When the world's most influential lymphoma study group speaks, the cancer community listens. At this year's annual meeting of the American Society of Radiation Oncology (ASTRO), that group has spoken: Patients with may be spared additional radiotherapy following chemotherapy if they have
Investigators from the German Hodgkin Study Group (GHSG) presented research that showed that the results of a positron-emission tomography (PET) scan should dictate treatment after the completion of chemotherapy for Hodgkin’s lymphoma. If the scan comes back negative, the Study Group believes that the patient can be spared the additional radiotherapy that would ordinarily follow.
To wit, the only patients who should be considered for radiotherapy after chemotherapy are advanced-stage Hodgkin's patients (III-IV) who have residual disease and come up with a positive PET scan.
This is a significant development since radiotherapy raises the risk of secondary cancer later in life. Any means of reducing that risk without compromising treatment efficacy is always welcome.
You can read a more detailed presentation of the GHSG data at Oncology Report.
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...
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...
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...