Publications by authors named "Hong-mei Jing"

Background: Peripheral T-cell lymphoma (PTCL) is a heterogeneous disease with dismal outcomes. We conducted an open-label, phase 2 nonrandomised, externally controlled study to evaluate the efficacy and safety of targeted agents plus CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone) (CHOPX) for PTCL in the front-line setting.

Methods: Eligible patients were ≥18 years of age and newly diagnosed PTCL.

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In this prospective, multicenter, Phase 2 clinical trial (NCT02987244), patients with peripheral T-cell lymphomas (PTCLs) who had responded to first-line chemotherapy with cyclophosphamide, doxorubicin or epirubicin, vincristine or vindesine, etoposide, and prednisone (Chi-CHOEP) were treated by autologous stem cell transplantation (ASCT) or with chidamide maintenance or observation. A total of 85 patients received one of the following interventions: ASCT (n = 15), chidamide maintenance (n = 44), and observation (n = 26). estimated 3 PFS and OS rates were 85.

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Objective: To summarize the clinical characteristics, therapeutic effect and prognostic factors of patients with Hodgkin's lymphoma (HL).

Methods: A total of 129 patients with HL diagnosed in Peking University Third Hospital from January 2010 to March 2021 who were given at least one efficacy assessment after treatment were enrolled, and their clinical data, including sex, age, pathological type, Ann Arbor stage, ECOG score, blood test, β-microglobulin, lactate dehydrogenase level, albumin level were collected. The clinical characteristics, therapeutic effect and long-term prognosis of the patients were summarized and analyzed.

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Article Synopsis
  • Scientists wanted to see if combining arsenic compounds with a medicine called imatinib could help people with chronic myeloid leukemia (CML) better than just using imatinib alone.
  • They did a study with 191 patients who were recently diagnosed, giving some a mix of arsenic and imatinib while others got a placebo with imatinib.
  • After following the patients for over four years, they found that while both treatments worked similarly, the combination treatment might help more people achieve better results after 12 months.
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Objective: To analyze the clinical characteristics, treatment, and prognosis of adult patients with early T-cell precursor acute lymphoblastic leukemia/lymphoma (ETP-ALL/LBL).

Methods: Clinical data of 113 T lymphoblastic leukemia/lymphoma (T-ALL/LBL) patients from January 2006 to January 2019 were collected from three hematology research centers, including Peking University Third Hospital, the First Medical Center of Chinese PLA General Hospital and Institute of Hematology and Blood Diseases Hospital, Chinese Medical University. The clinical characteristics and prognosis of ETP-ALL/LBL patients were analyzed compared with non-ETP-ALL/LBL patients.

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  • This study looked at how well two treatments (IRd and IDd) work for older, frail patients with a type of cancer called multiple myeloma.
  • 120 patients aged 65 and older participated and received different combinations of medicines to see which worked better and was safer.
  • Results showed that both treatments helped many patients, but there were different rates of side effects and how long patients stayed healthy after treatment.
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  • Blastoid or pleomorphic mantle cell lymphoma (B/P-MCL) is highly aggressive and often leads to poor outcomes, making it difficult to treat effectively.
  • A retrospective study conducted in China analyzed data from 693 patients, revealing a median age of 60 and highlighting common genetic mutations associated with this condition.
  • Results showed low 3-year progression-free and overall survival rates, with specific genetic mutations predicting poor prognosis, emphasizing the need for new treatment options and clinical trials for better management of B/P-MCL.
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  • The study focused on evaluating low-dose decitabine as a treatment for acute myeloid leukemia (AML) in patients aged 65 and older who were not eligible for intensive chemotherapy due to health concerns.
  • Conducted in Beijing, the research involved 47 patients, with a median age of 78 years, who were monitored over a median follow-up period of 22.2 months; 31.9% achieved complete remission, with an overall survival (OS) rate of 36.1% after one year.
  • Results indicated that patients who were deemed 'unfit' based on geriatric assessments had a median survival of 11.2 months, showcasing the potential effectiveness
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Objective: To analyze the factors affecting the long-term survival of patients with chronic lymphocytic leukemia (CLL).

Methods: The clinical data of 101 newly diagnosed CLL patients from January 2010 to January 2021 were retrospectively analyzed. Rai and Binet staging systems were used for clinical staging, and CLL-IPI was used for risk stratification of the patients.

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  • Mantle cell lymphoma (MCL) is a rare subtype of non-Hodgkin lymphoma with varying treatment approaches across regions, particularly in Asia and China, where specific data on treatment outcomes for Asian patients is limited.
  • This study analyzed 805 MCL patients in China from 1999 to 2019, using statistical methods to evaluate survival rates and factors influencing prognosis.
  • Findings indicate that treatments like high-dose cytarabine and autologous stem cell transplantation improve survival rates, emphasizing the importance of maintenance therapy and the potential benefits of newer drugs for relapsed/refractory MCL patients.
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Relapsed or refractory (r/r) mantle cell lymphoma (MCL) is an aggressive B-cell malignancy with a poor prognosis. Bruton tyrosine kinase (BTK) is a mediator of B-cell receptor signaling and is associated with the development of B-cell lymphomas. Patients with r/r MCL were enrolled in this phase 1/2 study and treated with orelabrutinib, a novel, highly selective BTK inhibitor.

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Objective: To investigate the influece of early relapse in the era of novel drugs on the prognosis of the patients with newly diagnosed multiple myeloma(NDMM) and risk factors, and to provide the basis for the early identification of the high-risk patients and guiding the treatment.

Methods: The clinical data of the patients with NDMM admitted to our hospital from November 2011 to May 2022 were retrospectively analyzed. According to whether the progression free survival(PFS) was more than 12 months, they were divided into early relapse group(≤12 months) and late relapse group(>12 months).

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Objective: To investigate the clinical characteristics and treatment outcome of patients with Burkitt lymphoma.

Methods: The clinical data of 27 patients with Burkitt Lymphoma were collected and retrospectively analyzed, the clinical characteristics, laboratory data, survival and the factors affecting the prognosis were also analyzed.

Results: Among the 27 patients (mainly for adults), the median age was 30 (15-83) years old, the ratio of male and female was 3.

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BACKGROUND The digestive tract is the most common site of extranodal involvement in diffuse large B cell lymphoma (DLBCL) and its prognostic evaluation is different from that of ordinary DLBCL. Currently, for gastrointestinal lymphoma, in addition to the Ann Arbor staging system, the Lugano and the TNM staging systems are commonly used. However, there is no effective prognostic model to identify poor prognosis in patients with localized gastrointestinal diffuse large B cell lymphoma (GI-DLBCL).

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In this study, we aimed to investigate treatment options and the prognosis of patients with WM in China. This retrospective study included 1141 patients diagnosed with symptomatic WM between January 2003 and December 2019 at 35 tertiary hospitals in 22 provinces of China. Fifty-four patients (7.

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Article Synopsis
  • R-CHOP is a common treatment used for a type of cancer called diffuse large B cell lymphoma, but it doesn't work for everyone, and there's no easy way to tell who it will help.
  • Researchers studied DNA from blood samples of 86 patients to find markers that could predict how well R-CHOP would work for them.
  • They discovered thirteen specific DNA markers that could help predict treatment success, and their prediction method was better than other existing tests used in clinics.
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Objective: To investigate the clinical features and prognostic factors of patients with extranodal NK/T cell lymphoma (ENKTL).

Methods: The clinical data of patients with ENKTL from November 2009 to November 2019 was collected and retrospectively analyzed to clarify the clinical features of ENKTL, and evaluate the factors that affected survival and prognosis.

Results: Forty-seven patients with ENKTL were collected, median age was 40 (12-82) years old, and more common in males than females, at the ratio of 1.

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Mantle cell lymphoma (MCL) is a unique subtype of B-cell non-Hodgkin lymphoma with a generally aggressive and heterogeneous clinical course. Chemokines are one of the complex components in the tumor microenvironment (TME), and they play a vital role in tumor progression and metastasis. There is no information about the monokine induced by gamma interferon (MIG)/CXC chemokine receptor 3 (CXCR3) axis in patients with MCL.

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  • The study aimed to assess FAM19A5 expression levels in mantle cell lymphoma (MCL) patients and evaluate its impact on patient prognosis.
  • Results showed that MCL patients had significantly higher serum concentrations of FAM19A5 compared to controls, and this expression was correlatively linked to survival rates.
  • The findings suggest that FAM19A5 can serve as a potential prognostic marker, indicating a higher risk of relapse or death in patients with elevated levels.
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  • The study aims to analyze abnormal signal patterns in Chronic Myeloid Leukemia (CML) and B-cell Acute Lymphoblastic Leukemia (B-ALL) patients using a specialized FISH probe to identify BCR/ABL fusion genes and ASS1 gene deletions.
  • A total of 100 newly diagnosed patients were tested, revealing a high prevalence of the BCR/ABL fusion gene in CML (100%) and variable findings in B-ALL cases (32%).
  • The findings suggest that the tricolor dual-fusion FISH probe is effective for detecting genetic abnormalities associated with these types of leukemia, which could aid in diagnosis and treatment planning.*
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Objective: To investigate the effect of sphingosine-1-phosphate receptor 2 (S1PR2) specific antagonist JTE-013 on the proliferation of human chronic myeloid leukemia (CML) cell line K562.

Methods: K562 cells were treated with JTE-013 (0, 0.5, 1, 5, 10, 20 μmol/L) for 24 and 48 hours respectively, CCK8 assay was used to detect the cell viability.

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Objective: To explore the clinical manifestation, pathological features and treatment regimen of blastic plasmacytoid dendritic cell neoplasm (BPDCN).

Methods: The clinical and pathologic features, diagnosis, treatment and prognosis of 5 BPDCN patients were analyzed retrospectively.

Results: 5 patients had skin lesions, and bone marrow involvement.

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We aimed to evaluate whether subcapsular injection of ultrasonic contrast agent (UCA) can distinguish between benign and malignant lymph node (LN) lesions exhibiting homogeneous enhancement in intravenous contrast-enhanced ultrasound (CEUS) images. From November 2012 to July 2015, 32 patients with superficial lymphadenopathy exhibiting homogeneous enhancement after intravenous CEUS were enrolled. A small amount of UCA was injected into LNs using a subcapsular approach, and perfusion characteristics were recorded.

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