Long-term oncological outcomes of endoscopic full-thickness resection after previous incomplete resection of low-risk T1 CRC (LOCAL-study): study protocol of a national prospective cohort study.


Journal

BMC gastroenterology
ISSN: 1471-230X
Titre abrégé: BMC Gastroenterol
Pays: England
ID NLM: 100968547

Informations de publication

Date de publication:
13 Dec 2022
Historique:
received: 25 08 2022
accepted: 21 11 2022
entrez: 13 12 2022
pubmed: 14 12 2022
medline: 16 12 2022
Statut: epublish

Résumé

T1 colorectal cancer (CRC) without histological high-risk factors for lymph node metastasis (LNM) can potentially be cured by endoscopic resection, which is associated with significantly lower morbidity, mortality and costs compared to radical surgery. An important prerequisite for endoscopic resection as definite treatment is the histological confirmation of tumour-free resection margins. Incomplete resection with involved (R1) or indeterminate (Rx) margins is considered a strong risk factor for residual disease and local recurrence. Therefore, international guidelines recommend additional surgery in case of R1/Rx resection, even in absence of high-risk factors for LNM. Endoscopic full-thickness resection (eFTR) is a relatively new technique that allows transmural resection of colorectal lesions. Local scar excision after prior R1/Rx resection of low-risk T1 CRC could offer an attractive minimal invasive strategy to achieve confirmation about radicality of the previous resection or a second attempt for radical resection of residual luminal cancer. However, oncologic safety has not been established and long-term data are lacking. Besides, surveillance varies widely and requires standardization. In this nationwide, multicenter, prospective cohort study we aim to assess feasibility and oncological safety of completion eFTR following incomplete resection of low-risk T1 CRC. The primary endpoint is to assess the 2 and 5 year luminal local tumor recurrence rate. Secondary study endpoints are to assess feasibility, percentage of curative eFTR-resections, presence of scar tissue and/or complete scar excision at histopathology, safety of eFTR compared to surgery, 2 and 5 year nodal and/or distant tumor recurrence rate and 5-year disease-specific and overall-survival rate. Since the implementation of CRC screening programs, the diagnostic rate of T1 CRC is steadily increasing. A significant proportion is not recognized as cancer before endoscopic resection and is therefore resected through conventional techniques primarily reserved for benign polyps. As such, precise histological assessment is often hampered due to cauterization and fragmentation and frequently leads to treatment dilemmas. This first prospective trial will potentially demonstrate the effectiveness and oncological safety of completion eFTR for patients who have undergone a previous incomplete T1 CRC resection. Hereby, substantial surgical overtreatment may be avoided, leading to treatment optimization and organ preservation. Trial registration Nederlands Trial Register, NL 7879, 16 July 2019 ( https://trialregister.nl/trial/7879 ).

Sections du résumé

BACKGROUND BACKGROUND
T1 colorectal cancer (CRC) without histological high-risk factors for lymph node metastasis (LNM) can potentially be cured by endoscopic resection, which is associated with significantly lower morbidity, mortality and costs compared to radical surgery. An important prerequisite for endoscopic resection as definite treatment is the histological confirmation of tumour-free resection margins. Incomplete resection with involved (R1) or indeterminate (Rx) margins is considered a strong risk factor for residual disease and local recurrence. Therefore, international guidelines recommend additional surgery in case of R1/Rx resection, even in absence of high-risk factors for LNM. Endoscopic full-thickness resection (eFTR) is a relatively new technique that allows transmural resection of colorectal lesions. Local scar excision after prior R1/Rx resection of low-risk T1 CRC could offer an attractive minimal invasive strategy to achieve confirmation about radicality of the previous resection or a second attempt for radical resection of residual luminal cancer. However, oncologic safety has not been established and long-term data are lacking. Besides, surveillance varies widely and requires standardization.
METHODS/DESIGN METHODS
In this nationwide, multicenter, prospective cohort study we aim to assess feasibility and oncological safety of completion eFTR following incomplete resection of low-risk T1 CRC. The primary endpoint is to assess the 2 and 5 year luminal local tumor recurrence rate. Secondary study endpoints are to assess feasibility, percentage of curative eFTR-resections, presence of scar tissue and/or complete scar excision at histopathology, safety of eFTR compared to surgery, 2 and 5 year nodal and/or distant tumor recurrence rate and 5-year disease-specific and overall-survival rate.
DISCUSSION CONCLUSIONS
Since the implementation of CRC screening programs, the diagnostic rate of T1 CRC is steadily increasing. A significant proportion is not recognized as cancer before endoscopic resection and is therefore resected through conventional techniques primarily reserved for benign polyps. As such, precise histological assessment is often hampered due to cauterization and fragmentation and frequently leads to treatment dilemmas. This first prospective trial will potentially demonstrate the effectiveness and oncological safety of completion eFTR for patients who have undergone a previous incomplete T1 CRC resection. Hereby, substantial surgical overtreatment may be avoided, leading to treatment optimization and organ preservation. Trial registration Nederlands Trial Register, NL 7879, 16 July 2019 ( https://trialregister.nl/trial/7879 ).

Identifiants

pubmed: 36513968
doi: 10.1186/s12876-022-02591-5
pii: 10.1186/s12876-022-02591-5
pmc: PMC9749288
doi:

Types de publication

Clinical Trial Protocol Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

516

Subventions

Organisme : Maarten van der Weijden foundation
ID : 2022-34

Informations de copyright

© 2022. The Author(s).

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Auteurs

L W Zwager (LW)

Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers Location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Amsterdam, The Netherlands.

L M G Moons (LMG)

Department of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands.

A Farina Sarasqueta (A)

Department of Pathology, Amsterdam University Medical Center, Amsterdam, The Netherlands.

M M Laclé (MM)

Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.

S C Albers (SC)

Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers Location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Amsterdam, The Netherlands.

R Hompes (R)

Department of Surgery, Amsterdam University Medical Center, Amsterdam, The Netherlands.

K C M J Peeters (KCMJ)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

F C Bekkering (FC)

Department of Gastroenterology and Hepatology, IJsselland Hospital, Capelle Aan Den Ijssel, The Netherlands.

J J Boonstra (JJ)

Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.

F Ter Borg (F)

Department of Gastroenterology and Hepatology, Deventer Hospital, Deventer, The Netherlands.

P R Bos (PR)

Department of Gastroenterology and Hepatology, Gelderse Vallei, Ede, The Netherlands.

G J Bulte (GJ)

Department of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, The Netherlands.

E A R Gielisse (EAR)

Department of Gastroenterology and Hepatology, Rode Kruis Hospital, Beverwijk, The Netherlands.

W L Hazen (WL)

Department of Gastroenterology and Hepatology, Elisabeth Tweesteden Hospital, Tilburg, The Netherlands.

W R Ten Hove (WR)

Department of Gastroenterology and Hepatology, Alrijne Medical Group, Leiden, The Netherlands.

M H M G Houben (MHMG)

Department of Gastroenterology and Hepatology, Haga Teaching Hospital, the Hague, The Netherlands.

M W Mundt (MW)

Department of Gastroenterology and Hepatology, Flevoziekenhuis, Almere, The Netherlands.

W B Nagengast (WB)

Department of Gastroenterology and Hepatology, University Medical Center Groningen, Groningen, The Netherlands.

L E Perk (LE)

Department of Gastroenterology and Hepatology, Haaglanden Medical Center, The Hague, The Netherlands.

R Quispel (R)

Department of Gastroenterology and Hepatology, Reinier de Graaf, Delft, The Netherlands.

S T Rietdijk (ST)

Department of Gastroenterology and Hepatology, OLVG, Amsterdam, The Netherlands.

F J Rando Munoz (FJ)

Department of Gastroenterology and Hepatology, Nij Smellinghe Hospital, Drachten, The Netherlands.

R J J de Ridder (RJJ)

Department of Gastroenterology and Hepatology, Maastricht University Medical Center, Maastricht, The Netherlands.

M P Schwartz (MP)

Department of Gastroenterology and Hepatology, Meander Medical Center, Amersfoort, The Netherlands.

R M Schreuder (RM)

Department of Gastroenterology and Hepatology, Catharina Hospital, Eindhoven, The Netherlands.

T C J Seerden (TCJ)

Department of Gastroenterology and Hepatology, Amphia Hospital, Breda, The Netherlands.

H van der Sluis (H)

Department of Gastroenterology and Hepatology, Isala Clinics, Zwolle, The Netherlands.

B W van der Spek (BW)

Department of Gastroenterology and Hepatology, Noordwest Hospital Group, Alkmaar, The Netherlands.

J W A Straathof (JWA)

Department of Gastroenterology and Hepatology, Màxima Medical Center, Veldhoven, The Netherlands.

J S Terhaar Sive Droste (JS)

Department of Gastroenterology and Hepatology, Jeroen Bosch Hospital, S' Hertogenbosch, The Netherlands.

M S Vlug (MS)

Department of Gastroenterology and Hepatology, Dijklander Hospital, Hoorn, The Netherlands.

W van de Vrie (W)

Department of Gastroenterology and Hepatology, Albert Schweitzer Hospital, Dordrecht, The Netherlands.

B L A M Weusten (BLAM)

Department of Gastroenterology and Hepatology, St. Antonius Hospital, Nieuwegein, The Netherlands.

T D de Wijkerslooth (TD)

Department of Gastrointestinal Oncology, Netherlands Cancer Institute/Antoni Van Leeuwenhoek, Amsterdam, The Netherlands.

H J Wolters (HJ)

Department of Gastroenterology and Hepatology, Martini Hospital, Groningen, The Netherlands.

P Fockens (P)

Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers Location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Amsterdam, The Netherlands.

E Dekker (E)

Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers Location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Amsterdam, The Netherlands.

B A J Bastiaansen (BAJ)

Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers Location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands. b.a.bastiaansen@amsterdamumc.nl.
Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam, The Netherlands. b.a.bastiaansen@amsterdamumc.nl.
Cancer Center Amsterdam, Amsterdam, The Netherlands. b.a.bastiaansen@amsterdamumc.nl.

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