- Open Access
Paediatric acute myeloid leukaemia with the t(7;12)(q36;p13) rearrangement: a review of the biological and clinical management aspects
© Tosi et al. 2015
Received: 19 May 2015
Accepted: 25 June 2015
Published: 5 October 2015
The presence of chromosomal abnormalities is one of the most important criteria for leukaemia diagnosis and management. Infant leukaemia is a rare disease that affects children in their first year of life. It has been estimated that approximately one third of infants with acute myeloid leukaemia harbour the t(7;12)(q36;p13) rearrangement in their leukaemic blasts. However, the WHO classification of acute myeloid leukaemia does not yet include the t(7;12) as a separate entity among the different genetic subtypes, although the presence of this chromosomal abnormality has been associated with an extremely poor clinical outcome. Currently, there is no consensus treatment for t(7;12) leukaemia patients. However, with the inferior outcome with the standard induction therapy, stem cell transplantation may offer a better chance for disease control. A better insight into the chromosome biology of this entity might shed some light into the pathogenic mechanisms arising from this chromosomal translocation, that at present are not fully understood. Further work is needed to improve our understanding of the molecular and genetic basis of this disorder. This will hopefully open some grounds for possible tailored treatment for this subset of very young patients with inferior disease outcome. This review aims at highlighting the cytogenetic features that characterise the t(7;12) leukaemias for a better detection of the abnormality in the diagnostic setting. We also review treatment and clinical outcome in the cases reported to date.
In the past three decades, there has been a considerable improvement in the cure of childhood leukaemia, reaching a long term survival rate of more than 90 % in ALL and approximately 70 % in AML [3, 4]. However, certain categories of childhood leukaemia are still considered high risk, and this level of risk is dictated by the presence of cytogenetic and molecular genetic markers. The amended world health organization (WHO) leukaemia classification includes the most relevant chromosomal rearrangements to allow proper risk stratification of leukaemia patients . To date, the t(7;12)(q36;p13) rearrangement found in infant AML has not been incorporated in the WHO classification, although it has been associated with poor clinical outcome [3, 6]. This cytogenetic entity has not been associated with a particular morphologic or immunophenotypic subtype [6, 7], but has been found in a range of AML types as well as a case of myelodysplastic syndrome . The scope of this review is to give the reader a comprehensive understanding of the t(7;12) rearrangement at the chromosomal level and the available methods for the detection of this cytogenetic marker for an improved diagnosis and a better estimate of the real incidence of this type of leukaemia. We also review the clinical outcome and the therapeutic approaches that have been adopted in the cases reported to date.
The t(7;12) rearrangement: chromosomal appearance and cytogenetic features
In the t(7;12)(q36;p13), the breakpoints on chromosome 12 are consistently at the 5′ end of ETV6, between exons 1 and 3, whereas the breakpoints on chromosome 7 are quite heterogeneous affecting band q36 in regions proximal to the Homeobox HB9 (HLXB9) gene [6, 12, 13], also known as MNX1 (motor neuron and pancreas homeobox 1). There have been descriptions of breakpoints in 7q31 , 7q32 [14, 15], and 7q35–36 . However, some of these findings were not validated using fluorescence in situ hybridisation (FISH). Informative FISH probes spanning 7q would have been helpful towards achieving a more accurate definition of the breakpoints in these cases.
Cryptic and complex rearrangements
To date, three cases of complex rearrangements harbouring the t(7;12) have been reported [16, 17]. These three way translocations were characterised by FISH and described as (i) t(5;7;12)(q31;q36;p13) ; (ii) t(1;7;12)(q25;q36;p13)  and (iii) t(7;12;16)(q36;p13;q12)  respectively. Due to the breakpoints affecting the terminal regions of both chromosomes 7 and 12, the t(7;12)(q36;p13) is considered a cryptic rearrangement. The use of appropriate FISH probes would surely improve the detection of this abnormality and might uncover a higher proportion of t(7;12) translocations masked by more complex rearrangements, as in the cases of the three way translocations previously described.
Interestingly, the majority of t(7;12) cases have been reported in association with specific aneusomies. A recent review of the literature reported that only 2 out of 44 cases harboured the t(7;12) as a sole abnormality . In particular, the presence of one or more additional copies of chromosomes 8, 19 and/or 22 have been recurrently described [6, 7, 15]. The presence of these additional abnormalities has been reported in samples at diagnosis and/or at relapse, indicating that the acquired aneusomies might be sign of clonal evolution and important for the establishment and the survival of the leukaemic clone.
Is there a fusion gene?
As a fusion transcript is detected in only approximately fifty per cent of t(7;12) AML patients, it is debatable that the formation of the fusion gene is the only contributor to leukaemogenesis in these cases. What all the t(7;12) leukaemias have in common is the over-expression of the HLXB9 gene, suggesting that this, rather than the formation of a fusion gene, might be the driver of leukaemogenesis in these patients. Expression of other genes mapping at 7q36 near the breakpoint has also been evaluated and quantified in t(7;12) patients. However, this analysis showed that expression of NOM1, LMBR1 and RNF32 in 7q36 as well as ETV6 on 12p13 was not different from that observed in AML patients without the t(7;12) and in normal bone marrow .
The expression of HLXB9 in healthy progenitor blood cells in the bone marrow has been investigated by several groups. Early expression studies performed in 1991 showed that bone marrow enriched for CD34-positive cells highly expressed HLXB9, whereas unfractionated bone marrow cells expressed HLXB9 in low levels, and bone marrow cells depleted of CD34-positive cells did not show detectable levels of HLXB9 . Later on, the same authors reported increased levels of HLXB9 expression in acute leukaemias that were not seen in the leukaemia patients at remission. These studies suggested a link between HLXB9 over-expression and leukaemogenesis . Other authors reported a relatively low HLXB9 expression in normal bone marrow by real time quantitative PCR (RT-Q-PCR) and did not observe HLXB9 expression in healthy CD34-positive bone marrow cells, but described increased levels in the bone marrow of leukaemia patients with the t(7;12) rearrangement [6, 24]. Observations from our group and by others confirmed elevated HLXB9 expression in t(7;12) leukaemias as well as in some patients with acute myeloid leukaemia with chromosomal abnormalities other than the t(7;12) [20, 25]. HLXB9 expression has been associated with hypo-methylation of its promoter in a series of paediatric AMLs. However, in the same study it was found that in childhood ALL the HLXB9 promoter was hyper-methylated leading to down-regulation of this gene. The authors suggest that HLXB9 might act as an oncogene in AML, whereas it would act as a tumour suppressor gene in ALL . Over-expression of HLXB9 has been also reported in lymphoma [27, 28] and cancer types other than haematological malignancies, such as breast cancer , testicular cancer [30, 31] and hepatocarcinoma . These studies support the idea that HLXB9 involvement might be pivotal in other tumours as well as leukaemia. Limited studies have been carried out on the HLXB9 expression at the protein level, whose presence has been demonstrated in bone marrow smear of leukaemia patients with the t(7;12) by immunohistochemistry . Further studies on leukaemia as well as other cancer types are needed in order to clarify whether the presence of elevated HLXB9 transcript corresponds to proportionate levels of the corresponding protein, or whether translation is regulated by RNA interference pathways .
HLXB9 over-expression and genome organisation
Gene expression signature of t(7;12) leukaemias and HLXB9 targets
The first study to investigate expression profiling of t(7;12) leukaemias was conducted by Wildenhain et al. , who compared leukaemic blasts of patients positive for the presence of the HLXB9/ETV6 fusion transcript with those with MLL rearrangements. It has to be said that these represent the two most common chromosomal rearrangements found in very young AML patients, including infants and mainly children younger than 2 years of age. The authors found that genes expressed in the MLL group of patients, were significantly down-regulated in the HLXB9/ETV6 positive patients. These included HOX genes and genes characteristic for the MLL-induced transformation process such as MEIS1, HOXA9 and C-MYB. On the other hand, together with over-expression of HLXB9, the HLXB9/ETV6 positive patients showed up-regulation of genes implicated in cell–cell interactions and cell adhesion such as EDIL3, CNTNAP5, ANGPT1, DSG2, ITGA9, ITGAV, KDR and SIGLEC6. These are known to be implicated in the maintenance of quiescent haematopoietic stem cells (HSC) and homeostasis of the HSC niche. Overall, this study implies that the mechanisms of leukaemogenesis in these two types of childhood leukaemia are fundamentally very different. Evidence would suggest that the HLXB9/ETV6 positive leukaemias might be initiated through an alterations of interactions between the HSC and the HSC niche. Balgobind et al.  used expression microarrays to examine a large cohort of samples from paediatric patients with AML including seven samples from patients with the t(7;12). The authors built a classifier based on 59 genes that enabled them to identify very specific expression profiling signatures predictive of cytogenetic and molecular subtypes. This classification tool, based on the genetic heterogeneity of paediatric AML, is of great diagnostic potential although its feasibility and implementation in the diagnostic setting will have to be further explored. The significance and the impact of HLXB9 up-regulation in the t(7;12) leukaemias merits further studies. These would shed some light on the pathways triggered by this chromosomal rearrangement. The only report to date to explore possible targets for HB9 (the transcription factor coded by the HLXB9 gene) in haematopoietic cells was performed on the HL-60 myeloid cell line using ChiP-on-chip and expression profiling analyses . This study describes binding of HB9 to the prostaglandin E receptor 2 (PGTER2) promoter resulting in down-regulation of PGTER2 and consequent reduction of intracellular cAMP level. This down-regulatory effect on PGTER2 expression was also observed in t(7;12) patients. Together with repression of PGTER2, Wildenhain et al. , found that HLXB9 expression in the HL60 cell line had mostly a down-regulatory effect on other genes, particularly ZYX and ETS1. Physiologically, expression of PGTER2 modulates differentiation of osteoclasts. Up-regulation of PTGER2 has been shown in immature myeloid precursors. PTGER2 becomes subsequently down-regulated after the cells have differentiated into osteoclasts . Further work is needed to clarify the implications of PTGER2 down-regulation on the bone marrow niche and on the differentiation of immature pre-leukaemic cells.
The t(7;12)(q36;p13) rearrangement affects the subtelomeric regions of chromosomes 7 and 12 respectively. Due to the small size of the genomic fragments translocated, this rearrangement is difficult to detect using the conventional methods of chromosome banding.
Fluorescence in situ hybridisation
Reverse transcription polymerase chain reaction
Specific primers have been designed for the detection of the HLXB9/ETV6 fusion at the cDNA level by reverse transcription polymerase chain reaction (RT-PCR) . However, the presence of a fusion transcript by RT-PCR has been identified only in approximately 50 % of t(7,12) leukaemia patients (Table 1). For this reason RT-PCR does not represent a reliable method for the detection of the t(7;12) rearrangements at diagnosis. However, in those patients positive for the HLXB9/ETV6 fusion transcript, RT-PCR would prove useful for the monitoring of minimal residual disease .
Studies based on expression microarrays have shown that the leukaemic cells of patients carrying the t(7;12) have a distinctive expression pattern that allows to discriminate this specific cytogenetic subgroup from other . Microarray based technologies combined with appropriate classifiers constitute potentially a very powerful diagnostic approach, although in a routine diagnostic laboratory the availability of specialised equipment and costs involved might impact on the choice of method.
A literature search has shown that at least 47 leukaemia patients with the t(7;12) have been reported to date, based on the presence of the chromosomal translocation and/or the fusion transcript . To date, there are a very limited number of studies to address the incidence of this translocation, with a quite comprehensive investigation considering a total of 345 paediatric patients . In this study, patients were subdivided in 289 ALL, of which 99 were infants, and 59 AML, of which 18 were infants. It emerged that 5 out of 18 infant AMLs (age 0–12 months) harboured the t(7;12) rearrangement, making the incidence of this rearrangement near one third of infant AML. In addition to the above, the t(7;12) was also found in one infant with ALL and one 18 month old child with AML. A previous study was conducted on a more selected series of leukaemia patients, chosen on the basis of age <20 months and the presence of additional copies of chromosomes 8 and/or 19, as well as abnormalities of 7q and/or 12p . This study showed that 10 out of 23 patients harboured a translocation between 7q and 12p. However, in only 7 cases ETV6 was involved in the translocation and of these, 6 cases had breakpoint in 7q36 and one in 7q22. Later studies confirmed that the incidence of t(7;12)(q36;p13) was low when considering AML paediatric patients enrolled for clinical trials. These studies reported four t(7;12) cases out of 729 enrolled in the UK MRC AML10 and AML 12; one case out of 454 in AML-BFM 98 and 8 cases out of 981 enrolled in the COG trial AAML0531 [54–56].
Prognostic significance and treatment options
Prognostic significance and clinical outcome
Summary of reports of t(7;12) leukaemias with treatments and clinical outcome
No. of patients
6 died of leukemia
1 died of leukemia and infection
1 died of infection
1 died of treatment related toxicity
1 alive, 22 months after BMT in CR1
1 relapsed in bone marrow with bilateral chloromas on the hips. Treated with radiation and BMT, but later died due to disease
1 relapsed twice, treated with BMT, alive after 2 years
Median EFS: 9 months
3-year EFS: 0 %
3-year OS: 0 %
Alive after 5 years, treated with chemotherapy only
1 received cord blood transplantation at 11 months, relapsed 4 months later, then died at 16 months
1 died during induction chemotherapy from multiple organ failure
1 achieved remission, but relapsed at 10 months, and died at 16 months
3-year EFS: 14 %
3-year OS: 28 %
2 of 7 evaluable patients are alive (1 after chemotherapy, 1 after BMT) (personal communication)
Standard treatment for paediatric patients with AML includes induction chemotherapy (remission induction) with an anthracycline based regimen which also contains cytarabine. The choice of the anthracycline drug used, as well as the total doses of chemotherapy differ between different centres and collaborative study groups. Most children achieve complete remission with rates of 80–90 % after 2 induction courses and the toxic death rate is in the region of 5 %, with the failures being due to resistant disease . Consolidation or Intensification chemotherapy (post-remission therapy) is essential for cure. It includes the administration of high dose cytarabine possibly in combination with other drugs. Doses, duration, number of drugs as well as scheduling differ between collaborative groups. Currently, treatment related death rates in AML paediatric patients, with the improvement of supportive care and the administration of treatment in experienced units, are now less than 10 % .
Stem cell transplantation
Haematopoietic stem cell transplantation (HSCT) is considered an effective therapy for treatment of high risk leukaemia. However, the high toxicity which includes a mortality rate reaching up to 20 % in some series, makes it not a standard therapy in the first line treatment of AML patients with favourable cytogenetics, where a high cure rate is achieved with chemotherapy alone. For patients with unfavourable cytogenetics, although the benefit of HSCT is still to be fully explored, HSCT is considered by many groups as the standard of care [57, 58]. When patients relapse, the most important prognostic factors that will determine the outcome of the salvage therapy are the length of first remission and cytogenetics. In the United Kingdom, HSCT is generally used as consolidation therapy as part of salvage treatment with a survival rate of around 40 % achieved irrespective of the source of stem cells. However, it is important to better understand molecular markers and cytogenetics of the disease to identify patients who would most likely benefit from this modality of treatment . To date, although there are no published guidelines about the management of this group, there is increasing interest among paediatric haematologists/study groups to consider intensification of therapy with allogeneic stem cell transplantation in first complete remission [13, 15, 16, 56]. Further study of this important subgroup of infant AML as well as the incorporation of t(7;12) in future risk stratification schemas are needed to better understand the best treatment approach.
The t(7;12)(q36;p13) is a rare cytogenetic abnormality in paediatric AML and difficult to identify using conventional karyotyping. The use of FISH with appropriate probe sets would enable diagnostic laboratories to identify this cytogenetic entity confidently and to give a better estimate of its occurrence. The incidence of t(7;12) leukaemias is low in overall paediatric AML, but significant in infant leukaemia. There are no published management guidelines for those patients, but it is now acknowledged as a high risk group with poor prognosis and accordingly many are being treated with HSCT in first complete remission. Better understanding of the genetic mechanisms at the basis of t(7;12) leukaemias and the role of HLXB9 in the establishment of this malignancies would provide grounds for possible tailored therapy.
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