A novel approach to inoperable or recurrent rectal cancer by chemoembolization. A new arrow in our quiver?
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Roberto Bini1, Simone Comelli2, Renzo Leli1, Giacomo Paolo Vaudano2, Daniele Savio2, Tiziana Viora1, Alfredo Addeo3
1General Surgery Department, SG Bosco Hospital, Turin, Italy
2Interventional Radiology- Neuroradiology Department, SG Bosco Hospital, Turin, Italy
3Oncology Department, Bristol Cancer Center, Bristol, UK
Roberto Bini, email: email@example.com
Keywords: debiri, rectal cancer, chemoembolization, cancer recurrence
Received: November 09, 2015 Accepted: May 20, 2016 Published: June 10, 2016
Purpose: Assess the feasibility, safety and efficacy of TACE with irinotecan loaded micro particles (debiri) for the treatment of locally advanced rectal cancer patients.
Results: We assessed the Edmonton Symptom Assessment System (ESAS). The tool is designed to assess nine common symptoms in cancer patients: pain, tiredness, nausea, depression, anxiety, drowsiness, appetite, wellbeing and shortness of breath. The ESAS score was 7 in 10/12 (83%) patients before treatment and 6 in 2/12 (16.5%) patients. After treatment in 6/12 (50%) patients the score dropped to 3; 3/12 (33%) reported 4, 1/12 (8%) reported 2. All patients experienced local control disease with a degree of citoreduction; in 4 cases (33%) we observed outstanding responses with a dramatic reduction in the tumors size which led us to surgical radical resections.
Materials and methods: We run a prospective mono-institutional study where we recruited, 12 non- consecutive patients with histology confirmation of rectal cancer, inoperable and not treatable due to severe comorbidities, or pelvic recurrence/progression after curative treatment, chemotherapy, radiotherapy and/or surgery. Their performance status (PS) ECOG was 2-3 . Twelve patients (10 male and 2 female) with a median age 71 (range 56-89) were recruited in the study.
Conclusions: The study has met the primary endpoint and showed encouraging activity. Debiri could be a possible option for locally advanced/inoperable or recurred rectal cancer patients. Further trials are warranted to validate this methodic in early stages.
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