Publications by authors named "Banghe Ding"

The introduction of tyrosine kinase inhibitors (TKIs) has revolutionized chronic myeloid leukemia (CML) treatment. The knowledge, attitude, and practice (KAP) of patients and their families play a significant role in treatment adherence and effectiveness. This study aimed to investigate the KAP of CML patients and their families regarding TKI therapy in China.

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Introduction: The aim of this study was to develop a prognostic model for chronic lymphocytic leukemia (CLL).

Methods: GEO2R was used to retrieve the gene expression data of CLL and normal B cells from the Gene Expression Omnibus (GEO; GSE22529 and GSE50006 datasets) database. Practical Extraction and Report Language was used to extract the gene expression and overall survival (OS) data of CLL patients from the Chronic Lymphocytic Leukemia - ES (CLLE-ES) project in the International Cancer Genome Consortium (ICGC) database.

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Objectives: Optimal post-remission treatment for individual favorable and intermediate risk acute myeloid leukemia (AML) patients has not yet been established. Human leukocyte antigen (HLA)-mismatched stem cell microtransplantation (MST), may improve outcomes and avoid graft-versus-host disease in patients with first complete remission of AML.

Methods: We retrospectively analyzed the efficacy, safety, and survival of 63 patients with favorable- or intermediate-risk AML who received MST, autologous stem cell transplantation (ASCT), or cytarabine single agent (CSA) as post-remission treatment from January 2014 to August 2021.

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Objective: To observe the efficacy and safety of CLAE intensive chemotherapy followed by allogeneic hematopoietic stem cell transplantation (allo-HSCT) in patients with relapsed/refractory acute leukemia (R/R AL).

Methods: CLAE regimen [cladribine 5 mg/(m·d), d 1-5; cytarabine 1.5 g/(m·d), d 1-5; etoposide 100 mg/(m·d), d 3-5] followed by allo-HSCT was used to treat 3 R/R AL patients.

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Recent studies have shown that microtransplant (MST) could improve outcome of patients with elderly acute myeloid leukemia (EAML). To further standardize the MST therapy and improve outcomes in EAML patients, based on analysis of the literature on MST, especially MST with EAML from January 1st, 2011 to November 30th, 2022, the International Microtransplant Interest Group provides recommendations and considerations for MST in the treatment of EAML. Four major issues related to MST for treating EAML were addressed: therapeutic principle of MST (1), candidates for MST (2), induction chemotherapy regimens (3), and post-remission therapy based on MST (4).

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Article Synopsis
  • The study investigates how the CXCR4 gene influences the effectiveness of Carfilzomib (CFZ) treatment in patients with multiple myeloma (MM).
  • Researchers analyzed data from CFZ-resistant and parental MM cell lines to identify key genes related to CFZ resistance using microarray data and protein-protein interaction networks.
  • Findings reveal that high levels of CXCR4 expression are linked to increased relapse rates and decreased overall survival in MM patients, suggesting CXCR4 could be a target for improving treatment responses in resistant cases.
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Objective: This study was conducted in order to study the clinical characteristics, prognostic factors, and treatment outcomes in patients with primary central nervous system lymphoma (PCNSL).

Materials And Methods: The data of a total of 5,166 PCNSL patients diagnosed between 2000 and 2018 from the Surveillance, Epidemiology, and End Results (SEER) database were obtained.

Results: The mean age was 63.

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Objectives: Acute myeloid leukaemia (AML) is a haematopoietic malignancy with a dismal outcome. Consequently, risk stratification based on more effective prognostic biomarkers is crucial to make accurate therapy decisions. T cell receptor gamma alternative reading frame protein (TARP) has been reported in prostate and breast cancers, but its correlation with AML remains unclear.

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Objective: To investigate the efficacy and safety of micro-transplantation in acute myeloid leukemia (AML).

Methods: The clinical data of 13 adult AML patients who received micro-transplantation as consolidation therapy from July 2014 to October 2019 was retrospectively analyzed, and the adverse reactions and efficacy of micro-transplantation were followed up.

Results: Eight patients received micro-transpantation were still in complete remission, 5 patients relapsed after micro-transplantation, 1 of them received umbilical cord blood micro-transplantation after remission by reinduction, and all of the 13 patients have survived till now.

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The prognosis of patients with relapsed/refractory acute myeloid leukemia (R/R AML) is poor, with a 3-year overall survival rate of 10%. Patients with translocation (t)(11;19)(q23;p13) have a higher risk of relapse and there is no optimal regimen for these patients. The present study treated two young patients with t(11;19)(q23;p13) AML, who relapsed after one or two cycles of consolidation, with a salvage treatment consisting of sequential cladribine, cytarabine and etoposide (CLAE) and allogeneic hematopoietic stem cell transplantation (allo-HSCT).

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Article Synopsis
  • The study aimed to evaluate the importance of a targeted next-generation sequencing test for diagnosing myeloid malignancies in patients with blood disorders.
  • A total of 39 patients were analyzed, with 70.8% of those diagnosed with myeloid malignancies showing positive mutations, particularly in genes like ASXL1, TET2, and RUNX1.
  • The findings indicated that the targeted sequencing can enhance diagnosis and potentially guide treatment for patients, especially for those with myelodysplastic syndromes.
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Retinoic acid receptor gamma (RARG) belongs to the nuclear receptor superfamily and has 90% homology to RAR alpha (RARA) and RAR beta. The () fusion gene has been implicated in acute promyelocytic leukemia (APL). gene rearrangement has been identified in a rare subtype of acute myeloid leukemia (AML) that resembles APL.

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Article Synopsis
  • The study aimed to analyze clinical characteristics of 66 newly diagnosed essential thrombocytopenia (ET) patients, focusing on their mutation status (JAK2, CALR, MPL, or none).
  • Results showed that 69.7% had JAK2 mutations, with the average age significantly higher (63.2 years) than those with CALR mutations (51.8 years) or negative mutations (50.2 years).
  • The CALR mutation group exhibited lower white blood cell (WBC) and hemoglobin (Hb) levels, while 30.3% of all patients experienced thrombus or embolism, with some also facing complications like hyperkalemia.
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It is common of chronic phase chronic myeloid leukemia (CML-CP) patients coexisting anemia at diagnosis, but the role of anemia on the prognosis is not clear. This study aims to explore impact of anemia on outcomes of CML-CP patients in TKI era. In the retrospective study, 258 newly diagnosed CML patients treated with TKIs were enrolled.

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  • The study aimed to analyze the effectiveness and prognosis of acute myeloid leukemia (AML) patients based on chromosome karyotype abnormalities by investigating clinical features and treatment responses in 91 patients.
  • Results showed that while there was no significant difference in complete remission and overall response rates between patients with normal and abnormal karyotypes, those with abnormal karyotypes experienced higher recurrence rates and longer relapse-free survival for normal karyotype patients.
  • The conclusion drawn indicates that having an abnormal karyotype is an independent prognostic factor in AML, with a particular mention that monosomal karyotypes are associated with poorer outcomes and higher recurrence rates.
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The FMS-like tyrosine kinase 3-internal tandem duplication () gene mutation is present in ~20% of patients with acute myeloid leukemia (AML). Patients with an mutation have a poor prognosis. However, the prognostic function of combined with other cytogenetic abnormalities are not clear.

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The specific prognostic factors and the long-term effects of different treatment options in APL remain unclear. In this retrospective study, 70 APL patients were treated with ATRA + DNR/DA or ATRA + ATO regimens for induction therapy and DA or ATRA + ATO for consolidation and maintenance therapy. The prognostic factors and treatment effects on outcome were analyzed.

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The relapse and resistance to cytarabine (Ara-C) therapy is still a dominating obstacle to the successful clinical treatment of acute myeloid leukemia (AML). Recent studies have shown that dysregulation of miRNAs might modulate the resistance of cancer cells to anticancer drugs; yet, the mechanism is not fully understood. In this study, we showed a significant downregulation of miR-134 in human multidrug-resistant leukemia cells and relapsed/refractory AML patient samples.

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Article Synopsis
  • The study investigates how combining inhibitors of mTORC2 and HSP90 affects the growth and death of multiple myeloma (MM) cells using the U266 cell line.
  • Treatment with rapamycin and 17-AAG showed that both drugs could slow down cell growth, with their combined use being more effective than each one alone or a control group.
  • The findings indicate that the combination therapy not only enhances apoptosis (cell death) but also alters key protein levels, suggesting a promising strategy for treating multiple myeloma.
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  • The study aimed to explore how the HSP90 inhibitor 17-AAG affects the growth of multiple myeloma cells (U266) and its underlying mechanisms.
  • Researchers treated U266 cells with various concentrations of 17-AAG over different time periods, measuring cell growth and the levels of specific proteins involved in cell proliferation.
  • Results showed that higher concentrations of 17-AAG significantly reduced cell growth and down-regulated key proteins (β-catenin and C-MYC), indicating that 17-AAG inhibits cell proliferation primarily through the Wnt/β-catenin signaling pathway and the inhibition of HSP90 expression.
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Acute promyelocytic leukemia (APL) is a common myeloid leukemia. At the newly diagnosed stage, it can be fatal because of the serious complication-disseminated intravascular coagulation. With the advent and early application of all-trans retinoic acid, most APL patients can achieve a long-term survival, and only a minority of patients will develop extramedullary relapse after remission.

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Reduced-intensity (RIT) conditioning regimens are gaining increased attention as a result of their advantages and efficacy. However, no data are available regarding whether these regimens improve patient quality of life (QoL). In our study, health-related QoL (HRQoL) was retrospectively assessed in 111 patients with hematological malignancies.

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This study was purposed to investigate the expression of Btk and NFκB in acute myeloid leukemia (AML) cells and its significance. Bone marrow mononuclear cell specimens were taken from 14 AML patients who were in new diagnosis and complete remission respectively, the expressions of Btk and NFκB at mRNA and protein levels were detected by RT-PCR and Western blot, respectively. The results showed that Btk and NFκB expressed in all the samples at RNA and protein levels.

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Background: At present, the treatment of polycythemia vera (PV) and essential thrombocythemia (ET) is still largely supportive and symptomatic. Homoharringtonine (HHT), a valid drug for treating chronic myelogenous leukemia, has shown some effect on leukemic stem cells. The aim of this study was to observe the effect of HHT on patients with high-risk PV and ET.

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