Monosomal karyotype in myeloid neoplasias: a literature review

Abstract

In 2008, the concept of the monosomal karyotype (MK) in adult acute myeloid leukemia (AML) patients was introduced, defined by the presence of a chromosomal aberration pattern characterized by the presence of at least two autosomal monosomies or of one monosomy plus one or more structural aberrations (not including loss of a chromosome). We present a systematic review of the literature about the influence of the MK on the outcome of patients affected by myeloid malignancies (AML, myelodysplastic syndromes, and primary myelofibrosis). For this review, a comprehensive literature search using the term “monosomal karyotype” was performed, considering articles listed in MEDLINE. This analysis of the literature confirms the negative prognostic impact on survival of the MK in myeloid neoplasias. The detrimental effect of MK on AML patients’ outcome is independent of other variables, including adverse cytogenetic features, supporting the identification of this entity as a challenging subgroup of patients with distinct biologic and clinical features.

Keywords:

• monosomal karyotype
• acute myeloid leukemia
• myelodysplastic syndromes
• primary myelofibrosis
• prognosis

Introduction

In the last few years, the application of cytogenetic and molecular disease markers has redefined the approach to the diagnosis, risk stratification, and treatment of myeloid malignancies, including acute myeloid leukemia (AML), myelodysplastic syndromes (MDS), and primary myelofibrosis (PMF). In 2008, in a cooperative study, the Dutch–Belgian Haemato-Oncology Cooperative Group/Swiss Group for Clinical Cancer Research (HOVON-SAKK)¹ proposed the concept of the monosomal karyotype (MK), defined by the presence of a chromosomal aberration pattern characterized by the presence of at least two autosomal monosomies or of one monosomy plus one or more structural aberrations (not including loss of a chromosome). We present a systematic review of the literature concerning the influence of the MK on the outcome of patients affected by myeloid malignancies.

MK in AML

AML is a clinically and biologically heterogeneous hematologic malignancy derived from a clonal transformation of hematopoietic precursors due to the acquisition of chromosomal rearrangements and gene mutations.

The World Health Organization 2008 classification firstly, and the 2016 revision later, incorporated genetic information into diagnostic algorithms for myeloid neoplasms with the aim of redefining clinically distinct disease subtypes that require specific therapeutic interventions.^2,3 In this context, subtypes of AML are classified and prognostically determined on the basis of their cytogenetic profiles.^4,5 Thus, in clinical practice, the metaphase cytogenetics obtained at the diagnosis of AML has allowed clinicians to classify patients into different risk groups.^6,7

In adult AML, cytogenetic risk is the most important independent prognostic factor, predictive of the probability of overall survival (OS) and progression-free survival.^4,5 Cytogenetic abnormalities are found in ~60% of patients with AML, and most cytogenetic risk stratification systems subdivide patients, by recurrent cytogenetic abnormalities, into favorable, intermediate, and unfavorable risk groups.^6–8

In the HOVON-SAKK study, MK+ AML was prevalent in about 9% of AML patients between 15 and 60 years of age.¹ In subsequent studies, MK+ AML has been reported in about 6%–10% patients with newly diagnosed AML and the prevalence rises with increasing age.^9–11 For example, the Southwest Oncology Group (SWOG)⁹ reported a frequency of MK+ AML of about 20% in newly diagnosed patients with AML of age >60 years, 4% in patients of age <31 years, 7% in patients aged between 31 and 40 years, 11% for patients with age ranging from 41 to 50 years, and 13% for patients aged 51–60 years. These data on the frequency of the MK were later confirmed in two other studies that showed frequency of 10% in patients with AML of age <60 years and 13%–15% in patients with AML of age >60 years.^10,11

Types of cytogenetic abnormalities

All studies are in agreement about the frequency of the different types of autosomal monosomies (Figure 1).

Figure 1 Frequency of autosomal monosomies in MK+ AML.

Abbreviations: AML, acute myeloid leukemia; MK, monosomal karyotype.

The most common monosomies involved in MK+ AML are −5 and −7. In the German–Austrian AML Study Group analysis of MK+ AML cases, the most frequent chromosome abnormalities were −5 or 5q (55%) and −7 (45%).¹² Another paper showed that the most frequent monosomy was −7, followed by monosomies 17, 18, 16, 5, and 3.⁴ Voutiadou et al also reported monosomy 7 as predominant in terms of frequency, being present in 22.6% of MK cases, followed by monosomy 5 in 21%.¹³ Furthermore, the HOVON-SAKK study showed, in multiple comparisons, that any type of monosomy in AML was associated with a poor outcome.¹ In fact, direct comparison between patients with a single monosomy 7 and other variable single autosomal monosomies revealed an identically poor OS. Therefore, no difference in the prognosis seems to result from the presence of any specific monosomy, in the context of the MK.

MK and TP53 alterations

The mechanisms responsible for MK+ AML are still unclear, but it may be associated with deletions or mutations in TP53 gene and multiple drug resistance. In fact, recent evidence indicated that TP53 alterations occur in 70% of MK+ AML patients and that these abnormalities are more frequent in patients with a complex karyotype (CK+)/MK+ AML than in those with CK+/MK− AML.¹⁴ They potentially lead to a chromosome instability pattern that is usually a result of a single catastrophic event known as chromothripsis.¹⁵ Moreover, it has been recently reported that chromothripsis-positive AML cases were characterized by a particularly high degree of karyotype complexity (CK, MK, abnl[5q], abnl[7q], and abnl[17p]), TP53 mutations, and dismal prognosis.¹⁶ Thus, TP53 alterations appear to be one molecular basis for this MK+ AML subset and, in particular, biallelic alterations suggest an important role for p53 in leukemogenesis. From a prognostic standpoint, TP53 abnormalities have a negative impact on the outcome of these patients due to chemoresistance (lower complete remission (CR) rates and higher rates of refractory disease).¹⁴

Prognostic impact of MK in AML

Several recent studies have revealed that AML with the MK are at the extreme end of the unfavorable risk category, and its presence is predictive of the worst possible outcome.

Two major cooperative trial groups, namely, the HOVON-SAKK and the SWOG groups, collected cytogenetic diagnostics at baseline in patients with AML enrolled in their treatment protocols. These works generated datasets in large series of homogeneously treated patients, in whom the prognostic contribution of various cytogenetic abnormalities such as CK could be evaluated. Statistical analysis revealed that the loss of a complete autosomal chromosome conferred a negative prognostic impact, while structural abnormalities negatively influenced the prognosis in association with an autosomal monosomy.¹

In particular, among 733 non-core-binding factor AML patients ranging in age from 15 to 60 years, the first HOVON-SAKK group¹ paper showed that the presence of a single autosomal monosomy conferred a poor prognosis, regardless of the chromosome involved, as compared with patients without monosomy. Similar results were later reported by the SWOG group;⁹ in their study, 1344 AML patients ranging in age from 16 to 88 years were included and treated with standard chemotherapy. One hundred seventy-six (13%) patients were classified as having the MK. The median age of patients bearing the MK was 61 years. The median OS of the MK group was 4 months. The CR rate in patients with unfavorable cytogenetics without the MK was 34% vs 18% in patients with the MK, and the 4-year OS of patients with unfavorable cytogenetics but without the MK was 13% vs 3% in the MK group. Thus, these data confirmed that the MK defines a subset of AML patients with unfavorable cytogenetics and poor prognosis.

In two HOVON-SAKK studies^10,11 and one by SWOG,⁹ the CR rates for MK+ AML were no more than 52% in patients aged <60 years and only 34% in those aged >60 years. In particular, a CR rate of 50% was reported in patients aged <31 years (a low percentage for young AML compared to historical controls), 27% in patients aged 31–40 years, 14% in patients from 41 to 50 years old, 24% for patients aged 51–60 years, and 13% in MK+ AML patients aged over 60 years.⁹ Apart from the CR rates, the survival estimates were also very poor in MK+ AML. In the original study, the HOVON-SAKK group¹ showed an OS of 4% at 4 years in patients with MK+ AML of age >60 years; subsequently, the SWOG study⁹ also reported an OS of 3% at 4 years in patients with MK+ AML aged between 16 and 88 years, compared to a 4-year OS of 13% in patients with an unfavorable karyotype but without the MK. The latest HOVON-SAKK group studies reported 4% OS at 2 years in MK+ patients aged >60 years¹¹ and 7% OS at 5 years in those aged <60 years.¹⁰ Of note, in the SWOG⁹ study, an estimated OS of <1% at 4 years was reported for patients with MK+ AML aged between 41 and 88 years, while in the HOVON-SAKK study, at 5 years, there were no long-term survivors among patients >60 years of age.¹¹ The very poor prognosis of MK+ AML in terms of OS was also shown in a large-scale study of AML patients aged between 16 and 59 years conducted by the UK Medical Research Council:⁷ the estimated OS at 10 years was 5%. Similarly, the Groupe Ouest Est des Leucemies Aigues et Autres Maladies du Sang¹⁷ made a retrospective study of patients aged >60 years with unfavorable cytogenetics. There was a significantly lower CR rate for MK+ AML than for the MK- group (37% vs 64%, respectively), and the OS rate at 2 years was also decreased (7% and 22%, respectively). Moreover, in the subgroup of CK patients, OS was dramatically decreased for MK+ patients (8% vs 28%). These results demonstrate that the MK is a major independent very poor prognosis factor in elderly AML. During the past few years, several large studies have been conducted to analyze the prognostic impact of the MK on the outcome of AML (summarized in Table 1), confirming the previously reported findings.^{1,5,9–13,17–24} Moreover, a recent report demonstrated that the combination of CK (defined in this study as unrelated chromosomal abnormalities ≥4) and the MK missed the least number of patients with unfavorable prognosis.¹⁸

Table 1 Main characteristics of AML patients with MK

Reference	Number of patients	Age (median, range)	MK frequency (%)	CR rate	OS	Comments
Breems et al^Citation1	1,975	NR, 15–60	9	48%	4% at 4 years
Medeiros et al^Citation9	1,344	NR, 16–88	13	18%	3% at 4 years	Monosomies of 5 and 7 were the most common
Grimwade et al^Citation7	1,612	44, 16–59	6	NR	5% at 10 years
Löwenberg et al^Citation11	813	67, 60–83	13	34%	4% at 2 years
Lowenberg et al^Citation10	860	49, 18–60	10	52%	7% at 5 years
Perrot et al^Citation17	186	68, 60–79	59	37%	7% at 2 years
Haferlach et al^Citation18	824*	NR, 15–60	19	NR	Median 5.7 months	All cases were analyzed by multicolor FISH
Voutiadou et al^Citation13	549	53, 6–88	11.3	27%	8% at 3 years	Predominant monosomies were −5 and −7
Kayser et al^Citation12	1,058*	57, 17–84	30	32.5%	9% at 4 years	NPM1, FLT3-ITD, FLT3-D835 less frequent in MK+ group
Yang et al^Citation19	1,147*	NR, 15–88	18.5	25%	Median 5 months	Monosomies of 5 and 7 were the most frequent
Ahn et al^Citation20	369	47 (18–85)	6.2	34.8%	8.7% at 3 years
Weinberg et al^Citation21	111	57 (17–83)	13	36%	Median 5.6 months	Most frequent chromosomes lost were 7 and 17
Manola et al^Citation22	140	13 (25–21)	12.1	NR	51.9% at 4 years	MK in children
Lu et al^Citation23	1,251	44 (15–89)	14.7	29.8%	Median 9 months
Lazarevic et al^Citation24	1,893	71 (18–80)	18	59% in <60 years 41% in >60 years	NR

Note:

* AML patients with t (15;17), t (8;21), inv (16), and normal karyotype were excluded.

Abbreviations: AML, acute myeloid leukemia; FISH, fluorescence in situ hybridization; MK, monosomal karyotype; NR, not reported; OS, overall survival.

With regard to the MK in AML, it should be remembered that many monosomies described in chromosome banding analysis may be not real monosomies, but part of chromosomal material hidden in unbalanced translocations or marker chromosomes.¹⁴

Therapeutic implications of MK in AML

MK+ AML patients respond poorly to conventional chemotherapy due to resistance to current treatments, resulting in a low CR rate or in an early relapse rate after CR. In the past, daunorubicin dose escalation was shown to yield a higher CR rate and improved survival in patients with AML under 65 years of age.²⁰ In the same way, two recent studies reported that high-dose cytarabine-based chemotherapeutic protocols could improve long-term survival in patients with MK+ AML and showed a potential survival benefit.^25–27 In particular, a study conducted by the HOVON-SAKK group²⁶ reported that no significant differences were noted between the intermediate- and the high-dose groups in terms of CR rates (80% and 82%, respectively), probability of relapse-free survival at 5 years (34% and 35%, respectively), or OS (40% and 42%, respectively). However, only in the MK+ subgroup (89 patients, 9% of the total population) were the 5-year event-free survival (13% vs 0%) and OS rates (16% vs 0%) better in the high-dose cytarabine group, compared with the standard-dose group. The impact of different postremission strategies on the outcome of these subsets of patients is not clear. A study by the Fred Hutchinson Cancer Research Center reviewed the experience of allogenic hematopoietic stem cell transplantation (alloHSCT) in 432 patients with AML.²⁸ They showed that alloHSCT could increase the 4-year disease-free survival rate of MK+ AML by up to 25%, and similar results were obtained with matched related and matched unrelated donors. Although this result is still lower than the 56% OS seen in patients without the MK, it is better than the 3%–9% OS seen in patients receiving chemotherapy alone. This study also showed that the OS rate was higher for patients who achieved CR before transplantation, and that the 4-year OS rate was 30% for patients in CR1, 25% for patients in CR2, and 16% for patients in other disease statuses before transplantation.²⁸

Subsequent studies also confirmed that transplantation could improve long-term survival in MK+ AML patients, but it was associated with disadvantages such as a high recurrence rate and a short median time to recurrence.^29,30 In 2012, a comparative analysis performed by the HOVON/SAKK group was reported, which included >300 MK+ patients.³¹ Among the 140 patients who achieved CR after two induction cycles, 107 (76%) proceeded to consolidation therapy and 45 (32%) subsequently received alloHSCT. Finally, MK+ patients in CR1 who received alloHSCT had a long-term OS of 19% at 5 years, compared to 8% among those receiving alternative consolidation chemotherapies.³¹

Moreover, a study reported by Moon et al confirmed these findings, showing that alloHSCT in MK+ patients with active disease at the time of transplantation had a negative impact on the outcomes.³² So, the remission status at the time of transplantation is critical for all patients, and particularly for MK+ AML patients.

However, allogeneic transplant remains the only potentially curative strategy for MK+ patients who were refractory to the initial therapy. In fact, while the median OS for MK+ patients refractory to induction therapy and who received an allogeneic transplant was 3–9 months, and 10% of patients achieved long-term survival, a shorter median OS and no long-term survivors were reported for refractory MK+ AML patients who did not proceed to transplantation.³¹

In conclusion, the data available suggest that alloHSCT in first CR is a reasonable treatment to improve the outcomes in this subset of patients. However, the MK+ AML prognosis remains poor even after alloHSCT, and this category of AML patients should be seen as candidates for clinical trials testing novel treatment strategies in order to improve their overall outcome.

MK in MDS

MDS are heterogeneous diseases characterized by bone marrow dysplasia, cytopenias, and a variable risk of evolution to AML.³³ The most widely used risk scoring system in MDS is the International Prognostic Scoring System (IPSS), which utilizes clinical and molecular features, including cytogenetics, percentage of blasts, and the number of cytopenias, to risk-stratify patients.³⁴ The IPSS was subsequently revised (IPSS-R) and this version maintained bone marrow cytogenetics, marrow blast percentage, and cytopenias as the basis of the scoring system, but introduced increased stratification within these categories.³⁵ While the IPSS includes only three cytogenetic patterns, the IPSS-R classifies cytogenetic information in MDS in five risk groups with correspondingly different median OS.³⁶

Prognostic impact of MK in MDS

An abnormal karyotype is seen in 50% of de novo MDS and 80%–92% of therapy-related MDS, and it is clear that the poor and the very poor IPSS-R cytogenetic groups include patients with the MK.^35,37 Several conflicting reports (summarized in Table 2) on the impact of the MK as an independent predictor of survival in MDS have drawn attention to the importance of considering the prognostic weight of complex aberrations in association with autosomal monosomies.^38–43 In a recent study including only CK MDS patients from the Mayo Clinic database, the authors suggested that MK+ is associated with a lower OS:³⁸ the OS was significantly inferior in patients with MK+ compared with those with a CK without monosomies, and the median survival of patients with a CK without monosomies was 13 months vs 7 months in patients with MK+. By contrast, the Spanish group of MDS (GESMD) analyzed 1054 MDS patients with an abnormal karyotype. In their cohort, MK+ was identified with a frequency of 16%, and the majority of these patients (88%) also had a CK.³⁹ To clarify the significance of the presence of MK+, the GESMD study analyzed its impact on both CK patients and those with only two chromosomal abnormalities (ie, at least two autosomal monosomies or of one monosomy plus one structural aberrations), being the minimum necessary to fulfill the criteria for MK+. In CK patients, the MK was not statistically associated with a lower OS in univariate or multivariate analysis, but the risk factors associated with a lower OS in patients with CK were the classic variables (refractory anemia with excess blasts, high IPSS, low hemoglobin level, and low platelet count) together with higher numbers of chromosomal abnormalities.³⁹ In patients with only two abnormalities, although MK+ patients showed a lower OS in univariate analysis, this effect did not persist in multivariate analysis, in which the only variable associated with a lower OS was a higher IPSS risk group. By contrast, the CK adverse prognostic value was retained in MK+ patients also. These results support the hypothesis regarding the predominant role of karyotype complexity in determining the prognosis in patients with MDS. Similarly, in 2013, a study analyzed 431 untreated MDS patients with two or more chromosomal abnormalities from an international MDS database and found that MK+ was associated with a worse OS only in those patients with four or fewer abnormalities, and that in the multivariate analysis, it was not independently associated with OS.⁴⁰ The authors concluded that the number of chromosomal abnormalities, rather than the presence of MK+, defined the MDS subgroups with a worse prognosis and that the number of chromosomal aberrations in MK+ subgroups of MDS was directly related to OS, and so MK+ was not reflected as an independent prognostic factor.

Table 2 Main characteristics of MDS patients with the MK

Reference	Number of patients	Age (median, range)	MK frequency (%)	Median OS	Comments
Schanz et al^Citation40	431	69 (21–90)	47	6.7 months	Patients included in the study were primary, untreated MDS
Valcarcel et al^Citation39	1,054	71 (16–96)	16	7.6 months	MK was not associated with poorest prognosis; 431 patients received therapy. The study results were not influenced by treatment
Belli et al^Citation41	421	71 (17–93)	5.4	16 months	MK had a similar prognostic impact to other poor cytogenetic findings. Most patients received treatment or supportive care
Gangat et al^Citation42	783	72 (18–98)	9.1	4.5 months	MK adversely affected survival in both the poor and very poor karyotype groups
Patnaik et al^Citation38	127	70 (18–89)	83	7 months	This study considered only MDS patients with a complex karyotype
Cluzeau et al^Citation43	154	72 (35–88)	15	9 months	Stratification with the MK has a value in the prognosis of azacitidine-treated patients

Abbreviations: MDS, myelodysplastic syndromes; MK, monosomal karyotype; OS, overall survival.

In conclusion, although the cytogenetic prognosis is very important in the IPSS-R, MK+ was not considered as a prognostic subgroup. The Mayo Clinic group suggested that the MK provides additional prognostic information in poor/very poor karyotypes: in their cohort of 783 patients with MDS, there was no significant difference in survival among IPSS-R subgroups (very good, intermediate, poor), but reclassification using MK+ allowed them to obtain a significant difference in OS.⁴²

Therapeutic implication of MK in MDS

Azacitidine (AZA) is a first-line treatment for higher IPSS risk patients with MDS who are ineligible for alloHSCT.⁴⁴ The prognostic impact of MK+ in AZA-treated patients is unclear. The French group has shown that the IPSS-R is a powerful tool to evaluate the outcome of previously untreated MDS patients treated with AZA.⁴⁵ A report in 2011 suggested that AZA might reduce the negative impact of MK+ in higher IPSS risk MDS patients:⁴⁶ in a cohort of 75 patients with high-risk MDS treated with AZA, the median OS was 7.1 months in MK+ and 8.7 months in non-MK patients (no statistically significant difference). Several studies have pointed out that high-risk patients are often referred for hematopoietic cell transplantation, the only potentially curative treatment for MDS.^47–49 Many recent studies evaluating the importance of MK+ in alloHCT have reported similar results. In a cohort of 261 MDS patients with chromosome 7 abnormalities, it was shown that MK+ was more predictive of progression-free survival and OS after alloHSCT than complex cytogenetics in 261 MDS patients.⁴⁹

It has also been reported that MK+ was more predictive of alloHSCT outcomes in MDS patients, compared to other established scoring systems.⁵⁰ Moreover, the presence of MK+, both at diagnosis and at alloHSCT, was predictive of a worse OS after alloHSCT; in fact, the presence of MK+ at diagnosis was associated with a poor 3-year disease-free survival (27% vs 39%) and OS (29% vs 47%). Therefore, MK+, particularly at diagnosis, seems to be the cytogenetic risk factor most predictive of post-alloHSCT outcomes. A large study by the International Blood and Marrow Transplant Research group analyzed the influence of MK+ on survival in a large cohort of patients with AML and MDS undergoing alloHSCT.⁵¹ Among patients with MDS, MK+ MDS was associated with higher disease relapse rates, higher transplant-related mortality, and a worse OS. Subset analyses comparing chromosome 7 abnormalities with or without MK+ demonstrated a higher mortality for MK+ MDS. Koichiro et al reported the outcome of 53 MDS patients; among them, 9 (17%) had MK+ and 4-year OS was 0%, significantly lower than that of MDS patients with a normal karyotype.⁵² However, the European Bone Marrow Transplantation group reported that the CK is a better predictor of a poor outcome than MK+ after alloHSCT in MDS patients;⁵³ in this study, the OS of patients with CK, with or without MK, was significantly worse than that of patients with isolated MK+.

A work by Gruppo Italiano Trapianto Midollo Osseo analyzed 519 patients with primary MDS undergoing alloHSCT and showed a 5-year OS of MK+ patients of only 10%, significantly worse than that of patients without the MK.⁵⁴ Moreover, the 5-year incidence of relapse was 49%, significantly greater than that of patients without the MK.

In summary, cytogenetic abnormalities remain the most important predictor of treatment outcome in MDS patients. MK+, which was not considered as a separate category in the scoring system, may represent another subset of high-risk MDS patients with a dismal outcome after alloHSCT. Further evaluation with prospective studies will help to define the importance of MK+ in MDS and improve treatment strategies for this subgroup of patients.

MK in PMF

In clinical practice, the IPSS is used to assess prognosis in PMF.⁵⁵ The IPSS score was later modified to the Dynamic IPSS (DIPSS) for use at any time during the disease course.⁵⁶ Most recently, DIPSS was further modified to the DIPSS-plus, with the incorporation of three additional DIPSS-independent risk factors: red cell transfusion need, platelet count <100×10⁹/L, and unfavorable karyotype.⁵⁷ This category includes CK or one or two abnormalities among +8, −7/7q-, i (17q), inv (3), -5/5q-, 12p-, or 11q23 rearrangement.

Two studies have analyzed the impact of MK+ in PMF patients. In the first, 793 patients were included; among them, 341 (43%) showed an abnormal karyotype, including 41 (12%) with CK and among these, 17 (41%) were classified as having an MK+.⁵⁸ To determine whether the presence of MK+ conferred additional prognostic significance, the authors compared groups with MK+, CK without monosomies, and with only trisomy 8: median survival was 6, 24, and 20 months, respectively, and the corresponding 2-year leukemic transformation rates were 29.4%, 8.3%, and 0%. Therefore, the study shows that MK+ is equally as bad as PMF in terms of both OS and leukemia-free survival. In fact, the presence of MK+ in PMF signified a worse survival than the rate associated with either the CK without monosomies or a sole trisomy 8, both of which had previously been identified as unfavorable cytogenetic findings in PMF.⁵⁹ More recently, a large cohort of Chinese patients with PMF⁶⁰ was analyzed: the MK was found in 12% of cases. The patients were divided into two cytogenetics-based cohorts: a favorable (subjects with a normal karyotype, a CK that was not an MK, +8 only or a balanced translocation only) and an unfavorable karyotype (all the others). The median OS was 52 vs 72 months in patients with a favorable and unfavorable karyotype, respectively.

These findings underscore the importance of paying attention to cytogenetic findings also in PMF and the prudence of early intervention with investigational drug therapy or allogeneic stem cell transplantation in MK+ PMF, although the value of such a treatment strategy in this particular patient population remains unproven.

Conclusion

This analysis of the literature confirms the negative prognostic impact on survival of the MK in myeloid neoplasias. The detrimental effect of the MK on AML patients’ outcome is independent of other variables, including adverse cytogenetic features such as monosomy 7 and CK, supporting the identification of this entity as a challenging subgroup of patients with distinct biologic and clinical features.

All studies on AML and MDS confirm that the MK classification scheme identifies a group with a very poor prognosis for all study endpoints, even after alloHSCT.

The last several years have seen marked improvements, thanks to standardized chemotherapy (including induction therapy and consolidation therapy), in the survival times of AML patients, while alloHSCT is currently used as a salvage therapy for patients with high-risk AML, including MK+ AML. However, MK+ has been shown to be significantly correlated with a worse OS among patients who have undergone alloHSCT.

In conclusion, the presence of MK+ is associated with a worse outcome (in terms of OS and CR rate) compared to other cytogenetic abnormalities. Therefore, research to identify more effective induction regimens, conditioning regimens, and posttransplant treatments for the prevention of relapse is warranted in this high-risk group of patients, in order to improve the number of patients who can benefit from alloHSCT and achieve a better outcome. Moreover, MK+ patients, mostly those with AML, should be enrolled to take part in clinical trials of novel treatment strategies in order to improve the OS in this very poor prognostic group.

Acknowledgments

This work was supported by “Associazione Italiana contro le Leucemie (AIL)-BARI”.

Disclosure

The authors report no conflicts of interest in this work.