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Tolerability and safety of adjuvant chemoradiotherapy with S-1 after limited surgery for T1 or T2 lower rectal cancer.
Tei, Mitsuyoshi; Noura, Shingo; Ohue, Masayuki; Kitakaze, Masatoshi; Takahashi, Hidekazu; Miyoshi, Norikatsu; Uemura, Mamoru; Mizushima, Tsunekazu; Murata, Kohei; Doki, Yuichiro; Eguchi, Hidetoshi.
  • Tei M; Department of Surgery, Osaka Rosai Hospital, 1179-3 Nagasonecho, Kita-ku, Sakai, 591-8025, Japan. mtei@live.jp.
  • Noura S; Department of Surgery, Toyonaka Municipal Hospital, Toyonaka, Japan.
  • Ohue M; Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan.
  • Kitakaze M; Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Suita, Japan.
  • Takahashi H; Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Suita, Japan.
  • Miyoshi N; Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Suita, Japan.
  • Uemura M; Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Suita, Japan.
  • Mizushima T; Department of Surgery, Osaka Rosai Hospital, 1179-3 Nagasonecho, Kita-ku, Sakai, 591-8025, Japan.
  • Murata K; Department of Surgery, Kansai Rosai Hospital, Amagasaki, Japan.
  • Doki Y; Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Suita, Japan.
  • Eguchi H; Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Suita, Japan.
Int J Clin Oncol ; 26(11): 2046-2052, 2021 Nov.
Article en En | MEDLINE | ID: mdl-34318389
ABSTRACT

BACKGROUND:

Chemo-radiotherapy (CRT) after local excision for pT1 with high-risk features or pT2 rectal cancer is recommended as an optional treatment to achieve both curability and maintenance of quality of life. The aim of this study was to evaluate the short-term safety of combining limited surgery with adjuvant CRT for T1 or T2 lower rectal cancer.

METHODS:

This was a multicenter, single-arm, prospective phase II trial. Patients diagnosed with lower rectal or anal canal cancer (clinical T1 or T2 with a maximum diameter of 30 mm and N0 and M0) underwent local excision or endoscopic resection. Patients received CRT with S-1 (tegafur/gimeracil/oteracil) after confirmation of well- or moderately differentiated adenocarcinoma, and negative margins, and/or depth of submucosal invasion ≥ 1000 µm or muscularis propria, and/or positive lymphovascular invasion, and/or tumor budding grade of 2/3. The primary endpoint was relapse-free survival. Secondary endpoints included overall and local relapse-free survival, safety, anal sphincter preservation rate, and anal function.

RESULTS:

Pathological diagnosis was T1 in 36 patients and T2 in 16 patients. Serious complications after surgery were not reported. The CRT completion rate per protocol was 86.5% (45/52). Thirty-two patients developed 54 events of CRT-related adverse events, including only one patient with a grade 3 event (stomatitis). The most common CRT-related adverse event was diarrhea (n = 14). No patients showed deterioration of anal function at 3 years postoperatively.

CONCLUSION:

CRT with S-1 after limited surgery for T1 or T2 lower rectal cancer resulted in a low incidence of toxicities and maintenance of anal function.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias del Recto / Quimioradioterapia Adyuvante Tipo de estudio: Clinical_trials / Guideline / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias del Recto / Quimioradioterapia Adyuvante Tipo de estudio: Clinical_trials / Guideline / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article