The NHS-Galleri trial has and will continue to provide critical insights to refine future MCED studies

Share on facebook
Share on twitter
Share on linkedin
Share on email
Share on print

The NHS-Galleri trial1 presented at ASCO was the largest, prospective, randomized trial of a multicancer early detection test (MCED) to date. The study enrolled approximately 143,000 asymptomatic adults (ages 50-77) and was the first of its kind to assess clinical utility of an MCED test for cancer screening. 

To access this subscriber-only content please log in or subscribe.

If your institution has a site license, log in with IP-login or register for a sponsored account.*
*Not all site licenses are enrolled in sponsored accounts.

Login Subscribe
Bryan Bassig, PhD
Saville Cancer Screening and Prevention Center at Inova Health
Catherine R. Marinac, PhD
Dana-Farber Cancer Institute
Elizabeth K. O'Donnell, MD
Dana-Farber Cancer Institute
Jennifer Keating Litton, MD, MHCM
University of Texas MD Anderson Cancer Center
Kennedy Ng Yao Yi, MBBS
National Cancer Centre Singapore, Duke-NUS Medical School, and Singapore General Hospital’s Division of Population Health and Integrated Care
Kurt Giles, PhD
University of California San Francisco (UCSF) Health
Nima Nabavizadeh, MD
Oregon Health & Science University
Ora K. Gordon, MD
Providence Center for Clinical Genetics and Genomics
Rebecca Kaltman, MD
Saville Cancer Screening and Prevention Center at Inova Health
Shawn Kothari, MD
Northwestern Medicine
Table of Contents

YOU MAY BE INTERESTED IN

The ASCERTAIN-V phase I/II clinical trial, which evaluated the first all-oral regimen of decitabine-cedazuridine plus venetoclax in patients with newly diagnosed acute myeloid leukemia who are ineligible for intensive induction chemotherapy, demonstrated favorable response rates and survival with expected myelosuppressive effects.
Talvey (talquetamab-tgvs), a GPRC5D bispecific antibody, in combination with Darzalez Faspro (daratumumab and hyaluronidase-fihj) with or without pomalidomide demonstrated significant reduction in the risk of disease progression or death of up to 72% and clinically meaningful reduction of up to 53% in the risk of death compared to the standard regimen of Darzalez Faspro, pomalidomide, and dexamethasone in patients with relapsed/refractory multiple myeloma, according to the results of the investigational phase III MonumenTAL-3 study. 
Jaypirca (pirtobrutinib), a non-covalent Bruton tyrosine kinase inhibitor, plus a two-year venetoclax and rituximab regimen versus venetoclax and rituximab in patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma reduced the risk of disease progression or death by 45% (HR=0.55 [95% CI, 0.40-0.75]; p=0.0001), according to the results of the phase III BRUIN CLL-322 trial. The study met its primary endpoint of independent review committee-assessed progression-free survival.
Bryan Bassig, PhD
Saville Cancer Screening and Prevention Center at Inova Health
Catherine R. Marinac, PhD
Dana-Farber Cancer Institute
Elizabeth K. O'Donnell, MD
Dana-Farber Cancer Institute
Jennifer Keating Litton, MD, MHCM
University of Texas MD Anderson Cancer Center
Kennedy Ng Yao Yi, MBBS
National Cancer Centre Singapore, Duke-NUS Medical School, and Singapore General Hospital’s Division of Population Health and Integrated Care
Kurt Giles, PhD
University of California San Francisco (UCSF) Health
Nima Nabavizadeh, MD
Oregon Health & Science University
Ora K. Gordon, MD
Providence Center for Clinical Genetics and Genomics
Rebecca Kaltman, MD
Saville Cancer Screening and Prevention Center at Inova Health
Shawn Kothari, MD
Northwestern Medicine

Never miss an issue!

Get alerts for our award-winning coverage in your inbox.

Login