TY - JOUR
T1 - Long-term outcomes for neoadjuvant versus adjuvant chemotherapy in early breast cancer
T2 - meta-analysis of individual patient data from ten randomised trials
AU - Early Breast Cancer Trialists' Collaborative Group (EBCTCG)
AU - Asselain, Bernard
AU - Barlow, William
AU - Bartlett, John
AU - Bergh, Jonas
AU - Bergsten-Nordström, Elizabeth
AU - Bliss, Judith
AU - Boccardo, Francesco
AU - Boddington, Clare
AU - Bogaerts, Jan
AU - Bonadonna, Gianni
AU - Bradley, Rosie
AU - Brain, Etienne
AU - Braybrooke, Jeremy
AU - Broet, Philippe
AU - Bryant, John
AU - Burrett, Julie
AU - Cameron, David
AU - Clarke, Mike
AU - Coates, Alan
AU - Coleman, Robert
AU - Coombes, Raoul Charles
AU - Correa, Candace
AU - Costantino, Joe
AU - Cuzick, Jack
AU - Danforth, David
AU - Davidson, Nancy
AU - Davies, Christina
AU - Davies, Lucy
AU - Di Leo, Angelo
AU - Dodwell, David
AU - Dowsett, Mitch
AU - Duane, Fran
AU - Evans, Vaughan
AU - Ewertz, Marianne
AU - Fisher, Bernard
AU - Forbes, John
AU - Ford, Leslie
AU - Gazet, Jean Claude
AU - Gelber, Richard
AU - Gettins, Lucy
AU - Gianni, Luca
AU - Gnant, Michael
AU - Godwin, Jon
AU - Goldhirsch, Aron
AU - Goodwin, Pamela
AU - Gray, Richard
AU - Hayes, Daniel
AU - Hill, Catherine
AU - Ingle, James
AU - Sparano, Joseph
N1 - Funding Information:
This study is supported by core funding to the Population Health Research Unit and Clinical Trial Service Unit, Nuffield Department of Population Health, University of Oxford, from Cancer Research UK, the British Heart Foundation, and the UK Medical Research Council, as well as by the UK Department of Health grant RRX108 and Cancer Research UK grant C8225/A21133. The chief acknowledgement is to the women in these trials and the trial personnel.
Publisher Copyright:
© 2018 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
PY - 2018/1
Y1 - 2018/1
N2 - Background Neoadjuvant chemotherapy (NACT) for early breast cancer can make breast-conserving surgery more feasible and might be more likely to eradicate micrometastatic disease than might the same chemotherapy given after surgery. We investigated the long-term benefits and risks of NACT and the influence of tumour characteristics on outcome with a collaborative meta-analysis of individual patient data from relevant randomised trials. Methods We obtained information about prerandomisation tumour characteristics, clinical tumour response, surgery, recurrence, and mortality for 4756 women in ten randomised trials in early breast cancer that began before 2005 and compared NACT with the same chemotherapy given postoperatively. Primary outcomes were tumour response, extent of local therapy, local and distant recurrence, breast cancer death, and overall mortality. Analyses by intention-to-treat used standard regression (for response and frequency of breast-conserving therapy) and log-rank methods (for recurrence and mortality). Findings Patients entered the trials from 1983 to 2002 and median follow-up was 9 years (IQR 5–14), with the last follow-up in 2013. Most chemotherapy was anthracycline based (3838 [81%] of 4756 women). More than two thirds (1349 [69%] of 1947) of women allocated NACT had a complete or partial clinical response. Patients allocated NACT had an increased frequency of breast-conserving therapy (1504 [65%] of 2320 treated with NACT vs 1135 [49%] of 2318 treated with adjuvant chemotherapy). NACT was associated with more frequent local recurrence than was adjuvant chemotherapy: the 15 year local recurrence was 21·4% for NACT versus 15·9% for adjuvant chemotherapy (5·5% increase [95% CI 2·4–8·6]; rate ratio 1·37 [95% CI 1·17–1·61]; p=0·0001). No significant difference between NACT and adjuvant chemotherapy was noted for distant recurrence (15 year risk 38·2% for NACT vs 38·0% for adjuvant chemotherapy; rate ratio 1·02 [95% CI 0·92–1·14]; p=0·66), breast cancer mortality (34·4% vs 33·7%; 1·06 [0·95–1·18]; p=0·31), or death from any cause (40·9% vs 41·2%; 1·04 [0·94–1·15]; p=0·45). Interpretation Tumours downsized by NACT might have higher local recurrence after breast-conserving therapy than might tumours of the same dimensions in women who have not received NACT. Strategies to mitigate the increased local recurrence after breast-conserving therapy in tumours downsized by NACT should be considered—eg, careful tumour localisation, detailed pathological assessment, and appropriate radiotherapy. Funding Cancer Research UK, British Heart Foundation, UK Medical Research Council, and UK Department of Health.
AB - Background Neoadjuvant chemotherapy (NACT) for early breast cancer can make breast-conserving surgery more feasible and might be more likely to eradicate micrometastatic disease than might the same chemotherapy given after surgery. We investigated the long-term benefits and risks of NACT and the influence of tumour characteristics on outcome with a collaborative meta-analysis of individual patient data from relevant randomised trials. Methods We obtained information about prerandomisation tumour characteristics, clinical tumour response, surgery, recurrence, and mortality for 4756 women in ten randomised trials in early breast cancer that began before 2005 and compared NACT with the same chemotherapy given postoperatively. Primary outcomes were tumour response, extent of local therapy, local and distant recurrence, breast cancer death, and overall mortality. Analyses by intention-to-treat used standard regression (for response and frequency of breast-conserving therapy) and log-rank methods (for recurrence and mortality). Findings Patients entered the trials from 1983 to 2002 and median follow-up was 9 years (IQR 5–14), with the last follow-up in 2013. Most chemotherapy was anthracycline based (3838 [81%] of 4756 women). More than two thirds (1349 [69%] of 1947) of women allocated NACT had a complete or partial clinical response. Patients allocated NACT had an increased frequency of breast-conserving therapy (1504 [65%] of 2320 treated with NACT vs 1135 [49%] of 2318 treated with adjuvant chemotherapy). NACT was associated with more frequent local recurrence than was adjuvant chemotherapy: the 15 year local recurrence was 21·4% for NACT versus 15·9% for adjuvant chemotherapy (5·5% increase [95% CI 2·4–8·6]; rate ratio 1·37 [95% CI 1·17–1·61]; p=0·0001). No significant difference between NACT and adjuvant chemotherapy was noted for distant recurrence (15 year risk 38·2% for NACT vs 38·0% for adjuvant chemotherapy; rate ratio 1·02 [95% CI 0·92–1·14]; p=0·66), breast cancer mortality (34·4% vs 33·7%; 1·06 [0·95–1·18]; p=0·31), or death from any cause (40·9% vs 41·2%; 1·04 [0·94–1·15]; p=0·45). Interpretation Tumours downsized by NACT might have higher local recurrence after breast-conserving therapy than might tumours of the same dimensions in women who have not received NACT. Strategies to mitigate the increased local recurrence after breast-conserving therapy in tumours downsized by NACT should be considered—eg, careful tumour localisation, detailed pathological assessment, and appropriate radiotherapy. Funding Cancer Research UK, British Heart Foundation, UK Medical Research Council, and UK Department of Health.
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U2 - 10.1016/S1470-2045(17)30777-5
DO - 10.1016/S1470-2045(17)30777-5
M3 - Article
C2 - 29242041
AN - SCOPUS:85037727699
SN - 1470-2045
VL - 19
SP - 27
EP - 39
JO - The Lancet Oncology
JF - The Lancet Oncology
IS - 1
ER -