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Regorafenib and Sintilimab in Combination With Electroacupuncture in MSS CRC

Not Applicable
Not yet recruiting
Conditions
Colorectal Cancer Metastatic
Interventions
Drug: Regorafenib and Sintilimab in combination with electroacupuncture
Registration Number
NCT06456515
Lead Sponsor
The First People's Hospital of Changzhou
Brief Summary

The aim of this clinical trial is to find out whether Regorafenib and Sintilimab in combination with electroacupuncture works in treating participants with microsatellite stable (MSS) advanced colorectal cancer who have failed one or more second-line standard chemotherapy regimens. It will also learn about the efficacy and safety of the combination therapy. The main questions the trial aims to answer are:

Does combination therapy reduce the overall survival time ? What medical problems do people have when they take combination therapy?

Participants will

Regorafenib, take for 2 weeks and stop for 1 week; Sintilimab, intravenous, every 3 weeks; Electroacupuncture was performed 1 day before, on the day of, and on the 2nd day after each cycle of Sintilimab administration, and patients completed 3 treatments in week 1, followed by 1 treatment per week for 2 weeks, with 5 treatments per dosing

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
40
Inclusion Criteria
  1. Fullly knowledge of the study and voluntarily sign the informed consent;
  2. Histologically and/or cytologically confirmed metastatic colorectal adenocarcinoma (Stage IV) with microsatellite stable (MSS)* confirmed by PCR or NGS;
  3. Receive at least two lines of standard chemotherapy in the past and have failed.
  4. No systemic chemotherapy or antitumor therapy such as radiotherapy, immunotherapy, biological or hormonal therapy in the past 4 weeks; and have never received VEGFR inhibitors
  5. Willing to receive electroacupuncture;
  6. Aged 18-75 years old (including 18 years old and 75 years old);
  7. Weighing more than 40 kg (including 40 kg);
  8. Able to take oral medication.
  9. Patients with adequate organ function at the time of enrollment are defined as follows: Neutrophil count ≥1500mm3 Platelet count ≥10.0 × 104/mm3 Hemoglobin (Hb) ≥ 9 g/dL Aspartate aminotransferase (AST), alanine aminotransferase (ALT) ≤100 U/L (≤100 U/L in patients with hepatocellular carcinoma, ≤250 U/L in patients with liver metastasis) Total bilirubin ≤1.5 mg /dL Creatinine ≤1.5 mg /dL Lipase ≤ 80 IU/L Urine Protein: one of the following (if any of the criteria are met, no other test may be performed) (i) Urine Protein (paper test) of 2+ or less (ii) UPC < 3.5 (iii) Urine Protein ≦ 3500 mg for 24 hour urine protein measurements. mg Prothrombin time (PT)-International Normalized Ratio (INR): ≤ 1.5 (≤ 3.0 for anticoagulant administration)
  10. Eastern Cooperative Oncology Group Physical Performance Score (ECOG PS) ≤ 1 (0-1);
  11. Cardiac function evaluation: left ventricular ejection fraction ≥ 50% (echocardiography);
  12. Clearly meet the criteria for evaluating the efficacy of solid tumors (e.g., echocardiograms) Measurable lesions that meet the requirements of RECIST 1.1;
  13. Expected survival of more than 12 weeks.
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Exclusion Criteria

Patients will be excluded from the study if any of the following criteria are met.

  1. Patients who have received systemic chemotherapy, radiotherapy, surgery, hormonal therapy or immunotherapy <2 weeks prior to enrolment. Immune checkpoint blockade pretreatment is permitted.
  2. Patients with a history of regorafenib administration.
  3. Patients with uncontrolled hypertension (systolic blood pressure ≥160 mmHg and diastolic blood pressure ≥90 mmHg) despite multiple antihypertensive medications; and
  4. Patients with acute coronary syndromes (including myocardial infarction and unstable angina) and a history of coronary angioplasty or stenting within 6 months prior to enrolment;
  5. Patients with a large pleural effusion or ascites requiring drainage; and
  6. Patients with grade ≥ 3 active infection according to NCI CTC AE version 4.03; patients with symptomatic brain metastases; and patients with a history of coronary artery angioplasty or stenting within the previous 6 months.
  7. Patients with symptomatic brain metastases;
  8. Patients with partial or complete gastrointestinal obstruction;
  9. Patients with interstitial lung disease with active signs or symptoms;
  10. Patients who test positive for anti-HIV-1 antibody, anti-HIV-2 antibody, hepatitis B surface antigen (HBsAg), or anti-hepatitis C virus (HCV)* *Patients who test positive for anti-hepatitis B surface (HBs) or anti-hepatitis B core (HBc) antibodies and patients with hepatitis B virus (HBV)-DNA measurements that are greater than the sensitivity of the test will also be excluded. Patients with concurrent autoimmune disease
  11. Patients with concurrent autoimmune disease or a history of chronic or recurrent autoimmune disease.
  12. Patients requiring systemic corticosteroids (excluding those given temporarily for testing, prophylactic administration for allergic reactions, or for the relief of swelling associated with radiotherapy) or immunosuppressive agents, or who have received such therapy <14 days prior to study participation;
  13. Patients with a history or finding of class ≥III congestive heart failure according to the New York Heart Association functional class;
  14. Patients with epilepsy requiring pharmacological treatment;
  15. Patients with grade 3 or greater bleeding within 4 weeks prior to enrolment.
  16. Patients who have undergone major surgery (open heart or caesarean section, etc.), caesarean biopsy, or trauma within 28 days prior to enrolment. the same day of the week prior to the 4-week period may be enrolled (however, in the case of manual anastomosis without bowel resection, this should be within 14 days prior to enrolment);
  17. Patients with non-healing wounds, non-healing ulcers or non-healing fractures.
  18. Patients with a history of hypersensitivity reaction to any investigational drug, analogue or excipient.
  19. Women who are pregnant or breastfeeding or have the potential to become pregnant.
  20. Patients with contraindications to electroacupuncture therapy or patients for whom electroacupuncture is contraindicated in accordance with TCM syndromes.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Regorafenib and Sintilimab in combination with electroacupunctureRegorafenib and Sintilimab in combination with electroacupuncture-
Primary Outcome Measures
NameTimeMethod
Overall survival (OS)Up to 2 years

The time from randomization to death

Secondary Outcome Measures
NameTimeMethod
Progression-free survival (PFS)Up to 2 years

The time from randomization until first evidence of disease progression or death

Time to progression (TTP)Up to 2 years

The time from randomization until first evidence of disease progression

Adverse events (AE)Up to 2 years

Use the Common Terminology Criteria for Adverse Events (CTCAE) v4.0. Grade refers to the severity of the AE. The CTCAE v4.0 assigns Grades 1 through 5 with unique clinical descriptions of severity for each AE based on this general guideline: Grade 1 Mild AE, Grade 2 Moderate AE, Grade 3 Severe AE, Grade 4 Life-threatening or disabling AE, Grade 5 Death related to AE.

Overall incidence of TEAE;

* Incidence of grade 3 or higher AE;

* Incidence of SAEs;

* Incidence of AEs leading to permanent discontinuation;

* Incidence of AEs leading to medication suspension or dose adjustment.

Immune-related adverse event (irAE)Up to 2 years
Disease control rate (DCR)Up to 2 years

Percentage of patients with advanced cancer whose therapeutic intervention has led to a complete response, partial response, or stable disease

Cancer-related fatigue(CRF)Up to 2 years

A distressing, persistent, subjective sense of physical, emotional, and/or cognitive tiredness or exhaustion related to cancer and/or cancer treatment that is not proportional to recent activity and interferes with usual functioning, use the Revised Piper Fatigue Scale (RPFS)

CmaxUp to 2 years

Based on non-compartmental PK evaluation.Cmax refers to the highest measured drug concentration which is obtained by collecting a series of blood samples and measuring the concentrations of drug in each sample.

Blood samples should be collected within 2 hours before electroacupuncture administration and 1 to 4 hours after electroacupuncture by weeks 2 and 3, and 2 hours before electroacupuncture in cycles 4-6

BiomarkerUp to 2 years

Biomarker analysis can be categorized as "non-genetic" (e.g., associated proteins) or "genetically relevant" (e.g., associated RNA or DNA).

Objective response rate (ORR)Up to 2 years

The proportion of patients that respond either partially or fully to therapy

Health-related quality of life (HRQoL)Up to 2 years

Assessment of patient quality of life with respect to health status

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