You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 142 No. 10, October 2006 TABLE OF CONTENTS
  Archives
  •  Online Features
  Study
 This Article
 •Full text
 •PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on ISI (5)
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Topic Collections
 •Hematology/ Hematologic Malignancies
 •Leukemias/ Lymphomas
 •Nutritional and Metabolic Disorders
 •Nutrition/ Malnutrition
 •Drug Therapy
 •Adverse Effects
 •Alert me on articles by topic

Dermatologic Adverse Effects of Lenalidomide Therapy for Amyloidosis and Multiple Myeloma

Hans P. Sviggum, BA; Mark D. P. Davis, MD; S. Vincent Rajkumar, MD; Angela Dispenzieri, MD

Arch Dermatol. 2006;142:1298-1302.

Objectives  To examine dermatologic adverse effects of lenalidomide in patients with amyloidosis and multiple myeloma and to determine whether the adverse effects are different when lenalidomide is used alone compared with when it is used in combination with dexamethasone.

Design  Retrospective review of medical records.

Setting  Tertiary referral center.

Patients  Seventy-five patients with multiple myeloma and 23 patients with amyloidosis participating in clinical trials.

Intervention  In the 75 patients with multiple myeloma, lenalidomide was the treatment in 24 and lenalidomide and dexamethasone in 51. In the 23 patients with amyloidosis, lenalidomide was used alone.

Main Outcome Measures  The frequency, type, severity, and time of onset of all skin eruptions that were temporally related to lenalidomide treatment were recorded.

Results  In the patients with amyloidosis treated with lenalidomide, 10 (43%) had rashes. In the patients with multiple myeloma, rashes occurred in 7 (29%) of those receiving lenalidomide alone and in 15 (29%) of those receiving lenalidomide and dexamethasone. The rashes were characterized as morbilliform, urticarial, dermatitic, acneiform, and undefined. Severe rashes required permanent discontinuation of lenalidomide therapy in 2 patients. In 23 patients (72%), rashes occurred in the first month after therapy was initiated; however, delayed-onset rashes occurred in 9 (28%).

Conclusions  The prevalence of dermatologic adverse effects in patients receiving lenalidomide was higher in those with amyloidosis than in those with multiple myeloma. The prevalence of skin eruptions was not diminished by the concurrent use of systemic corticosteroids. Most skin eruptions were mild and did not necessitate withdrawal of lenalidomide therapy.


Author Affiliations: Mayo Medical School, Mayo Clinic College of Medicine (Mr Sviggum), and Department of Dermatology (Dr Davis) and Division of Hematology (Drs Rajkumar and Dispenzieri), Mayo Clinic, Rochester, Minn.



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

The activity of lenalidomide with or without dexamethasone in patients with primary systemic amyloidosis
Dispenzieri et al.
Blood 2007;109:465-470.
ABSTRACT | FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2006 American Medical Association. All Rights Reserved.