FOLFIRI chemotherapy for metastatic colorectal cancer patients
Objectives: 1) To confirm the efficacy of irinotecan plus folinic acid/continuous 5-fluorouracil as bimonthly FOLFIRI regimen in metastatic colorectal cancer patients. Efficacy evaluations will include response rate, duration of response, and survival. 2) To evaluate safety profiles on patients rece...
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th-cmuir.6653943832-21272014-08-30T02:00:30Z FOLFIRI chemotherapy for metastatic colorectal cancer patients Kamnerdsupaphon P. Lorvidhaya V. Chitapanarux I. Tonusin A. Sukthomya V. Objectives: 1) To confirm the efficacy of irinotecan plus folinic acid/continuous 5-fluorouracil as bimonthly FOLFIRI regimen in metastatic colorectal cancer patients. Efficacy evaluations will include response rate, duration of response, and survival. 2) To evaluate safety profiles on patients receiving this combination. Material and Method: Nineteen patients with metastatic colorectal cancer received 180mg/m2 intravenous (iv) day 1 of irinotecan, 200 mg/m2 iv of folinic acid, 400 mg/m2 iv bolus days 1 to 2, 5-fluorouracil (5-FU), and 600 mg/m2 iv 5-FU infusion over 22 hours, days 1 to 2. Treatment was repeated every two weeks and one cycle contained three fortnightly administrations. Sites of disease were liver in nine patients, lungs in three patients, bowels in four patients, lymph nodes in three patients, and peritoneum in two patients. Two patients had >1 metastatic site. Previous treatments included adjuvant chemotherapy in seven cases and front-line chemotherapy for advanced disease in one case. Results: A median of six treatment cycles was completed (range, 2-13 cycles). All patients were assessable for toxicity and 16 patients were evaluable for treatment response. The non-hematological toxicity was mild. Most had grade 1 or 2. Only one patient experienced grade 3 fatigue and anorexia, and discontinued chemotherapy after the second cycle. There were no cases with grade 4 toxicity. Fourteen patients had at least grade 2 alopecia. The most common hematological toxicity was neutropenia. Grade 3 and 4 neutropenia were observed in three and two patients, respectively. There was no case of febrile neutropenia. Based on intention to treat analysis, there were no complete responses (CR), five (26.3%) partial response (PR), and 11 (57.9%) stable disease. With the median follow-up of 6.6 months, the median time to disease progression was 4.7 months and the median survival time was 10.6 months. Conclusion: Bimonthly irinotecan in combination with folinic acid and 5-fluorouracil was active with acceptable toxicities and a prolonged survival time in pretreated colorectal cancer. Additional trials to define the optimal dose and schedule of treatment are justified. 2014-08-30T02:00:30Z 2014-08-30T02:00:30Z 2007 Article 01252208 18041432 JMTHB http://www.scopus.com/inward/record.url?eid=2-s2.0-35848959497&partnerID=40&md5=c00a2c1fe2bf594897777d95f4e77f39 http://www.ncbi.nlm.nih.gov/pubmed/18041432 http://cmuir.cmu.ac.th/handle/6653943832/2127 English |
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Objectives: 1) To confirm the efficacy of irinotecan plus folinic acid/continuous 5-fluorouracil as bimonthly FOLFIRI regimen in metastatic colorectal cancer patients. Efficacy evaluations will include response rate, duration of response, and survival. 2) To evaluate safety profiles on patients receiving this combination. Material and Method: Nineteen patients with metastatic colorectal cancer received 180mg/m2 intravenous (iv) day 1 of irinotecan, 200 mg/m2 iv of folinic acid, 400 mg/m2 iv bolus days 1 to 2, 5-fluorouracil (5-FU), and 600 mg/m2 iv 5-FU infusion over 22 hours, days 1 to 2. Treatment was repeated every two weeks and one cycle contained three fortnightly administrations. Sites of disease were liver in nine patients, lungs in three patients, bowels in four patients, lymph nodes in three patients, and peritoneum in two patients. Two patients had >1 metastatic site. Previous treatments included adjuvant chemotherapy in seven cases and front-line chemotherapy for advanced disease in one case. Results: A median of six treatment cycles was completed (range, 2-13 cycles). All patients were assessable for toxicity and 16 patients were evaluable for treatment response. The non-hematological toxicity was mild. Most had grade 1 or 2. Only one patient experienced grade 3 fatigue and anorexia, and discontinued chemotherapy after the second cycle. There were no cases with grade 4 toxicity. Fourteen patients had at least grade 2 alopecia. The most common hematological toxicity was neutropenia. Grade 3 and 4 neutropenia were observed in three and two patients, respectively. There was no case of febrile neutropenia. Based on intention to treat analysis, there were no complete responses (CR), five (26.3%) partial response (PR), and 11 (57.9%) stable disease. With the median follow-up of 6.6 months, the median time to disease progression was 4.7 months and the median survival time was 10.6 months. Conclusion: Bimonthly irinotecan in combination with folinic acid and 5-fluorouracil was active with acceptable toxicities and a prolonged survival time in pretreated colorectal cancer. Additional trials to define the optimal dose and schedule of treatment are justified. |
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Article |
author |
Kamnerdsupaphon P. Lorvidhaya V. Chitapanarux I. Tonusin A. Sukthomya V. |
spellingShingle |
Kamnerdsupaphon P. Lorvidhaya V. Chitapanarux I. Tonusin A. Sukthomya V. FOLFIRI chemotherapy for metastatic colorectal cancer patients |
author_facet |
Kamnerdsupaphon P. Lorvidhaya V. Chitapanarux I. Tonusin A. Sukthomya V. |
author_sort |
Kamnerdsupaphon P. |
title |
FOLFIRI chemotherapy for metastatic colorectal cancer patients |
title_short |
FOLFIRI chemotherapy for metastatic colorectal cancer patients |
title_full |
FOLFIRI chemotherapy for metastatic colorectal cancer patients |
title_fullStr |
FOLFIRI chemotherapy for metastatic colorectal cancer patients |
title_full_unstemmed |
FOLFIRI chemotherapy for metastatic colorectal cancer patients |
title_sort |
folfiri chemotherapy for metastatic colorectal cancer patients |
publishDate |
2014 |
url |
http://www.scopus.com/inward/record.url?eid=2-s2.0-35848959497&partnerID=40&md5=c00a2c1fe2bf594897777d95f4e77f39 http://www.ncbi.nlm.nih.gov/pubmed/18041432 http://cmuir.cmu.ac.th/handle/6653943832/2127 |
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1681419799961272320 |