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dc.contributor.authorRustin, G
dc.contributor.authorVan der Burg, M
dc.contributor.authorGriffin, C
dc.contributor.authorGuthrie, D
dc.contributor.authorLamont, A
dc.contributor.authorJayson, Gordon C
dc.contributor.authorKristensen, G
dc.contributor.authorMediola, C
dc.contributor.authorCoens, C
dc.contributor.authorQian, W
dc.contributor.authorParmar, M
dc.contributor.authorSwart, A
dc.date.accessioned2010-11-18T15:55:21Z
dc.date.available2010-11-18T15:55:21Z
dc.date.issued2010-10-02
dc.identifier.citationEarly versus delayed treatment of relapsed ovarian cancer (MRC OV05/EORTC 55955): a randomised trial. 2010, 376 (9747):1155-63 Lanceten
dc.identifier.issn1474-547X
dc.identifier.pmid20888993
dc.identifier.doi10.1016/S0140-6736(10)61268-8
dc.identifier.urihttp://hdl.handle.net/10541/115828
dc.descriptionTumor Markers, Biologicalen
dc.description.abstractBACKGROUND: Serum CA125 concentration often rises several months before clinical or symptomatic relapse in women with ovarian cancer. In the MRC OV05/EORTC 55955 collaborative trial, we aimed to establish the benefits of early treatment on the basis of increased CA125 concentrations compared with delayed treatment on the basis of clinical recurrence. METHODS: Women with ovarian cancer in complete remission after first-line platinum-based chemotherapy and a normal CA125 concentration were registered for this randomised controlled trial. Clinical examination and CA125 measurement were done every 3 months. Patients and investigators were masked to CA125 results, which were monitored by coordinating centres. If CA125 concentration exceeded twice the upper limit of normal, patients were randomly assigned (1:1) by minimisation to early or delayed chemotherapy. Patients and clinical sites were informed of allocation to early treatment, and treatment was started as soon as possible within 28 days of the increased CA125 measurement. Patients assigned to delayed treatment continued masked CA125 measurements, with treatment commencing at clinical or symptomatic relapse. All patients were treated according to standard local practice. The primary outcome was overall survival. Analysis was by intention to treat. This study is registered, ISRCTN87786644. FINDINGS: 1442 patients were registered for the trial, of whom 529 were randomly assigned to treatment groups and were included in our analysis (265 early, 264 delayed). With a median follow-up of 56·9 months (IQR 37·4-81·8) from randomisation and 370 deaths (186 early, 184 delayed), there was no evidence of a difference in overall survival between early and delayed treatment (HR 0·98, 95% CI 0·80-1·20, p=0·85). Median survival from randomisation was 25·7 months (95% CI 23·0-27·9) for patients on early treatment and 27·1 months (22·8-30·9) for those on delayed treatment. INTERPRETATION: Our findings showed no evidence of a survival benefit with early treatment of relapse on the basis of a raised CA125 concentration alone, and therefore the value of routine measurement of CA125 in the follow-up of patients with ovarian cancer who attain a complete response after first-line treatment is not proven. FUNDING: UK Medical Research Council and the European Organisation for Research and Treatment of Cancer.
dc.language.isoenen
dc.subjectAnticancerous Combined Chemotherapy Protocolsen
dc.subjectCancer Recurrenceen
dc.subjectOvarian Canceren
dc.subjectBiological Tumour Markersen
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshCA-125 Antigen
dc.subject.meshCarcinoma
dc.subject.meshDrug Administration Schedule
dc.subject.meshEarly Detection of Cancer
dc.subject.meshEurope
dc.subject.meshEvidence-Based Medicine
dc.subject.meshFemale
dc.subject.meshFollow-Up Studies
dc.subject.meshHumans
dc.subject.meshKaplan-Meiers Estimate
dc.subject.meshMiddle Aged
dc.subject.meshNeoplasm Recurrence, Local
dc.subject.meshOvarian Neoplasms
dc.subject.meshPlatinum Compounds
dc.subject.meshQuality of Life
dc.subject.meshQuestionnaires
dc.subject.meshRussia
dc.subject.meshSouth Africa
dc.subject.meshTime Factors
dc.subject.meshTreatment Outcome
dc.subject.meshTumor Markers, Biological
dc.titleEarly versus delayed treatment of relapsed ovarian cancer (MRC OV05/EORTC 55955): a randomised trial.en
dc.typeArticleen
dc.contributor.departmentMount Vernon Cancer Centre, Northwood, UK.en
dc.identifier.journalLanceten
html.description.abstractBACKGROUND: Serum CA125 concentration often rises several months before clinical or symptomatic relapse in women with ovarian cancer. In the MRC OV05/EORTC 55955 collaborative trial, we aimed to establish the benefits of early treatment on the basis of increased CA125 concentrations compared with delayed treatment on the basis of clinical recurrence. METHODS: Women with ovarian cancer in complete remission after first-line platinum-based chemotherapy and a normal CA125 concentration were registered for this randomised controlled trial. Clinical examination and CA125 measurement were done every 3 months. Patients and investigators were masked to CA125 results, which were monitored by coordinating centres. If CA125 concentration exceeded twice the upper limit of normal, patients were randomly assigned (1:1) by minimisation to early or delayed chemotherapy. Patients and clinical sites were informed of allocation to early treatment, and treatment was started as soon as possible within 28 days of the increased CA125 measurement. Patients assigned to delayed treatment continued masked CA125 measurements, with treatment commencing at clinical or symptomatic relapse. All patients were treated according to standard local practice. The primary outcome was overall survival. Analysis was by intention to treat. This study is registered, ISRCTN87786644. FINDINGS: 1442 patients were registered for the trial, of whom 529 were randomly assigned to treatment groups and were included in our analysis (265 early, 264 delayed). With a median follow-up of 56·9 months (IQR 37·4-81·8) from randomisation and 370 deaths (186 early, 184 delayed), there was no evidence of a difference in overall survival between early and delayed treatment (HR 0·98, 95% CI 0·80-1·20, p=0·85). Median survival from randomisation was 25·7 months (95% CI 23·0-27·9) for patients on early treatment and 27·1 months (22·8-30·9) for those on delayed treatment. INTERPRETATION: Our findings showed no evidence of a survival benefit with early treatment of relapse on the basis of a raised CA125 concentration alone, and therefore the value of routine measurement of CA125 in the follow-up of patients with ovarian cancer who attain a complete response after first-line treatment is not proven. FUNDING: UK Medical Research Council and the European Organisation for Research and Treatment of Cancer.


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