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Total skin electron beam therapy for cutaneous T-cell lymphomas in the Netherlands: A retrospective analysis of treatment outcomes and selection for high or low dose schedule.
Smits, K; Quint, K D; Vermeer, M H; Daniëls, L A; Willemze, R; Jansen, P M; Jansen, W P A; Neelis, K J.
Afiliación
  • Smits K; Department of Radiotherapy, Leiden University Medical Center, Leiden, the Netherlands.
  • Quint KD; Department of Dermatology, Leiden University Medical Center, Leiden, the Netherlands.
  • Vermeer MH; Department of Dermatology, Leiden University Medical Center, Leiden, the Netherlands.
  • Daniëls LA; Department of Radiotherapy, Amsterdam University Medical Centre, Amsterdam, the Netherlands.
  • Willemze R; Department of Dermatology, Leiden University Medical Center, Leiden, the Netherlands.
  • Jansen PM; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
  • Jansen WPA; Radiotherapiegroep, Arnhem, the Netherlands.
  • Neelis KJ; Department of Radiotherapy, Leiden University Medical Center, Leiden, the Netherlands.
Clin Transl Radiat Oncol ; 33: 77-82, 2022 Mar.
Article en En | MEDLINE | ID: mdl-35106383
ABSTRACT

PURPOSE:

Total skin electron beam therapy (TSEBT) is used mostly in the treatment of cutaneous T cell lymphoma. In this study we describe the results of TSEBT applied in the Netherlands using two different schedules, a conventional dose schedule of 35 Gy and a low-dose schedule of 12 Gy. We aimed to evaluate the treatment results in and compare treatment outcomes between the two treatment groups and to further define indications for both doses.

METHODS:

In the LUMC, Leiden, we performed a retrospective analysis of 51 patients treated with TSEBT between January 2008 and December 2018, with follow-up untill December 2019. Thirty one patients were treated with 35 Gy and twenty with 12 Gy. The dose was chosen based on the severity of skin involvement. Outcome measures were time to meaningful progression, survival, response rate and toxicity.

RESULTS:

Time to meaningful progression was 5.1 months with no significant differences between dose groups (P = 0.77). Overall survival was 27.4 months. Both time to progression and survival were significantly better for T2 vs T3 stage. Overall response rate was 80.4 %. Both dose groups showed improvement of symptoms. Treatment was generally well tolerated.

CONCLUSIONS:

Both high-dose and low-dose TSEBT offer similar results for TMP and OS. It remains unclear which patients benefit most from a high-dose schedule. We propose to use the low-dose schedule as a standard for TSEBT and use supplementary boosts or escalation to high-dose treatment for patients unresponsive to the low-dose schedule.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Transl Radiat Oncol Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Transl Radiat Oncol Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos
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