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dc.contributor.authorThatcher, Nick
dc.contributor.authorCerny, T
dc.contributor.authorStout, Ronald
dc.contributor.authorAnderson, Heather
dc.contributor.authorBarber, Philip V
dc.contributor.authorWolstenholme, R J
dc.contributor.authorBarnes, P
dc.contributor.authorDeiraniya, A
dc.date.accessioned2010-07-14T15:11:11Z
dc.date.available2010-07-14T15:11:11Z
dc.date.issued1987-11-15
dc.identifier.citationIfosfamide, etoposide, and thoracic irradiation therapy in 163 patients with unresectable small cell lung cancer. 1987, 60 (10):2382-7 Canceren
dc.identifier.issn0008-543X
dc.identifier.pmid2822217
dc.identifier.urihttp://hdl.handle.net/10541/107626
dc.description.abstractOne hundred sixty-three patients with small cell lung cancer were treated with six courses, at 3-week intervals, of ifosfamide (5 g/m2) with mesna and etoposide. Thoracic radiotherapy was delivered to the limited stage (LS) patients. The complete response rate (CR, determined clinically and radiologically) was 76% for the 78 LS patients with a further 14% partial response (PR). The majority of the CRs were confirmed on a follow-up bronchoscopy. The CR rate was 27% for extensive stage (ES) patients with another 38% undergoing a partial response. The median survival for LS patients was 11 months, (16 months for CR confirmed by rebronchoscopy) and 8 months for ES patients. The 2-year actuarial survival for LS patients is 27%, follow-up ranges from 12 months to 30 months with a median of 22 months. Toxicity was not severe for the patient population, of whom only 20% had a good performance status before chemotherapy. Parental antibiotics were required on 4% of all 844 chemotherapy courses and 12% of courses were delayed due to side effects. The majority of responses occurred within the first two courses of chemotherapy and there was a corresponding improvement in the patients' symptoms and performance status. The regimen produced rapid tumor response with corresponding improvement in symptoms without marked toxicity and allowed further treatment development.
dc.language.isoenen
dc.subjectLung Canceren
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshCarcinoma, Small Cell
dc.subject.meshCombined Modality Therapy
dc.subject.meshEtoposide
dc.subject.meshEvaluation Studies as Topic
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshIfosfamide
dc.subject.meshLorazepam
dc.subject.meshLung Neoplasms
dc.subject.meshMale
dc.subject.meshMesna
dc.subject.meshMetoclopramide
dc.subject.meshMiddle Aged
dc.titleIfosfamide, etoposide, and thoracic irradiation therapy in 163 patients with unresectable small cell lung cancer.en
dc.typeArticleen
dc.contributor.departmentCRC Department of Medical Oncology, Christie Hospital & Holt Radium Institute, Manchester, United Kingdom.en
dc.identifier.journalCanceren
html.description.abstractOne hundred sixty-three patients with small cell lung cancer were treated with six courses, at 3-week intervals, of ifosfamide (5 g/m2) with mesna and etoposide. Thoracic radiotherapy was delivered to the limited stage (LS) patients. The complete response rate (CR, determined clinically and radiologically) was 76% for the 78 LS patients with a further 14% partial response (PR). The majority of the CRs were confirmed on a follow-up bronchoscopy. The CR rate was 27% for extensive stage (ES) patients with another 38% undergoing a partial response. The median survival for LS patients was 11 months, (16 months for CR confirmed by rebronchoscopy) and 8 months for ES patients. The 2-year actuarial survival for LS patients is 27%, follow-up ranges from 12 months to 30 months with a median of 22 months. Toxicity was not severe for the patient population, of whom only 20% had a good performance status before chemotherapy. Parental antibiotics were required on 4% of all 844 chemotherapy courses and 12% of courses were delayed due to side effects. The majority of responses occurred within the first two courses of chemotherapy and there was a corresponding improvement in the patients' symptoms and performance status. The regimen produced rapid tumor response with corresponding improvement in symptoms without marked toxicity and allowed further treatment development.


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