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Neoadjuvant chemoradiotherapy plus surgery versus active surveillance for oesophageal cancer: a stepped-wedge cluster randomised trial

BACKGROUND: Neoadjuvant chemoradiotherapy (nCRT) plus surgery is a standard treatment for locally advanced oesophageal cancer. With this treatment, 29% of patients have a pathologically complete response in the resection specimen. This provides the rationale for investigating an active surveillance...

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Autores principales: Noordman, Bo Jan, Wijnhoven, Bas P. L., Lagarde, Sjoerd M., Boonstra, Jurjen J., Coene, Peter Paul L. O., Dekker, Jan Willem T., Doukas, Michael, van der Gaast, Ate, Heisterkamp, Joos, Kouwenhoven, Ewout A., Nieuwenhuijzen, Grard A. P., Pierie, Jean-Pierre E. N., Rosman, Camiel, van Sandick, Johanna W., van der Sangen, Maurice J. C., Sosef, Meindert N., Spaander, Manon C. W., Valkema, Roelf, van der Zaag, Edwin S., Steyerberg, Ewout W., van Lanschot, J. Jan B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801846/
https://www.ncbi.nlm.nih.gov/pubmed/29409469
http://dx.doi.org/10.1186/s12885-018-4034-1
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author Noordman, Bo Jan
Wijnhoven, Bas P. L.
Lagarde, Sjoerd M.
Boonstra, Jurjen J.
Coene, Peter Paul L. O.
Dekker, Jan Willem T.
Doukas, Michael
van der Gaast, Ate
Heisterkamp, Joos
Kouwenhoven, Ewout A.
Nieuwenhuijzen, Grard A. P.
Pierie, Jean-Pierre E. N.
Rosman, Camiel
van Sandick, Johanna W.
van der Sangen, Maurice J. C.
Sosef, Meindert N.
Spaander, Manon C. W.
Valkema, Roelf
van der Zaag, Edwin S.
Steyerberg, Ewout W.
van Lanschot, J. Jan B.
author_facet Noordman, Bo Jan
Wijnhoven, Bas P. L.
Lagarde, Sjoerd M.
Boonstra, Jurjen J.
Coene, Peter Paul L. O.
Dekker, Jan Willem T.
Doukas, Michael
van der Gaast, Ate
Heisterkamp, Joos
Kouwenhoven, Ewout A.
Nieuwenhuijzen, Grard A. P.
Pierie, Jean-Pierre E. N.
Rosman, Camiel
van Sandick, Johanna W.
van der Sangen, Maurice J. C.
Sosef, Meindert N.
Spaander, Manon C. W.
Valkema, Roelf
van der Zaag, Edwin S.
Steyerberg, Ewout W.
van Lanschot, J. Jan B.
author_sort Noordman, Bo Jan
collection PubMed
description BACKGROUND: Neoadjuvant chemoradiotherapy (nCRT) plus surgery is a standard treatment for locally advanced oesophageal cancer. With this treatment, 29% of patients have a pathologically complete response in the resection specimen. This provides the rationale for investigating an active surveillance approach. The aim of this study is to assess the (cost-)effectiveness of active surveillance vs. standard oesophagectomy after nCRT for oesophageal cancer. METHODS: This is a phase-III multi-centre, stepped-wedge cluster randomised controlled trial. A total of 300 patients with clinically complete response (cCR, i.e. no local or disseminated disease proven by histology) after nCRT will be randomised to show non-inferiority of active surveillance to standard oesophagectomy (non-inferiority margin 15%, intra-correlation coefficient 0.02, power 80%, 2-sided α 0.05, 12% drop-out). Patients will undergo a first clinical response evaluation (CRE-I) 4–6 weeks after nCRT, consisting of endoscopy with bite-on-bite biopsies of the primary tumour site and other suspected lesions. Clinically complete responders will undergo a second CRE (CRE-II), 6–8 weeks after CRE-I. CRE-II will include 18F–FDG-PET-CT, followed by endoscopy with bite-on-bite biopsies and ultra-endosonography plus fine needle aspiration of suspected lymph nodes and/or PET- positive lesions. Patients with cCR at CRE-II will be assigned to oesophagectomy (first phase) or active surveillance (second phase of the study). The duration of the first phase is determined randomly over the 12 centres, i.e., stepped-wedge cluster design. Patients in the active surveillance arm will undergo diagnostic evaluations similar to CRE-II at 6/9/12/16/20/24/30/36/48 and 60 months after nCRT. In this arm, oesophagectomy will be offered only to patients in whom locoregional regrowth is highly suspected or proven, without distant dissemination. The main study parameter is overall survival; secondary endpoints include percentage of patients who do not undergo surgery, quality of life, clinical irresectability (cT4b) rate, radical resection rate, postoperative complications, progression-free survival, distant dissemination rate, and cost-effectiveness. We hypothesise that active surveillance leads to non-inferior survival, improved quality of life and a reduction in costs, compared to standard oesophagectomy. DISCUSSION: If active surveillance and surgery as needed after nCRT leads to non-inferior survival compared to standard oesophagectomy, this organ-sparing approach can be implemented as a standard of care.
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spelling pubmed-58018462018-02-14 Neoadjuvant chemoradiotherapy plus surgery versus active surveillance for oesophageal cancer: a stepped-wedge cluster randomised trial Noordman, Bo Jan Wijnhoven, Bas P. L. Lagarde, Sjoerd M. Boonstra, Jurjen J. Coene, Peter Paul L. O. Dekker, Jan Willem T. Doukas, Michael van der Gaast, Ate Heisterkamp, Joos Kouwenhoven, Ewout A. Nieuwenhuijzen, Grard A. P. Pierie, Jean-Pierre E. N. Rosman, Camiel van Sandick, Johanna W. van der Sangen, Maurice J. C. Sosef, Meindert N. Spaander, Manon C. W. Valkema, Roelf van der Zaag, Edwin S. Steyerberg, Ewout W. van Lanschot, J. Jan B. BMC Cancer Study Protocol BACKGROUND: Neoadjuvant chemoradiotherapy (nCRT) plus surgery is a standard treatment for locally advanced oesophageal cancer. With this treatment, 29% of patients have a pathologically complete response in the resection specimen. This provides the rationale for investigating an active surveillance approach. The aim of this study is to assess the (cost-)effectiveness of active surveillance vs. standard oesophagectomy after nCRT for oesophageal cancer. METHODS: This is a phase-III multi-centre, stepped-wedge cluster randomised controlled trial. A total of 300 patients with clinically complete response (cCR, i.e. no local or disseminated disease proven by histology) after nCRT will be randomised to show non-inferiority of active surveillance to standard oesophagectomy (non-inferiority margin 15%, intra-correlation coefficient 0.02, power 80%, 2-sided α 0.05, 12% drop-out). Patients will undergo a first clinical response evaluation (CRE-I) 4–6 weeks after nCRT, consisting of endoscopy with bite-on-bite biopsies of the primary tumour site and other suspected lesions. Clinically complete responders will undergo a second CRE (CRE-II), 6–8 weeks after CRE-I. CRE-II will include 18F–FDG-PET-CT, followed by endoscopy with bite-on-bite biopsies and ultra-endosonography plus fine needle aspiration of suspected lymph nodes and/or PET- positive lesions. Patients with cCR at CRE-II will be assigned to oesophagectomy (first phase) or active surveillance (second phase of the study). The duration of the first phase is determined randomly over the 12 centres, i.e., stepped-wedge cluster design. Patients in the active surveillance arm will undergo diagnostic evaluations similar to CRE-II at 6/9/12/16/20/24/30/36/48 and 60 months after nCRT. In this arm, oesophagectomy will be offered only to patients in whom locoregional regrowth is highly suspected or proven, without distant dissemination. The main study parameter is overall survival; secondary endpoints include percentage of patients who do not undergo surgery, quality of life, clinical irresectability (cT4b) rate, radical resection rate, postoperative complications, progression-free survival, distant dissemination rate, and cost-effectiveness. We hypothesise that active surveillance leads to non-inferior survival, improved quality of life and a reduction in costs, compared to standard oesophagectomy. DISCUSSION: If active surveillance and surgery as needed after nCRT leads to non-inferior survival compared to standard oesophagectomy, this organ-sparing approach can be implemented as a standard of care. BioMed Central 2018-02-06 /pmc/articles/PMC5801846/ /pubmed/29409469 http://dx.doi.org/10.1186/s12885-018-4034-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Noordman, Bo Jan
Wijnhoven, Bas P. L.
Lagarde, Sjoerd M.
Boonstra, Jurjen J.
Coene, Peter Paul L. O.
Dekker, Jan Willem T.
Doukas, Michael
van der Gaast, Ate
Heisterkamp, Joos
Kouwenhoven, Ewout A.
Nieuwenhuijzen, Grard A. P.
Pierie, Jean-Pierre E. N.
Rosman, Camiel
van Sandick, Johanna W.
van der Sangen, Maurice J. C.
Sosef, Meindert N.
Spaander, Manon C. W.
Valkema, Roelf
van der Zaag, Edwin S.
Steyerberg, Ewout W.
van Lanschot, J. Jan B.
Neoadjuvant chemoradiotherapy plus surgery versus active surveillance for oesophageal cancer: a stepped-wedge cluster randomised trial
title Neoadjuvant chemoradiotherapy plus surgery versus active surveillance for oesophageal cancer: a stepped-wedge cluster randomised trial
title_full Neoadjuvant chemoradiotherapy plus surgery versus active surveillance for oesophageal cancer: a stepped-wedge cluster randomised trial
title_fullStr Neoadjuvant chemoradiotherapy plus surgery versus active surveillance for oesophageal cancer: a stepped-wedge cluster randomised trial
title_full_unstemmed Neoadjuvant chemoradiotherapy plus surgery versus active surveillance for oesophageal cancer: a stepped-wedge cluster randomised trial
title_short Neoadjuvant chemoradiotherapy plus surgery versus active surveillance for oesophageal cancer: a stepped-wedge cluster randomised trial
title_sort neoadjuvant chemoradiotherapy plus surgery versus active surveillance for oesophageal cancer: a stepped-wedge cluster randomised trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801846/
https://www.ncbi.nlm.nih.gov/pubmed/29409469
http://dx.doi.org/10.1186/s12885-018-4034-1
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