PD-1 blockade in neoadjuvant setting of DNA mismatch repair-deficient/microsatellite instability-high colorectal cancer.
Ding-Xin LiuDan-Dan LiWan HeChuan-Feng KeWu JiangJing-Hua TangLing-Heng KongYuan LiQiao-Qi SuiBin-Yi XiaoWei-Rong LiZhi-Gang HongRui-Hua XuZhi-Zhong PanXiao-Shi ZhangPei-Rong DingPublished in: Oncoimmunology (2020)
Background: Although PD-1 blockade has significantly improved the survival of metastatic colorectal cancer with DNA Mismatch Repair-Deficient/Microsatellite Instability-High (MSI-H), the data on neoadjuvant setting is limited. Methods: In this retrospective study, we enrolled eight patients with advanced MSI-H colorectal cancer from three hospitals. Four patients are locally advanced and four are metastatic. All the patients received at least two doses of PD-1 antibody with or without chemotherapy as neoadjuvant therapy. The aim of the present study was to evaluate the short-term efficacy and toxicities of this strategy. Results: All the enrolled eight patients had a major response in imaging and/or pathological evaluation. Five of the seven resected patients were evaluated as pathological complete response. One patient without surgery has a clinical complete response (cCR) tumor response. Conclusions: Neoadjuvant PD-1 blockade induced tumor regression with a major clinical and pathological response in advanced dMMR/MSI-H colorectal cancer. Further studies are required to evaluate the long-term effect of this strategy.
Keyphrases
- locally advanced
- end stage renal disease
- rectal cancer
- newly diagnosed
- chronic kidney disease
- ejection fraction
- lymph node
- squamous cell carcinoma
- prognostic factors
- healthcare
- stem cells
- small cell lung cancer
- neoadjuvant chemotherapy
- endothelial cells
- machine learning
- cell free
- mass spectrometry
- deep learning
- regulatory t cells
- patient reported
- circulating tumor
- cell therapy
- photodynamic therapy
- data analysis
- replacement therapy
- atrial fibrillation