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- PMID: 10762745
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Article: A phase II study of ifosfamide, 5-fluorouracil and leucovorin in patients with recurrent nasopharyngeal carcinoma previously treated with platinum chemotherapy
Title | A phase II study of ifosfamide, 5-fluorouracil and leucovorin in patients with recurrent nasopharyngeal carcinoma previously treated with platinum chemotherapy |
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Authors | |
Keywords | 5-Fluorouracil Ifosfamide Leucovorin Nasopharyngeal carcinoma Palliative chemotherapy Recurrence |
Issue Date | 2000 |
Publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/ejca |
Citation | European Journal Of Cancer, 2000, v. 36 n. 6, p. 736-741 How to Cite? |
Abstract | The aim of this study was to evaluate the efficacy and toxicity of ifosfamide, 5-fluorouracil (5-FU) and leucovorin (IFL) as a second-line chemotherapy regimen in patients with recurrent undifferentiated nasopharyngeal carcinoma (NPC) previously treated with platinum/5-FU. Between June 1997 and February 1999, 18 patients were entered into the study. 3 patients had loco-regional recurrence, 12 had distant metastases and 3 had both loco-regional recurrence and distant metastases. All patients had previously received platinum/5-FU as adjuvant or palliative treatments. The IFL regimen consisting of ifosfamide 1.2 g/m2 (with mesna), 5-FU 375 mg/m2 and leucovorin 20 mg/m2 for 5 days and was repeated every 21 days. The dose of ifosfamide was escalated to 1.4 and 1.6 g/m2 in subsequent cycles according to the bone marrow toxicity, and the dose of 5-FU to 450 and 525 mg/m2 according to the severity of mucositis. Patients received a median of 3 cycles of IFL (range: 2-6), with a median total ifosfamide dose of 21 g/m2 (range: 13-46) and a median total 5-FU dose of 6.75 g/m2 (range: 4.1-14.7). The median follow-up was 10 months (range: 4-25). 9 patients (50%) achieved a partial response and 1 patient (6%) achieved a complete response, with an overall response rate of 56% (95% confidence interval (CI): 32-80%). For those patients who responded to IFL, 8 had subsequent disease progression on follow-up, with a median response duration of 7.1 months (95% CI: 5.3-8.9). The median time to progression for all patients was 6.5 months (95% CI: 4.2-8.7). 12 patients are still alive with an estimated 1-year survival probability rate of 51%. Treatments were well tolerated, only 1 patient had grade 3 emesis. None of the patients had grade 3/4 anaemia, leucopenia or thrombocytopenia, although IFL was discontinued in 1 patient because of persisting thrombocytopenia. IFL is an effective second-line regimen in patients with recurrent NPC and is well tolerated with mild toxicity. Combining platinum and IFL in chemonaive patients may further improve the overall response rate and duration and is worth investigating in future trials. Copyright (C) 2000 Elsevier Science Ltd. |
Persistent Identifier | http://hdl.handle.net/10722/150755 |
ISSN | 2023 Impact Factor: 7.6 2023 SCImago Journal Rankings: 2.501 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chua, DTT | en_HK |
dc.contributor.author | Kwong, DLW | en_HK |
dc.contributor.author | Sham, JST | en_HK |
dc.contributor.author | Au, GKH | en_HK |
dc.contributor.author | Choy, D | en_HK |
dc.date.accessioned | 2012-06-26T06:09:56Z | - |
dc.date.available | 2012-06-26T06:09:56Z | - |
dc.date.issued | 2000 | en_HK |
dc.identifier.citation | European Journal Of Cancer, 2000, v. 36 n. 6, p. 736-741 | en_HK |
dc.identifier.issn | 0959-8049 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/150755 | - |
dc.description.abstract | The aim of this study was to evaluate the efficacy and toxicity of ifosfamide, 5-fluorouracil (5-FU) and leucovorin (IFL) as a second-line chemotherapy regimen in patients with recurrent undifferentiated nasopharyngeal carcinoma (NPC) previously treated with platinum/5-FU. Between June 1997 and February 1999, 18 patients were entered into the study. 3 patients had loco-regional recurrence, 12 had distant metastases and 3 had both loco-regional recurrence and distant metastases. All patients had previously received platinum/5-FU as adjuvant or palliative treatments. The IFL regimen consisting of ifosfamide 1.2 g/m2 (with mesna), 5-FU 375 mg/m2 and leucovorin 20 mg/m2 for 5 days and was repeated every 21 days. The dose of ifosfamide was escalated to 1.4 and 1.6 g/m2 in subsequent cycles according to the bone marrow toxicity, and the dose of 5-FU to 450 and 525 mg/m2 according to the severity of mucositis. Patients received a median of 3 cycles of IFL (range: 2-6), with a median total ifosfamide dose of 21 g/m2 (range: 13-46) and a median total 5-FU dose of 6.75 g/m2 (range: 4.1-14.7). The median follow-up was 10 months (range: 4-25). 9 patients (50%) achieved a partial response and 1 patient (6%) achieved a complete response, with an overall response rate of 56% (95% confidence interval (CI): 32-80%). For those patients who responded to IFL, 8 had subsequent disease progression on follow-up, with a median response duration of 7.1 months (95% CI: 5.3-8.9). The median time to progression for all patients was 6.5 months (95% CI: 4.2-8.7). 12 patients are still alive with an estimated 1-year survival probability rate of 51%. Treatments were well tolerated, only 1 patient had grade 3 emesis. None of the patients had grade 3/4 anaemia, leucopenia or thrombocytopenia, although IFL was discontinued in 1 patient because of persisting thrombocytopenia. IFL is an effective second-line regimen in patients with recurrent NPC and is well tolerated with mild toxicity. Combining platinum and IFL in chemonaive patients may further improve the overall response rate and duration and is worth investigating in future trials. Copyright (C) 2000 Elsevier Science Ltd. | en_HK |
dc.language | eng | en_US |
dc.publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/ejca | en_HK |
dc.relation.ispartof | European Journal of Cancer | en_HK |
dc.subject | 5-Fluorouracil | en_HK |
dc.subject | Ifosfamide | en_HK |
dc.subject | Leucovorin | en_HK |
dc.subject | Nasopharyngeal carcinoma | en_HK |
dc.subject | Palliative chemotherapy | en_HK |
dc.subject | Recurrence | en_HK |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols - Therapeutic Use | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Fluorouracil - Administration & Dosage | en_US |
dc.subject.mesh | Follow-Up Studies | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Ifosfamide - Administration & Dosage | en_US |
dc.subject.mesh | Leucovorin - Administration & Dosage | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Nasopharyngeal Neoplasms - Drug Therapy - Radiography | en_US |
dc.subject.mesh | Neoplasm Metastasis | en_US |
dc.subject.mesh | Neoplasm Recurrence, Local - Drug Therapy | en_US |
dc.subject.mesh | Platinum Compounds - Administration & Dosage | en_US |
dc.subject.mesh | Tomography, X-Ray Computed | en_US |
dc.title | A phase II study of ifosfamide, 5-fluorouracil and leucovorin in patients with recurrent nasopharyngeal carcinoma previously treated with platinum chemotherapy | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Chua, DTT: dttchua@hkucc.hku.hk | en_HK |
dc.identifier.email | Kwong, DLW: dlwkwong@hku.hk | en_HK |
dc.identifier.authority | Chua, DTT=rp00415 | en_HK |
dc.identifier.authority | Kwong, DLW=rp00414 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/S0959-8049(00)00008-3 | en_HK |
dc.identifier.pmid | 10762745 | - |
dc.identifier.scopus | eid_2-s2.0-0034106426 | en_HK |
dc.identifier.hkuros | 52957 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0034106426&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 36 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | 736 | en_HK |
dc.identifier.epage | 741 | en_HK |
dc.identifier.isi | WOS:000086811800014 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Chua, DTT=7006773480 | en_HK |
dc.identifier.scopusauthorid | Kwong, DLW=15744231600 | en_HK |
dc.identifier.scopusauthorid | Sham, JST=7101655565 | en_HK |
dc.identifier.scopusauthorid | Au, GKH=7003748615 | en_HK |
dc.identifier.scopusauthorid | Choy, D=7102939127 | en_HK |
dc.identifier.issnl | 0959-8049 | - |