Introduction
8p11 myeloproliferative syndrome (EMS), first reported by Macdonald et al (1) in 1995, is a rare atypical myeloproliferative disease, and is also termed stem cell leukemia/lymphoma syndrome. The disease is characterized by a significantly higher peripheral white blood cell count (WBC), myeloid cell hyperplasia and eosinophilia in the bone marrow, lymph node pathology for lymphoblastic lymphoma and involvement of the short arm of chromosome 8 (8p11) for fibroblast growth factor-1 (FGFR1) gene translocation. Furthermore, EMS can progress to acute leukemia in the short term (2–4). The World Health Organization (WHO) designated EMS for myeloid/lymphoid neoplasms with FGFR1 rearrangement (MLNAF) in 2008. The designation was maintained in the fourth edition of the WHO classification of hematopoietic and lymphoid tissue tumors revised in 2016 (5).
Globally, there have been only ~100 cases of MLNAF reported to date. In 1992, Abruzzo et al (6), for the first time, reported the cases of 3 patients with T lymphoblastic lymphoma and peripheral blood eosinophilia. All patients subsequently developed myeloid malignancy, and were gradually diagnosed with EMS. The occurrence of MLNAF is closely associated with FGFR1 gene abnormalities. FGFR1 encodes a receptor tyrosine kinase transmembrane protein and belongs to the FGFR family. Under normal conditions, FGFR1 exists in the form of an oligomer, which binds to its ligand and induces homologous dimerization and self-phosphorylation of FGFR1, thereby activating multiple effectors and producing signals for proliferation and survival (7). FGFR1 gene abnormalities in patients with MLNAF often manifest as translocation or insertion mutations, with gene translocation being the most common. At present, 15 partner genes have been identified for MLNAF, including ZNF198 (13p12), BCR (22q11), CEP110 (9q33), FGFR1OP2 (12p11), FOP (6q27), TRIM24 (7q34), HERVK (19q13), MYO18A (17q11), NUP98 (11p15), CPSF6 (12p11), CUX1 (7q22), RANBP2 (2q12), TPR (1q25), SQSTM 1 (5q35) and LRRFIPI (2q37) (3,8). In addition, two types of insertion changes, insertion (13;8)(q12;p11p23) and insertion (12;8)(p11;p11;p22) (9,10) have been observed. At present, no gene amplification or deletion mutations have been reported. The products formed by balanced translocation or insertion after FGR1 gene break exhibit ligand independent FGFR1 tyrosine kinase activity, and multiple downstream signaling pathways, including the Ras/mitogen-activated protein kinase (Ras/MAPK), phosphatidylinositol 3-kinase (PI3K), phospholipase C (PLC) 7 and signal transducer and activator of transcription (STAT) pathways, are continuously activated, leading to the development of MLNAF (11).
Few cases concerning MLNAF with t(8;13)(p11;q12) have been reported in the literature, and the outcome of most cases of EMS is poor, even in patients that have been treated with allogeneic stem cell transplantation. In the present study, the case of a patient with MLNAF with t(8;13)(p11;q12) who was treated with a tyrosine kinase inhibitor (TKI) combined with chemotherapy was reported. The aim of the present study is to improve the understanding of EMS.
Case report
A 62-year-old female with no history of hematological disease was admitted to the Department of Hematology, The Second Hospital of Hebei Medical University (Shijiazhuang, China) in November 2019 due to a painless groin mass that had been present for >2 months and a repeating recurrent rash lasting for 1 month. The patient had a history of an elevated peripheral leukocyte level, first reported 11 months prior (range, 11.1–61.8×109/l; normal range, 3.5–9.5×109/l), which was left untreated. Physical examination revealed extensive red papules and maculopapules on the skin, as well as enlarged lymph nodes in the neck, armpits and groin. The largest lymph node was located in the right groin, measuring ~4×4 cm, with a hard texture and no tenderness. The liver palpation indicated a protrusion of ~1 cm below the costal margin, while the splenic palpation discerned an extension of ~6 cm below the costal margin. The palpitations were homogeneous and had no tenderness.
At admission, the initial peripheral blood analysis revealed a WBC of 136.9×109/l (normal range, 3.5–9.5×109/l), with neutrophils accounting for 93.06% (normal range, 40–75%) and eosinophils for 0.97% (normal range, 0.4–8%), a hemoglobin level of 151 g/l (normal range, 115–150 g/l) and a platelet count of 208×109/l (normal range, 125–350×109/l). The eosinophil count, several serum analysis results and eosinophil percentages in the bone marrow at different stages of diagnosis, remission, relapse and AML transformation are summarized in Table I. The bone marrow was hypercellular, with an increased percentage of granules associated with eosinophilia, thus indicating that the patient did not have chronic myeloid leukemia (Fig. 1).
Analyses of the breakpoint cluster region-abelson leukemia virus (BCR-ABL) fusion gene, Janus kinase 2 (JAK2)-V617F, calreticulin (CALR) and myeloproliferative leukemia virus oncogene (MPL) mutations, and the next-generation sequencing of gene mutations related to myeloid tumors all gave negative results. The BCR-ABL fusion gene testing process was as follows: First, 0.8% ammonium chloride red blood cell lysate was added to the bone marrow fluid and centrifuged at 1,000 × g for 10 min at room temperature to obtain white blood cells. RNA was extracted using the RNA pred Pure Hi-Blood kit (Tiangen Biotech Co., Ltd.; cat. no. DP443), according to the manufacturer's instructions. A total of 1 ml Trizol was added to a 50-µl leukocyte suspension and mixed. The solution was incubated at room temperature for 5 min, followed by the addition of 0.2% chloroform. After shaking for 30 sec, it was left undisturbed for 3 min and further centrifuged at 16,000 × g for 15 min at 4°C. The supernatant was transferred into a diethylpyrocarbonatetreated EP tube and mixed with isopropyl alcohol, and left at room temperature for 10 min. RNA was obtained by centrifugation again at 16,000 × g for 5 min at 4°C. RNA amplification was performed using the BCR-ABL fusion gene detection kit (Bio-Rad Laboratories, Inc.; cat. no. 171V37145) in strict accordance with the instructions provided. The LightCycler 480 fluorescence detector (Roche Diagnostics) was used, and the amplification conditions included a temperature of 42°C for 30 min, 94°C for 5 min and 40 cycles. Fluorescence signals were collected at 60°C during the second step of the PCR cycle, and data analysis software Opticon Monitor realtime v2.02 (Bio-Rad Laboratories, Inc.) was utilized. The JAK2V617F, MPL and CALR testing process was as follows: First, 0.8% ammonium chloride red blood cell lysate was added into the bone marrow fluid and centrifuged at 1,000 × g for 10 min at room temperature to obtain white blood cells. The Tianamp genomic DNA kit (Tiangen Biotech Co., Ltd.; cat. no. DP304) was used to extract intracellular DNA in strict accordance with the instructions provided by the kit. A total of ~20 µl white blood cells and 18 µl protease were mixed well. After which, 200 µl buffer solution was added and the mixture was heated at 70°C for 10 min. A total of 200 µl anhydrous ethanol was added to the mixture, mixed until white flocculent appeared and then transferred to the centrifugal column. The sample was centrifuged at 13,400 × g for 1 min at room temperature and the waste liquid was discarded from the collection pipe. A total of 500 µl GD was added to the centrifugal column, and the sample was centrifuged at room temperature for 1 min at 13,400 × g. The waste liquid was discarded again and 500 µl bleach solution per wash was added to the centrifugal column, and centrifuged at room temperature for 1 min at 13,400 × g. The waste liquid was discarded once more and centrifuged at 13,400 × g for two min at room temperature. The centrifugal column was placed into a new EP tube, 200 µl TE solution was added and at room temperature centrifuged for 2 min at 13,400 × g in order to obtain DNA. The mutations of JAK2V617F (Exon12), CALR (Exon9) and MPL (Exon10) were qualitatively detected using the ipsogen JAK2 RGQ PCR Kit, ipsogen MPL W515L/K MutaScreen Kit and CALR RGQ PCR Kit (Qiagen AB; cat. nos. 673633, 676413 and 674013, respectively) The instructions of the kit were strictly followed, and ABI PRISM fluorescent PCR detector was used for detection. Amplification conditions included 40 cycles at 42°C for 5 min and 94°C for 3 min, and fluorescencemyoproliferative tumor-related gene mutation detection kit signals were collected at 60°C in the second step of the PCR cycle. The analysis software used was Opticon Monitor realtime v2.02 (Bio-Rad Laboratories, Inc.). The extraction steps of DNA and RNA in next-generation sequencing were as aforementioned. The DNA and RNA were extracted by commercial kits (Tiangen Biotech, Co., Ltd.; cat. nos. is DP340, DP304 and DP431). The purities and concentrations of DNA and RNA were confirmed by Nanodrop 2000 (Thermo Scientific Scientific, Inc.) and Qubit 3.0 Fluorometer (Thermo Fisher Scientific, Inc.). The Qsep400 nucleic acid fragment analyzer (Hangzhou Houze Bio-Technology Co., Ltd.,) was utilized to evaluate the integrity of DNA and RNA. The DNA were transformed into libraries using KAPA EvoPlus Kits (Kapa Biosystems; Roche Diagnostics; cat. no. 9420053001). The libraries were analyzed on the Illumina sequencing platform NextSeq550 using 150-bp paired-end sequencing. Sequencing was performed using the NextSeq 500/550 High output kit v2.5 (300 cycles; cat. no. 20024908; Illumina Inc). To quantify the final library concentration, the Qubit 3.0 Fluorometer was employed. The loading concentration of the final library was ~14 pM.
Fluorescence in situ hybridization (FISH) analysis of the bone marrow showed positive FGFR1 gene rearrangement (positive rate, 94%), with negative platelet-derived growth factor receptor A (PDGFRA) and PDGFRB gene rearrangements (Fig. 2). The preparation of the peripheral bone marrow samples from patients for FGFR1, PDGFRA, PDGFRB FISH detection was performed as follows: Initially, the samples were fixed in a fixed solution consisting of methanol to acetic acid (3:1), one pre-fixation step was performed using a 10% fixed solution, and the sample was fixed three times. Next, the fixed cells were placed onto a glass slide to create a sample slide, allowed to air dry, the fragments were washed with 2X saline sodium citrate buffer solution at 37°C for 30 min, and dehydrated sequentially in 75, 85 and 100% alcohol for 1 min each. The FISH probes FGFR1/D8Z2 (Anbiping; cat. no. F.01109–01), PDGFRA (Anbiping; cat. no. F.01162–01) and PDGFRB (Anbiping; cat. no. F.01033–01) were utilized with a hybridization instrument (Thermos; cat. no. S500-24) for hybridization, denaturing at 78°C for 8 min, and hybridizing at 42°C for 16 h. On the following day, the samples were washed with 0.3% NP40 wash solution at 68°C for 2 min, followed by washing with deionized water at 37°C for 1 min. DAPI nuclear staining was performed for 20 min at room temperature, and the results were observed using a fluorescence microscope (Olympus; cat. no. BX63). Metasystem ISIS V5.8.11 (Metasystem Co., Ltd.) FISH analysis software was used for photography and analysis purposes. The karyotype showed a balanced translocation between chromosome 8 and chromosome 13: t(8;13)(p11;q12) (Fig. 3). Positron emission tomography (PET)/computed tomography (CT) scans showed a diffuse increase in bone marrow metabolic activity, multiple high metabolic lymph nodes above and below the diaphragm, and splenomegaly with increased metabolic activity, consistent with the manifestation of lymphoma (Fig. S1).
A right inguinal lymph node biopsy revealed disruption of the normal structure with diffuse infiltration by lymphoblasts. The immunophenotype was as follows: CD3(+), CD5(+), CD43(+), CD99(+), terminal deoxynucleotidyl transferase (partial +), CD34(−), Ki-67(+ 70%), CD20(−), CD21(−), CD56(−), myeloperoxidase(−), CD68 (loose +), BCL-2(−), BCL-6(−), CD10(−), CD117(−), CD15(−), cyclinD1(−), mutated melanoma-associated antigen 1(−), paired box protein Pax-5(−) and Epstein-Barr virus-encoded small RNA(−). In order to further investigate the expression of immature markers in this patient with T lymphoblastic lymphoma, the immunohistochemical staining of CD1A, CD4 and CD8 was also performed. The results indicated that the samples were partially positive for CD1A, positive for CD4 and negative for CD8 (Fig. 4). The lymph nodes were immersed in a 4% formaldehyde solution and fixed overnight at 4 °C. The following day the tissue was dehydrated and embedded in paraffin wax. The embedded material was cut into 4-µm slices, dewaxed and rehydrated, and the antigens were extracted. The slices were incubated with 3% hydrogen peroxide at room temperature for 4 min. After washing with PBS, they were blocked with 5–10% normal goat serum (cat. no. ab7481; Abcam) in PBS, incubated at room temperature for 10 min, and the serum was removed. The following primary antibodies were added: Anti-CD1A (cat. no. ab313875; 0.1 µg/ml; Abcam), anti-CD4 (cat. no. ab133616; 0.2 µg/ml; Abcam), anti-CD8 (cat. no. ab245118; 0.4 µg/ml; Abcam), anti-CD3 (cat. no. ab243874; 0.2 µg/ml; Abcam), anti-CD43 (cat. no. ab101533; 0.5 µg/ml; Abcam), anti-CD5 (cat. no. ab75877; 0.2 µg/ml; Abcam), anti-CD68 (cat. no. ab213363; 0.08 µg/ml; Abcam), anti-CD99 (cat. no. ab108297; 0.5 µg/ml; Abcam), anti-terminal deucleotide transferase (cat. no. ab183341; 1 ug/ml; Abcam), anti-Ki-67 (cat. no. ab92742; 1 µg/ml; Abcam), anti-Bcl-2 (cat. no. ab32124; 1 µg/ml; Abcam), anti-Bcl-6 (cat. no. ab172610; 0.5 µg/ml; Abcam), anti-CD10 (cat. no. ab208778; 0.1 µg/ml; Abcam), anti-CD117 (cat. no. ab32363; 1 µg/ml; Abcam), anti-CD15 (cat. no. ab218403; 5 µg/ml; Abcam), anti-CD20 (cat. no. ab219329; 1 µg/ml; Abcam), anti-CD21 (cat. no. ab315160; 2 µg/ml; Abcam), anti-CD34 (cat. no. ab315820; 0.1 µg/ml; Abcam), anti-CD56 (cat. no. ab313779; 0.2 µg/ml; Abcam), anti-cyclind1 (cat. no. ab273608; 1 µg/ml; Abcam), anti-myeloperoxidase (cat. no. ab134142; 0.1 µg/ml; Abcam), anti-mutated melanoma-associated antigen 1 (cat. no. ab247079; 0.5 µg/ml; Abcam), anti-pin-box protein Pax-5 (cat. no. ab234402; 0.5 µg/ml; Abcam) and incubated at 3°C for 1–2 h or 4°C overnight. After washing with PBS for three times, biotin-labeled secondary antibody (HRP marker; cat. no. ab6721; 1 µg/ml; Abcam) was added to the working solution and incubated at 37°C for 20–40 min. The sample was washed with PBS three times, streptavidin coupled alkaline phosphatase was added and incubated at 37°C for 15–25 min. The sample was rinsed again with PBS and 3,3′-diaminobenzidine was added at room temperature for 3–15 min for color development. Section cleaning, hematoxylin reverse staining, dehydration, cleaning and mounting was performed. In situ hybridization was used to detect encoded small RNA (EBER) of Epstein-Barr virus. EBER in situ hybridization kit (cat. no. ISH 7001) from ZSBG-Bio was used. The dewaxed and hydrated lymph node sections were added with 1X protease K working solution and incubated at room temperature for 5 min. After which, EBER hybrid solution was added and incubated at 55°C for 60 min, and finally transferred to 37°C for overnight incubation. After washing with PBS, HRP-marked digoxin antibody was added. After incubation at 37°C for 30 min, DAB color developing solution was added, and hematoxylin was re-stained at room temperature for 1–2 min, dehydrated and sealed. Representative images are taken with a light microscope (Japan). This was consistent with the immunophenotype of typical T lymphoblastic lymphoma. Based on the aforementioned immunohistochemical staining, the biopsy of the right inguinal lymph node was consistent with T lymphoblastic lymphoma. FGFR1 gene rearrangement was also positive in the right inguinal lymph node tissue sections, as indicated by FISH (Fig. 5). Therefore, a diagnosis of MLNAF with t(8;13)(p11;q12) was made. At that time, the FGFR1 partner gene was not detected. Previously, paraffin-embedded samples of the lymph nodes of patient were used to detect the presence of the FGFR1-ZNF198 fusion gene by reverse transcription polymerase chain reaction quantification (RT-qPCR. The lymph node paraffin-embedded specimen was sliced and placed in a centrifuge tube. The tissue was dewaxed using xylene. RNA was extracted using the RNA pred Pure Hi-Blood kit (Tiangen Biotech Co., Ltd.; cat. no. DP443), in strict accordance with the kit instructions. A total of 1 ml of Trizol (Invitrogen; Thermo Fisher Scientific, Inc.) was added to 1×107 cell suspension and mixed. The mixture was incubated at room temperature for 5 min, followed by the addition of 0.2% chloroform. After shaking for 30 sec, it was left undisturbed for 3 min and then centrifuged at 2–8°C at 12,000 × g for 15 min. The supernatant was transferred into a DECP-treated EP tube and mixed with isopropyl alcohol, which was left at room temperature for 10 min. RNA was obtained by centrifugation again at 2–8°C at 12,000 × g for 5 min. cDNA was synthesized from 2 µg total RNA using a first-strand cDNA synthesis kit (cat. no. K1622; Thermo Fisher Scientific, Inc.). The PCR primers of the FGFR1-ZNF198 fusion gene and normalization control β-actin gene were designed based on the corresponding gene structure using Primer-BLAST (http://www.ncbi.nlm.nih.gov/tools/primer-blast), and the sequences were follows: FGFR1-ZNF198, Forward, 5′-TCCCTGTGCCTGTGTATATCCC-3′ and reverse, 5′-CGGGAAGCTCATACTCAGAGAC-3′; and β-actin forward, 5′-AAGGCCAACCGCGAGAAGAT-3′ and reverse, 5′-TCGGTGAGGATCTTCATGAG-3′. Using SYBR Green (Thermo Fisher Scientific, Inc.) as the fluorophore, the amplification conditions included a temperature of 42°C for 30 min, 94°C for 5 min and 40 cycles. The method of quantification was 2−ΔΔCq (Livak and Schmittgen 2001). Due to the prolonged placement of the specimen, the mRNA was severely degraded and could not be effectively reverse transcribed into cDNA, thus the RT-qPCR could not be completed.
The TKI dasatinib in combination with the CHOPE chemotherapy (2 mg/m2 vindesine on day 1 + 750 mg/m2 cyclophosphamide on day 1 + 20 mg/m2 doxorubicin hydrochloride liposome on day 1 + 60 mg/m2 etoposide on days 1–3 + 1 mg/kg prednisone tablet on days 1–5) was initiated for 1 cycle, every 21 days. After 4 cycles, the enlarged lymph nodes of the patient disappeared, the liver returned to normal and the spleen shrank to 1 cm below the left costal margin. Furthermore, the peripheral blood count returned to normal, and the proportion of FGFR1 gene rearrangement detected by bone marrow FISH analysis decreased to 36% (Fig. 2). Finally, PET/CT scans showed partial metabolic remission in April 2021 (Fig. 1). The flow cytometry results of the patient's bone marrow at diagnosis and remission are presented in Fig. 6. EDTA anticoagulant marrow blood and the following antibodies were added: CD45 (cat. no. ab40763; Abcam), CD38 (cat. no. ab108403; Abcam), CD117 (cat. no. ab317843; Abcam), CD7 (cat. no. ab109296; Abcam), HLA-DR (cat. no. ab92511; Abcam), CD16 (cat. no. ab223200; Abcam), CD13 (cat. no. ab317440; Abcam), CD33 (cat. no. ab134115; Abcam), CD56 (cat. no. ab220360; Abcam), CD64 (cat. no. ab109449; Abcam), CD11c (cat. no. ab254183; Abcam), CD15 (cat. no. ab241552; Abcam), CD11b (cat. no. ab224805; Abcam), MPO (cat. no. ab208670; Abcam) and CD79a (cat. no. ab133483; Abcam) at 100 µl/each into the tube, shaken, and kept in darkness at room temperature for 20 min. A total of 3% paraformaldehyde was added and incubated in darkness 10 min at room temperature. A total of 1 ml purified water was added and the solution was kept in darkness at room temperature for 10 min after shaking. The solution was centrifuged at 160 × g for 5 min at room temperature and the supernatant was discarded. A total of 2 ml of PBS solution was added, shaken and centrifuged at 160 × g for 5 min at room temperature. The supernatant was discarded and 500 µl PBS was added. Specimens were examined using Flow cytometer (Beckman Coulter, Inc.) after mixing. The detected data was analyzed by Kaluza 2.1.1 software(Beckman Coulter, Inc). The fluorescent dyes were all obtained from Beckman Coulter, Inc, including fluorescein isothiocyanate (FITC), phycoerythrin (PE), peridinin chlorophy II protion (PreCP) and allophycocyanin (APC). The aforementioned reagents and labeling methods were used to detect known positive specimens as positive controls and the negative cell population of the specimen was used as the negative control. However, upon continuation of the regimen for a further two cycles, the disease relapsed and new enlarged lymph nodes were found in the neck, and the spleen notably increased in size. An adjusted treatment regimen, including BCL2 inhibitor (venetoclax, 100 mg on day 1, 200 mg on day 2 and 400 mg on days 3–14) + demethylated agent (75 mg/m2 azacitidine on days 1–7) + histone deacetylase inhibitors (20 mg chidamide twice a week for 2 weeks), was administered. During the treatment process, the WBC count of the patient gradually increased to 60×109/l, and as confirmed by bone marrow cell morphology and flow cytometry, the patient was diagnosed with AML (Fig. 7). The proportion of FGFR1 gene rearrangement detected by peripheral blood FISH analysis increased to 90%. After diagnosis, the patient was changed to the IA chemotherapy regimen (10 mg/m2 idarubicin on days 1–3 + 150 mg/m2 arabinoside on days 1–7) and entered the myelosuppression phase 1 week after chemotherapy. The patient subsequently experienced a severe lung infection and died in August 2021.
Discussion
MLNAF is a malignant tumor originating from hematopoietic stem cells, with various clinical manifestations and aggressive progression; it is slightly more common in men than women, with a median age of 32 years (range, 3–84 years). MLNAF often presents with systemic symptoms such as fatigue, night sweating, emaciation or fever. At initial diagnosis, local or systemic lymph node enlargement and hepatic/splenomegaly are commonly found, and some patients may have extranodal organ involvement, such as that of the tonsils, lungs and mammary glands (3). Approximately one-half of patients with MLNAF possess the t(8;13)(p11;q12) mutation, forming the ZNF198-FGFR1 fusion gene (3). These patients often show a significant increase in WBC count, and increased eosinophils in the peripheral blood and bone marrow, presenting the coexistence of myeloproliferative neoplasm and T-cell lymphoma. Most of the patients rapidly progress to acute leukemia, commonly AML, within 1–2 years (4). The molecular pathogenesis of MLNAF is characterized by FGFR1 rearrangement, which forms a fusion gene through translocation, insertion, inversion or deletion (12). This genetic variation impacts FGFR1 mRNA transcription, thereby promoting the oncogenicity and genetic diversity of the FGFR1 protein. FGFR1 fusion genes can be divided into two types: Type I and type II. Type I refers to the FGFR1 gene located at the 3′ end of the fusion gene, and the FGFR1 tyrosine kinase domain is fused to the N-terminal oligomerization domain of the partner protein. This fusion type protein that cannot bind to the FGF ligand and causes a conformational change in the FGFR1 tyrosine kinase domain. This stimulates the function of FGFR1 oncogene and constitutively activates its tyrosine kinase function, changes its localization, and subsequently activates PI3K-AKT, RAS/MAPK, STAT and PLC/PKC in the downstream cell pathways to transmit abnormal signals, which ultimately leads to the transition from MLNAF to AML (4,13). The fusion genes of FGFR1 and its partners in MLNAF belong to type I. Conversely, type II fusion proteins retain the extracellular domain of FGFR1, allowing them to bind to FGF ligands, a characteristic commonly observed in solid tumors. Even though the domains in the fusion proteins retained by FGFR rearrangement are different, in all cases the protein retains a complete kinase domain, suggesting that the kinase domain plays a vital role in the function of the fusion protein. The expression of ZNF198-FGFR1 is related to specific plasminogen activator inhibitor-2-mediated anti-apoptosis, which is possibly one of the reasons for the high malignancy of leukemia cells (14). The numbers and common phenotypes of reported cases for MLNAF, and the reported response for chemotherapy and TKIs have been described in the literature (Table II) (15–36). A review of this literature showed that the cohort of patients with MNLF harboring ZNF198-FGFR1, representing the most prevalent cases, predominantly exhibit resistance to chemotherapy (15). While a subset of patients may experience transient responses to TKIs such as imatinib and midostaurin, sustained efficacy remains elusive (16,17). Notably, allogeneic hematopoietic stem cell transplantation was pursued by 9 patients, resulting in remission for 7 patients; however, 2 still experienced disease relapse (4). These findings underscore the insufficiency of traditional chemotherapy and TKIs in addressing this condition.
The patient described in the present study was an elderly woman. The combination of chemotherapy and TKI treatment achieved temporary complete remission; however, the condition rapidly progressed to AML 6 months after the diagnosis, which is consistent with previous literature reports (4,9). At present, there is no unified standard for MLNAF treatment, and conventional cytotoxic drugs have poor therapeutic effects, with the overall survival rate in the literature reportedly <20% (3). FGFR1, as a tyrosine kinase inhibitor receptor, is hypothesized to be a therapeutic target, but neither imatinib nor dasatinib have achieved ideal efficacy. New TKIs, such as pemigatinib and futibatinib, which selectively inhibit FGFR1 tyrosine kinase activity, have shown some efficacy in in vitro and animal experiments (37,38), but the exact therapeutic effect still needs to be verified by further clinical trials. Hu et al (39) found that the activation of FGFR1 is related to the upregulation of MYC, and there is a synergistic effect between FGFR1 inhibitors and MYC-targeted inhibitors, suggesting a new approach for MLNAF treatment. Currently, these new targeted drugs are still in the experimental stage, and at present, allogeneic hematopoietic stem cell transplantation (allo-HSCT) is still considered to be the best option for the treatment of MLNAF. A previous case study reported that patients with MLNAF achieved disease-free survival times of up to 16 years when treated with allo-HSCT (40). In addition, another patient with refractory MLNAF received dual umbilical cord blood transplantation and achieved 5 years of disease-free survival (41). In the present study, the patient obtained CR after combination chemotherapy + TKI, and was recommended to receive allo-HSCT. However, due to economic constraints, the patient did not receive the treatment and the disease progressed to AML. Finally, the patient died of a pulmonary infection after induction of remission treatment. The present study further confirms that conventional TKIs combined with chemotherapy have limited efficacy in the treatment of MLNAF, and that allo-HSCT should be performed as early as possible after diagnosis.
In conclusion, MLNAF is a rare malignancy originating from hematopoietic stem cells, which has diverse clinical manifestations and may develop into multiple lineage hematopoietic system tumors. The condition is easily misdiagnosed in the early stage, and diagnostic gold-standard genetic examination reveals FGFR1 gene breakage and chromosome 8p11 translocation. Conventional TKI chemotherapy has poor efficacy, and new targeted drugs are still under research, which may bring hope for the long-term survival of patients. However, at present, allo-HSCT remains the first choice for MLNAF treatment.