Abstract
B/T mixed phenotype acute leukemia (MPAL), which represents only 2–3% of all MPAL cases, is classified as a high-risk leukemia subtype. Adults diagnosed with B/T MPAL have a notably low 3-year survival rate, estimated at 20–40%. The rarity and undercharacterization of B/T MPAL present substantial challenges in identifying an optimal treatment protocol. This report aims to shed light on this issue by presenting a case in which a patient with a complex karyotype was treated using a combination of venetoclax, azacitidine, and blinatumomab. This novel, chemo-free regimen resulted in the patient achieving both hematologic and molecular complete remission, with no severe organ or hematological toxicity observed. Notably, the patient continued to maintain molecular remission for 1 year following the transplantation. Based on these findings, the combination of venetoclax, azacitidine, and blinatumomab could be considered a potential therapeutic approach for B/T MPAL patients, meriting further investigation.
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Background
B/T mixed phenotype acute leukemia (MPAL) is a rare and prognostically unfavorable leukemia subtype characterized by simultaneous immunophenotypic features of both B and T lymphoid lineages. It demonstrates significantly inferior clinical outcomes, with median overall survival (OS) and disease-free survival (DFS) recorded at 8 and 6 months, respectively [1,2,3]. Furthermore, the 3-year survival rate for adults with MPAL is alarmingly low, ranging from 20 to 40% [4, 5].
The therapeutic landscape for MPAL predominantly relies on standard combination chemotherapy, which includes acute lymphoblastic leukemia (ALL) regimen, acute myeloid leukemia (AML) regimen, or “hybrid” regimens that integrate elements from both. However, the establishment of an optimal treatment strategy remains a significant clinical challenge. Research indicates that while ALL-like induction chemotherapy results in higher rates of complete remission (CR) for MPAL, it fails to confer a survival advantage in terms of long-term OS. Additionally, the propensity for high relapse rates and the substantially reduced CR rates post-relapse in MPAL may be linked to the presence of minimal residual disease (MRD) and subclonal populations [6,7,8,9,10].
In the absence of an international treatment consensus, targeted therapies like the BCL-2 inhibitor venetoclax and blinatumomab, a bispecific T-cell engaging antibody construct targeting CD19, have emerged as promising therapeutic options. Empirical evidence supports their sensitivity and potential efficacy in MPAL treatment [11, 12].
Herein, we present the first report, as we know, of using a chemo-free regimen in a B/T MPAL patient, comprising a combination of venetoclax, azacitidine, and blinatumomab. This innovative approach aims to address the unmet clinical need in MPAL treatment, opening avenues for potential new treatment strategies.
Case presentation
A 47-year-old male presented with chest tightness and shortness of breath with palpitations after activity for 3 months. The patient had a previous history of hypertension and diabetes mellitus. Complete blood count: WBC 4.82 × 109/L,NE 1.76 × 109/L, HGB 80 g/L, PLT 56 × 109/L. Bone marrow aspiration showed 24% of morphological blast population. Flow cytometry showed 42.5% blasts with a mixed expression of B/T lymphoid lineage, including CD19: 95.69%, CD79a: 59.17%, cCD3 + : 42.99% (Fig. 1A). Karyotype: 46, XY. Next Generation Sequencing (NGS): ASXL1/RUNX1/EZH2/NOTCH1/JAK1/JAK3/NRAS mutations. RNA-sequence: negative. Fluorescence in situ hybridization(FISH):BCR/ABL and ABL1/ABL2/ JAK2/CRLF2/CSF1R/EPOR/PDGFR were all negative. Cytoscan: multiple CNVs were detected including 1p36 gain (2.8 Mb), 1p36 loss (5.9 Mb), 1p36 loss (2.4 Mb), 2q31 loss (3.7 Mb), 2q31q32 loss (7.8 Mb), 2p23p22 loss (2.9 Mb), 5q35 gain (1.7 Mb), 5q32q33 loss (7.9 Mb), 6p22 gain (4 Mb), 10p15p14 gain (9.1 Mb), 13q14 loss (1.6 Mb), 13q14 loss (2.1 Mb), 17q25 gain (2.5 Mb), 19q13 gain (2.1 Mb), 19p12p11 gain (3.9 Mb), and 22q13 gain (1.3 Mb). Sixteen CNVs were present in nine chromosomes, all with fragment sizes > 1 Mb, seven of them > 3 Mb, which suggested complex karyotypes (Fig. 1B). Additionally, the difference between the proportion of 13q-abnormal clones and other abnormalities in this patient was over 30%, suggesting the possible existence of subclones.
The patient was treated with venetoclax and azacitidine to reduce tumor load as follows: venetoclax: 100 mg d1, 200 mg d2, 400 mg d3–d21; azacitidine: 75 mg/m2/d IH d1–d7 (Fig. 2A). Then he achieved hematologic CR and the MRD was 1.9 × 10−4 (Fig. 3). Considering the presence of subclones and complex karyotypes, blinatumomab 9 ug d1–3, 28 ug d4–d14 was given after the end of the VA (venetoclax and azacitidine) regimen. There were no significant adverse therapeutic effects during the whole treatment with the neutropenia status for 3 days and the platelets consistently above 30 × 109/L (Fig. 2B). Bone marrow aspiration after the end of treatment indicated that the patient achieved hematologic and molecular CR which means the mutations found initially and the cytoscan turned negative. The MRD was < 1.0 × 10−4, which suggested the blinatumomab could reduce undetectable MRD (Fig. 3). Besides, no primitive leukemia cells were found in the cerebrospinal fluid (CSF) from the time of diagnosis until now. Peripheral stem cells from an unrelated donor were subsequently transplanted to patient after two consolidation therapy and the modified Bu-Cy conditioning regimen (Supplementary Material). Cyclosporine A (CsA), short-course methotrexate (MTX), mycophenolate mofetil (MMF), and rabbit antithymocyte globulin (Thymoglobulin™) were adopted for graft-versus-host disease (GVHD) prophylaxis (Supplementary Material 2 for usage). Now the patient has remained without evidence of disease for 1 year after transplantation.
Discussion and conclusions
The B-cell lymphoma 2 (BCL-2) protein family plays a pivotal role as regulators of the intrinsic mitochondrial apoptotic pathway through direct protein–protein interactions. Enhanced expression of BCL-2 family proteins has been observed in leukemia blasts, with a significant proportion of leukemia stem cells exhibiting abnormally high levels of BCL-2, relying on it for survival. Moreover, heightened expression of BCL-2 proteins correlates with disease progression and chemotherapeutic resistance in leukemia patients [13, 14]. Venetoclax, a potent and selective oral BCL-2 inhibitor, has emerged as a new standard in the treatment of AML in elderly and unfit patients when combined with hypomethylating agents like azacitidine, markedly improving overall survival and quality of life [15, 16]. Studies also indicate the potential benefits of the synergistic effects of venetoclax with demethylating agents for ALL [17, 18]. Furthermore, blinatumomab, a bispecific monoclonal antibody, has shown efficacy in enhancing response, survival, and rates of undetectable MRD in B-ALL [19, 20].
B/T MPAL, a rare leukemia subtype meeting criteria for both B-cell and T-cell lineages, presents a grim prognosis with a 3-year survival rate of merely 20–40%. While studies suggest that ALL-like induction chemotherapy yields higher CR rates compared to AML-like regimens for MPAL, it does not confer a long-term OS advantage. However, allogeneic hematopoietic stem cell transplantation (Allo-HSCT) post-chemotherapy significantly enhances survival, especially for patients achieving CR before transplantation [21, 22].
Motivated by these challenges, we explored a chemo-free regimen for B/T MPAL, aiming to achieve CR1 and minimize adverse effects for subsequent HSCT. Herein, we report, to our knowledge, the first successful application of a chemo-free regimen in B/T MPAL, comprising venetoclax, azacitidine, and blinatumomab. Given the lack of consensus on MPAL treatment, transitioning from retrospective studies to prospective trials is imperative. Our report on the effective treatment of this B/T MPAL case may provide valuable insights for the management of similar patients and could potentially influence future therapeutic strategies for this rare leukemia subtype.
Data availability
No datasets were generated or analysed during the current study.
Abbreviations
- ALL :
-
Acute lymphoblastic leukemia
- Allo-HSCT :
-
Allogeneic hematopoietic stem cell transplantation
- AML :
-
Acute myeloid leukemia
- BCL-2 :
-
B-cell lymphoma 2
- CR :
-
Complete remission
- FISH :
-
Fluorescence in situ hybridization (FISH)
- MPAL :
-
Mixed phenotype acute leukemia
- MRD :
-
Minimal residual disease
- NGS :
-
Next generation sequencing (NGS)
- OS :
-
Overall survival
- VA :
-
Venetoclax and azacitidine
- CSF :
-
Cerebrospinal fluid
- CsA :
-
Cyclosporine
- MTX :
-
Methotrexate
- MMF :
-
Mycophenolate mofetil
- GVHD :
-
Graft-versus-host disease
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Funding
This work was supported by research grants from National Natural Science Foundation of China (81873443 and 82070162), Translational Research Grant of NCRCH (2020ZKZC04), Natural Science Foundation of Jiangsu Province (BK20201169), The Key Science Research Project of Jiangsu Commission of Health (K2019022), Frontier Clinical Technical Project of Suzhou Science and Technology plan (SKY2022001), Bethune Charitable Foundation (BCF-IBW-XY-20220930–13), Suzhou diagnosis and treatment project of Clinical Key Diseases (LCZX202201), and the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD).
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DW, XT and SL were responsible for the study concept and design. SL collected and analyzed the data and wrote the first draft of the manuscript. XT, QC, ML, ZL, and SC treated the patients and assisted in the data collection. QC, ML and SL provided input for the figures. XT, QC, and ML helped write part of the case report and edited the case report. XT, QC, ML and SL wrote the final draft of the manuscript. SL and QC contributed equally to this manuscript. All authors read and approved the final manuscript.
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This clinical trial was approved by the Ethics Committee of the First Affiliated Hospital of Soochow University. The patients/participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.
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Liu, S., Cui, Q., Li, M. et al. Successful treatment of a B/T MPAL patient by chemo-free treatment with venetoclax, azacitidine, and blinatumomab. Ann Hematol 103, 1397–1402 (2024). https://doi.org/10.1007/s00277-024-05644-9
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DOI: https://doi.org/10.1007/s00277-024-05644-9