Leukemia Society Offers Patient Information on Use of STI-571

Publication
Article
Oncology NEWS InternationalOncology NEWS International Vol 10 No 7
Volume 10
Issue 7

n WHITE PLAINS, NY-The Leukemia & Lymphoma Society has joined in a collaborative partnership with Novartis to educate the public about imatinib mesylate (Gleevec, also known as STI-571), Novartis’ new oral medication approved by the FDA for patients with Philadelphia-chromosome-positive chronic myelogenous leukemia (CML) who have failed interferon therapy.

n WHITE PLAINS, NY—The Leukemia & Lymphoma Society has joined in a collaborative partnership with Novartis to educate the public about imatinib mesylate (Gleevec, also known as STI-571), Novartis’ new oral medication approved by the FDA for patients with Philadelphia-chromosome-positive chronic myelogenous leukemia (CML) who have failed interferon therapy.

The Society’s Information Resource Center (IRC) can be reached directly by calling 1-800-955-4572 from 9 am to 6 pm Eastern Standard Time, or via email at infocenter@leukemia-lymphoma.org.

IRC staff can provide callers with information on CML, imatinib, and the vast array of free patient services programs available nationwide through the Society’s 58 chapters, designed to help patients cope with living with leukemia.

For Medicare and other patients eligible for treatment with imatinib who are concerned about the cost of the drug, the IRC staff has information about the Novartis Patient Assistance Program (PAP), which will help patients assess their own funding resources to determine their eligibility for reimbursement for the cost of the drug.

In selected cases in which sufficient funding is not available, the Novartis PAP will help patients to obtain the drug who might not otherwise be able to do so. For information on Novartis PAP, call 1-877-GLEEVEC (1-877-453-3832).

Newsletter

Stay up to date on recent advances in the multidisciplinary approach to cancer.

Recent Videos
Increasing the use of patient-reported outcomes may ensure that practitioners can fully ascertain the impact of treatment for rare lymphomas.
Retrospective and real-world registry studies may be necessary to guide clinical decision-making for rarer lymphomas with insufficient prospective data.
Ongoing studies seek to evaluate immunotherapy in earlier lines of therapy for patients with early-stage Hodgkin lymphoma.
A paucity of prospective, well-vetted data to guide therapy in patients with rare lymphomas may result in a reliance on expert consensus guidelines.
Both clinicians and patients should have as much information as possible to participate in shared decision-making for CLL care, says Jacob D. Soumerai, MD.
Sequencing different treatments in the first 3 lines of therapy represents a challenge in chronic lymphocytic leukemia, according to Deborah Stephens, DO.
Related Content