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

Author:

Cao Wuteng123ORCID,Hu Huabin234ORCID,Li Jiao123ORCID,Wu Qianyu123ORCID,Shi Lishuo235ORCID,Li Biao123ORCID,Zhou Jie123ORCID,Wang Xinhua123ORCID,Chen Junhong6ORCID,Wang Chao237ORCID,Wang Huaiming238ORCID,Deng Weihao237ORCID,Huang Yan237ORCID,Deng Yanhong234ORCID

Affiliation:

1. Department of Radiology, The Sixth Affiliated Hospital Sun Yat‐sen University Guangzhou Guangdong China

2. Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, The Sixth Affiliated Hospital Sun Yat‐sen University Guangzhou Guangdong China

3. Biomedical Innovation Center, The Sixth Affiliated Hospital Sun Yat‐sen University Guangzhou Guangdong China

4. Department of Medical Oncology, The Sixth Affiliated Hospital Sun Yat‐sen University Guangzhou Guangdong China

5. Clinical Research Center, The Sixth Affiliated Hospital Sun Yat‐sen University Guangzhou Guangdong China

6. School of Public Health (Shenzhen) Shenzhen Campus of Sun Yat‐sen University Shenzhen Guangdong China

7. Department of Pathology, The Sixth Affiliated Hospital Sun Yat‐sen University Guangzhou Guangdong China

8. Department of Colorectal Surgery, Department of General Surgery, The Sixth Affiliated Hospital Sun Yat‐sen University Guangzhou Guangdong China

Abstract

AbstractNeoadjuvant 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 (NCT 03926338). 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.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cancer Research,Oncology

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