Rapid T-cell lymphoma progression associated with immune checkpoint inhibitors

Ohmoto, Akihiro; Fuji, Shigeo

doi:10.1080/17474086.2023.2215424

Cited by 4 publications

(1 citation statement)

References 40 publications

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“…In assessing ICI activity in r/r PTCL, investigators unexpectedly saw a subset of patients experience disease hyper-progression, defined as progression within 2 months of treatment initiation, resulting in halting of clinical studies. Small studies have reported rates of hyper-progression as high as 50% while other have been terminated after interim analysis showed futility (46)(47)(48). Thus far, studies evaluating anti-PD-1-based therapy in r/r PTCL (as either monotherapy or in combination) have reported ORRs ranging from 36.4-50% and CRs from 0-35.7% (49)(50)(51).…”

Section: T-cell Lymphomasmentioning

confidence: 99%

Checkpoint inhibition in hematologic malignancies

Tsumura,

Levis,

Tuscano

2023

Front. Oncol.

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Checkpoint inhibitor therapy has emerged as an effective therapeutic strategy for many types of malignancies, especially in solid tumors. Within the last two decades, numerous monoclonal antibody drugs targeting the CTLA-4 and PD-1/PD-L1 checkpoint pathways have seen FDA approval. Within hematologic malignancies, Hodgkin Lymphoma has seen the greatest clinical benefits thus far with more recent data showing efficacy in the front-line setting. As our understanding of checkpoint inhibition expands, using these pathways as a therapeutic target has shown some utility in the treatment of other hematologic malignancies as well, primarily in the relapsed/refractory settings. Checkpoint inhibition also appears to have a role as a synergistic agent to augment clinical responses to other forms of therapy such as hematopoietic stem cell transplant. Moreover, alternative checkpoint molecules that bypass the well-studied CTLA-4 and PD-1/PD-L1 pathways have emerged as exciting new therapeutic targets. Most excitingly is the use of anti-CD47 blockade in the treatment of high risk MDS and TP-53 mutated AML. Overall, there has been tremendous progress in understanding the benefits of checkpoint inhibition in hematologic malignancies, but further studies are needed in all areas to best utilize these agents. This is a review of the most recent developments and progress in Immune Checkpoint Inhibition in Hematologic Malignancies in the last decade.

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Section: T-cell Lymphomasmentioning

confidence: 99%

Checkpoint inhibition in hematologic malignancies

Tsumura,

Levis,

Tuscano

2023

Front. Oncol.

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Impact of the WHO-5 classification of haematolymphoid tumours on clinical practice

Brand,

Simonitsch-Klupp

2024

memo

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SummaryThe long-awaited 2022 World Health Organization Classification of Haematolymphoid Tumours (WHO-5-HAEM) has finally been published as part of the IARC Blue Book series. This two-volume edition is significantly more comprehensive than its predecessors, reflecting the integration of extensive advancements in genetic and molecular understanding, alongside clinically relevant findings. This brief review will highlight the key changes in the classification of the most common B‑cell lymphoproliferative disorders, specifically follicular lymphomas and large B‑cell lymphomas (LBCL). It will also introduce new entities and summarize the most critical updates within these lymphoma categories.

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Spontaneous regression in mature T-cell non-Hodgkin lymphoma

Ohmoto,

Fuji

2024

Expert Review of Hematology

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Rapid T-cell lymphoma progression associated with immune checkpoint inhibitors

Cited by 4 publications

References 40 publications

Checkpoint inhibition in hematologic malignancies

Checkpoint inhibition in hematologic malignancies

Impact of the WHO-5 classification of haematolymphoid tumours on clinical practice

Spontaneous regression in mature T-cell non-Hodgkin lymphoma

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