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)

Author:

Sun Myint Arthur1ORCID,Rao Christopher23,Barbet Nicolas4,Thamphya Brice5,Pace‐Loscos Tanguy5,Schiappa Renaud5,Magné Nicolas6,Martel‐Lafay Isabelle7,Mineur Laurent8,Deberne Melanie9,Zilli Thomas10,Dhadda Amandeep11,Gerard Jean Pierre5

Affiliation:

1. Clatterbridge Cancer Centre Liverpool UK

2. Department of Surgery and Cancer Imperial College London London UK

3. Department of Colorectal Surgery The Cumberland Infirmary Carlisle UK

4. ORLAM Lyon‐Villeurbanne‐Mâcon Villeurbanne France

5. Departement of Epidemiology, Biostatistic, and Health Data, Centre Antoine Lacassagne Université Côte d'Azur Nice France

6. Department of Radiation Oncology Saint‐Priest‐en‐Jarez France

7. Léon Bérard Cancer Center Lyon France

8. Department of Radiation Oncology Institute Sainte Catherine Avignon France

9. Centre Hospitalier Lyon‐Sud Lyon France

10. Department of Oncology University of Genève Genève Switzerland

11. Queen's Centre for Oncology Castle Hill Hospital Hull UK

Abstract

AbstractAimNonsurgical 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.

Publisher

Wiley

Subject

Gastroenterology

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Low energy contact X‐ray brachytherapy for treatment of rectal cancer: a health technology appraisal by Health Technology Wales;Colorectal Disease;2024-03-11

2. State of the Art Rektumchirurgie;Zentralblatt für Chirurgie - Zeitschrift für Allgemeine, Viszeral-, Thorax- und Gefäßchirurgie;2024-02

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