2023
DOI: 10.1007/s10388-023-00998-x
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Prognostic impact of endoscopic response evaluation after neoadjuvant chemotherapy for esophageal squamous cell carcinoma: a nationwide validation study

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Cited by 5 publications
(2 citation statements)
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“…We employed a stricter criterion to exclude any residual disease based on endoscopic findings, resulting in high specificity (0.88) and moderate sensitivity (0.67) in predicting MPR. Previous neoadjuvant chemotherapy studies have demonstrated a strong correlation between endoscopic response according to post-neoadjuvant macroscopic findings and pathologic response, with higher percentages of histological responders in endoscopic responders (45−58%) compared to endoscopic non-responders (7-16%) [46][47][48]. While the specificity and sensitivity of endoscopic evaluation slightly differ from our study due to different evaluation criteria, these Japanese studies support our findings.…”
Section: Discussionsupporting
confidence: 86%
“…We employed a stricter criterion to exclude any residual disease based on endoscopic findings, resulting in high specificity (0.88) and moderate sensitivity (0.67) in predicting MPR. Previous neoadjuvant chemotherapy studies have demonstrated a strong correlation between endoscopic response according to post-neoadjuvant macroscopic findings and pathologic response, with higher percentages of histological responders in endoscopic responders (45−58%) compared to endoscopic non-responders (7-16%) [46][47][48]. While the specificity and sensitivity of endoscopic evaluation slightly differ from our study due to different evaluation criteria, these Japanese studies support our findings.…”
Section: Discussionsupporting
confidence: 86%
“…Furthermore, the τ value of the binary variable has a theoretical upper limit of 0.75; hence, there is also the problem that a high value cannot be obtained. It was reported previously that pathological grade is a reliable predictor of prognosis 39 , and that endoscopic response is correlated with prognosis 40 . In the future, early postoperative outcomes, such as pCR, may be used as the primary endpoint to shorten the duration of clinical trials, such as phase II trials.…”
Section: Discussionmentioning
confidence: 96%