China special issue on gastrointestinal tumors-Radiological features of pathological complete response in mismatch repair deficient colorectal cancer after neoadjuvant PD-1 blockade : A post hoc analysis of the PICC phase II trial
© 2023 UICC..
Neoadjuvant programmed cell death protein 1 (PD-1) blockade exhibits promising efficacy in patients with mismatch repair deficient (dMMR) colorectal cancer (CRC). However, discrepancies between radiological and histological findings have been reported in the PICC phase II trial (NCT03926338). Therefore, we strived to discern radiological features associated with pathological complete response (pCR) based on computed tomography (CT) images. Data were obtained from the PICC trial that included 36 tumors from 34 locally advanced dMMR CRC patients, who received neoadjuvant PD-1 blockade for 3 months. Among the 36 tumors, 28 (77.8%) tumors achieved pCR. There were no statistically significant differences in tumor longitudinal diameter, the percentage change in tumor longitudinal diameter from baseline, primary tumor sidedness, clinical stage, extramural venous invasion status, intratumoral calcification, peritumoral fat infiltration, intestinal fistula and tumor necrosis between the pCR and non-pCR tumors. Otherwise, tumors with pCR had smaller posttreatment tumor maximum thickness (median: 10 mm vs 13 mm, P = .004) and higher percentage decrease in tumor maximum thickness from baseline (52.9% vs 21.6%, P = .005) compared to non-pCR tumors. Additionally, a higher proportion of the absence of vascular sign (P = .003, odds ratio [OR] = 25.870 [95% CI, 1.357-493.110]), nodular sign (P < .001, OR = 189.000 [95% CI, 10.464-3413.803]) and extramural enhancement sign (P = .003, OR = 21.667 [2.848-164.830]) was observed in tumors with pCR. In conclusion, these CT-defined radiological features may have the potential to serve as valuable tools for clinicians in identifying patients who have achieved pCR after neoadjuvant PD-1 blockade, particularly in individuals who are willing to adopt a watch-and-wait strategy.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:153 |
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Enthalten in: |
International journal of cancer - 153(2023), 11 vom: 01. Dez., Seite 1894-1903 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Cao, Wuteng [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 16.10.2023 Date Revised 16.10.2023 published: Print-Electronic ClinicalTrials.gov: NCT03926338 Citation Status MEDLINE |
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doi: |
10.1002/ijc.34647 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM359107087 |
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245 | 1 | 0 | |a China special issue on gastrointestinal tumors-Radiological features of pathological complete response in mismatch repair deficient colorectal cancer after neoadjuvant PD-1 blockade |b A post hoc analysis of the PICC phase II trial |
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500 | |a published: Print-Electronic | ||
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500 | |a Citation Status MEDLINE | ||
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520 | |a Neoadjuvant programmed cell death protein 1 (PD-1) blockade exhibits promising efficacy in patients with mismatch repair deficient (dMMR) colorectal cancer (CRC). However, discrepancies between radiological and histological findings have been reported in the PICC phase II trial (NCT03926338). Therefore, we strived to discern radiological features associated with pathological complete response (pCR) based on computed tomography (CT) images. Data were obtained from the PICC trial that included 36 tumors from 34 locally advanced dMMR CRC patients, who received neoadjuvant PD-1 blockade for 3 months. Among the 36 tumors, 28 (77.8%) tumors achieved pCR. There were no statistically significant differences in tumor longitudinal diameter, the percentage change in tumor longitudinal diameter from baseline, primary tumor sidedness, clinical stage, extramural venous invasion status, intratumoral calcification, peritumoral fat infiltration, intestinal fistula and tumor necrosis between the pCR and non-pCR tumors. Otherwise, tumors with pCR had smaller posttreatment tumor maximum thickness (median: 10 mm vs 13 mm, P = .004) and higher percentage decrease in tumor maximum thickness from baseline (52.9% vs 21.6%, P = .005) compared to non-pCR tumors. Additionally, a higher proportion of the absence of vascular sign (P = .003, odds ratio [OR] = 25.870 [95% CI, 1.357-493.110]), nodular sign (P < .001, OR = 189.000 [95% CI, 10.464-3413.803]) and extramural enhancement sign (P = .003, OR = 21.667 [2.848-164.830]) was observed in tumors with pCR. In conclusion, these CT-defined radiological features may have the potential to serve as valuable tools for clinicians in identifying patients who have achieved pCR after neoadjuvant PD-1 blockade, particularly in individuals who are willing to adopt a watch-and-wait strategy | ||
650 | 4 | |a Clinical Trial, Phase II | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a colorectal cancer | |
650 | 4 | |a computed tomography | |
650 | 4 | |a neoadjuvant PD-1 blockade | |
650 | 4 | |a pathological complete response | |
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650 | 7 | |a Immune Checkpoint Inhibitors |2 NLM | |
700 | 1 | |a Hu, Huabin |e verfasserin |4 aut | |
700 | 1 | |a Li, Jiao |e verfasserin |4 aut | |
700 | 1 | |a Wu, Qianyu |e verfasserin |4 aut | |
700 | 1 | |a Shi, Lishuo |e verfasserin |4 aut | |
700 | 1 | |a Li, Biao |e verfasserin |4 aut | |
700 | 1 | |a Zhou, Jie |e verfasserin |4 aut | |
700 | 1 | |a Wang, Xinhua |e verfasserin |4 aut | |
700 | 1 | |a Chen, Junhong |e verfasserin |4 aut | |
700 | 1 | |a Wang, Chao |e verfasserin |4 aut | |
700 | 1 | |a Wang, Huaiming |e verfasserin |4 aut | |
700 | 1 | |a Deng, Weihao |e verfasserin |4 aut | |
700 | 1 | |a Huang, Yan |e verfasserin |4 aut | |
700 | 1 | |a Deng, Yanhong |e verfasserin |4 aut | |
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