Karen L. Reckamp

ORCID: 0000-0002-9213-0325
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About
Contact & Profiles
Research Areas
  • Lung Cancer Treatments and Mutations
  • Lung Cancer Research Studies
  • Cancer Genomics and Diagnostics
  • Cancer Immunotherapy and Biomarkers
  • Colorectal Cancer Treatments and Studies
  • Lung Cancer Diagnosis and Treatment
  • Cancer therapeutics and mechanisms
  • HER2/EGFR in Cancer Research
  • PI3K/AKT/mTOR signaling in cancer
  • Immunotherapy and Immune Responses
  • CAR-T cell therapy research
  • Inflammatory mediators and NSAID effects
  • Cancer Mechanisms and Therapy
  • Gastric Cancer Management and Outcomes
  • Pancreatic and Hepatic Oncology Research
  • Cancer Research and Treatments
  • Radiomics and Machine Learning in Medical Imaging
  • Genetic factors in colorectal cancer
  • Peptidase Inhibition and Analysis
  • SARS-CoV-2 and COVID-19 Research
  • Immune cells in cancer
  • Cancer survivorship and care
  • Cytokine Signaling Pathways and Interactions
  • COVID-19 and healthcare impacts
  • Palliative Care and End-of-Life Issues

Cedars-Sinai Medical Center
2012-2025

Faculty of 1000 (United States)
2023

Molecular Oncology (United States)
2023

RELX Group (United States)
2023

City of Hope
2013-2022

City Of Hope National Medical Center
2012-2021

University of California, Los Angeles
2005-2018

Amgen (United States)
2006-2018

Pfizer (United States)
2018

Novartis (Germany)
2018

Patients with advanced squamous-cell non-small-cell lung cancer (NSCLC) who have disease progression during or after first-line chemotherapy limited treatment options. This randomized, open-label, international, phase 3 study evaluated the efficacy and safety of nivolumab, a fully human IgG4 programmed death 1 (PD-1) immune-checkpoint-inhibitor antibody, as compared docetaxel in this patient population.We randomly assigned 272 patients to receive at dose mg per kilogram body weight every 2...

10.1056/nejmoa1504627 article EN New England Journal of Medicine 2015-05-31

This selection from the NCCN Guidelines for Non–Small Cell Lung Cancer (NSCLC) focuses on targeted therapies and immunotherapies metastatic NSCLC, because therapeutic recommendations are rapidly changing disease. For example, new were added atezolizumab, ceritinib, osimertinib, pembrolizumab 2017 updates.

10.6004/jnccn.2017.0050 article EN Journal of the National Comprehensive Cancer Network 2017-04-01

The NCCN Guidelines for Non-Small Cell Lung Cancer (NSCLC) address all aspects of management NSCLC. These Insights focus on recent updates in immunotherapy. For the 2020 update, systemic therapy regimens have been categorized using a new preference stratification system; certain are now recommended as "preferred interventions," whereas others either "other interventions" or "useful under circumstances."

10.6004/jnccn.2019.0059 article EN Journal of the National Comprehensive Cancer Network 2019-12-01

Purpose Nivolumab, a programmed death-1 inhibitor, prolonged overall survival compared with docetaxel in two independent phase III studies previously treated patients advanced squamous (CheckMate 017; ClinicalTrials.gov identifier: NCT01642004) or nonsquamous 057; NCT01673867) non-small-cell lung cancer (NSCLC). We report updated results, including pooled analysis of the studies. Methods Patients stage IIIB/IV (N = 272) 582) NSCLC and disease progression during after prior platinum-based...

10.1200/jco.2017.74.3062 article EN Journal of Clinical Oncology 2017-10-12

RET fusions are oncogenic drivers in 1 to 2% of non-small-cell lung cancers (NSCLCs). In patients with fusion-positive NSCLC, the efficacy and safety selective inhibition unknown.We enrolled advanced NSCLC who had previously received platinum-based chemotherapy those were untreated separately a phase 1-2 trial selpercatinib. The primary end point was an objective response (a complete or partial response) as determined by independent review committee. Secondary points included duration...

10.1056/nejmoa2005653 article EN New England Journal of Medicine 2020-08-26

Abstract Naturally occurring CD4+CD25+ regulatory T cells (T reg) are pivotal in suppressing immune responses and maintaining tolerance. The identification of molecules controlling reg differentiation function is important understanding host malignancy autoimmunity. In this study we show that PGE2 enhances the vitro inhibitory human purified cells. Moreover, induces a phenotype CD4+CD25− PGE2-treated cell-mediated inhibition anti-CD3-stimulated lymphocyte proliferation did not require cell...

10.4049/jimmunol.175.3.1483 article EN The Journal of Immunology 2005-08-01

Purpose Most crizotinib-treated patients with anaplastic lymphoma kinase gene ( ALK)–rearranged non–small-cell lung cancer (ALK-positive NSCLC) eventually experience disease progression. We evaluated two regimens of brigatinib, an investigational next-generation ALK inhibitor, in crizotinib-refractory ALK-positive NSCLC. Patients and Methods were stratified by brain metastases best response to crizotinib. They randomly assigned (1:1) oral brigatinib 90 mg once daily (arm A) or 180 a 7-day...

10.1200/jco.2016.71.5904 article EN Journal of Clinical Oncology 2017-05-05

Abstract Cyclooxygenase (COX)-2 and its product prostaglandin (PG) E2 underlie an immunosuppressive network that is important in the pathogenesis of non–small cell lung cancer. CD4+CD25+ T regulatory (Treg) cells play role maintenance immunologic self-tolerance. Treg activities increase cancer appear to a suppressing antitumor immune responses. Definition pathways controlling will enhance our understanding limitation host Tumor-derived COX-2/PGE2 induced expression cell-specific...

10.1158/0008-5472.can-05-0141 article EN Cancer Research 2005-06-15

Abstract Purpose: Complete and timely tissue genotyping is challenging, leading to significant numbers of patients with newly diagnosed metastatic non–small cell lung cancer (mNSCLC) being undergenotyped for all eight genomic biomarkers recommended by professional guidelines. We aimed demonstrate noninferiority comprehensive cell-free DNA (cfDNA) relative physician discretion standard-of-care (SOC) identify guideline-recommended in mNSCLC. Patients Methods: Prospectively enrolled previously...

10.1158/1078-0432.ccr-19-0624 article EN Clinical Cancer Research 2019-04-16

Non-small-cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 20 insertion (Exon20ins) mutations exhibits inherent resistance to approved tyrosine kinase inhibitors. Amivantamab, an EGFR-MET bispecific antibody immune cell-directing activity, binds each receptor's extracellular domain, bypassing at the inhibitor binding site.CHRYSALIS is a phase I, open-label, dose-escalation, and dose-expansion study, which included population EGFR Exon20ins NSCLC. The primary end...

10.1200/jco.21.00662 article EN cc-by-nc-nd Journal of Clinical Oncology 2021-08-02

These NCCN Guidelines Insights focus on recent updates to the 2015 for Non-Small Cell Lung Cancer (NSCLC). Appropriate targeted therapy is very effective in patients with advanced NSCLC who have specific genetic alterations. Therefore, it important test tumor tissue from determine whether they alterations that make them candidates therapies. describe different testing methods currently available determining 2 most commonly actionable alterations, notably anaplastic lymphoma kinase (ALK) gene...

10.6004/jnccn.2015.0071 article EN Journal of the National Comprehensive Cancer Network 2015-05-01

These NCCN Guidelines Insights focus on recent updates in the 2016 for Non–Small Cell Lung Cancer (NSCLC; Versions 1–4). will discuss new immunotherapeutic agents, such as nivolumab and pembrolizumab, patients with metastatic NSCLC. For update, panel recommends immune checkpoint inhibitors preferred agents (in absence of contraindications) second-line beyond (subsequent) therapy NSCLC (both squamous nonsquamous histologies). Nivolumab pembrolizumab are based improved overall survival rates,...

10.6004/jnccn.2016.0031 article EN Journal of the National Comprehensive Cancer Network 2016-03-01

Approximately 3% to 10% of EGFR (epidermal growth factor receptor) -mutant non-small cell lung cancers (NSCLCs) undergo transformation small-cell cancer (SCLC), but their clinical course is poorly characterized.We retrospectively identified patients with EGFR-mutant SCLC and other high-grade neuroendocrine carcinomas seen at our eight institutions. Demographics, disease features, outcomes were analyzed.We included 67 patients-38 women 29 men; mutations exon 19 deletion (69%), L858R (25%),...

10.1200/jco.18.01585 article EN Journal of Clinical Oncology 2018-12-14

Most patients with non–small cell lung cancer (NSCLC) are diagnosed advanced cancer. These guidelines only include information about stage IV NSCLC. Patients widespread metastatic disease (stage IV) candidates for systemic therapy, clinical trials, and/or palliative treatment. The goal is to identify before initiating aggressive treatment, thus sparing these from unnecessary futile If discovered during surgery, then extensive surgery often aborted. Decisions treatment should be based on...

10.6004/jnccn.2012.0130 article EN Journal of the National Comprehensive Cancer Network 2012-10-01

In approximately 60% of patients with NSCLC who are receiving EGFR tyrosine kinase inhibitors, resistance develops through the acquisition T790M mutation. We aimed to demonstrate that a highly sensitive and quantitative next-generation sequencing analysis mutations from urine plasma specimens is feasible.Short footprint mutation enrichment assays were used interrogate activating in or enrolled TIGER-X (NCT01526928), phase 1/2 clinical study rociletinib previously treated mutant-positive...

10.1016/j.jtho.2016.05.035 article EN cc-by-nc-nd Journal of Thoracic Oncology 2016-07-25

This selection from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) for Non-Small Cell Lung Cancer (NSCLC) focuses on principles of radiation therapy (RT), which include following: (1) general early-stage, locally advanced, and advanced/metastatic NSCLC; (2) target volumes, prescription doses, normal tissue dose constraints advanced/palliative RT; (3) RT simulation, planning, delivery. Treatment recommendations should be made by a multidisciplinary team, including...

10.6004/jnccn.2014.0176 article EN Journal of the National Comprehensive Cancer Network 2014-12-01

Abstract Purpose: A phase I study was conducted to determine safety, clinical efficacy, and antitumor immune responses in patients with advanced non–small cell lung carcinoma (NSCLC) following intratumoral administration of autologous dendritic cells (DC) transduced an adenoviral (Ad) vector expressing the CCL21 gene (Ad-CCL21-DC). We evaluated safety tumor antigen–specific situ vaccination (ClinicalTrials.gov: NCT01574222). Experimental Design: Sixteen stage IIIB/IV NSCLC subjects received...

10.1158/1078-0432.ccr-16-2821 article EN Clinical Cancer Research 2017-05-04

Purpose: Evaluate safety and determine the recommended phase II dose (RP2D) of ensartinib (X-396), a potent anaplastic lymphoma kinase (ALK) tyrosine inhibitor (TKI), evaluate preliminary pharmacokinetics antitumor activity in first-in-human, I/II clinical trial primarily patients with non-small cell lung cancer (NSCLC).Patients Methods: In escalation, was administered at doses 25 to 250 mg once daily advanced solid tumors; expansion, ALK-positive NSCLC were 225 daily. Patients who had...

10.1158/1078-0432.ccr-17-2398 article EN Clinical Cancer Research 2018-03-21

PURPOSE Resistance to immune checkpoint inhibition (ICI) in advanced non–small-cell lung cancer (NSCLC) represents a major unmet need. Combining ICI with vascular endothelial growth factor (VEGF)/VEGF receptor has yielded promising results multiple tumor types. METHODS In this randomized phase II Lung-MAP nonmatch substudy (S1800A), patients ineligible for biomarker-matched NSCLC previously treated and platinum-based chemotherapy progressive disease at least 84 days after initiation of were...

10.1200/jco.22.00912 article EN cc-by-nc-nd Journal of Clinical Oncology 2022-06-03

Despite initial effectiveness of ALK receptor tyrosine kinase inhibitors (TKIs) in patients with ALK+ NSCLC, therapeutic resistance will ultimately develop. Serial tracking genetic alterations detected circulating tumor DNA (ctDNA) can be an informative strategy to identify response and resistance. This study evaluated the utility analyzing ctDNA as a function ensartinib, potent second-generation TKI.Pre-treatment plasma was collected from 76 NSCLC who were TKI-naive or had received prior...

10.1016/j.jtho.2019.08.003 article EN publisher-specific-oa Journal of Thoracic Oncology 2019-08-22
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