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Sequential adjuvant chemotherapy and radiotherapy in endometrial cancer - Results from two randomised studies

Authors :
Högberg, Thomas
Signorelli, Mauro
de Oliveira, Carlos Freire
Fossati, Roldano
Lissoni, Andrea Alberto
Sorbe, Bengt
Andersson, Håkan
Grenman, Seija
Lundgren, Caroline
Rosenberg, Per
Boman, Karin
Tholander, Bengt
Scambia, Giovanni
Reed, Nicholas
Cormio, Gennaro
Tognon, Germana
Clarke, Jackie
Sawicki, Tomasz
Zola, Paolo
Kristensen, Gunnar
Högberg, Thomas
Signorelli, Mauro
de Oliveira, Carlos Freire
Fossati, Roldano
Lissoni, Andrea Alberto
Sorbe, Bengt
Andersson, Håkan
Grenman, Seija
Lundgren, Caroline
Rosenberg, Per
Boman, Karin
Tholander, Bengt
Scambia, Giovanni
Reed, Nicholas
Cormio, Gennaro
Tognon, Germana
Clarke, Jackie
Sawicki, Tomasz
Zola, Paolo
Kristensen, Gunnar
Publication Year :
2010

Abstract

Introduction: Endometrial cancer patients with high grade tumours, deep myometrial invasion or advanced stage disease have a poor prognosis. Randomised studies have demonstrated the prevention of loco-regional relapses with radiotherapy (RT) with no effect on overall survival (OS). The possible additive effect of chemotherapy (CT) remains unclear. Two randomised clinical trials (NSGO-EC-9501/EORTC-55991 and MaNGO ILIADE-III) were undertaken to clarify if sequential combination of chemotherapy and radiotherapy improves progression-free survival (PFS) in high-risk endometrial cancer. The two studies were pooled. Methods: Patients (n = 540; 534 evaluable) with operated endometrial cancer International Federation of Obstetrics and Gynaecology (FIGO) stage I-III with no residual tumour andprognostic factors implying high-risk were randomly allocated to adjuvant radiotherapy with or without sequential chemotherapy. Results: In the NSGO/EORTC study, the combined modality treatment was associated with 36% reduction in the risk for relapse or death (hazard ratio (HR) 0.64, 95% confidence interval (CI) 0.41-0.99; P = 0.04); two-sided tests were used. The result from the Gynaecologic Oncology group at the Mario Negri Institute (MaNGO)-study pointed in the same direction (HR 0.61), but was not significant. In the combined analysis, the estimate of risk for relapse or death was similar but with narrower confidence limits (HR 0.63, CI 0.44 0.89; P = 0.009). Neither study showed significant differences in the overall survival. In the combined analysis, overall survival approached statistical significance (HR 0.69, CI 0.46-1.03; P = 0.07) and cancer-specific survival (CSS) was significant (HR 0.55, CI 0.35-0.88; P = 0.01). Conclusion: Addition of adjuvant chemotherapy to radiation improves progression-free survival in operated endometrial cancer patients with no residual tumour and a high-risk profile. A remaining question for future studies is if addition of radiotherapy to chemot

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1235104344
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1016.j.ejca.2010.06.002