Ifosfamide, etoposide, and thoracic irradiation therapy in 163 patients with unresectable small cell lung cancer.
dc.contributor.author | Thatcher, Nick | |
dc.contributor.author | Cerny, T | |
dc.contributor.author | Stout, Ronald | |
dc.contributor.author | Anderson, Heather | |
dc.contributor.author | Barber, Philip V | |
dc.contributor.author | Wolstenholme, R J | |
dc.contributor.author | Barnes, P | |
dc.contributor.author | Deiraniya, A | |
dc.date.accessioned | 2010-07-14T15:11:11Z | |
dc.date.available | 2010-07-14T15:11:11Z | |
dc.date.issued | 1987-11-15 | |
dc.identifier.citation | Ifosfamide, etoposide, and thoracic irradiation therapy in 163 patients with unresectable small cell lung cancer. 1987, 60 (10):2382-7 Cancer | en |
dc.identifier.issn | 0008-543X | |
dc.identifier.pmid | 2822217 | |
dc.identifier.uri | http://hdl.handle.net/10541/107626 | |
dc.description.abstract | One 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.iso | en | en |
dc.subject | Lung Cancer | en |
dc.subject.mesh | Adult | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols | |
dc.subject.mesh | Carcinoma, Small Cell | |
dc.subject.mesh | Combined Modality Therapy | |
dc.subject.mesh | Etoposide | |
dc.subject.mesh | Evaluation Studies as Topic | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Ifosfamide | |
dc.subject.mesh | Lorazepam | |
dc.subject.mesh | Lung Neoplasms | |
dc.subject.mesh | Male | |
dc.subject.mesh | Mesna | |
dc.subject.mesh | Metoclopramide | |
dc.subject.mesh | Middle Aged | |
dc.title | Ifosfamide, etoposide, and thoracic irradiation therapy in 163 patients with unresectable small cell lung cancer. | en |
dc.type | Article | en |
dc.contributor.department | CRC Department of Medical Oncology, Christie Hospital & Holt Radium Institute, Manchester, United Kingdom. | en |
dc.identifier.journal | Cancer | en |
html.description.abstract | One 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. |