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EBMT ALWP recommendations for transplantation in patients with FLT3-ITD AML

May 1, 2020

Patients with FLT3-mutated AML represent 25 30% of all newly diagnosed AML cases, and their overall prognosis is poor due to the aggressive course of the disease and the risk of early relapse. While there is general agreement on the incorporation of FLT3 inhibitors in frontline treatment and the use of measurable residual disease (MRD) assays, the strategy for allogeneic hematopoietic stem cell transplantation (allo-HSCT) differs between centers.

Globally, hematologists agree on quick treatment initiation followed by allo-HSCT once patients have achieved their first complete remission (CR1). However, clinical protocols vary regarding indication for allo-HSCT according to risk profiles, modalities of allo-HSCT, and post-transplant maintenance. Therefore, the Acute Leukaemia Working Party (ALWP) of the European Society for Blood and Marrow Transplantation (EBMT) recently published in Haematologica their position statement on allo-HSCT for patients with FLT3internal tandem duplication ( FLT3-ITD) AML. 1

A panel of 32 members mostly from the EBMT was selected by the chairs, Professor Ali Bazarbachi and Professor Mohamed Mohty, based on their expertise in research and clinical practice in AML and allo-HSCT. Using the Delphi technique, three panelists provided statements addressing key questions to the remaining panel members who scored their agreement with those statements and suggested rephrasing where necessary. Available evidence from public databases was used to rate the strength of recommendations and evidence level.

Indication for allo-HSCT in FLT3-mutated AML

As a rule, allo-HSCT in CR1 should be performed in patients with FLT3-ITD AML when feasible. Nevertheless, many additional variables can influence the indication for allo-HSCT in this subgroup of patients, such as allelic ratio, concomitant mutations, or MRD status post-induction. The authors state that at the moment, there is insufficient data to provide a rigorous recommendation taking into consideration every possible combination of these variables.

However, the need for transplantation in CR1 is debatable for the small subgroup of patients with FLT3-ITD low(allelic ratio < 0.5) AML and co-existing NPM1mutations, who achieved MRD-negativity after induction therapy. Given the favorable risk profile of this group, many European cooperative groups recommend withholding allo-HSCT for later stages of the disease, while the National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology (NCCN Guidelines®) still recommend allo-HSCT in CR1 for these patients. Overall, changes in the allelic ratio during the evolution of the disease, along with the variability in assessment techniques and the lack of a precise cut-off level, make it difficult to draw any firm conclusions from the published data.

Stem cell transplantation and predictive factors for outcome

Patients with FLT3-ITD mutated AML tend to benefit from allo-HSCT performed in CR1, leading to a 2-year leukemia-free survival (LFS) of 50-60%, but the authors advocate for the need to identify predictive factors which can help to better determine the outcome of transplantation. For instance, the presence of NPM1mutation and the in vivoT cell depletion with anti-thymocyte globulin (ATG) have a positive impact on the outcome. On the other hand, conditioning intensity and the type of donor do not correlate with the outcome and should be selected based on the patient's age, donor type, and disease status.

When selecting a stem cell donor, it is advised to follow the EBMT general guidelines, 2which may include the use of cord blood or a haploidentical donor if a matched sibling donor cannot be identified.

The authors highlight a recent large EBMT registry study published by Bazarbachi et al. 3where data from 462 patients with FLT3-mutated AML were analyzed. The results suggest that the use of ATG after transplant decreased the rate of chronic graft- versus-host disease (GvHD) and significantly improved LFS, overall survival (OS), and GvHD-free relapse-free survival (GRFS), without increasing the risk of relapse. Therefore, this procedure can now be considered a safe and effective option for these patients.

Post-transplant maintenance in FLT3mutated AML

There are limited treatment options for patients with FLT3-ITD AML who relapse, as standard chemotherapy and FLT3 inhibitors, also combined with donor lymphocyte infusions, show little efficacy in this setting. A second allo-HSCT is a hazardous option and only feasible in a minority of patients.

Therefore, the aim of adding FLT3 inhibitors as maintenance therapy is to delay relapse after the first allo-HSCT. After reviewing the available published data, the panel recommends the addition of post-transplant maintenance therapy with an FLT3 inhibitor (in the absence of a clinical trial) for all patients, except for those with active acute GvHD. Pending the results and approval of other FLT3 inhibitors, at the moment, sorafenib is the preferred option. The initiation of the maintenance therapy should be done as soon as possible after allo-HSCT and hematologic reconstitution.

Even in this high-risk setting, sorafenib seems to be safe and effective in improving progression-free survival (PFS) and OS, with manageable toxicities, as reported in different studies such as the SORMAIN trial. The recommended dose is 400 mg/day administered in two divided doses for a minimum of two years. Patients presenting with MRD-positive disease can also be initially treated with a higher dose (800 mg/day). The dose should be adapted gradually, according to tolerance. In the case of GvHD requiring corticosteroids, sorafenib should be discontinued and may be cautiously resumed when GvHD is in remission.

You can find more information about maintenance therapies being investigated for patients with AML in the monthly editorial theme published recently on the AML Hub.

Conclusion

The main limitation of these recommendations is the lack of data in the subgroup of patients with FLT3-ITD AML. Therefore, the panel was only able to review results from retrospective cohort studies and several phase II trials.

Regardless, the authors firmly recommend that allo-HSCT at CR1 should generally be offered to all patients with FLT3-ITD AML. However, there are some controversies about whether patients with FLT3-ITD lowand NPM1mutations who achieved MRD-negativity should proceed to transplantation, or save it for later stages of the disease where there are less therapeutic options available. More work is required to identify standards for assessing the FLT3-ITD allelic ratio and cut-off level.

Although maintenance therapy with FLT3 inhibitors is recommended in patients with FLT3-ITD AML after transplantation, many questions remain to be answered. There are still uncertainties around, for example, the duration of the maintenance (a minimum of two years is recommended but not established), the effect on immune reconstitution, the use of pre-emptive versusprophylactic donor lymphocyte infusion, possible combinations with other drugs, or the safest time for immunosuppression withdrawal.

Large prospective randomized trials are currently on-going that may shed light and provide additional evidence to support the optimal treatment of patients with FLT3-ITD AML.

Expert Opinion

If we focus on the management of GvHD in patients with FLT3-ITD AML, analysis of published data demonstrated that patients who underwent an in vivoT cell depletion with ATG had a decreased risk of chronic GvHD without an apparent increase in the risk of relapse.

Additionally, the EBMT ALWP makes a clear recommendation for post-transplant maintenance therapy with FLT3 inhibitors in patients with FLT3-ITD AML, except for patients with active acute GvHD. Similarly, if GvHD is reactivated during maintenance and corticoids need to be administered, the FLT3 inhibitor should be discontinued until GvHD is resolved.

  1. Bazarbachi A, Bug G, Baron F, et al. Clinical practice recommendation on hematopoietic stem cell transplantation for acute myeloid leukemia patients with FLT3 internal tandem duplication: a position statement from the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation. Haematologica.2020;105. DOI: 3324/haematol.2019.243410
  2. Ayuk F, Balduzzi A. Chapter 12: Donor selection for adults and pediatrics. In: Carreras E, Dufour C, Mohty M, Kröger N, editors. The EBMT Handbook: Hematopoietic Stem Cell Transplantation and Cellular Therapies. 7th edition. Cham: Springer; 2019. DOI: 1007/978-3-030-02278-5
  3. Bazarbachi A, Labopin M, Battipaglia G. Allogeneic stem cell transplantation for FLT3-mutated acute myeloid leukemia: in vivo T-cell depletion and posttransplant sorafenib maintenance improve survival. A retrospective Acute Leukemia Working Party-European Society for Blood and Marrow Transplant Study. Clin Hematol Int.2019;1(1):58– DOI: 10.2991/chi.d.190310.001