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. 135 No. 10, October 1999 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 (11)
 •Contact me when this article is cited
 Related Content
 •Related article
 •Similar articles in this journal
 Topic Collections
 •Prognosis/ Outcomes
 •Hematology/ Hematologic Malignancies
 •Leukemias/ Lymphomas
 •Immunologic Disorders
 •Alert me on articles by topic

Tumor Burden Index as a Prognostic Tool for Cutaneous T-Cell Lymphoma

A New Concept

Monika Hess Schmid, MD; Patricia Bird, MD; Reinhard Dummer, MD; Werner Kempf, MD; Günter Burg, MD

Arch Dermatol. 1999;135:1204-1208.

Objectives  To introduce a prognostic tool for cutaneous T-cell lymphoma that takes into account the tumor burden and to compare the prognostic value of this tumor burden index (TBI) with that of other prognostic factors.

Design  Retrospective clinical and statistical study.

Patients  One hundred sixteen patients with cutaneous T-cell lymphoma.

Methods  A TBI was designed that takes into account the types, numbers, and severity of skin lesions with the use of the Cox proportional hazard model.

Results  Models of the TBI were developed to test the relative contributions of patches, plaques, and tumors to the total tumor burden and, hence, survival time. Weighting factors reflecting the severity of each skin lesion were tested and incorporated. The best prognostic correlation was a dichotomized index with the following formula: TBI=1+(patchesx2)+(plaquesx2)+(tumorx1.3), where the patches factor equals 0 if 30% or less of the skin area is involved and 1 if greater than 30% of the skin area is involved and where the plaque or tumor factor equals 1 if plaques or tumors are present. Both the TBI and TNM provided predictive information. Discrimination of survival curves and significance of differences was better for TBI (P<.001) than for TNM (P=.009). Sex was also statistically related to survival (males had a better prognosis; P<.04), whereas neither age at first symptoms (P=.35) nor age at time of diagnosis (P=.36) was of prognostic value.

Conclusions  The TBI offers a simple prognostic index for the evaluation of cutaneous T-cell lymphoma. It may become a valuable tool for designing therapeutic strategies for patients according to their specific survival expectancies. However, this model is preliminary and has to be validated on a larger number of patients.


From the Department of Dermatology, University Hospital of Zürich, Zürich, Switzerland.


RELATED ARTICLE

Archives of Dermatology Reader's Choice: Continuing Medical Education
Arch Dermatol. 1999;135(10):1282-1283.
FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Vaccination of patients with cutaneous T-cell lymphoma using intranodal injection of autologous tumor-lysate-pulsed dendritic cells
Maier et al.
Blood 2003;102:2338-2344.
ABSTRACT | FULL TEXT  

Long-term Outcome of 525 Patients With Mycosis Fungoides and Sezary Syndrome: Clinical Prognostic Factors and Risk for Disease Progression
Kim et al.
Arch Dermatol 2003;139:857-866.
ABSTRACT | FULL TEXT  

Quantifying Skin Disease Burden in Mycosis Fungoides-Type Cutaneous T-Cell Lymphomas: The Severity-Weighted Assessment Tool (SWAT)
Stevens et al.
Arch Dermatol 2002;138:42-48.
ABSTRACT | FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1999 American Medical Association. All Rights Reserved.