New phase III trial of Velcade in newly diagnosed myeloma

Publication
Article
Oncology NEWS InternationalOncology NEWS International Vol 16 No 8
Volume 16
Issue 8

Millennium Pharmaceuticals, Inc. has initiated a randomized, multicenter, company-sponsored phase III trial to determine the most effective Velcade (bortezomib)-based combination therapy with approved agents for the treatment of newly diagnosed multiple myeloma patients who are ineligible for stem cell transplantation

CAMBRIDGE, Massachusetts—Millennium Pharmaceuticals, Inc. has initiated a randomized, multicenter, company-sponsored phase III trial to determine the most effective Velcade (bortezomib)-based combination therapy with approved agents for the treatment of newly diagnosed multiple myeloma patients who are ineligible for stem cell transplantation.

The trial, named UPFRONT and conducted primarily at community physician networks nationwide, will compare three Velcade-based therapies. Principal investigator is Ruben Niesvizky, MD, associate professor of medicine, New York-Presbyterian Hospital/Weill Cornell Medical Center. Velcade is currently approved for myeloma patients who have received at least one prior therapy.

UPFRONT will evaluate the safety and efficacy of Velcade and dexamethasone (VD); Velcade, thalidomide (Thalomid), and dexamethasone (VTD); and Velcade, melphalan, and prednisone (VMP). The primary endpoint is progression-free survival, with secondary endpoints including duration of response, overall survival, and overall safety/tolerability. Target enrollment is up to 500 patients, who will be treated for up to 1 year.

UPFRONT has a unique adaptive design, providing the flexibility to modify the therapies (following an interim analysis) should a new standard of care be established. The adaptive design will help ensure that the most effective treatment options are evaluated in the most efficient way, the company said.

For more information, patients and physicians can contact the Millennium Medical Product Information Department at 1-866-835-2233 (1-866-VELCADE). Additional information can also be found at www.velcade.com.

Recent Videos
“Every patient [with multiple myeloma] should be offered CAR T before they’re offered a bispecific, with some rare exceptions,” said Barry Paul, MD.
Barry Paul, MD, listed cilta-cel, anito-cel, and arlo-cel as 3 of the CAR T-cell therapies with the most promising efficacy in patients with multiple myeloma.
Elucidating nonresponses to bispecific T-cell engagers may be an important research consideration in the multiple myeloma field.
Fixed treatment durations with bispecific antibodies followed by observation may help in mitigating infection-related AEs, according to Shebli Atrash, MD.
Shebli Atrash, MD, stated that MRD should be considered carefully as an end point, given potential recurrence despite MRD negativity.
The National ICE-T Conference may inspire future collaboration between community and academic oncologists in the management of different cancers.
Long-term toxicities like infections and secondary primary malignancies remain a concern when sequencing novel agents for those with multiple myeloma.
Management of adverse effects and access to cellular therapies among community oncologists represented key points of discussion in multiple myeloma.
“If you have a [patient in the] fourth or fifth line, [JNJ-5322] could be a valid drug of choice,” said Rakesh Popat, BSc, MBBS, MRCP, FRCPath, PhD.
Earlier treatment with daratumumab may be better tolerated for patients with pretreated MRD-negative multiple myeloma.
Related Content