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Customized or randomized trials for relapsed refractory pediatric Burkitt lymphomas? A retrospective analysis of two clinical cases with comprehensive molecular profiling: Possible explanation for different treatment outcomes after similar targeted therapies

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F18%3A00069596" target="_blank" >RIV/65269705:_____/18:00069596 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0923753419323312" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0923753419323312</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1093/annonc/mdy314.037" target="_blank" >10.1093/annonc/mdy314.037</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Customized or randomized trials for relapsed refractory pediatric Burkitt lymphomas? A retrospective analysis of two clinical cases with comprehensive molecular profiling: Possible explanation for different treatment outcomes after similar targeted therapies

  • Original language description

    Background: Current standard chemoimmunotherapy achieves survival in almost 95% children with mature B-NHL. However, children with relapses still carry very poor prognosis. Methods: Molecular profiling consisted of whole exome NGS, gene expression profiling and peripheral blood phosphoflow. Results: Both cases had identical clinical presentation and histology, progressed early during standard therapy and did not respond to intensive retrieval chemotherapy. In the first patient, a germ line variant of c.935C&gt;G in the PI3K-delta subunit was found. Activation of PI3K downstream signaling pathway was detected using flow cytometry in patient&apos;s peripheral blood lymphocytes. Increased levels of PI3K were confirmed also by gene expression profiling together with an increased expression of HR23B. Immunohistochemistry revealed strong expression of PD-1L. Therapy was changed to a single agent idelalisib window. In two weeks there was markedly decreased PI3K pathway activation in patient&apos;s lymphocytes, but the disease still showed a radiological progression. During the time, ibrutinib, valproic acid, nivolumab and metronomic cyclophosphamide was added and local 21Gy radiation to the site of the abdominal relapse was used. Partial remission was documented and personalized immunotherapy with autologous dendritic cell-based vaccine was given. Residual tumor resected after 11 months did not show any viable tumor and treatment was gradually tapered down. His 3rd EFS 31 months on personalized treatment is the longest he ever experienced. The second patient died 11 months form diagnosis. Conclusions: The first case was successfully treated with targeted and immune therapy that matched the molecular signature of the tumor, but in the second case, the therapy &quot;missed&quot; the target, because his molecular signature was not known at the time retrieval therapy. The findings suggest that molecular signatures among clinically and histologically similar patients could be unique, and a tissue biomarker-based customized therapy may be the best approach to address these poor prognosis patients.

  • Czech name

  • Czech description

Classification

  • Type

    O - Miscellaneous

  • CEP classification

  • OECD FORD branch

    30204 - Oncology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů