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    Home > Medical News > Latest Medical News > Lymphoma Express: The first XPO1 inhibitor to treat r/r DLBCL; how is CAR-T treatment progress

    Lymphoma Express: The first XPO1 inhibitor to treat r/r DLBCL; how is CAR-T treatment progress

    • Last Update: 2021-09-05
    • Source: Internet
    • Author: User
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    Article source: Med

    Author: MedWatch×

    Based on PubMed, Clinicaltrials.


    1.


    1.


    In July 2020, the study was officially published in Lancet Haematology (ORR: 28%).


    SADAL research key data (source: NextMed database)

    OS subgroup analysis (Source: J Hematol Oncol)

    The results show that for patients with relapsed or refractory DLBCL who have previously received ≥2 lines of chemoimmunotherapy, the oral monotherapy Selinesor can induce sustained anti-tumor activity, and adverse reactions can be controlled


    2.


    2.


    In July of this year, J Hematol Oncol reported a single-center, retrospective study conducted by Professor Han Weidong’s team from the Chinese People’s Liberation Army General Hospital.


    Two patients achieved complete remission after receiving PD-1 blockade therapy, one patient had partial remission, and the other two patients had disease progression


    The study shows that PD-1 blockade therapy is effective for DLBCL patients who have failed the treatment of CAR-T cells expressed by tumor cells PD-1, and it is worthy of further study


    3.


    3.


    The median age of the patients was 64 years old, 90% had advanced disease, 81% of patients received an anthracycline-based treatment regimen, and 13% of patients received consolidated autologous stem cell transplantation (ASCT) at the first complete remission


    Multivariate analysis showed that age ≥60 years, ECOG PS >2, elevated C-reactive protein and elevated β2 microglobulin were associated with poor prognosis


    This large-scale prospective observational study shows that the demand for AITL treatment is still unmet, and there is an urgent need to find new and effective treatment options


    4.


    4.
    Extracellular vesicle miRNA can predict the FDG-PET response of patients with classic Hodgkin's lymphoma after treatment

    FDG-PET imaging is the gold standard for the mid-term evaluation of patients with classic Hodgkin’s lymphoma (cHL).
    However, due to its radioactivity and high cost, FDG-PET imaging cannot be used repeatedly and repeatedly.
    Therefore, a new, micro Innovative assessment methods are necessary
    .
    In July of this year, J Extracell Vesicles published the latest research by D Michiel Pegtel's team from Vrije Universiteit Amsterdam, Netherlands, and found that extracellular vesicles (EVs) miRNA can effectively predict the FDG-PET CT response of cHL patients after treatment
    .

    The study included a total of 193 samples of 31 cHL patients and 19 healthy donors as controls.
    Small RNA sequencing and qRT-PCR analysis showed that compared with patients with complete metabolic remission of PET, patients with active disease (before treatment or partial remission) ) The levels of five miRNAs (miR-127-3p, miR-155-5p, miR-21-5p, miR-24-3p and let-7a-5p) in plasma EVs increased significantly
    .
    Further analysis showed that the combination of these five miRNAs predicted the AUC (area under the ROC curve) of PET-positive and PET-negative patients to be 0.
    855, while the combined AUC of miR-127-3p and miR-24-3p was 0.
    872
    .

    Since serum TARC is a known and definite cHL biomarker, the authors further combined TARC with EV-miRNAl and found that when serum TARC was combined with five miRNAs, the AUC was 0.
    924, the sensitivity was 96%, and the negative predictive value (NPV) was 97%
    .
    When combined with EV-miR-127-3p and/or EV-let-7a-5p levels and serum TARC, the AUC can reach 0.
    93, the sensitivity is 93.
    5%, the specificity is 83.
    8/85.
    0%, and the NPV is 96%
    .

    This study suggests that miRNA in plasma extracellular vesicles is a reliable predictor of PET response (metabolism) in patients with classic Hodgkin’s lymphoma after treatment
    .

    Reference materials:

    1.
    Blood (IF: 22.
    11) 2021Jul Doi: 10.
    1182/blood.
    2020010387

    2.
    J Hematol Oncol (IF:17.
    38) 2021 Jul Doi: 10.
    1186/s13045-021-01122-1

    3.
    J Hematol Oncol (IF:17.
    38) 2021 Jul Doi: 10.
    1186/s13045-021-01120-

    4.
    J Extracell Vesicles (IF: 25.
    842) 2021 Jul Doi: 10.
    1002/jev2.
    12121.

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