123 results match your criteria: "Weill Cornell Medicine and New York-Presbyterian Hospital[Affiliation]"

Objective: To assess the feasibility and efficacy of group text messaging as a teaching tool to improve neurology resident knowledge and clinical pearl dissemination in an outpatient setting enriched with headache encounters, and to evaluate if learning points from this teaching method would influence resident care of subsequent patients.

Background: Inpatient neurology teaching during training is most often accomplished in team settings during rounds or conferences such as morning report, but outpatient teaching where headache is more likely encountered may be less consistently performed in such a setting where learning points may be shared. Few studies have evaluated whether group text messaging can be an innovative tool for teaching in residency training.

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Article Synopsis
  • The ROS1 proto-oncogene is linked with receptor tyrosine kinases and plays a significant role in treating ROS1 fusion-positive non-small cell lung cancer (NSCLC) using FDA-approved TKIs like crizotinib and entrectinib, though these medications face challenges such as resistance and limited brain penetration.
  • Repotrectinib, a new macrocyclic TKI, was created to tackle resistance mutations and enhance brain distribution, showing strong effectiveness in the TRIDENT-1 trial with high response rates in both TKI-naïve and TKI-pretreated patients.
  • The trial showed that 79% of TKI-naïve patients achieved an objective response and had longer progression
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  • The study investigated the feasibility and safety of active surveillance for patients with multiple ground glass opacities (GGOs) in the lungs, which are a common concern in medical imaging.
  • A total of 337 patients, primarily older adults with a significant history of smoking, were enrolled and monitored over time, with each GGO documented via CT scans every 6 to 12 months.
  • Preliminary findings suggest that active surveillance is a viable management option for patients, with ongoing assessments planned to evaluate long-term safety and outcomes over five years.
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Phase 2 Trial of Regorafenib in Recurrent/Metastatic Adenoid Cystic Carcinoma.

Clin Cancer Res

December 2024

Head and Neck Medical Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Article Synopsis
  • - The study tested regorafenib, a multi-targeted tyrosine kinase inhibitor, for treating patients with recurrent/metastatic adenoid cystic carcinoma (ACC), aiming to evaluate its effectiveness and identify biomarkers related to treatment response.
  • - Among 38 patients, no objective responses were observed, but 45% achieved 6-month progression-free survival (PFS), with longer PFS linked to specific immune-related tumor profiles and the presence of NOTCH1 or KDM6A alterations associated with poorer outcomes.
  • - The findings suggest that combining CDK4/6 inhibitors with VEGFR-TKIs might improve treatment efficacy, emphasizing the need to consider the role of the immune microenvironment in ACC treatment resistance.
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Introduction: The comparative efficacy and safety of lorlatinib, a third-generation anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitor (TKI), versus second-generation ALK TKIs as a first-line treatment for ALK+ advanced/metastatic nonsmall cell lung cancer (NSCLC) remains uncertain as there are no head-to-head clinical trials.

Methods: Matching-adjusted indirect comparisons (MAICs) were conducted using phase III trial data demonstrating superior efficacy over crizotinib, a first-generation ALK TKI. MAICs were conducted to compare lorlatinib (CROWN) versus alectinib (ALEX and ALESIA) and brigatinib (ALTA-1L) with matching based on prespecified effect modifiers.

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  • Racial and ethnic minorities are significantly underrepresented in cancer clinical trials, particularly due to restrictive eligibility criteria that often exclude patients who might benefit the most from treatments.
  • A study found that up to 24% of patients with diffuse large B-cell lymphoma would be disqualified from recent trials based on five specific lab criteria, leading to worse outcomes and increased deaths among these excluded groups.
  • Analysis revealed that Black/African American and Hispanic patients experienced higher rates of ineligibility compared to non-Hispanic White patients, highlighting a critical need to reevaluate how eligibility criteria are established to ensure equitable access to clinical trials across all demographics.
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Ivosidenib is a first-in-class mutant isocitrate dehydrogenase 1 (mIDH1) inhibitor with efficacy and tolerability in patients with advanced mIDH1 hematologic malignancies, leading to approval in frontline and relapsed/refractory (R/R) mIDH1 acute myeloid leukemia. We report final data from a phase 1 single-arm substudy of once-daily ivosidenib in patients with R/R mIDH1 myelodysplastic syndrome (MDS) after failure of standard-of-care therapies. Primary objectives were to determine safety, tolerability, and clinical activity.

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Safety and Toxicity Profiles of CAR T Cell Therapy in Non-Hodgkin Lymphoma: A Systematic Review and Meta-Analysis.

Clin Lymphoma Myeloma Leuk

June 2024

Division of Hematology and Medical Oncology, Weill Cornell Medicine, New York, NY.

Background: The application of CD19-directed chimeric antigen receptor T (CAR T) cell therapy has improved outcomes for thousands of patients with non-Hodgkin B cell lymphoma (NHL). The toxicities associated with various CAR T cell products, however, can be severe and difficult to anticipate.

Methods: In this systematic review and meta-analysis, we set out to determine whether there are measurable differences in common toxicities, including cytokine release syndrome (CRS), immune effector cell associated neurotoxicity syndrome (ICANS), cytopenias, and infections, between CAR T products that are commercially available for the treatment of NHL.

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  • The study investigates the distinct regions of the germinal center (GC)—the dark zone (DZ) and light zone (LZ)—which are crucial for B-cell expansion and antibody maturation, yet lack a clear understanding of their immune composition differences.
  • Researchers discovered specific DNA damage responses and chromatin features that explain why T-cells are excluded from the DZ region, providing insights into its immune-repulsive characteristics.
  • The findings highlight the role of the ATR kinase in regulating responses in the DZ, suggesting that targeting ATR could enhance immunotherapy effectiveness for aggressive types of lymphoma like Diffuse Large B-cell Lymphomas (DLBCL).
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Objective: Evaluate the longitudinal stability of six pregnancy contexts, including intention, in a diverse cohort of individuals experiencing delivery, abortion, or miscarriage.

Methods: We enrolled individuals 16-44 years of age with pregnancies <24 weeks gestation in this longitudinal study between June 2014 and June 2015 in four US urban clinics. We assessed six pregnancy contexts (intention, wantedness, planning, timing, desirability, and happiness) at enrollment and 3-month follow-up.

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A signature of enhanced proliferation associated with response and survival to anti-PD-L1 therapy in early-stage non-small cell lung cancer.

Cell Rep Med

March 2024

Meyer Cancer Center, Weill Cornell Medicine and New York Presbyterian Hospital, New York, NY 10065, USA; Department of Cardiothoracic Surgery, Weill Cornell Medicine and New York Presbyterian Hospital, New York, NY 10065, USA; Department of Biochemistry, Weill Cornell Medicine, New York, NY 10065, USA. Electronic address:

In early-stage non-small cell lung cancer, the combination of neoadjuvant anti-PD-L1 and subablative stereotactic body radiation therapy (SBRT) is associated with higher rates of major pathologic response compared to anti-PD-L1 alone. Here, we identify a 140-gene set, enriched in genes characteristic of highly proliferating cells, associated with response to the dual therapy. Analysis of on-treatment transcriptome data indicate roles for T and B cells in response.

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  • - The study investigated the effects of the AKT inhibitor MK-2206 on patients with recurrent/metastatic adenoid cystic carcinoma (ACC), a rare and incurable cancer, aiming to reduce MYB expression and induce tumor regression.
  • - Sixteen patients were treated but there were no confirmed responses; however, 13 maintained stable disease, with a median progression-free survival of 9.7 months and overall survival of 18 months.
  • - While MK-2206 did decrease MYB levels in some patients, its clinical efficacy was limited, suggesting a need for new strategies to target MYB in ACC.
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  • Unilateral laminotomy for bilateral decompression (ULBD) is a minimally invasive surgery that effectively relieves symptoms of lumbar spinal stenosis while minimizing risks like blood loss, muscle damage, and pain compared to traditional methods.
  • The study highlights a technique called slalom unilateral laminotomy for bilateral decompression with navigation, detailing ten steps to perform the surgery and reporting on a case series of seven patients who underwent the procedure.
  • Results showed significant pain reduction post-surgery, with average pain scores dropping from 4.71 to 1.50 for back pain and 4.33 to 1.21 for leg pain, indicating it is a safe and efficient option for treating multi-segmental lumbar spinal stenosis.
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  • A study evaluated the impact of diabetes and obesity on ten-year outcomes after coronary artery bypass graft (CABG) surgery, focusing on all-cause mortality and other health complications.
  • Results indicated that patients with diabetes, especially those with insulin-dependent diabetes, faced a significantly higher risk of mortality and sternal wound complications compared to those without diabetes, regardless of obesity status.
  • Interestingly, obesity alone did not increase long-term mortality risk, suggesting that it may have a "protective" effect when coupled with diabetes in CABG patients.
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In this real-world evaluation of tafasitamab-lenalidomide (TL) in relapsed or refractory LBCL, patients receiving TL had higher rates of comorbidities and high-risk disease characteristics, and substantially lower progression-free survival and overall survival, compared with the L-MIND registration clinical trial for TL.

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A multi-stem cell basis for craniosynostosis and calvarial mineralization.

Nature

September 2023

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.

Craniosynostosis is a group of disorders of premature calvarial suture fusion. The identity of the calvarial stem cells (CSCs) that produce fusion-driving osteoblasts in craniosynostosis remains poorly understood. Here we show that both physiologic calvarial mineralization and pathologic calvarial fusion in craniosynostosis reflect the interaction of two separate stem cell lineages; a previously identified cathepsin K (CTSK) lineage CSC (CTSK CSC) and a separate discoidin domain-containing receptor 2 (DDR2) lineage stem cell (DDR2 CSC) that we identified in this study.

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Nine-year follow-up of lenalidomide plus rituximab as initial treatment for mantle cell lymphoma.

Blood Adv

November 2023

Division of Hematology and Medical Oncology, Weill Cornell Medicine, New York, NY.

Article Synopsis
  • * After 9 years, the study shows 47% of patients remain in remission, with 51% progression-free survival and 66% overall survival, but some patients experienced significant side effects.
  • * A notable percentage developed secondary malignancies, and two patients stopped treatment due to COVID-19 concerns, but overall, LR continues to show promising long-term results.
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  • Follicular lymphoma (FL) varies greatly among patients, with some needing immediate treatment due to aggressive disease while others can monitor their condition without intervention.
  • A study analyzed the genetic alterations in FL across 370 patients, discovering that higher mutation burdens were present in relapsed or transformed FL but not linked to better outcomes in newly diagnosed cases.
  • A set of 7 specific gene mutations (MAP signature) was identified that indicates a shorter progression-free survival in newly diagnosed FL, which could help better predict patient outcomes beyond existing prognostic tools.
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Peripheral T-cell lymphomas (PTCLs) are associated with poor prognosis when treated with cytotoxic chemotherapy. We report the findings of a phase 2 study evaluating a chemotherapy-free combination of romidepsin plus lenalidomide as initial treatment for patients with PTCL who were aged >60 years or noncandidates for chemotherapy. Treatment was initiated with romidepsin 10 mg/m2 IV on days 1, 8, and 15 and lenalidomide 25 mg taken orally from days 1 to 21 of 28-day cycle for up to 1 year.

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In the last decade, there has been increased understanding of the pathologic features and biology of peripheral T cell lymphomas (PTCLs) through development of multi omics and molecular profiling techniques. In addition, international collaborations through multi center trials as well as prospective registry studies have improved our knowledge of host and tumor genomic factors and treatment factors affecting disease outcomes. In our review today, we aim to highlight the current epidemiology, latest advances in classification, disease biology and the evolving treatment landscape for nodal PTCLs.

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  • The study investigates the safety and effectiveness of CAR T cell therapy in patients who have had solid organ transplants, noting limited existing data on this topic.
  • It highlights the potential risks, such as harming the transplanted organ, while also exploring how post-transplant immunosuppression can affect CAR T cell function.
  • Results from 10 studies showed that 69% of patients responded to therapy, with 83% experiencing cytokine release syndrome (CRS) and 60% developing immune effector cell-associated neurotoxicity syndrome (ICANS), indicating significant side effects alongside treatment benefits.
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Background: The repair of lateral sphenoid sinus cerebrospinal fluid leaks is routinely accomplished through the use of the endonasal endoscopic approach (EEA) with a transpterygoidal extension. This approach can incur sinus morbidity, damage to the vidian, palatine and trigeminal nerves, and the contents of the pterygopalatine fossa, particularly if the encephalocele is lateral to the foramen rotundum (FR) and V2.

Objective: To investigate the use of the lateral transorbital approach (LTOA) as an alternative approach for repair of lateral sphenoid sinus encephaloceles that avoids the potential morbidity of EEA.

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Relapsed/refractory (R/R) Acute Myeloid Leukemia (AML) is a genetically complex and heterogeneous disease with a poor prognosis and limited treatment options. Thus, there is an urgent need to develop therapeutic combinations to overcome drug resistance in AML. This open-label, multicenter, international, phase 1b study evaluated the safety, efficacy, and pharmacokinetics of venetoclax in combination with alvocidib in patients with R/R AML.

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