
- Oncology NEWS International Vol 5 No 1
- Volume 5
- Issue 1
Vesanoid, First Retinoid to Receive a Cancer Indication,Is Approved for Treatment of APL
NUTLEY, NJ--Vesanoid (treti-noin, all-trans-retinoic acid) has become the first retinoid to receive a cancer treatment indication from the US Food and Drug Administration. The new agent, from Hoffmann-La Roche, is indicated for induction of remission in patients with acute promyelocytic leukemia (APL) who are refractory to or have relapsed from anthracycline chemotherapy, or for whom anthracy-cline chemotherapy is contraindicated.
NUTLEY, NJ--Vesanoid (treti-noin, all-trans-retinoic acid) hasbecome the first retinoid to receive a cancer treatment indicationfrom the US Food and Drug Administration. The new agent, fromHoffmann-La Roche, is indicated for induction of remission inpatients with acute promyelocytic leukemia (APL) who are refractoryto or have relapsed from anthracycline chemotherapy, or for whomanthracy-cline chemotherapy is contraindicated.
Vesanoid is for induction of remission only, and it should befollowed by an accepted form of remission consolidation and/ormaintenance therapy.
In APL patients achieving complete remission, the agent producesan initial maturation of the primitive promye-locytes derivedfrom the leukemic clone, followed by marrow repopulation by normal,polyclonal hematopoietic cells.
In an open-label, uncontrolled study from Memorial Sloan-KetteringCancer Center and two cohorts of compassionate cases treated bymultiple investigators under the auspices of the NCI, completeremissions among previously treated patients ranged from 50% to80%, compared with rates of 30% to 50% previously reported forcytotoxic chemotherapy of APL in relapse.
Median survival for Vesanoid-treated patients ranged from 5.8to 10.8 months, compared with less than 6 months in studies ofcytotoxic chemotherapy.
In clinical trials, about 25% of Vesanoid-treated patients experiencedretinoic acid-APL (RA-APL) syndrome, which is characterized byfever, dyspnea, weight gain, radiographic pulmonary infiltrates,and pleural or pericardial effusions. High-dose steroids givenat the first suspicion of the syndrome appear to reduce morbidityand mortality.
During Vesanoid treatment, about 40% of patients will developrapidly evolving leukocytosis. Patients who present with leukocytosisat diagnosis have an increased risk of a further rapid increasein WBC counts, which is associated with a higher risk of life-threateningcomplications. In these cases, adding full-dose chemotherapy tothe Vesanoid regimen may be recommended.
Vesanoid is teratogenic, and adequate contraception is essentialfor women of childbearing potential.
Articles in this issue
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HCFA Reevaluations May Affect Chemo Administration Cost Codesalmost 30 years ago
Breast Cancer Info Now on Internetalmost 30 years ago
HDC/ABMT Has Benefits in Multiple Myelomaalmost 30 years ago
Clinical Trial to Study MoAb 17-1A as An Adjuvant to Colon Cancer Therapyalmost 30 years ago
Reporting of Study Comparing Casodex, Eulexin Is Questionedalmost 30 years ago
Limits on Tamoxifen Duration Questionedalmost 30 years ago
ACRO Forecasts Radiologist Surplusalmost 30 years ago
Potency Status Before RT, Not Dose, Determines Post-RT Functionalmost 30 years ago
Dr. Klausner Outlines Goals for NCIalmost 30 years ago
Difficulties in Translating Relative Risks Into Absolute RiskNewsletter
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