Rectal cancer is one of the common malignant tumors of the digestive tract. Some patients with rectal cancer are already advanced tumors when they are first diagnosed. At this time, the tumor has local infiltration, the probability of recurrence and metastasis after surgical resection is high, and even radical tumor resection cannot be performed. Neoadjuvant chemotherapy and radiotherapy have become one of the important treatment methods for these patients to increase the rate of radical tumor resection. However, a series of side effects of neoadjuvant radiotherapy can even continue after the end of radiotherapy, and even increase the incidence of postoperative complications. Superselective arterial interventional chemotherapy has been widely used in preoperative neoadjuvant chemotherapy for various tumors, and its efficacy in rectal cancer has also been confirmed. In addition, as a hot spot in tumor treatment, tumor immunotherapy has shown exciting effects in the NICHE study of neoadjuvant immunotherapy before colon cancer surgery. Moreover, Oxaliplatin is a classic chemotherapeutic drug that induces Immunogenic cell death effects, which induce antitumor immunity. Therefore, in order to optimize the preoperative neoadjuvant therapy plan, the investigators propose a treatment method of superselective arterial chemoembolization combined with immunotherapy and systemic chemotherapy, in order to obtain better preoperative conversion therapy effect and reduce the adverse reactions of neoadjuvant therapy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
83
The blood supplying artery of the tumor is selected for drug injection with Oxaliplatin 85mg/m2 combined Raltitrexed 3mg/m2. After drug injection, gelatin sponge is used for embolization.
Tislelizumab Injection 200mg i.v. q3w, A total of 3 cycles are administered.
Capecitabine 1,000 mg/m2 bid, po, on days 1-14 Oxaliplatin: 130 mg/m2, i.v. day 1 Cycles are repeated on day 22. A total of 3 cycles are administered.
Pelvic MRI to evaluate efficacy
Surgical treatment for patients who meet the surgical conditions
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Yiwu, Zhejiang, China
RECRUITINGImaging Tumor Regression Rate
Tumor regression on imaging after neoadjuvant therapy
Time frame: From date of the start of drugs treatment until the end of drugs treatment (nearly 3 weeks)
Pathologic Complete Response
There is no histological evidence of malignancy in the primary tumor and metastatic regional lymph nodes, or there is only a carcinoma in situ component
Time frame: From date of the start of drugs treatment until the operation is completed (nearly 4 weeks)
Disease Free Survival
Time from postoperative disease-free survival to disease recurrence or metastasis
Time frame: 36 months
Safety (The side effects)
The side effects of this study
Time frame: 36 months
Pathological Tumor Regression Rate
Tumor regression on pathology after neoadjuvant therapy
Time frame: From date of the start of drugs treatment until the end of drugs treatment (nearly 3 weeks)
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