The safety and efficacy of total mesorectal excision ( TME ) surgery following dose‐escalation: Surgical outcomes from the organ preservation in early rectal adenocarcinoma ( OPERA ) trial, a European multicentre phase 3 randomised trial ( NCT02505750 )
AimNonsurgical treatment with chemoradiotherapy for rectal cancer is gaining interest as it avoids total mesorectal excision (TME) surgery and stoma. The OPERA trial aims to evaluate whether dose escalation with contact X‐ray brachytherapy (CXB) boost improves organ preservation compared to external...
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creator | Sun Myint, Arthur Rao, Christopher Barbet, Nicolas Thamphya, Brice Pace‐Loscos, Tanguy Schiappa, Renaud Magné, Nicolas Martel‐Lafay, Isabelle Mineur, Laurent Deberne, Melanie Zilli, Thomas Dhadda, Amandeep Gerard, Jean Pierre |
description | AimNonsurgical treatment with chemoradiotherapy for rectal cancer is gaining interest as it avoids total mesorectal excision (TME) surgery and stoma. The OPERA trial aims to evaluate whether dose escalation with contact X‐ray brachytherapy (CXB) boost improves organ preservation compared to external beam radiotherapy (EBRT) boost. It has been suggested that dose escalation adversely affects surgical outcomes and therefore we report outcomes following TME in OPERA at 36 months.MethodsOPERA is a European multicentre phase 3 trial (NCT02505750) which randomises patients with cT2‐3a‐b, cN0‐1, M0 to EBCRT (45 Gy in 25 fractions over 5 weeks with oral capecitabine 825 mg/m2) followed by EBRT boost (9 Gy in 5 fractions over 5 days) versus EBCRT followed by CXB boost (90 Gy in 3 fractions over 4 weeks). Patients were assessed at 14, 20 and 24 weeks from the start of treatment. Watch and wait management was adopted for patients who achieved a clinical complete response (cCR) at 24 weeks following treatment. Either local excision (LE) or TME surgery was offered for residual disease or local regrowth, according to patient and surgeon preference. Surgical morbidity and mortality were recorded prospectively.ResultsBetween July 2015 and June 2020, 148 patients were randomised of which 141 were evaluable in March 2022. At median follow‐up of 38.2 months (range: 34.2–42.5), surgery was performed for 66 (47%) patients. A total of 27 (20%) patients had local excision and 39 (29%) had TME surgery, 22/39 (56%) underwent anterior resection and 17/39 (44%) underwent abdominoperineal excision of the rectum. The R0 resection rate was 87%. There were no deaths, and six patients (15%) had Clavien‐Dindo IIIb complications. Whilst there was a statistically significant decrease in the TME rate following CXB boost (HR 0.38, 95% CI: 0.19–0.74, p = 0.00419) there was no difference in surgical outcomes between patients who received EBRT and CXB boost.ConclusionDose escalation can facilitate nonsurgical treatment for cT2‐3 rectal cancer patients who are fit but wish to avoid TME surgery and stoma. If TME surgery is required, then it can be performed safely and effectively. |
doi_str_mv | 10.1111/codi.16773 |
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The OPERA trial aims to evaluate whether dose escalation with contact X‐ray brachytherapy (CXB) boost improves organ preservation compared to external beam radiotherapy (EBRT) boost. It has been suggested that dose escalation adversely affects surgical outcomes and therefore we report outcomes following TME in OPERA at 36 months.MethodsOPERA is a European multicentre phase 3 trial (NCT02505750) which randomises patients with cT2‐3a‐b, cN0‐1, M0 to EBCRT (45 Gy in 25 fractions over 5 weeks with oral capecitabine 825 mg/m2) followed by EBRT boost (9 Gy in 5 fractions over 5 days) versus EBCRT followed by CXB boost (90 Gy in 3 fractions over 4 weeks). Patients were assessed at 14, 20 and 24 weeks from the start of treatment. Watch and wait management was adopted for patients who achieved a clinical complete response (cCR) at 24 weeks following treatment. Either local excision (LE) or TME surgery was offered for residual disease or local regrowth, according to patient and surgeon preference. Surgical morbidity and mortality were recorded prospectively.ResultsBetween July 2015 and June 2020, 148 patients were randomised of which 141 were evaluable in March 2022. At median follow‐up of 38.2 months (range: 34.2–42.5), surgery was performed for 66 (47%) patients. A total of 27 (20%) patients had local excision and 39 (29%) had TME surgery, 22/39 (56%) underwent anterior resection and 17/39 (44%) underwent abdominoperineal excision of the rectum. The R0 resection rate was 87%. There were no deaths, and six patients (15%) had Clavien‐Dindo IIIb complications. Whilst there was a statistically significant decrease in the TME rate following CXB boost (HR 0.38, 95% CI: 0.19–0.74, p = 0.00419) there was no difference in surgical outcomes between patients who received EBRT and CXB boost.ConclusionDose escalation can facilitate nonsurgical treatment for cT2‐3 rectal cancer patients who are fit but wish to avoid TME surgery and stoma. If TME surgery is required, then it can be performed safely and effectively.</description><identifier>ISSN: 1462-8910</identifier><identifier>EISSN: 1463-1318</identifier><identifier>DOI: 10.1111/codi.16773</identifier><language>eng</language><publisher>Chichester: Wiley Subscription Services, Inc</publisher><subject>Adenocarcinoma ; Brachytherapy ; Chemoradiotherapy ; Colorectal cancer ; Morbidity ; Ostomy ; Patients ; Preservation ; Radiation therapy ; Rectum ; Statistical analysis ; Surgery ; Surgical outcomes</subject><ispartof>Colorectal disease, 2023-11, Vol.25 (11), p.2160-2169</ispartof><rights>2023. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c328t-77a1ee8e90abfb83fda5749084cb31f4b02f038f3839ba60c446fe1c3014fded3</citedby><cites>FETCH-LOGICAL-c328t-77a1ee8e90abfb83fda5749084cb31f4b02f038f3839ba60c446fe1c3014fded3</cites><orcidid>0000-0001-5323-5696</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Sun Myint, Arthur</creatorcontrib><creatorcontrib>Rao, Christopher</creatorcontrib><creatorcontrib>Barbet, Nicolas</creatorcontrib><creatorcontrib>Thamphya, Brice</creatorcontrib><creatorcontrib>Pace‐Loscos, Tanguy</creatorcontrib><creatorcontrib>Schiappa, Renaud</creatorcontrib><creatorcontrib>Magné, Nicolas</creatorcontrib><creatorcontrib>Martel‐Lafay, Isabelle</creatorcontrib><creatorcontrib>Mineur, Laurent</creatorcontrib><creatorcontrib>Deberne, Melanie</creatorcontrib><creatorcontrib>Zilli, Thomas</creatorcontrib><creatorcontrib>Dhadda, Amandeep</creatorcontrib><creatorcontrib>Gerard, Jean Pierre</creatorcontrib><title>The safety and efficacy of total mesorectal excision ( TME ) surgery following dose‐escalation: Surgical outcomes from the organ preservation in early rectal adenocarcinoma ( OPERA ) trial, a European multicentre phase 3 randomised trial ( NCT02505750 )</title><title>Colorectal disease</title><description>AimNonsurgical treatment with chemoradiotherapy for rectal cancer is gaining interest as it avoids total mesorectal excision (TME) surgery and stoma. The OPERA trial aims to evaluate whether dose escalation with contact X‐ray brachytherapy (CXB) boost improves organ preservation compared to external beam radiotherapy (EBRT) boost. It has been suggested that dose escalation adversely affects surgical outcomes and therefore we report outcomes following TME in OPERA at 36 months.MethodsOPERA is a European multicentre phase 3 trial (NCT02505750) which randomises patients with cT2‐3a‐b, cN0‐1, M0 to EBCRT (45 Gy in 25 fractions over 5 weeks with oral capecitabine 825 mg/m2) followed by EBRT boost (9 Gy in 5 fractions over 5 days) versus EBCRT followed by CXB boost (90 Gy in 3 fractions over 4 weeks). Patients were assessed at 14, 20 and 24 weeks from the start of treatment. Watch and wait management was adopted for patients who achieved a clinical complete response (cCR) at 24 weeks following treatment. Either local excision (LE) or TME surgery was offered for residual disease or local regrowth, according to patient and surgeon preference. Surgical morbidity and mortality were recorded prospectively.ResultsBetween July 2015 and June 2020, 148 patients were randomised of which 141 were evaluable in March 2022. At median follow‐up of 38.2 months (range: 34.2–42.5), surgery was performed for 66 (47%) patients. A total of 27 (20%) patients had local excision and 39 (29%) had TME surgery, 22/39 (56%) underwent anterior resection and 17/39 (44%) underwent abdominoperineal excision of the rectum. The R0 resection rate was 87%. There were no deaths, and six patients (15%) had Clavien‐Dindo IIIb complications. Whilst there was a statistically significant decrease in the TME rate following CXB boost (HR 0.38, 95% CI: 0.19–0.74, p = 0.00419) there was no difference in surgical outcomes between patients who received EBRT and CXB boost.ConclusionDose escalation can facilitate nonsurgical treatment for cT2‐3 rectal cancer patients who are fit but wish to avoid TME surgery and stoma. If TME surgery is required, then it can be performed safely and effectively.</description><subject>Adenocarcinoma</subject><subject>Brachytherapy</subject><subject>Chemoradiotherapy</subject><subject>Colorectal cancer</subject><subject>Morbidity</subject><subject>Ostomy</subject><subject>Patients</subject><subject>Preservation</subject><subject>Radiation therapy</subject><subject>Rectum</subject><subject>Statistical analysis</subject><subject>Surgery</subject><subject>Surgical outcomes</subject><issn>1462-8910</issn><issn>1463-1318</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdks9u1DAQxiMEEqVw4QlG4tIiUuw4u3G4Vavlj1QoguUcTZzx1pVjb20HyI1H4Bl5EfDu9oQvnsNvvm9G8xXFc84ueH6vlR_MBV82jXhQnPB6KUouuHx4qKtStpw9Lp7EeMtYhrg8Kf5ubggiakozoBuAtDYK1QxeQ_IJLYwUfSC1L-mnMtF4B2ew-biGc4hT2FKYQXtr_Q_jtjD4SH9-_aao0GLK7Bv4mqGsacFPSfksBzr4EVI29mGLDnaBIoXvBxyMA8JgZ7j3xIGcVxiUcX7E7Hz9ef3lMnunYNC-AoT1FPyOss442WQUuRQIdjcYCQSEvJQfTaTh2JAFPq02rFqwRbNgcP60eKTRRnp2_58W396uN6v35dX1uw-ry6tSiUqmsmmQE0lqGfa6l0IPuGjqlsla9YLrumeVZkJqIUXb45Kpul5q4kowXuuBBnFanB11d8HfTRRTl4dSZC068lPsKplvJtta8Iy--A-99VNwebpMtTWTrWhYpl4eKRV8jIF0twtmxDB3nHX7LHT7LHSHLIh_IeSqsw</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Sun Myint, Arthur</creator><creator>Rao, Christopher</creator><creator>Barbet, Nicolas</creator><creator>Thamphya, Brice</creator><creator>Pace‐Loscos, Tanguy</creator><creator>Schiappa, Renaud</creator><creator>Magné, Nicolas</creator><creator>Martel‐Lafay, Isabelle</creator><creator>Mineur, Laurent</creator><creator>Deberne, Melanie</creator><creator>Zilli, Thomas</creator><creator>Dhadda, Amandeep</creator><creator>Gerard, Jean Pierre</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5323-5696</orcidid></search><sort><creationdate>20231101</creationdate><title>The safety and efficacy of total mesorectal excision ( TME ) surgery following dose‐escalation: Surgical outcomes from the organ preservation in early rectal adenocarcinoma ( OPERA ) trial, a European multicentre phase 3 randomised trial ( NCT02505750 )</title><author>Sun Myint, Arthur ; Rao, Christopher ; Barbet, Nicolas ; Thamphya, Brice ; Pace‐Loscos, Tanguy ; Schiappa, Renaud ; Magné, Nicolas ; Martel‐Lafay, Isabelle ; Mineur, Laurent ; Deberne, Melanie ; Zilli, Thomas ; Dhadda, Amandeep ; Gerard, Jean Pierre</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c328t-77a1ee8e90abfb83fda5749084cb31f4b02f038f3839ba60c446fe1c3014fded3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adenocarcinoma</topic><topic>Brachytherapy</topic><topic>Chemoradiotherapy</topic><topic>Colorectal cancer</topic><topic>Morbidity</topic><topic>Ostomy</topic><topic>Patients</topic><topic>Preservation</topic><topic>Radiation therapy</topic><topic>Rectum</topic><topic>Statistical analysis</topic><topic>Surgery</topic><topic>Surgical outcomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun Myint, Arthur</creatorcontrib><creatorcontrib>Rao, Christopher</creatorcontrib><creatorcontrib>Barbet, Nicolas</creatorcontrib><creatorcontrib>Thamphya, Brice</creatorcontrib><creatorcontrib>Pace‐Loscos, Tanguy</creatorcontrib><creatorcontrib>Schiappa, Renaud</creatorcontrib><creatorcontrib>Magné, Nicolas</creatorcontrib><creatorcontrib>Martel‐Lafay, Isabelle</creatorcontrib><creatorcontrib>Mineur, Laurent</creatorcontrib><creatorcontrib>Deberne, Melanie</creatorcontrib><creatorcontrib>Zilli, Thomas</creatorcontrib><creatorcontrib>Dhadda, Amandeep</creatorcontrib><creatorcontrib>Gerard, Jean Pierre</creatorcontrib><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Colorectal disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun Myint, Arthur</au><au>Rao, Christopher</au><au>Barbet, Nicolas</au><au>Thamphya, Brice</au><au>Pace‐Loscos, Tanguy</au><au>Schiappa, Renaud</au><au>Magné, Nicolas</au><au>Martel‐Lafay, Isabelle</au><au>Mineur, Laurent</au><au>Deberne, Melanie</au><au>Zilli, Thomas</au><au>Dhadda, Amandeep</au><au>Gerard, Jean Pierre</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The safety and efficacy of total mesorectal excision ( TME ) surgery following dose‐escalation: Surgical outcomes from the organ preservation in early rectal adenocarcinoma ( OPERA ) trial, a European multicentre phase 3 randomised trial ( NCT02505750 )</atitle><jtitle>Colorectal disease</jtitle><date>2023-11-01</date><risdate>2023</risdate><volume>25</volume><issue>11</issue><spage>2160</spage><epage>2169</epage><pages>2160-2169</pages><issn>1462-8910</issn><eissn>1463-1318</eissn><abstract>AimNonsurgical treatment with chemoradiotherapy for rectal cancer is gaining interest as it avoids total mesorectal excision (TME) surgery and stoma. The OPERA trial aims to evaluate whether dose escalation with contact X‐ray brachytherapy (CXB) boost improves organ preservation compared to external beam radiotherapy (EBRT) boost. It has been suggested that dose escalation adversely affects surgical outcomes and therefore we report outcomes following TME in OPERA at 36 months.MethodsOPERA is a European multicentre phase 3 trial (NCT02505750) which randomises patients with cT2‐3a‐b, cN0‐1, M0 to EBCRT (45 Gy in 25 fractions over 5 weeks with oral capecitabine 825 mg/m2) followed by EBRT boost (9 Gy in 5 fractions over 5 days) versus EBCRT followed by CXB boost (90 Gy in 3 fractions over 4 weeks). Patients were assessed at 14, 20 and 24 weeks from the start of treatment. Watch and wait management was adopted for patients who achieved a clinical complete response (cCR) at 24 weeks following treatment. Either local excision (LE) or TME surgery was offered for residual disease or local regrowth, according to patient and surgeon preference. Surgical morbidity and mortality were recorded prospectively.ResultsBetween July 2015 and June 2020, 148 patients were randomised of which 141 were evaluable in March 2022. At median follow‐up of 38.2 months (range: 34.2–42.5), surgery was performed for 66 (47%) patients. A total of 27 (20%) patients had local excision and 39 (29%) had TME surgery, 22/39 (56%) underwent anterior resection and 17/39 (44%) underwent abdominoperineal excision of the rectum. The R0 resection rate was 87%. There were no deaths, and six patients (15%) had Clavien‐Dindo IIIb complications. Whilst there was a statistically significant decrease in the TME rate following CXB boost (HR 0.38, 95% CI: 0.19–0.74, p = 0.00419) there was no difference in surgical outcomes between patients who received EBRT and CXB boost.ConclusionDose escalation can facilitate nonsurgical treatment for cT2‐3 rectal cancer patients who are fit but wish to avoid TME surgery and stoma. If TME surgery is required, then it can be performed safely and effectively.</abstract><cop>Chichester</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/codi.16773</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-5323-5696</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma Brachytherapy Chemoradiotherapy Colorectal cancer Morbidity Ostomy Patients Preservation Radiation therapy Rectum Statistical analysis Surgery Surgical outcomes |
title | The safety and efficacy of total mesorectal excision ( TME ) surgery following dose‐escalation: Surgical outcomes from the organ preservation in early rectal adenocarcinoma ( OPERA ) trial, a European multicentre phase 3 randomised trial ( NCT02505750 ) |
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