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Total Neoadjuvant Therapy for Rectal Cancer in the CAO/ARO/AIO-12 Randomized Phase 2 Trial: Early Surrogate Endpoints Revisited.
Diefenhardt, Markus; Schlenska-Lange, Anke; Kuhnt, Thomas; Kirste, Simon; Piso, Pompiliu; Bechstein, Wolf O; Hildebrandt, Guido; Ghadimi, Michael; Hofheinz, Ralf-Dieter; Rödel, Claus; Fokas, Emmanouil.
Afiliación
  • Diefenhardt M; Department of Radiotherapy and Oncology, University of Frankfurt, 60596 Frankfurt, Germany.
  • Schlenska-Lange A; Frankfurt Cancer Institute, 60596 Frankfurt, Germany.
  • Kuhnt T; Department of Haematology and Oncology, Barmherzige Brüder Hospital Regensburg, 93049 Regensburg, Germany.
  • Kirste S; Department of Radiation Oncology, University Hospital Leipzig, 04103 Leipzig, Germany.
  • Piso P; Department of Radiation Oncology, Faculty of Medicine, Medical Center University of Freiburg, 79098 Freiburg, Germany.
  • Bechstein WO; German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), Partner Site: Freiburg, 69120 Heidelberg, Germany.
  • Hildebrandt G; Department of General and Visceral Surgery, Barmherzige Brüder Hospital, 93049 Regensburg, Germany.
  • Ghadimi M; Department of General and Visceral Surgery, University of Frankfurt, 60596 Frankfurt, Germany.
  • Hofheinz RD; Department of Radiotherapy, University of Rostock, 18051 Rostock, Germany.
  • Rödel C; Department of General and Visceral Surgery, University Medical Center Göttingen, 37075 Göttingen, Germany.
  • Fokas E; Department of Medical Oncology, University Hospital Mannheim, 68167 Mannheim, Germany.
Cancers (Basel) ; 14(15)2022 Jul 27.
Article en En | MEDLINE | ID: mdl-35954320
BACKGROUND: Early efficacy outcome measures in rectal cancer after total neoadjuvant treatment are increasingly investigated. We examined the prognostic role of pathological complete response (pCR), tumor regression grading (TRG) and neoadjuvant rectal (NAR) score for disease-free survival (DFS) in patients with rectal carcinoma treated within the CAO/ARO/AIO-12 randomized phase 2 trial. METHODS: Distribution of pCR, TRG and NAR score was analyzed using the Pearson's chi-squared test. Univariable analyses were performed using the log-rank test, stratified by treatment arm. Discrimination ability of non-pCR for DFS was assessed by analyzing the ROC curve as a function of time. RESULTS: Of the 311 patients enrolled, 306 patients were evaluable (Arm A:156, Arm B:150). After a median follow-up of 43 months, the 3-year DFS was 73% in both groups (HR, 0.95, 95% CI, 0.63-1.45, p = 0.82). pCR tended to be higher in Arm B (17% vs. 25%, p = 0.086). In both treatment arms, pCR, TRG and NAR were significant prognostic factors for DFS, whereas survival in subgroups defined by pCR, TRG or NAR did not significantly differ between the treatment arms. The discrimination ability of non-pCR for DFS remained constant over time (C-Index 0.58) but was slightly better in Arm B (0.61 vs. 0.56). CONCLUSION: Although pCR, TRG and NAR were strong prognostic factors for DFS in the CAO/ARO/AIO-12 trial, their value in selecting one TNT approach over another could not be confirmed. Hence, the conclusion of a long-term survival benefit of one treatment arm based on early surrogate endpoints should be stated with caution.
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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies Idioma: En Revista: Cancers (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies Idioma: En Revista: Cancers (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Alemania