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DOI: 10.1055/a-2032-3646
Magnifying endoscopy with narrow-band imaging and salvage endoscopic submucosal dissection of a locally advanced rectal adenocarcinoma after neoadjuvant chemoradiotherapy
A 61-year-old man underwent colonoscopy because of bloody stools. Colonoscopy showed an elevated lesion of 25 × 15 mm about 3 cm from the anus ([Fig. 1 a]). Histological examination of the biopsy indicated that this was an adenocarcinoma. Endoscopic ultrasound (EUS) showed that the lesion was involving the muscularis propria. Computed tomography (CT) and rectal magnetic resonance imaging (MRI) resulted in a staging classification of T2N0M0.


The patient had a strong desire for his anus to be preserved, so neoadjuvant chemoradiotherapy (nCRT) was carried out first. The patient received 45 Gy of radiotherapy in 25 fractions to the pelvic lymph node drainage area and 50.4 Gy in three fractions to the rectal tumor. He then took capecitabine orally. Follow-up colonoscopy 4 months later showed that the tumor had regressed significantly. The residual tumor appeared to be a 0-IIa lesion of 6 × 8 mm with a white scar ([Fig. 1 b, c]). Under magnifying endoscopy with narrow-band imaging (ME-NBI), the surface and vascular patterns looked like type 2B on JNET typing ([Fig. 2]; [Video 1]). EUS revealed that the lesion was located within the mucosa ([Fig. 1 d]). There was no evidence of metastasis on CT imaging ([Fig. 1 e]). Rectal MRI showed that the lower segment of the rectum was slightly thickened, but no suspicious lymph nodes were seen ([Fig. 1 f]). With the signs indicating tumor downstaging, the patient still declined surgery. It was agreed that he would undergo salvage endoscopic submucosal dissection (ESD) to assess the pathologic response.


Video 1 Endoscopic features and salvage endoscopic submucosal dissection procedure for a locally advanced rectal adenocarcinoma that had been treated with neoadjuvant chemoradiotherapy.
Quality:
Although the lesion was locally scarred, salvage ESD was performed successfully ([Fig. 3]) and was not as difficult as expected. The pathological results showed that the residual adenocarcinoma was confined within the mucosa ([Fig. 4]) and that the lateral and vertical margins were negative, meaning partial pathological complete response and an R0 resection. After further discussion with surgeons and oncologists, the patient chose follow-up and observation and, 4 months later, rectal MRI showed no signs of residual disease or recurrence ([Fig. 5]). The patient is still being closely followed up.






Salvage ESD for locally advanced rectal cancer after nCRT is technically feasible [1] [2]. There should be a diagnostic role for salvage ESD in assessing the pathologic response to nCRT and a possible therapeutic role in resecting residual lesions, with the potential to avoid surgery.
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Competing interests
The authors declare that they have no conflict of interest.
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References
- 1 Ali F, Keshinro A, Weiser M. Advances in the treatment of locally advanced rectal cancer. Ann Gastroenterol Surg 2020; 5: 32-38
- 2 Leung G, Nishimura M, Hingorani N. et al. Technical feasibility of salvage endoscopic submucosal dissection after chemoradiation for locally advanced rectal adenocarcinoma. Gastrointest Endosc 2022; 96: 359-367
Corresponding author
Publication History
Article published online:
30 March 2023
© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 Ali F, Keshinro A, Weiser M. Advances in the treatment of locally advanced rectal cancer. Ann Gastroenterol Surg 2020; 5: 32-38
- 2 Leung G, Nishimura M, Hingorani N. et al. Technical feasibility of salvage endoscopic submucosal dissection after chemoradiation for locally advanced rectal adenocarcinoma. Gastrointest Endosc 2022; 96: 359-367









