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Clinical advantage and outcomes of computed tomography-based transvaginal hybrid brachytherapy performed only by sedation without general or saddle block anesthesia.
Okonogi, Noriyuki; Murata, Kazutoshi; Matsui, Toshiaki; Iwai, Yuma; Mori, Yasumasa; Kaneko, Takashi; Wakatsuki, Masaru; Tsuji, Hiroshi.
Afiliação
  • Okonogi N; QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.
  • Murata K; QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.
  • Matsui T; QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.
  • Iwai Y; QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.
  • Mori Y; QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.
  • Kaneko T; QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.
  • Wakatsuki M; QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.
  • Tsuji H; QST Hospital, National Institutes for Quantum Science and Technology, Chiba, Japan.
Cancer Rep (Hoboken) ; 5(11): e1607, 2022 11.
Article em En | MEDLINE | ID: mdl-35229494
BACKGROUND: Three-dimensional image-guided brachytherapy is the standard of care in cervical cancer radiotherapy. In addition, the usefulness of the so-called "hybrid brachytherapy (HBT)" has been reported, which involves the addition of needle applicators to conventional intracavitary brachytherapy for interstitial irradiation. AIM: To evaluate the clinical outcomes of CT-based HBT consisting of transvaginal insertion of needle applicators (CT-based transvaginal HBT) and only intravenous sedation without general or saddle block anesthesia. METHODS AND RESULTS: This is a retrospective chart review of patients who received definitive radiotherapy, including CT-based transvaginal HBT, between February 2012 and July 2019. The inclusion criteria were as follows: (i) histologically diagnosed disease, (ii) untreated cervical cancer, (iii) International Federation of Gynecology and Obstetrics (FIGO) stage IB1-IVA disease in the 2008 FIGO staging system, and (iv) patients who underwent CT-based transvaginal HBT at least once in a series of intracavitary brachytherapy. Overall, 54 patients fulfilled the eligibility criteria in the present study. The median follow-up period was 32 (IQR, 19-44) months. No patient complained of symptoms such as persistent bleeding or abdominal pain after the treatment. The 3-year local control (LC), disease-free survival, and overall survival rates for all 54 patients were 86.6%, 60.3%, and 90.7% (95% CI [81.3%-100.0%]), respectively. The 3-year LC rate was 87.7% in patients with FIGO III-IVA and 90.4% in tumor size >6.0 cm. The incidence rate of late adverse events, grade ≥3, in the rectum and bladder was 0% and 1.8%, respectively. In the dose-volume histogram analyses, transvaginal HBT increased the dose of HR-CTVD90 by ~7.5% without significantly increasing the dose of organs at risk. CONCLUSION: Considering the favorable clinical outcomes, CT-based transvaginal HBT may be a good option for treating cervical cancer.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Braquiterapia / Neoplasias do Colo do Útero / Anestesia Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: Cancer Rep (Hoboken) Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Braquiterapia / Neoplasias do Colo do Útero / Anestesia Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: Cancer Rep (Hoboken) Ano de publicação: 2022 Tipo de documento: Article