Capecitabine Initially Concomitant to Radiotherapy Then Perioperatively Administered in Locally Advanced Rectal Cancer

Purpose To evaluate the impact of neoadjuvant capecitabine, concomitant to radiotherapy, followed by capecitabine monotherapy, in operable locally advanced rectal cancer (LARC) by measuring pathologic response and conservative surgery rate, toxicity profile, and disease-free survival (DFS). Methods...

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Published inInternational journal of radiation oncology, biology, physics Vol. 75; no. 2; pp. 421 - 427
Main Authors Zampino, Maria Giulia, M.D, Magni, Elena, M.D, Leonardi, Maria Cristina, M.D, Petazzi, Elena, M.D, Santoro, Luigi, M.Sc, Luca, Fabrizio, M.D, Chiappa, Antonio, M.D, Petralia, Giuseppe, M.D, Trovato, Cristina, M.D, Fazio, Nicola, M.D, Orecchia, Roberto, M.D, Nolè, Franco, M.D, de Braud, Filippo, M.D
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.10.2009
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Summary:Purpose To evaluate the impact of neoadjuvant capecitabine, concomitant to radiotherapy, followed by capecitabine monotherapy, in operable locally advanced rectal cancer (LARC) by measuring pathologic response and conservative surgery rate, toxicity profile, and disease-free survival (DFS). Methods and Materials From October 2002 to July 2006, a total of 51 patients affected by LARC (T3–T4 or any node positive tumor), received capecitabine (825 mg/m2 , orally, twice daily continuously) concomitant to radiotherapy on the pelvis (50.4 Gy/ 28 fractions), followed by two cycles of capecitabine (1,250 mg/m2 , orally, twice daily, 14 days on 7 days off) up until 2 weeks before surgery. Tailored adjuvant systemic treatment was discussed according to pathologic stage. Results Of 51 patients, (median age 61 years, range 38–82 years; 19 women and 32 men; ECOG performance status 0/1/2: 46/4/1), 50 were evaluable for response: 18% complete pathologic remission; 12% T-downstaging, and 30% N-downstaging. One patient died before surgery from mesenteric stroke. Grade 3 acute toxicities were 2% diarrhea, 8% dermatitis, 2% liver function test elevation, and 2% hand–foot syndrome. Sphincter preservation rates for tumors ≤6 cm from the anal verge were 62% and 80% for the whole population. Median follow up was 43.0 months (range 0.8–68.6 months). Five-years DFS was 85.4% (95% CI = 75.3–95.4%). Conclusions Based on our study results, we conclude that this regimen is well tolerated and active and compares favorably with existing capecitabine-based approaches.
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ISSN:0360-3016
1879-355X
DOI:10.1016/j.ijrobp.2008.11.002