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Jeremy J. Pappacena

Researcher at Memorial Sloan Kettering Cancer Center

Publications -  7
Citations -  82

Jeremy J. Pappacena is an academic researcher from Memorial Sloan Kettering Cancer Center. The author has contributed to research in topics: Leukemia & Pentostatin. The author has an hindex of 3, co-authored 7 publications receiving 49 citations. Previous affiliations of Jeremy J. Pappacena include Allegheny Health Network.

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Blinatumomab administered concurrently with oral tyrosine kinase inhibitor therapy is a well-tolerated consolidation strategy and eradicates measurable residual disease in adults with Philadelphia chromosome positive acute lymphoblastic leukemia

TL;DR: This small series suggests blinatumomab’s concurrent with commercially available TKIs as consolidative therapy to spare toxicities of conventional chemotherapy is a safe and effective consolidation strategy for patients with Ph’+ ALL to achieve or maintain CMR.
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Drug interactions with Bruton's tyrosine kinase inhibitors: clinical implications and management.

TL;DR: The relevant drug–drug and drug–food interactions associated with ibrutinib, acalabrutinIB, and zanubrut inib are discussed and clinical practice recommendations for managing these interactions are provided based on the available literature.
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Tolerability and toxicity of pegaspargase in adults 40 years and older with acute lymphoblastic leukemia.

TL;DR: This study suggests that while hepatotoxicity and other known adverse effects are common, with careful monitoring, pegaspargase can safely be administered to adults with ALL age ≥40 years old.
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No Loose Ends: A Review of the Pharmacotherapy of Hairy Cell and Hairy Cell Leukemia Variant.

TL;DR: HCL and HCLv are uncommon lymphoid neoplasms that lead to a characteristic constellation of symptoms, and the emergence of PAs and novel targeted agents have improved the likelihood and durability of responses for these patients.
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Blinatumomab Administered Concurrently with Oral Tyrosine Kinase Inhibitor Therapy Is a Well-Tolerated Consolidation Strategy and Eradicates Measurable Residual Disease in Adults with Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia

TL;DR: The primary objectives were to characterize the safety/toxicity profile and rates of MRD negativity by flow cytometry (FACS) and/or quantitative real-time PCR for BCR-ABL1 transcripts following consolidation or re-induction w/ BLIN+TKI, and to deepen responses.