We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
INTEGRA BIOSCIENCES AG

Download Mobile App




FDA Approves First of its Kind Companion Dx for Lung Cancer Patients

By LabMedica International staff writers
Posted on 02 Nov 2015
The US Food and Drug Administration (FDA) have approved the first complementary diagnostic test to support use of OPDIVO (nivolumab) for non-squamous non-small-cell lung cancer (NSCLC) therapy.

Historically, the one-year overall survival in the second-line treatment of NSCLC has been about 26%. More...
The new test, “PD-L1 IHC 28-8 pharmDx” from Dako Denmark A/S (Glostrup, Denmark), an Agilent Technologies company, is a qualitative immunohistochemical (IHC) assay that can identify PD-L1 expression levels on the surface of NSCLC tumor cells and provide information on the survival benefit of therapy with OPDIVO for patients with non-squamous NSCLC. Dako developed the diagnostic through collaboration with Bristol-Myers Squibb, maker of OPDIVO, an immuno-oncology therapy FDA-approved for treatment of patients with previously treated NSCLC.

Dako’s test was used to assess PD-L1 expression in the Phase-3 CheckMate 057 trial, in which OPDIVO demonstrated superior overall survival in patients with previously treated metastatic non-squamous NSCLC compared to chemotherapy. The FDA on October 9, 2015, expanded the indication for OPDIVO to include previously treated non-squamous NSCLC in addition to the squamous NSCLC indication. PD-L1 IHC 28-8 pharmDx is the first and only diagnostic assay FDA-approved to assess survival benefit associated with OPDIVO. PD-L1 testing is not required for use of OPDIVO, but it may provide additional information for physicians and inform patient dialogue.

"We are excited about Agilent's involvement in these advancements and the potential PD-L1 IHC 28-8 pharmDx has in helping to provide information to oncologists considering OPDIVO for patients with non-squamous NSCLC," said Jacob Thaysen, president, Diagnostics and Genomics Group, Agilent.

"We are proud to announce the recent FDA approval of OPDIVO based upon overall survival in an expanded indication for all appropriate patients with previously treated metastatic NSCLC," added Michael Giordano, senior vice president and head of Development, Oncology, Bristol-Myers Squibb, "Our collaboration with Dako underscores our leadership in cancer innovation and our commitment to advancing research evaluating the potential role of PD-L1 in multiple tumor types."

Related Links:

Dako 
PD-L1 IHC 28-8 pharmDx
Agilent Technologies



Platinum Member
Automated Coagulation Analyzer
Hemolumi H6
Gold Member
Platelet Function Analyzer
PL-12
Platinum Member
Integrated Biochemical & Immunological System
Biolumi CX Solution X10+C10
New
Gold Member
Serum Indices Control
Acusera Serum Indices Control
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Clinical Chemistry

view channel
Image: Researchers from the Department of Chemistry at Aarhus University have developed and tested a new technology that can identify and measure the concentration of pharmaceuticals in under 10 minutes. Today, this process takes up to an hour. That is critical waiting time for patients suffering from a stroke. (Image Credit: Aarhus University)

Point-of-Care Blood Test Could Speed Treatment Decisions in Acute Stroke

Minutes can shape treatment decisions in emergency stroke care, particularly when physicians need to know whether a patient is taking anticoagulants before administering clot-dissolving therapy.... Read more

Microbiology

view channel
Image: The clearance also broadens QIAstat-Dx\'s infectious disease testing menu in the U.S., which already includes panels for respiratory and gastrointestinal infections, as well as meningitis and encephalitis (Photo courtesy of Qiagen)

One-Hour Molecular Panel Expands Bloodstream Infection Testing for Gram-Negative Pathogens

Bloodstream infections can progress rapidly and lead to sepsis, organ failure, and death. In the United States, about 1.7 million adults develop sepsis each year, and at least 350,000 die during hospitalization... Read more

Industry

view channel
Image

Collaboration Combines AI Cognitive Assessment and RNA Blood Testing for Earlier Alzheimer’s Detection

Alzheimer’s disease is often identified only after substantial neurodegeneration, partly because current diagnostic pathways are fragmented and difficult to scale. As treatment shifts toward earlier intervention,... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.