Durable Response to Venetoclax Monotherapy in Richter's Syndrome: A Case Report and Review of Literature.

Chronic lymphocytic leukemia Richter transformation Venetoclax

Journal

Journal of hematology
ISSN: 1927-1212
Titre abrégé: J Hematol
Pays: Canada
ID NLM: 101635099

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 21 12 2018
accepted: 15 02 2019
entrez: 18 4 2020
pubmed: 18 4 2020
medline: 18 4 2020
Statut: ppublish

Résumé

In 2017, 20,110 people in the United States were diagnosed with chronic lymphocytic leukemia (CLL). Of these patients, 5-15% will ultimately undergo Richter's syndrome (RS), a transformation to a more aggressive lymphoma, most commonly diffuse large B-cell lymphoma (DLBCL) type. Particularly when the transformation is clonally related, prognosis is poor in these individuals with a median survival of only 5 - 14 months. This is an area of unmet need, and as such, the benefits of novel approaches with targeted therapies should be explored. Our patient is a 70-year-old female who was diagnosed with CLL in 2010. In 2016, she presented to her general practitioner with new B symptoms and leukocytosis. Cytogenetics on peripheral blood was notable for known trisomy 12 (52.8% of cells) and new 17p deletion (93.4% of cells). She received five cycles of ofatumumab with complete resolution of systemic symptoms but mixed response on interim computed tomography (CT) scan with ensuing rise in her white blood cell (WBC) and lactic acid dehydrogenase (LDH). A positron emission tomography (PET) scan had disproportionate uptake in the porta hepatis lymph nodes and subsequent lymph node biopsy confirmed transformation. She was started on R-CHOP chemotherapy but tolerated it very poorly. She was transitioned to venetoclax monotherapy in April 2017 and achieved a partial response by CT and bone marrow biopsy. This has been maintained over the last 12 months allowing the patient to travel and maintain a high quality of life. While the pathogenesis to RS is poorly understood, there have been several studies to identify tumor genetic changes predisposing to transformation. Of the proposed factors, a review of the literature consistently suggests

Identifiants

pubmed: 32300445
doi: 10.14740/jh473
pmc: PMC7153679
doi:

Types de publication

Case Reports

Langues

eng

Pagination

60-63

Informations de copyright

Copyright 2019, Kollipara et al.

Déclaration de conflit d'intérêts

Parmeswaran Venugopal is a consultant for Bayer and AbbVie pharmaceuticals. Brett Mahon is the director of Pathology for Tempus Laboratories and has equity interest. He is a consultant for AbbVie. Revathi Kollipara and Kelly Szymanski have no disclosures.

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Auteurs

Revathi Kollipara (R)

Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.

Kelly Szymanski (K)

Division of Hematology, Oncology and Cell Therapy, Rush University Medical Center, Chicago, IL, USA.

Brett Mahon (B)

Department of Pathology, Rush University Medical Center, Chicago, IL, USA.

Parameswaran Venugopal (P)

Division of Hematology, Oncology and Cell Therapy, Rush University Medical Center, Chicago, IL, USA.

Classifications MeSH