Publications by authors named "Deanna H Wong"

Purpose: To identify patient and hospital characteristics associated with extended surgical cytoreduction in the treatment of ovarian cancer.

Methods: A retrospective analysis using the National Inpatient Sample (NIS) database identified women hospitalized for surgery to remove an ovarian malignancy between 2013 and 2017. Extended cytoreduction (ECR) was defined as surgery involving the bowel, liver, diaphragm, bladder, stomach, or spleen.

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Background And Objectives: Postoperative readmissions are often used to assess quality of surgical care. This study compared 30-day vs 31- to 90-day readmission following surgery for ovarian, fallopian tube, or primary peritoneal cancer.

Methods: This retrospective study of the 2010-2015 Nationwide Readmissions Database characterized 90-day readmissions following cytoreductive surgery for these cancers.

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The clinical efficacy displayed by ibrutinib in chronic lymphocytic leukemia (CLL) has been challenged by the frequent emergence of resistant clones. The ibrutinib target, Bruton's tyrosine kinase (BTK), is essential for B-cell receptor signaling, and most resistant cases carry mutations in or , a downstream effector target of BTK. Recent findings show that MI-2, a small molecule inhibitor of the para-caspase MALT1, is effective in preclinical models of another type of BCR pathway-dependent lymphoma.

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Multi-gene panel testing has expanded the genetic information available to cancer patients. The objective was to assess provider behaviors and attitudes and patient knowledge and attitudes towards genetic counseling and testing. An online survey was distributed to Society of Gynecologic Oncology members and a written questionnaire was administered to patients diagnosed with epithelial ovarian cancer at a tertiary care referral center.

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Purpose: Chronic lymphocytic leukemia (CLL) cells depend on microenvironmental interactions for proliferation and survival that are at least partially mediated through B-cell receptor (BCR) signaling. Ibrutinib, a Bruton tyrosine kinase inhibitor, disrupts BCR signaling and leads to the egress of tumor cells from the microenvironment. Although the on-target effects on CLL cells are well defined, the impact on the microenvironment is less well studied.

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Article Synopsis
  • Ibrutinib, a treatment for chronic lymphocytic leukemia (CLL), causes a rapid increase in blood lymphocytes, mainly due to CLL cells moving from lymphoid tissues into the bloodstream.
  • In a clinical trial, patients taking ibrutinib showed a significant reduction in CLL cell adhesion to fibronectin within days, while the effect on migration to other signals was less pronounced.
  • The study suggests that inhibiting specific adhesion pathways (BTK and VLA-4) may lead to a better understanding of how ibrutinib induces lymphocytosis and potentially weakens CLL cell survival signals in their environment.
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