Adjuvant chemotherapy with folinic acid and 5-fluorouracil in patients with locally advanced rectal cancer previously treated by preoperative radiochemotherapy and curative tumor resection |
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Authors: | Bert Hildebrandt Beate Rau Jürgen Löffel Peter Wust Annett Nicolaou Johanna Gellermann Philipp Le Coutre Peter Neuhaus Roland Felix Klaus-Dieter Wernecke Bernd Dörken Hanno Riess |
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Affiliation: | 1. Medizinische Klinik für H?matologie und Onkologie, Charité, Campus Virchow Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany 6. Medizinische Klinik für H?matologie und Onkologie Charite, Campus Virchow Klinikum, D-13344, Berlin, Germany 2. Klinik für Chirurgie und Chirurgische Onkologie, Charité, Campus Berlin-Buch, Lindenberger Weg 80, 13125, Berlin, Germany 3. Klinik für Strahlenheilkunde, Charité, Campus Virchow Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany 4. Klinik für Allgemein-, Viszeral- und Transplantationschirurgie, Charité, Campus Virchow Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany 5. Institut für Medizinische Biometrie, Charité, Campus Mitte, Luisenstrasse 65, 10117, Berlin, Germany
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Abstract: | BACKGROUND AND AIMS: The role of postoperative adjuvant chemotherapy in patients with rectal cancer pretreated by preoperative radiochemotherapy (RCT) and curative surgery is still poorly investigated. PATIENTS AND METHODS: We pooled data from both arms of a phase III trial in which patients with locally advanced (T3/4) rectal cancer were randomized to preoperative RCT alone or combined with pelvic radio-frequency hyperthermia. After surgery, R0-resected patients were scheduled to adjuvant chemotherapy with four monthly courses of 50 mg folinic acid (FA) and gradually escalated 5-fluorouracil (5-FU, 350-500 mg/m2, days 1-5). Reasons preventing initiation of chemotherapy and treatment-related toxicities were evaluated. Patients' characteristics and survival parameters were compared between the treated and untreated patient groups. RESULTS: Out of 93 patients, 73 (79%) started adjuvant chemotherapy, whereas 19 (21%) did not, mostly due to perioperative complications and refusal. Chemotherapy-related toxicities were mild to moderate in most cases, but--together with protracted postoperative complications--prevented the intended dose escalation of 5-FU in 71% of patients. Distant-failure-free (p=0.03) and overall survival (p=0.03) were improved in the chemotherapy group, although there was a negative selection of patients with unfavourable characteristics into the untreated patient group. INTERPRETATION/CONCLUSION: Adjuvant chemotherapy using FA and 5-FU can be safely applied to the majority of patients with rectal cancer pretreated by RCT and surgery. Survival data are not suitable to allow far-reaching conclusions, but are in line with suggestions of a favourable effect of adjuvant chemotherapy in these patients. |
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Keywords: | Rectal neoplasms Chemotherapy Adjuvant Neoadjuvant therapy Colorectal surgery Fluorouracil Randomised control trial Hyperthermia, induced |
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