Replacing Vincristine with Velcade Looks Good Against Mantle Cell Lymphoma

Changing R-CHOP improved outcomes in patients with mantle cell lymphoma (MCL), according to a new study presented at at the annual meeting of the American Society of Clinical Oncology.

Dr. Franco Cavalli of the Oncology Institute of Southern Switzerland and colleagues conducted the LYM-3002 trial, a randomized, open label phase III study in 487 patients with newly diagnosed MCL who are not eligible for a bone marrow transplant.

The patients received the VR-CAP regimen, a combination of rituximab, doxorubicin, bortezomib (Velcade), cyclophosphamide, and prednisone, or the standard R-CHOP. Patients in the first arm experienced better progression-free survival than patients treated with R-CHOP.

The only difference between the regimens is that VR-CAP uses Velcade in place of vincristine in R-CHOP.

At a median follow-up of 40 months, median progression-free survival was 24.7 months in the Velcade group compared to 14.4 months in the R-CHOP group.

"[The VR-CAP regimen] could be considered a new standard of care for newly diagnosed MCL patients not considered for intensive treatment and bone marrow transplant," said Cavalli.

Source: Oncologypractice

More Articles

More Articles

Amazon.com is pleased to have the Lymphoma Information Network in the family of Amazon.com associates. We've agreed to ship items...

The question ought to be what are myelodysplastic syndromes (MDS), since this is a group of similar blood and bone marrow diseases that...

Merkel Cell Carcinoma (MCC) is a very rare and aggressive skin cancer that usually develops when a person is in his or her 70s. It is...

Radiation Therapy Topics

...

At some point, the Seattle biotech company Cell Therapeutics Inc (CTI) should earn an entry in the Guinness Book of World Records for utter and...

Site Beginnings

This site was started as Lymphoma Resource Page(s) in 1994. The site was designed to collect lymphoma...

Three papers appearing in the journal Blood and pointing towards a regulator-suppressor pill could offer hope to blood cancer...

The US Food and Drug Administration (FDA) has granted a third so-called Breakthrough Therapy Designation for the investigational oral...

The US Food and Drug Administration today has approved an expanded use of Imbruvica (ibrutinib) in patients with...

The U.S. Food and Drug Administration has announced that it has granted "Breakthrough Therapy Designation" for the investigational agent...

According to a new study published in the Proceedings of the National Academy of Sciences, a team from the University of California, San...

Pharmacyclics has announced that the company has submitted a New Drug Application (NDA) to the US Food and Drug Administration (FDA) for...

New research suggests that frontline radioimmunotherapy...

Gilead Sciences has announced results of the company's Phase II study of its investigational compound idelalisib, an oral inhibitor of...

Sitemap