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Urinary toxicity after salvage re-irradiation for prostate cancer local failure after definitive radiotherapy: a clinical and dosimetric prognostic factors analysis.
Dipasquale, Giovanna; Zilli, Thomas; Fiorino, Claudio; Achard, Vérane; Rouzaud, Michel; Miralbell, Raymond.
Afiliação
  • Dipasquale G; Division of Radiation Oncology, Geneva University Hospital, Geneva, Switzerland.
  • Zilli T; Division of Radiation Oncology, Geneva University Hospital, Geneva, Switzerland, Geneva University Faculty of Medicine, Geneva Switzerland.
  • Fiorino C; Medical Physics San Raffaele Scientific Institute, Milan, Italy.
  • Achard V; Division of Radiation Oncology, Geneva University Hospital, Geneva, Switzerland, Geneva University Faculty of Medicine, Geneva, Switzerland.
  • Rouzaud M; Division of Radiation Oncology, Geneva University Hospital, Geneva, Switzerland.
  • Miralbell R; Geneva University Faculty of Medicine, Geneva, Switzerland.
J Contemp Brachytherapy ; 14(3): 222-226, 2022 Jun.
Article em En | MEDLINE | ID: mdl-36199992
ABSTRACT

Purpose:

Predictors of long-term toxicity after prostate cancer re-irradiation are scarce. In this study, we retrospectively assessed the impact of clinical/dosimetric data on late genitourinary (GU) toxicity on fourteen radio-recurrent prostate cancer patients treated with salvage radiotherapy (RT). Material and

methods:

To identify dose parameters and clinical factors potentially associated to severe long-term GU toxicity, study population was stratified in two groups according to toxicity, including one low-grade group (grade ≤ 2, n = 6) and one high-grade group (grade ≥ 3, n = 8). Dose prescription at primary and salvage-RT in 2 Gy equivalent dose (EQD2Gy) per fraction, treatment techniques, and clinical factors potentially associated to severe GU toxicity were analyzed.

Results:

At salvage-RT, the median EQD2Gy α/ß = 3 Gy was significantly higher in the high-toxicity group (85 Gy, range, 71-85 Gy) compared to the low-toxicity group (77 Gy, range, 61-85 Gy) (p = 0.01). All patients treated using salvage-RT with a brachytherapy (BT) boost and with a baseline Framingham risk-score of > 20% (n = 8) developed severe GU toxicity, while none of the remaining patients developed a grade 3 or more GU toxicity (p = 0.0003). V70 > 0 and V75 > 0 of the primary treatment were associated with an increased rate of toxicity.

Conclusions:

Our analysis shows that the delivery of doses up to 75-80 Gy (EQD2Gy, α/ß = 3 Gy) in salvage-RT can be safe in terms of severe GU toxicity avoidance. Furthermore, concomitant cardiovascular comorbidities seem to increase the risk to develop severe GU toxicity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Contemp Brachytherapy Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Contemp Brachytherapy Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suíça