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- Publisher Website: 10.1016/j.clon.2007.11.008
- Scopus: eid_2-s2.0-39049165189
- PMID: 18155454
- WOS: WOS:000254160500009
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Article: Efficacy of Combination Chemotherapy with Irinotecan (CPT-11) plus Capecitabine in Patients with Metastatic or Advanced Colorectal Carcinoma - a Dual-centre Phase II Study: the MAC-6
Title | Efficacy of Combination Chemotherapy with Irinotecan (CPT-11) plus Capecitabine in Patients with Metastatic or Advanced Colorectal Carcinoma - a Dual-centre Phase II Study: the MAC-6 |
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Authors | |
Keywords | Capecitabine CPT-11 irinotecan metastatic colorectal cancer |
Issue Date | 2008 |
Publisher | WB Saunders Co Ltd. The Journal's web site is located at http://www.elsevier.com/locate/clon |
Citation | Clinical Oncology, 2008, v. 20 n. 2, p. 168-175 How to Cite? |
Abstract | Aims: A phase II trial was initiated to evaluate the efficacy and toxicity of combination chemotherapy with irinotecan (CPT-11) plus capecitabine in patients with metastatic colorectal cancer. Patients and methods: Patients received a combination of CPT-11 plus capecitabine. CPT-11 was infused intravenously on day 1 every 2 weeks and oral capecitabine was taken twice daily for 5 days every 7 days. Efficacy and toxicities were assessed. Results: Between 2004 and 2005, 43 patients were enrolled. The overall response rate was 51.35%. With a median follow-up of 13 months, the median time to progression was 10 months (95% confidence interval 7.6-12.3 months); the median survival was 15 months (95% confidence interval 13.9-16.9 months). The most common grade 3 haematological and non-haematological toxicities were neutropenia (5.4%), diarrhoea (8.1%) and hand-foot syndrome (2.7%). Conclusions: CPT-11 plus capecitabine with a 14 day cycle showed a comparable response with international phase II data with a 3 weekly regimen and was well tolerated as a first-line palliative chemotherapy in patients with metastatic colorectal cancer. The data should be interpreted with caution due to the limited sample size and should be further confirmed by a phase III randomised trial. © 2007 The Royal College of Radiologists. |
Persistent Identifier | http://hdl.handle.net/10722/83520 |
ISSN | 2023 Impact Factor: 3.2 2023 SCImago Journal Rankings: 0.907 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Choi, CKK | en_HK |
dc.contributor.author | Chan, RTT | en_HK |
dc.contributor.author | Tung, SY | en_HK |
dc.contributor.author | Lui, L | en_HK |
dc.contributor.author | Siu, S | en_HK |
dc.contributor.author | Au, GKH | en_HK |
dc.contributor.author | Ho, JWC | en_HK |
dc.contributor.author | Law, WL | en_HK |
dc.date.accessioned | 2010-09-06T08:42:01Z | - |
dc.date.available | 2010-09-06T08:42:01Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Clinical Oncology, 2008, v. 20 n. 2, p. 168-175 | en_HK |
dc.identifier.issn | 0936-6555 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/83520 | - |
dc.description.abstract | Aims: A phase II trial was initiated to evaluate the efficacy and toxicity of combination chemotherapy with irinotecan (CPT-11) plus capecitabine in patients with metastatic colorectal cancer. Patients and methods: Patients received a combination of CPT-11 plus capecitabine. CPT-11 was infused intravenously on day 1 every 2 weeks and oral capecitabine was taken twice daily for 5 days every 7 days. Efficacy and toxicities were assessed. Results: Between 2004 and 2005, 43 patients were enrolled. The overall response rate was 51.35%. With a median follow-up of 13 months, the median time to progression was 10 months (95% confidence interval 7.6-12.3 months); the median survival was 15 months (95% confidence interval 13.9-16.9 months). The most common grade 3 haematological and non-haematological toxicities were neutropenia (5.4%), diarrhoea (8.1%) and hand-foot syndrome (2.7%). Conclusions: CPT-11 plus capecitabine with a 14 day cycle showed a comparable response with international phase II data with a 3 weekly regimen and was well tolerated as a first-line palliative chemotherapy in patients with metastatic colorectal cancer. The data should be interpreted with caution due to the limited sample size and should be further confirmed by a phase III randomised trial. © 2007 The Royal College of Radiologists. | en_HK |
dc.language | eng | en_HK |
dc.publisher | WB Saunders Co Ltd. The Journal's web site is located at http://www.elsevier.com/locate/clon | en_HK |
dc.relation.ispartof | Clinical Oncology | en_HK |
dc.subject | Capecitabine | en_HK |
dc.subject | CPT-11 | en_HK |
dc.subject | irinotecan | en_HK |
dc.subject | metastatic colorectal cancer | en_HK |
dc.title | Efficacy of Combination Chemotherapy with Irinotecan (CPT-11) plus Capecitabine in Patients with Metastatic or Advanced Colorectal Carcinoma - a Dual-centre Phase II Study: the MAC-6 | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0936-6555&volume=20&issue=2&spage=168&epage=175&date=2008&atitle=Efficacy+of+combination+chemotherapy+with+irinotecan+(CPT-11)+plus+capecitabine+in+patients+with+metastatic+or+advanced+colorectal+carcinoma+-+a+dual-centre+phase+II+study:+the+MAC-6 | en_HK |
dc.identifier.email | Law, WL: lawwl@hkucc.hku.hk | en_HK |
dc.identifier.authority | Law, WL=rp00436 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.clon.2007.11.008 | en_HK |
dc.identifier.pmid | 18155454 | - |
dc.identifier.scopus | eid_2-s2.0-39049165189 | en_HK |
dc.identifier.hkuros | 141229 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-39049165189&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 20 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 168 | en_HK |
dc.identifier.epage | 175 | en_HK |
dc.identifier.isi | WOS:000254160500009 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Choi, CKK=22952868600 | en_HK |
dc.identifier.scopusauthorid | Chan, RTT=8663654400 | en_HK |
dc.identifier.scopusauthorid | Tung, SY=7102858954 | en_HK |
dc.identifier.scopusauthorid | Lui, L=8232203800 | en_HK |
dc.identifier.scopusauthorid | Siu, S=12040146600 | en_HK |
dc.identifier.scopusauthorid | Au, GKH=7003748615 | en_HK |
dc.identifier.scopusauthorid | Ho, JWC=7402649983 | en_HK |
dc.identifier.scopusauthorid | Law, WL=7103147867 | en_HK |
dc.identifier.issnl | 0936-6555 | - |