Radical surgery versus organ preservation via short-course radiotherapy followed by transanal endoscopic microsurgery for early-stage rectal cancer (TREC): a randomised, open-label feasibility study

Radical surgery via total mesorectal excision might not be the optimal first-line treatment for early-stage rectal cancer. An organ-preserving strategy with selective total mesorectal excision could reduce the adverse effects of treatment without substantially compromising oncological outcomes. We i...

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Veröffentlicht in:The lancet. Gastroenterology & hepatology 2021-02, Vol.6 (2), p.92-105
Hauptverfasser: Bach, Simon P, Gilbert, Alexandra, Korsgen, Stephan, Geh, Ian, Hill, James, Gill, Talvinder, Tutton, Matthew G, Khan, Jim, Robinson, Jonathan, Steward, Mark, Cunningham, Christopher, Beveridge, Alan, Handley, Kelly, Vince, Alex, Hilken, Nick, Sidile, Chakanaka, Wilcockson, Adrian, Peto, Richard, Crosby, Tom, Olliff, Julie, Ashok, Katti, Slawik, Simone, Smethurst, Andrew, Sripadam, Rajaram, Tagore, Veena, Terlizzo, Monica, Nisar, Pasha, Stewart, Alexandra, Trickett, Jonathan, Ashish, Bansal, Billings, Peter, Chandran, Palanichamy, Corr, Conor, Favill, Edward, Gollins, Simon, Marsh, Peter, Rajagopal, Ramesh, Cooper, Rachel, Hatfield, Paul, Lowe, Andy, Ostrowski, Julian, Simpson, Rhian, Adams, Richard, Bleehen, Robert, Morgan, Meleri, Boone, Darren, Lacey, Nicola, Stunell, Helen, Wu, Shaobin, Hadaki, Maher, Blunt, Dominic, Cleator, Susan, Darzi, Ara, Goldin, Robert, Dobson, Mike, Pitt, Mark, Susnerwala, Shabbir, Williamson, Deborah, Howarth, Georgina, Horgan, Alan, McDonald, Fiona, Scott, John, Simmons, Timothy, Biswas, Debashis, Hernon, James, Kapur, Sandeep, Sington, James, Speakman, Christopher, Williams, Stuart, Garg, Dharmendra, Hegab, Mohammed, Hobday, Catherine, Shrimankar, Jyotsna, Jones, Oliver, Mortensen, Neil, Slater, Andrew, Wang, Lai, Warren, Bryan, Weaver, Andrew, Flubacher, Maxine, Tarver, David, Beable, Richard, Cowlishaw, David, Vogiatzis, Prokopios, Saunders, Mark, Teo, Mark, Glaholm, John, Goldstein, Mark, Langman, Gerald, Morton, Dion, Falk, Stephen, Thomas, Michael, Haba, Yasser, Harris, Guy, Hookway, Max, Skull, Angela, Umar, Tijani
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container_title The lancet. Gastroenterology & hepatology
container_volume 6
creator Bach, Simon P
Gilbert, Alexandra
Korsgen, Stephan
Geh, Ian
Hill, James
Gill, Talvinder
Tutton, Matthew G
Khan, Jim
Robinson, Jonathan
Steward, Mark
Cunningham, Christopher
Beveridge, Alan
Handley, Kelly
Vince, Alex
Hilken, Nick
Sidile, Chakanaka
Wilcockson, Adrian
Peto, Richard
Crosby, Tom
Olliff, Julie
Ashok, Katti
Slawik, Simone
Smethurst, Andrew
Sripadam, Rajaram
Tagore, Veena
Terlizzo, Monica
Nisar, Pasha
Stewart, Alexandra
Trickett, Jonathan
Ashish, Bansal
Billings, Peter
Chandran, Palanichamy
Corr, Conor
Favill, Edward
Gollins, Simon
Marsh, Peter
Rajagopal, Ramesh
Cooper, Rachel
Hatfield, Paul
Lowe, Andy
Ostrowski, Julian
Robinson, Jonathan
Simpson, Rhian
Adams, Richard
Bleehen, Robert
Morgan, Meleri
Boone, Darren
Lacey, Nicola
Stunell, Helen
Wu, Shaobin
Hadaki, Maher
Blunt, Dominic
Cleator, Susan
Darzi, Ara
Goldin, Robert
Dobson, Mike
Pitt, Mark
Susnerwala, Shabbir
Williamson, Deborah
Howarth, Georgina
Horgan, Alan
McDonald, Fiona
Scott, John
Simmons, Timothy
Biswas, Debashis
Hernon, James
Kapur, Sandeep
Sington, James
Speakman, Christopher
Williams, Stuart
Garg, Dharmendra
Gill, Talvinder
Hegab, Mohammed
Hobday, Catherine
Shrimankar, Jyotsna
Jones, Oliver
Mortensen, Neil
Slater, Andrew
Wang, Lai
Warren, Bryan
Weaver, Andrew
Flubacher, Maxine
Tarver, David
Beable, Richard
Cowlishaw, David
Vogiatzis, Prokopios
Saunders, Mark
Teo, Mark
Geh, Ian
Glaholm, John
Goldstein, Mark
Langman, Gerald
Morton, Dion
Falk, Stephen
Thomas, Michael
Haba, Yasser
Harris, Guy
Hookway, Max
Skull, Angela
Umar, Tijani
description Radical surgery via total mesorectal excision might not be the optimal first-line treatment for early-stage rectal cancer. An organ-preserving strategy with selective total mesorectal excision could reduce the adverse effects of treatment without substantially compromising oncological outcomes. We investigated the feasibility of recruiting patients to a randomised trial comparing an organ-preserving strategy with total mesorectal excision. TREC was a randomised, open-label feasibility study done at 21 tertiary referral centres in the UK. Eligible participants were aged 18 years or older with rectal adenocarcinoma, staged T2 or lower, with a maximum diameter of 30 mm or less; patients with lymph node involvement or metastases were excluded. Patients were randomly allocated (1:1) by use of a computer-based randomisation service to undergo organ preservation with short-course radiotherapy followed by transanal endoscopic microsurgery after 8–10 weeks, or total mesorectal excision. Where the transanal endoscopic microsurgery specimen showed histopathological features associated with an increased risk of local recurrence, patients were considered for planned early conversion to total mesorectal excision. A non-randomised prospective registry captured patients for whom randomisation was considered inappropriate, because of a strong clinical indication for one treatment group. The primary endpoint was cumulative randomisation at 12, 18, and 24 months. Secondary outcomes evaluated safety, efficacy, and health-related quality of life assessed with the European Organisation for Research and Treatment of Cancer (EORTC) QLQ C30 and CR29 in the intention-to-treat population. This trial is registered with the ISRCTN Registry, ISRCTN14422743. Between Feb 22, 2012, and Dec 19, 2014, 55 patients were randomly assigned at 15 sites; 27 to organ preservation and 28 to radical surgery. Cumulatively, 18 patients had been randomly assigned at 12 months, 31 at 18 months, and 39 at 24 months. No patients died within 30 days of initial treatment, but one patient randomly assigned to organ preservation died within 6 months following conversion to total mesorectal excision with anastomotic leakage. Eight (30%) of 27 patients randomly assigned to organ preservation were converted to total mesorectal excision. Serious adverse events were reported in four (15%) of 27 patients randomly assigned to organ preservation versus 11 (39%) of 28 randomly assigned to total mesorectal excision (p=
doi_str_mv 10.1016/S2468-1253(20)30333-2
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Gilbert, Alexandra ; Korsgen, Stephan ; Geh, Ian ; Hill, James ; Gill, Talvinder ; Tutton, Matthew G ; Khan, Jim ; Robinson, Jonathan ; Steward, Mark ; Cunningham, Christopher ; Beveridge, Alan ; Handley, Kelly ; Vince, Alex ; Hilken, Nick ; Sidile, Chakanaka ; Wilcockson, Adrian ; Peto, Richard ; Crosby, Tom ; Olliff, Julie ; Ashok, Katti ; Slawik, Simone ; Smethurst, Andrew ; Sripadam, Rajaram ; Tagore, Veena ; Terlizzo, Monica ; Nisar, Pasha ; Stewart, Alexandra ; Trickett, Jonathan ; Ashish, Bansal ; Billings, Peter ; Chandran, Palanichamy ; Corr, Conor ; Favill, Edward ; Gollins, Simon ; Marsh, Peter ; Rajagopal, Ramesh ; Cooper, Rachel ; Hatfield, Paul ; Lowe, Andy ; Ostrowski, Julian ; Robinson, Jonathan ; Simpson, Rhian ; Adams, Richard ; Bleehen, Robert ; Morgan, Meleri ; Boone, Darren ; Lacey, Nicola ; Stunell, Helen ; Wu, Shaobin ; Hadaki, Maher ; Blunt, Dominic ; Cleator, Susan ; Darzi, Ara ; Goldin, Robert ; Dobson, Mike ; Pitt, Mark ; Susnerwala, Shabbir ; Williamson, Deborah ; Howarth, Georgina ; Horgan, Alan ; McDonald, Fiona ; Scott, John ; Simmons, Timothy ; Biswas, Debashis ; Hernon, James ; Kapur, Sandeep ; Sington, James ; Speakman, Christopher ; Williams, Stuart ; Garg, Dharmendra ; Gill, Talvinder ; Hegab, Mohammed ; Hobday, Catherine ; Shrimankar, Jyotsna ; Jones, Oliver ; Mortensen, Neil ; Slater, Andrew ; Wang, Lai ; Warren, Bryan ; Weaver, Andrew ; Flubacher, Maxine ; Tarver, David ; Beable, Richard ; Cowlishaw, David ; Vogiatzis, Prokopios ; Saunders, Mark ; Teo, Mark ; Geh, Ian ; Glaholm, John ; Goldstein, Mark ; Langman, Gerald ; Morton, Dion ; Falk, Stephen ; Thomas, Michael ; Haba, Yasser ; Harris, Guy ; Hookway, Max ; Skull, Angela ; Umar, Tijani</creator><creatorcontrib>Bach, Simon P ; Gilbert, Alexandra ; Korsgen, Stephan ; Geh, Ian ; Hill, James ; Gill, Talvinder ; Tutton, Matthew G ; Khan, Jim ; Robinson, Jonathan ; Steward, Mark ; Cunningham, Christopher ; Beveridge, Alan ; Handley, Kelly ; Vince, Alex ; Hilken, Nick ; Sidile, Chakanaka ; Wilcockson, Adrian ; Peto, Richard ; Crosby, Tom ; Olliff, Julie ; Ashok, Katti ; Slawik, Simone ; Smethurst, Andrew ; Sripadam, Rajaram ; Tagore, Veena ; Terlizzo, Monica ; Nisar, Pasha ; Stewart, Alexandra ; Trickett, Jonathan ; Ashish, Bansal ; Billings, Peter ; Chandran, Palanichamy ; Corr, Conor ; Favill, Edward ; Gollins, Simon ; Marsh, Peter ; Rajagopal, Ramesh ; Cooper, Rachel ; Hatfield, Paul ; Lowe, Andy ; Ostrowski, Julian ; Robinson, Jonathan ; Simpson, Rhian ; Adams, Richard ; Bleehen, Robert ; Morgan, Meleri ; Boone, Darren ; Lacey, Nicola ; Stunell, Helen ; Wu, Shaobin ; Hadaki, Maher ; Blunt, Dominic ; Cleator, Susan ; Darzi, Ara ; Goldin, Robert ; Dobson, Mike ; Pitt, Mark ; Susnerwala, Shabbir ; Williamson, Deborah ; Howarth, Georgina ; Horgan, Alan ; McDonald, Fiona ; Scott, John ; Simmons, Timothy ; Biswas, Debashis ; Hernon, James ; Kapur, Sandeep ; Sington, James ; Speakman, Christopher ; Williams, Stuart ; Garg, Dharmendra ; Gill, Talvinder ; Hegab, Mohammed ; Hobday, Catherine ; Shrimankar, Jyotsna ; Jones, Oliver ; Mortensen, Neil ; Slater, Andrew ; Wang, Lai ; Warren, Bryan ; Weaver, Andrew ; Flubacher, Maxine ; Tarver, David ; Beable, Richard ; Cowlishaw, David ; Vogiatzis, Prokopios ; Saunders, Mark ; Teo, Mark ; Geh, Ian ; Glaholm, John ; Goldstein, Mark ; Langman, Gerald ; Morton, Dion ; Falk, Stephen ; Thomas, Michael ; Haba, Yasser ; Harris, Guy ; Hookway, Max ; Skull, Angela ; Umar, Tijani ; TREC collaborators</creatorcontrib><description>Radical surgery via total mesorectal excision might not be the optimal first-line treatment for early-stage rectal cancer. An organ-preserving strategy with selective total mesorectal excision could reduce the adverse effects of treatment without substantially compromising oncological outcomes. We investigated the feasibility of recruiting patients to a randomised trial comparing an organ-preserving strategy with total mesorectal excision. TREC was a randomised, open-label feasibility study done at 21 tertiary referral centres in the UK. Eligible participants were aged 18 years or older with rectal adenocarcinoma, staged T2 or lower, with a maximum diameter of 30 mm or less; patients with lymph node involvement or metastases were excluded. Patients were randomly allocated (1:1) by use of a computer-based randomisation service to undergo organ preservation with short-course radiotherapy followed by transanal endoscopic microsurgery after 8–10 weeks, or total mesorectal excision. Where the transanal endoscopic microsurgery specimen showed histopathological features associated with an increased risk of local recurrence, patients were considered for planned early conversion to total mesorectal excision. A non-randomised prospective registry captured patients for whom randomisation was considered inappropriate, because of a strong clinical indication for one treatment group. The primary endpoint was cumulative randomisation at 12, 18, and 24 months. Secondary outcomes evaluated safety, efficacy, and health-related quality of life assessed with the European Organisation for Research and Treatment of Cancer (EORTC) QLQ C30 and CR29 in the intention-to-treat population. This trial is registered with the ISRCTN Registry, ISRCTN14422743. Between Feb 22, 2012, and Dec 19, 2014, 55 patients were randomly assigned at 15 sites; 27 to organ preservation and 28 to radical surgery. Cumulatively, 18 patients had been randomly assigned at 12 months, 31 at 18 months, and 39 at 24 months. No patients died within 30 days of initial treatment, but one patient randomly assigned to organ preservation died within 6 months following conversion to total mesorectal excision with anastomotic leakage. Eight (30%) of 27 patients randomly assigned to organ preservation were converted to total mesorectal excision. Serious adverse events were reported in four (15%) of 27 patients randomly assigned to organ preservation versus 11 (39%) of 28 randomly assigned to total mesorectal excision (p=0·04, χ2 test). Serious adverse events associated with organ preservation were most commonly due to rectal bleeding or pain following transanal endoscopic microsurgery (reported in three cases). Radical total mesorectal excision was associated with medical and surgical complications including anastomotic leakage (two patients), kidney injury (two patients), cardiac arrest (one patient), and pneumonia (two patients). Histopathological features that would be considered to be associated with increased risk of tumour recurrence if observed after transanal endoscopic microsurgery alone were present in 16 (59%) of 27 patients randomly assigned to organ preservation, versus 24 (86%) of 28 randomly assigned to total mesorectal excision (p=0·03, χ2 test). Eight (30%) of 27 patients assigned to organ preservation achieved a complete response to radiotherapy. Patients who were randomly assigned to organ preservation showed improvements in patient-reported bowel toxicities and quality of life and function scores in multiple items compared to those who were randomly assigned to total mesorectal excision, which were sustained over 36 months’ follow-up. The non-randomised registry comprised 61 patients who underwent organ preservation and seven who underwent radical surgery. Non-randomised patients who underwent organ preservation were older than randomised patients and more likely to have life-limiting comorbidities. Serious adverse events occurred in ten (16%) of 61 non-randomised patients who underwent organ preservation versus one (14%) of seven who underwent total mesorectal excision. 24 (39%) of 61 non-randomised patients who underwent organ preservation had high-risk histopathological features, while 25 (41%) of 61 achieved a complete response. Overall, organ preservation was achieved in 19 (70%) of 27 randomised patients and 56 (92%) of 61 non-randomised patients. Short-course radiotherapy followed by transanal endoscopic microsurgery achieves high levels of organ preservation, with relatively low morbidity and indications of improved quality of life. These data support the use of organ preservation for patients considered unsuitable for primary total mesorectal excision due to the short-term risks associated with this surgery, and support further evaluation of short-course radiotherapy to achieve organ preservation in patients considered fit for total mesorectal excision. Larger randomised studies, such as the ongoing STAR-TREC study, are needed to more precisely determine oncological outcomes following different organ preservation treatment schedules. Cancer Research UK.</description><identifier>ISSN: 2468-1253</identifier><identifier>EISSN: 2468-1253</identifier><identifier>DOI: 10.1016/S2468-1253(20)30333-2</identifier><identifier>PMID: 33308452</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adenocarcinoma - pathology ; Adenocarcinoma - radiotherapy ; Adenocarcinoma - surgery ; Adolescent ; Adult ; Aged ; Aged, 80 and over ; Feasibility Studies ; Female ; Follow-Up Studies ; Humans ; Male ; Middle Aged ; Neoplasm Staging ; Organ Sparing Treatments ; Proctectomy ; Radiotherapy, Adjuvant ; Rectal Neoplasms - pathology ; Rectal Neoplasms - radiotherapy ; Rectal Neoplasms - surgery ; Transanal Endoscopic Microsurgery ; Treatment Outcome ; Young Adult</subject><ispartof>The lancet. Gastroenterology &amp; hepatology, 2021-02, Vol.6 (2), p.92-105</ispartof><rights>2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license</rights><rights>Copyright © 2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.</rights><rights>2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-cfffe4967f5e1733358d8676f4e75eb66e99787372050aacf17f4e35e4ca4b0d3</citedby><cites>FETCH-LOGICAL-c467t-cfffe4967f5e1733358d8676f4e75eb66e99787372050aacf17f4e35e4ca4b0d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33308452$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bach, Simon P</creatorcontrib><creatorcontrib>Gilbert, Alexandra</creatorcontrib><creatorcontrib>Korsgen, Stephan</creatorcontrib><creatorcontrib>Geh, Ian</creatorcontrib><creatorcontrib>Hill, James</creatorcontrib><creatorcontrib>Gill, 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Sandeep</creatorcontrib><creatorcontrib>Sington, James</creatorcontrib><creatorcontrib>Speakman, Christopher</creatorcontrib><creatorcontrib>Williams, Stuart</creatorcontrib><creatorcontrib>Garg, Dharmendra</creatorcontrib><creatorcontrib>Gill, Talvinder</creatorcontrib><creatorcontrib>Hegab, Mohammed</creatorcontrib><creatorcontrib>Hobday, Catherine</creatorcontrib><creatorcontrib>Shrimankar, Jyotsna</creatorcontrib><creatorcontrib>Jones, Oliver</creatorcontrib><creatorcontrib>Mortensen, Neil</creatorcontrib><creatorcontrib>Slater, Andrew</creatorcontrib><creatorcontrib>Wang, Lai</creatorcontrib><creatorcontrib>Warren, Bryan</creatorcontrib><creatorcontrib>Weaver, Andrew</creatorcontrib><creatorcontrib>Flubacher, Maxine</creatorcontrib><creatorcontrib>Tarver, David</creatorcontrib><creatorcontrib>Beable, Richard</creatorcontrib><creatorcontrib>Cowlishaw, David</creatorcontrib><creatorcontrib>Vogiatzis, Prokopios</creatorcontrib><creatorcontrib>Saunders, Mark</creatorcontrib><creatorcontrib>Teo, Mark</creatorcontrib><creatorcontrib>Geh, Ian</creatorcontrib><creatorcontrib>Glaholm, John</creatorcontrib><creatorcontrib>Goldstein, Mark</creatorcontrib><creatorcontrib>Langman, Gerald</creatorcontrib><creatorcontrib>Morton, Dion</creatorcontrib><creatorcontrib>Falk, Stephen</creatorcontrib><creatorcontrib>Thomas, Michael</creatorcontrib><creatorcontrib>Haba, Yasser</creatorcontrib><creatorcontrib>Harris, Guy</creatorcontrib><creatorcontrib>Hookway, Max</creatorcontrib><creatorcontrib>Skull, Angela</creatorcontrib><creatorcontrib>Umar, Tijani</creatorcontrib><creatorcontrib>TREC collaborators</creatorcontrib><title>Radical surgery versus organ preservation via short-course radiotherapy followed by transanal endoscopic microsurgery for early-stage rectal cancer (TREC): a randomised, open-label feasibility study</title><title>The lancet. Gastroenterology &amp; hepatology</title><addtitle>Lancet Gastroenterol Hepatol</addtitle><description>Radical surgery via total mesorectal excision might not be the optimal first-line treatment for early-stage rectal cancer. An organ-preserving strategy with selective total mesorectal excision could reduce the adverse effects of treatment without substantially compromising oncological outcomes. We investigated the feasibility of recruiting patients to a randomised trial comparing an organ-preserving strategy with total mesorectal excision. TREC was a randomised, open-label feasibility study done at 21 tertiary referral centres in the UK. Eligible participants were aged 18 years or older with rectal adenocarcinoma, staged T2 or lower, with a maximum diameter of 30 mm or less; patients with lymph node involvement or metastases were excluded. Patients were randomly allocated (1:1) by use of a computer-based randomisation service to undergo organ preservation with short-course radiotherapy followed by transanal endoscopic microsurgery after 8–10 weeks, or total mesorectal excision. Where the transanal endoscopic microsurgery specimen showed histopathological features associated with an increased risk of local recurrence, patients were considered for planned early conversion to total mesorectal excision. A non-randomised prospective registry captured patients for whom randomisation was considered inappropriate, because of a strong clinical indication for one treatment group. The primary endpoint was cumulative randomisation at 12, 18, and 24 months. Secondary outcomes evaluated safety, efficacy, and health-related quality of life assessed with the European Organisation for Research and Treatment of Cancer (EORTC) QLQ C30 and CR29 in the intention-to-treat population. This trial is registered with the ISRCTN Registry, ISRCTN14422743. Between Feb 22, 2012, and Dec 19, 2014, 55 patients were randomly assigned at 15 sites; 27 to organ preservation and 28 to radical surgery. Cumulatively, 18 patients had been randomly assigned at 12 months, 31 at 18 months, and 39 at 24 months. No patients died within 30 days of initial treatment, but one patient randomly assigned to organ preservation died within 6 months following conversion to total mesorectal excision with anastomotic leakage. Eight (30%) of 27 patients randomly assigned to organ preservation were converted to total mesorectal excision. Serious adverse events were reported in four (15%) of 27 patients randomly assigned to organ preservation versus 11 (39%) of 28 randomly assigned to total mesorectal excision (p=0·04, χ2 test). Serious adverse events associated with organ preservation were most commonly due to rectal bleeding or pain following transanal endoscopic microsurgery (reported in three cases). Radical total mesorectal excision was associated with medical and surgical complications including anastomotic leakage (two patients), kidney injury (two patients), cardiac arrest (one patient), and pneumonia (two patients). Histopathological features that would be considered to be associated with increased risk of tumour recurrence if observed after transanal endoscopic microsurgery alone were present in 16 (59%) of 27 patients randomly assigned to organ preservation, versus 24 (86%) of 28 randomly assigned to total mesorectal excision (p=0·03, χ2 test). Eight (30%) of 27 patients assigned to organ preservation achieved a complete response to radiotherapy. Patients who were randomly assigned to organ preservation showed improvements in patient-reported bowel toxicities and quality of life and function scores in multiple items compared to those who were randomly assigned to total mesorectal excision, which were sustained over 36 months’ follow-up. The non-randomised registry comprised 61 patients who underwent organ preservation and seven who underwent radical surgery. Non-randomised patients who underwent organ preservation were older than randomised patients and more likely to have life-limiting comorbidities. Serious adverse events occurred in ten (16%) of 61 non-randomised patients who underwent organ preservation versus one (14%) of seven who underwent total mesorectal excision. 24 (39%) of 61 non-randomised patients who underwent organ preservation had high-risk histopathological features, while 25 (41%) of 61 achieved a complete response. Overall, organ preservation was achieved in 19 (70%) of 27 randomised patients and 56 (92%) of 61 non-randomised patients. Short-course radiotherapy followed by transanal endoscopic microsurgery achieves high levels of organ preservation, with relatively low morbidity and indications of improved quality of life. These data support the use of organ preservation for patients considered unsuitable for primary total mesorectal excision due to the short-term risks associated with this surgery, and support further evaluation of short-course radiotherapy to achieve organ preservation in patients considered fit for total mesorectal excision. Larger randomised studies, such as the ongoing STAR-TREC study, are needed to more precisely determine oncological outcomes following different organ preservation treatment schedules. Cancer Research UK.</description><subject>Adenocarcinoma - pathology</subject><subject>Adenocarcinoma - radiotherapy</subject><subject>Adenocarcinoma - surgery</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Organ Sparing Treatments</subject><subject>Proctectomy</subject><subject>Radiotherapy, Adjuvant</subject><subject>Rectal Neoplasms - pathology</subject><subject>Rectal Neoplasms - radiotherapy</subject><subject>Rectal Neoplasms - surgery</subject><subject>Transanal Endoscopic Microsurgery</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>2468-1253</issn><issn>2468-1253</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUctu1DAUjRCIVqWfAPKylQg4cWxnWIDQqC1IlZBKWVs39vWMkSeO7CQoP8h34enQUVmxsuV7Hr7nFMXrir6raCXef68b0ZZVzdlFTS8ZZYyV9bPi9Pj8_Mn9pDhP6SeltJJMCNa-LE4ynrYNr0-L33dgnAZP0hQ3GBcyY0xTIiFuoCdDxIRxhtGFnswOSNqGOJY6TDEhiZkaxi1GGBZig_fhFxrSLWSM0Cfosyr2JiQdBqfJzukYHl1siAQh-qVMI2yyFOoxwzX0GiO5uL-7Wl9-IJAtssDOJTRvSRiwLz106IlFSK5z3o0LSeNkllfFCws-4fnf86z4cX11v_5S3n67-br-fFvqRsj8cWstNishLcecBmO8Na2QwjYoOXZC4GolW8lkTTkF0LaSecQ4Nhqajhp2Vnw86A5Tt0Ojsc-7ejVEt4O4qABO_Tvp3VZtwqxkS2te8SzADwL7MFJEe-RWVO27VQ_dqn1xqqbqoVtVZ96bp8ZH1mOTGfDpAMC8_uwwqqQd5jiN24erTHD_sfgDaV67Bw</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Bach, Simon P</creator><creator>Gilbert, Alexandra</creator><creator>Korsgen, Stephan</creator><creator>Geh, Ian</creator><creator>Hill, 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Dion</creator><creator>Falk, Stephen</creator><creator>Thomas, Michael</creator><creator>Haba, Yasser</creator><creator>Harris, Guy</creator><creator>Hookway, Max</creator><creator>Skull, Angela</creator><creator>Umar, Tijani</creator><general>Elsevier Ltd</general><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20210201</creationdate><title>Radical surgery versus organ preservation via short-course radiotherapy followed by transanal endoscopic microsurgery for early-stage rectal cancer (TREC): a randomised, open-label feasibility study</title><author>Bach, Simon P ; Gilbert, Alexandra ; Korsgen, Stephan ; Geh, Ian ; Hill, James ; Gill, Talvinder ; Tutton, Matthew G ; Khan, Jim ; Robinson, Jonathan ; Steward, Mark ; Cunningham, Christopher ; Beveridge, Alan ; Handley, Kelly ; Vince, Alex ; Hilken, Nick ; Sidile, Chakanaka ; Wilcockson, Adrian ; Peto, Richard ; Crosby, Tom ; Olliff, Julie ; Ashok, Katti ; Slawik, Simone ; Smethurst, Andrew ; Sripadam, Rajaram ; Tagore, Veena ; Terlizzo, Monica ; Nisar, Pasha ; Stewart, Alexandra ; Trickett, Jonathan ; Ashish, Bansal ; Billings, Peter ; Chandran, Palanichamy ; Corr, Conor ; Favill, Edward ; Gollins, Simon ; Marsh, Peter ; Rajagopal, Ramesh ; Cooper, Rachel ; Hatfield, Paul ; Lowe, Andy ; Ostrowski, Julian ; Robinson, Jonathan ; Simpson, Rhian ; Adams, Richard ; Bleehen, Robert ; Morgan, Meleri ; Boone, Darren ; Lacey, Nicola ; Stunell, Helen ; Wu, Shaobin ; Hadaki, Maher ; Blunt, Dominic ; Cleator, Susan ; Darzi, Ara ; Goldin, Robert ; Dobson, Mike ; Pitt, Mark ; Susnerwala, Shabbir ; Williamson, Deborah ; Howarth, Georgina ; Horgan, Alan ; McDonald, Fiona ; Scott, John ; Simmons, Timothy ; Biswas, Debashis ; Hernon, James ; Kapur, Sandeep ; Sington, James ; Speakman, Christopher ; Williams, Stuart ; Garg, Dharmendra ; Gill, Talvinder ; Hegab, Mohammed ; Hobday, Catherine ; Shrimankar, Jyotsna ; Jones, Oliver ; Mortensen, Neil ; Slater, Andrew ; Wang, Lai ; Warren, Bryan ; Weaver, Andrew ; Flubacher, Maxine ; Tarver, David ; Beable, Richard ; Cowlishaw, David ; Vogiatzis, Prokopios ; Saunders, Mark ; Teo, Mark ; Geh, Ian ; Glaholm, John ; Goldstein, Mark ; Langman, Gerald ; Morton, Dion ; Falk, Stephen ; Thomas, Michael ; Haba, Yasser ; Harris, Guy ; Hookway, Max ; Skull, Angela ; Umar, Tijani</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-cfffe4967f5e1733358d8676f4e75eb66e99787372050aacf17f4e35e4ca4b0d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adenocarcinoma - pathology</topic><topic>Adenocarcinoma - radiotherapy</topic><topic>Adenocarcinoma - surgery</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and 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Gastroenterology &amp; hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bach, Simon P</au><au>Gilbert, Alexandra</au><au>Korsgen, Stephan</au><au>Geh, Ian</au><au>Hill, James</au><au>Gill, Talvinder</au><au>Tutton, Matthew G</au><au>Khan, Jim</au><au>Robinson, Jonathan</au><au>Steward, Mark</au><au>Cunningham, Christopher</au><au>Beveridge, Alan</au><au>Handley, Kelly</au><au>Vince, Alex</au><au>Hilken, Nick</au><au>Sidile, Chakanaka</au><au>Wilcockson, Adrian</au><au>Peto, Richard</au><au>Crosby, Tom</au><au>Olliff, Julie</au><au>Ashok, Katti</au><au>Slawik, Simone</au><au>Smethurst, Andrew</au><au>Sripadam, Rajaram</au><au>Tagore, Veena</au><au>Terlizzo, Monica</au><au>Nisar, Pasha</au><au>Stewart, Alexandra</au><au>Trickett, Jonathan</au><au>Ashish, Bansal</au><au>Billings, Peter</au><au>Chandran, Palanichamy</au><au>Corr, Conor</au><au>Favill, Edward</au><au>Gollins, Simon</au><au>Marsh, Peter</au><au>Rajagopal, Ramesh</au><au>Cooper, Rachel</au><au>Hatfield, Paul</au><au>Lowe, Andy</au><au>Ostrowski, Julian</au><au>Robinson, Jonathan</au><au>Simpson, Rhian</au><au>Adams, Richard</au><au>Bleehen, Robert</au><au>Morgan, Meleri</au><au>Boone, Darren</au><au>Lacey, Nicola</au><au>Stunell, Helen</au><au>Wu, Shaobin</au><au>Hadaki, Maher</au><au>Blunt, Dominic</au><au>Cleator, Susan</au><au>Darzi, Ara</au><au>Goldin, Robert</au><au>Dobson, Mike</au><au>Pitt, Mark</au><au>Susnerwala, Shabbir</au><au>Williamson, Deborah</au><au>Howarth, Georgina</au><au>Horgan, Alan</au><au>McDonald, Fiona</au><au>Scott, John</au><au>Simmons, Timothy</au><au>Biswas, Debashis</au><au>Hernon, James</au><au>Kapur, Sandeep</au><au>Sington, James</au><au>Speakman, Christopher</au><au>Williams, Stuart</au><au>Garg, Dharmendra</au><au>Gill, Talvinder</au><au>Hegab, Mohammed</au><au>Hobday, Catherine</au><au>Shrimankar, Jyotsna</au><au>Jones, Oliver</au><au>Mortensen, Neil</au><au>Slater, Andrew</au><au>Wang, Lai</au><au>Warren, Bryan</au><au>Weaver, Andrew</au><au>Flubacher, Maxine</au><au>Tarver, David</au><au>Beable, Richard</au><au>Cowlishaw, David</au><au>Vogiatzis, Prokopios</au><au>Saunders, Mark</au><au>Teo, Mark</au><au>Geh, Ian</au><au>Glaholm, John</au><au>Goldstein, Mark</au><au>Langman, Gerald</au><au>Morton, Dion</au><au>Falk, Stephen</au><au>Thomas, Michael</au><au>Haba, Yasser</au><au>Harris, Guy</au><au>Hookway, Max</au><au>Skull, Angela</au><au>Umar, Tijani</au><aucorp>TREC collaborators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Radical surgery versus organ preservation via short-course radiotherapy followed by transanal endoscopic microsurgery for early-stage rectal cancer (TREC): a randomised, open-label feasibility study</atitle><jtitle>The lancet. Gastroenterology &amp; hepatology</jtitle><addtitle>Lancet Gastroenterol Hepatol</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>6</volume><issue>2</issue><spage>92</spage><epage>105</epage><pages>92-105</pages><issn>2468-1253</issn><eissn>2468-1253</eissn><abstract>Radical surgery via total mesorectal excision might not be the optimal first-line treatment for early-stage rectal cancer. An organ-preserving strategy with selective total mesorectal excision could reduce the adverse effects of treatment without substantially compromising oncological outcomes. We investigated the feasibility of recruiting patients to a randomised trial comparing an organ-preserving strategy with total mesorectal excision. TREC was a randomised, open-label feasibility study done at 21 tertiary referral centres in the UK. Eligible participants were aged 18 years or older with rectal adenocarcinoma, staged T2 or lower, with a maximum diameter of 30 mm or less; patients with lymph node involvement or metastases were excluded. Patients were randomly allocated (1:1) by use of a computer-based randomisation service to undergo organ preservation with short-course radiotherapy followed by transanal endoscopic microsurgery after 8–10 weeks, or total mesorectal excision. Where the transanal endoscopic microsurgery specimen showed histopathological features associated with an increased risk of local recurrence, patients were considered for planned early conversion to total mesorectal excision. A non-randomised prospective registry captured patients for whom randomisation was considered inappropriate, because of a strong clinical indication for one treatment group. The primary endpoint was cumulative randomisation at 12, 18, and 24 months. Secondary outcomes evaluated safety, efficacy, and health-related quality of life assessed with the European Organisation for Research and Treatment of Cancer (EORTC) QLQ C30 and CR29 in the intention-to-treat population. This trial is registered with the ISRCTN Registry, ISRCTN14422743. Between Feb 22, 2012, and Dec 19, 2014, 55 patients were randomly assigned at 15 sites; 27 to organ preservation and 28 to radical surgery. Cumulatively, 18 patients had been randomly assigned at 12 months, 31 at 18 months, and 39 at 24 months. No patients died within 30 days of initial treatment, but one patient randomly assigned to organ preservation died within 6 months following conversion to total mesorectal excision with anastomotic leakage. Eight (30%) of 27 patients randomly assigned to organ preservation were converted to total mesorectal excision. Serious adverse events were reported in four (15%) of 27 patients randomly assigned to organ preservation versus 11 (39%) of 28 randomly assigned to total mesorectal excision (p=0·04, χ2 test). Serious adverse events associated with organ preservation were most commonly due to rectal bleeding or pain following transanal endoscopic microsurgery (reported in three cases). Radical total mesorectal excision was associated with medical and surgical complications including anastomotic leakage (two patients), kidney injury (two patients), cardiac arrest (one patient), and pneumonia (two patients). Histopathological features that would be considered to be associated with increased risk of tumour recurrence if observed after transanal endoscopic microsurgery alone were present in 16 (59%) of 27 patients randomly assigned to organ preservation, versus 24 (86%) of 28 randomly assigned to total mesorectal excision (p=0·03, χ2 test). Eight (30%) of 27 patients assigned to organ preservation achieved a complete response to radiotherapy. Patients who were randomly assigned to organ preservation showed improvements in patient-reported bowel toxicities and quality of life and function scores in multiple items compared to those who were randomly assigned to total mesorectal excision, which were sustained over 36 months’ follow-up. The non-randomised registry comprised 61 patients who underwent organ preservation and seven who underwent radical surgery. Non-randomised patients who underwent organ preservation were older than randomised patients and more likely to have life-limiting comorbidities. Serious adverse events occurred in ten (16%) of 61 non-randomised patients who underwent organ preservation versus one (14%) of seven who underwent total mesorectal excision. 24 (39%) of 61 non-randomised patients who underwent organ preservation had high-risk histopathological features, while 25 (41%) of 61 achieved a complete response. Overall, organ preservation was achieved in 19 (70%) of 27 randomised patients and 56 (92%) of 61 non-randomised patients. Short-course radiotherapy followed by transanal endoscopic microsurgery achieves high levels of organ preservation, with relatively low morbidity and indications of improved quality of life. These data support the use of organ preservation for patients considered unsuitable for primary total mesorectal excision due to the short-term risks associated with this surgery, and support further evaluation of short-course radiotherapy to achieve organ preservation in patients considered fit for total mesorectal excision. Larger randomised studies, such as the ongoing STAR-TREC study, are needed to more precisely determine oncological outcomes following different organ preservation treatment schedules. Cancer Research UK.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>33308452</pmid><doi>10.1016/S2468-1253(20)30333-2</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 2468-1253
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issn 2468-1253
2468-1253
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7802515
source MEDLINE; Alma/SFX Local Collection
subjects Adenocarcinoma - pathology
Adenocarcinoma - radiotherapy
Adenocarcinoma - surgery
Adolescent
Adult
Aged
Aged, 80 and over
Feasibility Studies
Female
Follow-Up Studies
Humans
Male
Middle Aged
Neoplasm Staging
Organ Sparing Treatments
Proctectomy
Radiotherapy, Adjuvant
Rectal Neoplasms - pathology
Rectal Neoplasms - radiotherapy
Rectal Neoplasms - surgery
Transanal Endoscopic Microsurgery
Treatment Outcome
Young Adult
title Radical surgery versus organ preservation via short-course radiotherapy followed by transanal endoscopic microsurgery for early-stage rectal cancer (TREC): a randomised, open-label feasibility study
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