MRD Connect
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Treatment for a B-cell acute lymphoblastic leukemia patient carrying a rare TP53 c.C275T mutation: A case report - PubMed

Treatment for a B-cell acute lymphoblastic leukemia patient carrying a rare TP53 c.C275T mutation: A case report - PubMed

Source : https://pubmed.ncbi.nlm.nih.gov/36798689/

TP53 mutations are associated with poor prognosis in the vast majority of cancers. In this study, we present a pediatric B-cell acute lymphoblastic leukemia (B-ALL) patient carrying a rare TP53...


Conclusions: Our report suggests that the TP53 c.C275T mutation is associated with poor prognosis in B-ALL. Fortunately, bortezomib combined with chemotherapy could achieve a better therapeutic effect than conventional regimens in this type of ALL.

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A glycolysis-related gene signatures in diffuse large B-Cell lymphoma predicts prognosis and tumor immune microenvironment

A glycolysis-related gene signatures in diffuse large B-Cell lymphoma predicts prognosis and tumor immune microenvironment

Source : https://www.frontiersin.org/articles/10.3389/fcell.2023.1070777/full

Background: Diffuse large B-cell lymphoma (DLBCL) is the most common type of lymphoma which that highly aggressive and heterogeneous. Glycolysis has been implicated in the regulation of tumor microenvironment (TME)...


Conclusions: These results suggested that the glycolytic risk model could accurately and stably predict the prognosis of patients with DLBCL and might unearth the possible explanation for the glycolysis-related poor prognosis.

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    Key Points • Source: Frontiers in Cell and Developmental Biology • Conclusion: “These results suggested that the glycolytic risk model could accurately and stably predict the prognosis of patients with DLBCL and might unearth Show More
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Identification of microtubule-associated biomarkers in diffuse large B-cell lymphoma and prognosis prediction

Identification of microtubule-associated biomarkers in diffuse large B-cell lymphoma and prognosis prediction

Source : https://www.frontiersin.org/articles/10.3389/fgene.2022.1092678/full

Background: Diffuse large B-cell lymphoma (DLBCL) is a genetically heterogeneous disease with a complicated prognosis. Even though various prognostic evaluations have been applied currently, they usually only use the clinical...


Conclusions: The novel MAGs prognostic model has a well predictive capability, which may as a supplement for the current assessments. Furthermore, candidate TMEM63A gene has therapeutic target potentially in DLBCL.


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Case report: Successful management of a refractory double-expressor diffuse large B-cell lymphoma patient under the guidance of in vitro high-throughput drug sensitivity test

Case report: Successful management of a refractory double-expressor diffuse large B-cell lymphoma patient under the guidance of in vitro high-throughput drug sensitivity test

Source : https://www.frontiersin.org/articles/10.3389/fonc.2022.1079890/full

IntroductionDouble-expressor diffuse large B-cell lymphoma (DEL), harboring double expression of MYC and BCL2, has an inferior prognosis following standard first-line therapy with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP).


Conclusions: In this article, we present a first-line chemoresistant DEL patient with ATM and CD58 mutations who was treated successfully with VTD plus gemcitabine under the guidance of in vitro high-throughput drug sensitivity test.


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Cytogenetics and Molecular Genetics in Pediatric Acute Lymphoblastic Leukemia (ALL) and Its Correlation with Induction Outcomes

Cytogenetics and Molecular Genetics in Pediatric Acute Lymphoblastic Leukemia (ALL) and Its Correlation with Induction Outcomes

Source : https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0042-1754337

CC BY-NC-ND 4.0 · South Asian J Cancer 2022; 11(04): 353-360DOI: 10.1055/s-0042-1754337 Leukemia, Lymphoma, Myeloma 1   Department of Pediatric Hematology and Oncology, Kanchi Kamakoti Childs Trust Hospital, Chennai, Tamil...


Conclusions: Cytogenetic and molecular genetic subgrouping prognosticates ALL outcomes. Although 25% of TEL–AML   children had MRD positivity, larger studies are required to validate the same. End-of-induction MRD outcomes did not correlate with chromosomal aberrations.