Andrew Crabbe

ORCID: 0009-0003-3655-3344
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About
Contact & Profiles
Research Areas
  • Lymphoma Diagnosis and Treatment
  • T-cell and Retrovirus Studies
  • Galectins and Cancer Biology
  • CAR-T cell therapy research
  • Colorectal Cancer Surgical Treatments
  • Genetic factors in colorectal cancer
  • Cancer Immunotherapy and Biomarkers
  • Colorectal Cancer Treatments and Studies
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Hematological disorders and diagnostics
  • Acute Myeloid Leukemia Research
  • Colorectal and Anal Carcinomas
  • Immune Cell Function and Interaction

Massachusetts General Hospital
2021-2024

Akron General Medical Center
2022-2024

Cleveland Clinic
2022-2024

Abstract Purpose: Develop a novel therapeutic strategy for patients with subtypes of mature T-cell and NK-cell neoplasms. Experimental Design: Primary specimens, cell lines, patient-derived xenograft models, commercially available, proprietary anti-KLRG1 antibodies were used screening, target, functional validation. Results: Here we demonstrate that surface KLRG1 is highly expressed on tumor cells in subsets extranodal NK/T-cell lymphoma (ENKTCL), T-prolymphocytic leukemia (T-PLL),...

10.1158/1078-0432.ccr-23-3504 article EN cc-by-nc-nd Clinical Cancer Research 2024-01-22

Micropapillary carcinoma (MPC) is a recognised WHO variant of colonic (CC), although little known about its prognosis, immune microenvironment and molecular alterations. We investigated clinical, pathological immunological characteristics.

10.1136/jcp-2023-208895 article EN Journal of Clinical Pathology 2023-05-31

Serrated adenocarcinoma (SAC), a recognised WHO variant of colonic adenocarcinoma, is the purported end-product serrated neoplasia. However, diagnosis SAC infrequently rendered, and little known about its prognosis, immune microenvironment molecular alterations.We assessed 903 consecutive colon carcinomas tumours with ≥ 5% (n = 77) 50% patterns 13). We precursor polyps synchronous polyps. recorded demographic/clinical parameters, histological features mismatch repair (MMR) status. performed...

10.1111/his.14719 article EN Histopathology 2022-07-05

<div>AbstractPurpose:<p>Develop a novel therapeutic strategy for patients with subtypes of mature T-cell and NK-cell neoplasms.</p>Experimental Design:<p>Primary specimens, cell lines, patient-derived xenograft models, commercially available, proprietary anti-KLRG1 antibodies were used screening, target, functional validation.</p>Results:<p>Here we demonstrate that surface KLRG1 is highly expressed on tumor cells in subsets extranodal NK/T-cell lymphoma...

10.1158/1078-0432.c.7265752 preprint EN 2024-06-03

<div>AbstractPurpose:<p>Develop a novel therapeutic strategy for patients with subtypes of mature T-cell and NK-cell neoplasms.</p>Experimental Design:<p>Primary specimens, cell lines, patient-derived xenograft models, commercially available, proprietary anti-KLRG1 antibodies were used screening, target, functional validation.</p>Results:<p>Here we demonstrate that surface KLRG1 is highly expressed on tumor cells in subsets extranodal NK/T-cell lymphoma...

10.1158/1078-0432.c.7265752.v1 preprint EN 2024-06-03

A 49-year-old man was evaluated because of relapsed acute myeloid leukemia that occurred 14 months after the initial diagnosis and treatment. Molecular genetic profiling at time relapse identified a new internal tandem duplication mutation in FLT3 (FLT3-ITD). bone marrow biopsy performed, management decisions were made.

10.1056/nejmcpc2103458 article EN New England Journal of Medicine 2021-08-25
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