CD30+ Cutaneous T Cell Lymphoma: Response to Rotational Total Skin Electron Irradiation
Introduction Rotational total skin electron irradiation (RTSEI) is an effective therapy for cutaneous T cell lymphoma (CTCL). CD30 expression has been identified as a prognostic factor in CTCL. Therefore, we investigated CD30 status, treatment response, and survival in our cohort of patients with CT...
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Veröffentlicht in: | Dermatology and therapy 2016-06, Vol.6 (2), p.251-263 |
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Sprache: | eng |
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Zusammenfassung: | Introduction
Rotational total skin electron irradiation (RTSEI) is an effective therapy for cutaneous T cell lymphoma (CTCL). CD30 expression has been identified as a prognostic factor in CTCL. Therefore, we investigated CD30 status, treatment response, and survival in our cohort of patients with CTCL treated with RTSEI.
Methods
Patients with CTCL treated with RTSEI (≥30 Gy) between 2000 and 2013 at our institution were identified, and clinical and pathologic data were retrospectively reviewed. Primary outcomes were complete clinical response (CCR; >90% reduction of skin disease burden), relapse-free survival (RFS), and overall survival (OS).
Results
Sixty-eight patients with CTCL treated with RTSEI were identified. Median age at diagnosis was 51 years with median follow-up of 61 months. Median OS was 76 months and median RFS was 11 months. Thirteen patients (19%) had CD30+ lymphocytes on initial pathology. In the CD30+ cohort, there were no T2, eight T3, and five T4 cases. In comparison, in the CD30− cohort, there were 18 T2, 29 T3, and 8 T4 cases (
P
= 0.01). Six weeks post-RTSEI, CCR was 85% in CD30+ and 81% in CD30− cases (
P
= 1). Six months post-RTSEI, CCR was 23% in CD30+ and 50% in CD30− cases (
P
= 0.083).
Conclusion
RTSEI resulted in excellent CCR at 6 weeks in our cohort of patients with CTCL, with a median RFS of 11 months. We found CD30+ patients presented with significantly higher T stage at time of RTSEI and trended towards decreased CCR at 6 months post-RTSEI compared with the CD30− group. |
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ISSN: | 2193-8210 2190-9172 |
DOI: | 10.1007/s13555-016-0115-8 |