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Three‐year outcomes with brentuximab vedotin plus bendamustine as first salvage therapy in relapsed or refractory Hodgkin lymphoma

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TLDR
Influence of DNMT3A R882 mutations on AML prognosis determined by the allele ratio in Chinese patients is determined byThe allele ratio is defined as the sum of the following: A.J.F., Wilson, R.K.
Abstract
F., Wilson, R.K., Ley, T.J. & Ding, L. (2014) Age-related mutations associated with clonal hematopoietic expansion and malignancies. Nature Medicine, 20, 1472–1478. Yuan, X.Q., Chen, P., Du, Y.X., Zhu, K.W., Zhang, D.Y., Yan, H., Liu, H., Liu, Y.L., Cao, S., Zhou, G., Zeng, H., Chen, S.P., Zhao, X.L., Yang, J., Zeng, W.J. & Chen, X.P. (2019) Influence of DNMT3A R882 mutations on AML prognosis determined by the allele ratio in Chinese patients. Journal of Translational Medicine, 17, 220.

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LAG-3 is expressed on a majority of tumor infiltrating lymphocytes in pediatric Hodgkin lymphoma.

TL;DR: Patient tumor samples from Children’s Oncology Group clinical trial AHOD0031 with matched patient outcome data were analyzed and there was a positive statistically significant relationship between presence of LAG-3 and PD-L1 expression.
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Bendamustine: A review of pharmacology, clinical use and immunological effects

TL;DR: The current knowledge on the use of bendamustine in oncology, its pharmacokinetics, mechanism of action and toxicity was summarized, and its immune-modulating effects that have not been fully elucidated so far are emphasized to encourage further investigations of this unique drug.
Journal ArticleDOI

Brentuximab vedotin in combination with bendamustine in pediatric patients or young adults with relapsed or refractory Hodgkin lymphoma

TL;DR: Brentuximab vedotin in combination with bendamustine may represent a suitable salvage therapy in patients with primary refractory disease and some subsets of relapsed patients still have a dismal outcome.
References
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Revised response criteria for malignant lymphoma

TL;DR: New guidelines incorporating PET, IHC, and flow cytometry for definitions of response in non-Hodgkin's and Hodgkin's lymphoma are presented and it is hoped that they will be adopted widely by study groups, pharmaceutical and biotechnology companies, and regulatory agencies to facilitate the development of new and more effective therapies to improve the outcome of patients with lymphoma.
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