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FDA Approves Alectinib for Early-Stage ALK+ NSCLC
FDA Approves Alectinib for Early-Stage ALK+ NSCLC

April 18th 2024

The FDA has approved alectinib for the adjuvant treatment of patients with ALK-positive non-small cell lung cancer with tumors that are least 4 cm or node positive, as detected by an FDA-approved test.

Forging a Path in Thoracic Surgery to Create a Stellar Career
Forging a Path in Thoracic Surgery to Create a Stellar Career

March 25th 2024

Results from a phase 2 trial support the safety and tolerability of VGT-309 in patients with suspected lung cancer who undergo standard-of-care surgical resection.
VGT-309 Helps Visualize Tumors During Robotic-Assisted Lung Cancer Surgery

February 14th 2024

Defining a Space for NRG1 Fusion–Positive Tumors in Lung and GI Cancers
Defining a Space for NRG1 Fusion–Positive Tumors in Lung and GI Cancers

January 17th 2024

New Lung Cancer Treatment Options Combine Neoadjuvant and Adjuvant Therapies
New Lung Cancer Treatment Options Combine Neoadjuvant and Adjuvant Therapies

December 30th 2023

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Equalizing Inequities™ in Multiple Myeloma Care: Shining a Light on Current Barriers and Opportunities for Improved Outcomes

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Breaking Down Biomarkers in Non–Small Cell Lung Cancer: A Case-Based Discussion for the Oncology Nurse

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Go To PER in Chicago

May 31, 2024 - June 2, 2024

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The Top 10 Oncogenic Drivers in NSCLC for 2023: What You Need to Know on Tumor Testing, Targets, and Treatment Strategies to Move the Field Forward

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Expanding the Armamentarium of Actionable Mutations in NSCLC: Uncovering the Potential of CEACAM5 as a Therapeutic Target

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Pathology Implications for CEACAM5 as a Therapeutic Target in Advanced NSCLC

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Medical Crossfire®: What Are Effective Strategies for Onco-Nurses to Improve Outcomes in Patients with Small Cell Lung Cancer?

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Virtual Show Me the Data™: How HER2, HER3, and TROP2 Targeted Strategies Will Impact Evolving Paradigms in NSCLC

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42nd Annual CFS®: Innovative Cancer Therapy for Tomorrow®

November 13-15, 2024

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How CEACAM5 Expression Can Be Measured and Leveraged in NSCLC Care: Current Developments & Future Therapeutic Opportunities

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Medical Crossfire®: Where Are We in the World of ADCs? From HER2 to CEACAM5, TROP2, HER3, CDH6, B7H3, c-MET and Beyond!

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Community Oncology Connections™: Overcoming Barriers to Testing, Trial Access, and Equitable Care in Cancer

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22nd Annual Winter Lung Cancer Conference®

January 31, 2025 - February 2, 2025

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Dialogues With the Surgeon on Integration of Systemic Therapies in Perioperative Settings for NSCLC: Looking at EGFR, ALK, IO, and Beyond…

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Community Practice Connections™: 5th Annual Precision Medicine Symposium – An Illustrated Tumor Board

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p53 Tumor Suppressor Gene Therapy for Cancer

October 1st 1999

Gene therapy has the potential to provide cancer treatments based on novel mechanisms of action with potentially low toxicities. This therapy may provide more effective control of locoregional recurrence in diseases like non–small-cell lung cancer (NSCLC) as well as systemic control of micrometastases. Despite current limitations, retroviral and adenoviral vectors can, in certain circumstances, provide an effective means of delivering therapeutic genes to tumor cells. Although multiple genes are involved in carcinogenesis, mutations of the p53 gene are the most frequent abnormality identified in human tumors. Preclinical studies both in vitro and in vivo have shown that restoring p53 function can induce apoptosis in cancer cells. High levels of p53 expression and DNA-damaging agents like cisplatin (Platinol) and ionizing radiation work synergistically to induce apoptosis in cancer cells. Phase I clinical trials now show that p53 gene replacement therapy using both retroviral and adenoviral vectors is feasible and safe. In addition, p53 gene replacement therapy induces tumor regression in patients with advanced NSCLC and in those with recurrent head and neck cancer. This article describes various gene therapy strategies under investigation, reviews preclinical data that provide a rationale for the gene replacement approach, and discusses the clinical trial data available to date. [ ONCOLOGY 13(Suppl 5):148-154, 1999]