Copenhagen, Denmark
Onsite/Online

ESTRO 2022

Session Item

Monday
May 09
11:40 - 12:40
Room D1
Highlights of Proffered Papers - Latest Clinical Trials
Anna Kirby, United Kingdom;
Ben Slotman, The Netherlands
Proffered Papers
Interdisciplinary
12:20 - 12:30
Total neoadjuvant therapy for Organ Preservation in Rectal Cancer: The CAO/ARO/AIO-16 phase II trial
Cihan Gani, Germany
OC-0833

Abstract

Total neoadjuvant therapy for Organ Preservation in Rectal Cancer: The CAO/ARO/AIO-16 phase II trial
Authors:

Cihan Gani1, Bülent Polat2, Oliver Ott3, Elisabeth Germer4, Alfred Königsrainer5, Andreas Kirschniak6, Stephan Clasen7, Ulrich Grosse8, Markus Diefenhardt9, Michael Bitzer10, Joachim Reibetanz11, Peter Martus12, Michael Flentje2, Rainer Fietkau3, Emmanouil Fokas9, Daniel Zips1, Claus Michael Rödel9

1University Hospital Tübingen, Department of Radiation Oncology, Tübingen, Germany; 2University Hospital Würzburg, Department of Radiation Oncology, Würzburg, Germany; 3University Hospital Erlangen, Department of Radiation Oncology, Erlangen, Germany; 4University Hospital Würzburg, Comprehensive Cancer Center, Würzburg, Germany; 5University Hospital Tübingen, Department of general, visceral and transplant surgery, Tübingen, Germany; 6Kliniken Maria Hilf , Surgical Department, Mönchengladbach, Germany; 7Klinikum am Steinenberg, Institute for Diagnostic and Interventional Radiology, Reutlingen, Germany; 8Spital Thurgau , Radiology, Frauenfeld, Switzerland; 9University Hospital Frankfurt, Department of Radiation Oncology, Frankfurt, Germany; 10University Hospital Tübingen, Department of Gastroenterology, Tübingen, Germany; 11University Hospital Würzburg, Department of general, visceral and transplant surgery, Würzburg, Germany; 12University Hospital Tübingen, Institute for clinical epidemiology and applied biometry, Tübingen, Germany

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Purpose or Objective

Total neoadjuvant therapy (TNT) has recently shown to considerably increase pathological complete response (pCR) rates after surgery. However, data on the impact of TNT on clinical complete response (cCR) rates to facilitate subsequent organ preservation remain limited.

Material and Methods

This multicenter phase II trial assessed the clinical response after long-course radiochemotherapy (50.4 Gy and concomitant 5-FU/Oxaliplatin) followed by three cycles of consolidation chemotherapy with mFOLFOX6. Patients with stage II or III rectal cancer were enrolled. The primary endpoint was cCR rate on day 106 or day 196 (in case of a near CR on d106) after the start of treatment. Secondary endpoints include compliance, toxicity, pathological complete response, and long-term oncologic outcomes.

Results

A total of 93 patients were enrolled, 91 patients were evaluable. Of those 91 patients, 99% received full-dose radiotherapy, 70.3% received full-dose concomitant chemotherapy and 83% received all three cycles of consolidative chemotherapy. Grade III- IV toxicity during TNT was observed in 45% of patients. On day 106, 15% of patients had achieved a cCR and 38% were found to have a near cCR. After re-assessment on day 196, 21 of the 30 (70%) patients with a near cCR on day 106 had further regressed to a cCR. Another two patients underwent local excision after restaging on day 196 and were found to have a pCR. In total 36 of 91 (40%) patients qualified for omission of major surgery after TNT. 

Conclusion

TNT with long-course radiotherapy and consolidative chemotherapy results in high cCR rate in patients with locally advanced rectal cancer. Results for sustained cCR and local regrowth rates require longer follow-up.  

ClinicalTrials.gov Identifier: NCT03561142