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Case Reports
. 2020 Nov 11:2020:8867461.
doi: 10.1155/2020/8867461. eCollection 2020.

Dasatinib and FLAG-IDA Is an Effective Therapy for Initial Myeloid Blast Crisis but Involves a High Risk of Opportunistic Infections

Affiliations
Case Reports

Dasatinib and FLAG-IDA Is an Effective Therapy for Initial Myeloid Blast Crisis but Involves a High Risk of Opportunistic Infections

Jorge Labrador et al. Case Rep Hematol. .

Abstract

Blast crisis (BC) continues to be the major challenge in the treatment of chronic myeloid leukemia. Best results have been observed in a few patients who were successfully transplanted after returning to chronic phase. Recent studies focus on the combination of chemotherapy with imatinib, but results remain unsatisfactory. Since dasatinib induces deeper and faster responses, a reasonable strategy might be to combine it with chemotherapy, taking into account the alterations in T-cell response induced by dasatinib. However, there are no published studies or case reports supporting the use of dasatinib as first line treatment for initial myeloid BC, and very little is known about infectious complications associated with this drug. Based on this, we present the case of a patient diagnosed with an initial nonlymphoid phenotype BC, who achieved molecular response (MR4.5) with dasatinib and FLAG-IDA, but he suffered a pulmonary aspergillosis, CMV infection, and a CMV reactivation, prior to an allogeneic hematopoietic stem cell transplantation (HSCT). In conclusion, dasatinib and FLAG-IDA is an effective therapy for initial BC. However, a warning call is needed owing to the high risk of opportunistic infections, such as CMV.

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Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

Figure 1
Figure 1
Erythematous, round, well-grouped plaques located at the rear right costal arch. A biopsy of the skin lesions was performed and reported as compatible with leukemia cutis.
Figure 2
Figure 2
Flow cytometry at diagnosis showed 33% of blasts distributed in 3 populations. 1st population, myeloid without differentiation (15%), in red: CD34++, CD117 +, HLA-DR +, CD45 + d, CD13+, CD64 −, CD35−/+ d, CD36−, CD33 +, CD71−/ +, CD105 + d, CD7−/ +, CD15−/ +, CD22−, CD38 +, CD123 +, CD4+d, and cMPO−. 2nd population, dendritic (13%), in blue: CD34+d, CD117−/+, HLA-DR++, CD45+d, CD13 +, CD64−/ +, CD35−, CD36−/ +, CD33++, CD71−/+, CD105 + d, CD7−/+, CD15−/+, CD22−, CD38 +, CD123++, CD4 + d, and cMPO−/ +. 3rd population, myeloid (5%), in yellow: CD34 + d, CD117 + d, HLA-DR−/+, CD45 + d, CD13 +, CD64−, CD35−, CD36−, CD33−, CD71−, CD105−, CD7−, CD15−, CD22 +, CD38−, CD123−, CD4−/+d, and cMPO−. Blasts were negative for CD10, CD16, CD11b, CD14, IREM-2, nTdT, CD56, CD19, 7.1, CD42, CD61, CD203c, cCD79a, cCD3, and CD3.
Figure 3
Figure 3
Chest X-ray showing a triangular consolidation in the right superior lobule.

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