Adcetris Performs Well Against Anaplastic Large Cell Lymphoma

Phase II clinical trial results of Seattle Genetics' antibody drug conjugate Adcetris (brentuximab vedotin) have been published in the Journal of Clinical Oncology and indicate good things about the breakthrough lymphoma treatment against a specific subtype, systemic anaplastic large cell lymphoma (ALCL).

Researchers from Philadelphia's Fox Chase Cancer Center carried out a prospective clinical trial evaluating Adcetris in 58 patients diagnosed with ALCL whose disease had proven recurrent after at least one previous therapy.

The primary end point of the study was overall objective response rate.

Patients were given an infusion of Adcetris every three weeks on an outpatient basis, and investigators reported the following:

-- 86 percent achieved an objective response
-- 57 percent achieved a complete remission
-- 29 percent achieved a partial remission

Median duration for overall response was 12.6 months.

Patients reported neutropenia, thrombocytopenia, and peripheral sensory neuropathy.

"Targeted therapy with this CD30-directed antibody-drug conjugate may be an effective treatment for relapsed or refractory systemic ALCL and warrants further studies in front-line therapy," the study authors wrote.

Source: JCO

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