHT. Good recovery of normal haematopoietic cells showing nucleus-restricted NPM1 positivity (indicative of NPM1 wild-type). A small cluster of residual leukaemic cells with cytoplasmic NPM1 is seen (arrow) (BM biopsy, APAAP immunostaining, x100). F Higher magnification of the small cluster of NPM1 cytoplasmic leukaemic cells (arrow) shown in Fig. 4E (BM biopsy, APAAP immunostaining, x400).

Questions and recommendations

NPM1 mutations have been reported in de novo AML with BCR-ABL1 but not in chronic myeloid leukaemia in blastic phase [74,75,76]. How should this patient be classified? In the 2017 WHO classification [5], NPM1-mutated AML and AML with BCR-ABL1 represent a ‘distinct’ and a ‘provisional’ entity, respectively [5]. Therefore, NPM1 mutations supersede BCR-ABL1 and our case should be diagnosed as NPM1-mutated AML, annotating the presence of BCR-ABL1 [5]. Notably, leukaemic cells showed CD34 negativity that is more consistent with NPM1-mutated AML [3] than with BCR-ABL1 AML [5]. The relative contribution of the two genetic abnormalities to leukaemogenesis remains to be established.

What is the prognostic impact of these genetic alterations? In the 2017 ELN model, AML with BCR-ABL1 is regarded as high-risk disease [77] whilst NPM1-mutated AML without FLT3-ITD has a relatively good outcome [6]. ELN recommendations [6] do not comment on the combination of NPM1 mutations and BCR-ABL1. Interestingly, two patients carrying NPM1 mutation and BCR-ABL1 were alive 36 and 71 months after diagnosis [74], suggesting that they may behave more like a NPM1-mutated AML than as de novo AML with BCR-ABL1. However, further studies are required.

Practical recommendations for the clinical management of NPM1-mutated AML patient

NPM1-mutated AML should be suspected in a middle-age or older patient who presents with M4-M5 morphology [3], cup-like nuclei [78] or multilineage involvement [26] (case 1), a yet relatively preserved number of platelets despite high WBC count and negativity for CD34. Hyperleukocytosis usually associates with a concomitant mutation of FLT3 or RAS. A low WBC count does not exclude NPM1-mutated AML since cases with FLT3 wild-type may have this presentation, despite the BM tends to remain not hypocellular [79]. Independently of high WBC count, NPM1 or/and FLT3-ITD mutations may associate with disseminated intravascular coagulation [80]. Extramedullary involvement may occur [7], especially in skin (case 2).

In haematological centers performing BM biopsy at presentation, demonstration by IHC of cytoplasmic NPM1 may serve as surrogate to molecular techniques in case of dry tap or myeloid sarcoma [7] (case 2). Moreover, as discussed in case 5, IHC could predict even rare NPM1 mutations occurring at exons other than 12 and even NPM1-containg fusion transcripts [81].

Confirmation of diagnosis requires the identification of NPM1 mutation by Sanger or the more sensitive NGS technique (detecting 1–5% of mutated cells, depending on the allele coverage). NGS can also identify concomitant driver mutations, even within subclones. Identifying the exact type of NPM1 mutation [11, 82] is critical for setting-up the strategy of MRD monitoring (see below).

Once a NPM1 mutation has been recognized, the definitive diagnosis of NPM1-mutated AML requires that other distinct and provisional AML entities of the 2017 WHO classification, such as AML-MRC (case 2), AML with BCR-ABL1 (case 6, Fig. 6) and AML with RUNX1 mutations (Fig. 6) are excluded. According to WHO 2017, the diagnosis of NPM1-mutated AML requires ≥20% BM blasts [5] (Fig. 6). However, the rare cases diagnosed as NPM1-mutated MDS show rapid transformation to AML [83] and respond better to CHT than to HMAs [84], suggesting that NPM1 mutations may define AML irrespective of blast percentage [85]. Similarly, NPM1-mutated chronic myelomonocytic leukaemia (CMML) cases [86, 87] often carry a normal karyotype and tend to evolve rapidly to AML [86], especially those with high NPM1 mutation allelic burden [87]. In our experience, they usually represent NPM1-mutated AML presenting with marked monocytosis.

Fig. 6: Differential diagnosis of NPM1-mutated AML.
figure 6

Decisional algorithm for distinguishing NPM1-mutated AML from AML with BCR-ABL1 and AML with RUNX1 mutations (two provisional entities of the 2017 WHO classification of haematopoietic tumors).

Once the diagnosis of NPM1-mutated AML has been established, the patient should be assigned to one of the ELN categories, either favorable (if FLT3 is wild-type or low ratio) or intermediate (FLT3-ITDhigh). Cases co-mutated for NPM1 and FLT3 should be possibly analyzed for DNMT3A to exclude the triple mutated genotype, which shows a particularly adverse outcome. As discussed in cases 1, 2, 3 and 4, risk stratification is important in guiding frontline (whether to use or not a FLT3 inhibitor) and post-remission therapeutic decisions (whether to perform or not allo-HSCT). Patient’s age and fitness are other important parameters to be considered for choosing between CHT and venetoclax-based regimens or for deciding whether to perform or not allo-HSCT.

As discussed in cases 1 and 2, MRD monitoring (Fig. 7) during and after completion of CHT + /- allo-HSCT is a critical step in NPM1-mutated AML [24]. In fact, progressive raising of MRD levels is a reliable predictor of impending haematological relapse [15, 24, 88]. Patients in molecular relapse (as case 2) are candidates for pre-emptive therapy [31,32,33], although it still remains uncertain whether converting pre-transplant MRD positivity into negativity is clinically relevant. Relapse without detectable NPM1 mutation points to a second AML [89,90,91] (Fig. 7).

Fig. 7: Decisional algorithm for the molecular diagnosis of NPM1-mutated AML and monitoring of MRD.
figure 7

Immunohistochemical analysis (IHC) on BM trephine discriminates between AML with nuclear localization of nuclephosmin (predictive of wild-type NPM1 gene), and AML with cytoplasmic staining for NPM1 (predictive of NPM1 mutations). Standard Sanger sequencing of NPM1 exon 12 (involved in almost all cases) allows identification of the specific NPM1 mutations. The discrepancy between IHC (cytoplasmic NPM1) and conventional molecular analysis of exon 12 (absence of NPM1 mutation) should prompt to study the entire NPM1 coding sequence to exclude mutations in other exons. Application of RT-qPCR to monitor MRD to be performed during CHT and at interval of 3 months for at least 2 years after the end of CHT + /− allo-HSCT. NGS has the potential to identify all NPM1 mutations but the commercially available panels should be implemented to include, together with exon 12, at least exon 11, 9 and 5. *Should the entire coding sequence be wild-type, FISH to exclude very rare NPM1 fusions should be considered. RNA sequencing should be also performed in these cases to identify novel NPM1 translocations. NGS can be used also for MRD monitoring. Relapse with no detectable NPM1 mutation points towards a diagnosis of second AML.

Conclusions and future perspectives

Although the presence of NPM1 mutations cannot overcome the prognostic relevance of high-risk cytogenetic abnormalities (e.g. monosomy 7 defining AML-MRC), available data suggest that it probably supersedes the value of blast count. Indeed, the rare cases diagnosed as NPM1-mutated MDS or CMML often show features overlapping with AML [83,84,85,86,87]. Therefore, we envision that future issues of the WHO classification will identify NPM1 mutations as genetic abnormalities sufficient to diagnose acute myeloid leukaemia regardless of the blast count, joining t(8;21), inv(16), t(16;16), and t(15;17).

Despite great progresses, improving standardization of MRD monitoring and therapy of NPM1-mutated AML remain a medical need. MRD monitoring is usually done by RT-qPCR [11]. However, highly sensitive NGS techniques for monitoring NPM1 MRD have become available [92,93,94]. Digital droplet PCR may be an alternative, even for assessing rare NPM1 mutations [95].

Incorporation of gemtuzumab ozogamicin has been advocated in the frontline treatment of NPM1-mutated AML [96,97,98]. Potential of venetoclax plus CHT [99,100,101] and mechanisms of resistance to venetoclax [102] should be further explored in NPM1-mutated AML. The good outcome of NPM1-mutated AML with FLT3-ITDlow was questioned in recent CHT-based studies [103,104,105], whilst clearly emerged in trials using CHT plus midostaurin [106]. Thus, the best post-remission therapy for this genotype remains controversial. Translation into clinic of XPO1 [107] and MLL-Menin inhibitors [27, 108], alone or combined with FLT3 inhibitors [109] is warranted. Finally, NPM1 mutant neoantigens complex may be a potential target for immunotherapy [110].