Effects of Fasting Strategies on Postoperative Recovery and Long-term Prognosis in Patients With Colorectal Cancer

August 9, 2020 updated by: Changhong Miao, Fudan University

Effects of Different Fasting Strategies in Perioperative Period on Postoperative Recovery, Immune Function, and Long-term Prognosis in Patients With Radical Resection of Colorectal Cancer

In 2018, colorectal cancer is the third most common malignant tumor in terms of morbidity and second mortality in the world. Surgical resection is still the main treatment for colorectal cancer.With the introduction of the ERAS, the latest international and domestic guidelines for fasting before surgery all advocate shortening the fasting time. For example, 2 hours before surgery, oral take cleared fluids, including water, sugar water, fruit juice, tea and black coffee (without milk) is allowed.Solid food can be consumed 4 hours before surgery, and oral diet should be resumed as soon as possible after surgery. Changes in diet, nutritional status, and physical activity are closely related to the incidence of colorectal cancer. Therefore, we believe that the intestine may be very sensitive to different fasting times during the perioperative period. Prolonging the fasting time may improve the prognosis by improving postoperative insulin resistance, reducing inflammation and protecting anti-tumor immune function in patients with colorectal cancer.Prolonged fasting time seems to be contrary to the results of some studies, and whether it is applicable to patients with tumor surgery is unclear. Therefore, there is an urgent need to conduct large-scale, prospective, randomized controlled clinical studies to clarify the most suitable perioperative fasting strategy (including composition, interval, and amount) for cancer patients, which can not only reduce surgical stress and speed up postoperative rehabilitation,reduce postoperative metastasis and recurrence and improve mid- and long-term prognosis.

Study Overview

Status

Active, not recruiting

Intervention / Treatment

Detailed Description

As early as a century ago, Investigators proved that diet restriction can prevent the occurrence of transplanted tumors in mice. Following this milestone, many animal studies (from mice to primates) have confirmed that diet restriction can slow the development of spontaneous tumors and transplanted tumors. A study of macaque monkeys for more than 20 years revealed that restricting diet by 30% can reduce the incidence of tumors by 50%, which makes people see the potential value of restricting diet to humans. However, whether diet restriction can also reduce the incidence of human tumors is not entirely clear. The growth of tumor cells requires a nutrient-rich environment, and the lack of glucose and amino acids caused by diet restrictions is very detrimental to tumor cells. Unlike normal cells, tumor cells mainly rely on glycolysis (Warburg effect) rather than energy and biosynthetic precursors provided by oxidative phosphorylation for proliferation. These characteristics make tumor cells extremely sensitive to changes in the surrounding environment, which is called differential stress sensitization (DSS).Investigators found that the use of low sugar and low serum in a cell model to simulate periodic fasting can enhance the sensitivity of human or animal tumor cells to doxorubicin and cyclophosphamide, and also found that they were transplanted subcutaneously in mice Melanoma or breast cancer, diet combined with chemotherapy is better than chemotherapy alone; in the mouse metastatic neuroblastoma model, fasting before high-dose chemotherapy can successfully reduce the toxic side effects of chemotherapy drugs and reduce metastasis and prolong the tumor-free survival. Surgery and stress are twin brothers. Surgical resection, blood flow blockage, ischemia-reperfusion injury, tissue damage, local inflammatory factor release, and changes in systemic neuroendocrine and metabolism all affect blood flow, blood coagulation, and immune function. Investgators found restricted diet can reduce the inflammatory response after myocardial ischemia-reperfusion injury in mice. Many animal experiments have confirmed that perioperative fasting can effectively protect the liver, kidneys, and brain from organ damage. The specific mechanism may be related to fasting increasing antioxidant enzyme activity, reducing insulin-like growth factor-1 (IGF-1), and activating the autophagy pathway. Similar to chemotherapy, there is currently no randomized clinical controlled study to evaluate the impact of individualized perioperative dietary regimens (such as restricted diet) on the prognosis of tumor surgery.

In 2018, colorectal cancer is the third most common malignant tumor in terms of morbidity and second mortality in the world. Surgical resection is still the main treatment for colorectal cancer.With the introduction of the ERAS, the latest international and domestic guidelines for fasting before surgery all advocate shortening the fasting time. For example, 2 hours before surgery, oral take cleared fluids, including water, sugar water, fruit juice, tea and black coffee (without milk) is allowed.Solid food can be consumed 6 hours before surgery, and oral diet should be resumed as soon as possible after surgery. Changes in diet, nutritional status, and physical activity are closely related to the incidence of colorectal cancer. Therefore, we believe that the intestine may be very sensitive to different fasting times during the perioperative period. Prolonging the fasting time may improve the prognosis by improving postoperative insulin resistance, reducing inflammation and protecting anti-tumor immune function in patients with colorectal cancer.Prolonged fasting time seems to be contrary to the results of some studies, and whether it is applicable to patients with tumor surgery is unclear. Therefore, there is an urgent need to conduct large-scale, prospective, randomized controlled clinical studies to clarify the most suitable perioperative fasting strategy (including composition, interval, and amount) for cancer patients, which can not only reduce surgical stress and speed up postoperative rehabilitation,reduce postoperative metastasis and recurrence and improve mid- and long-term prognosis.

Study Type

Interventional

Enrollment (Anticipated)

2400

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Shanghai
      • Shanghai, Shanghai, China, 200032
        • Fudan University Shanghai Cancer Center
      • Shanghai, Shanghai, China, 200032
        • Department of Biostatistics, School of Public Health, Fudan University,
      • Shanghai, Shanghai, China, 200032
        • Fudan University Huashan Hospital
      • Shanghai, Shanghai, China, 200032
        • Fudan University,ZhongShan Hospital
      • Shanghai, Shanghai, China, 200032
        • Shanghai Changhai Hospital, Naval Medical University,
      • Shanghai, Shanghai, China, 200032
        • Shanghai First People's Hospital,Shanghai Jiaotong University
      • Shanghai, Shanghai, China, 200032
        • Shanghai Tongji Hospital,Tongji University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 70 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Age 20 ~ 70 years old
  2. With BMI 20.5-25.0 kg/m2
  3. Without any Endocrine and metabolic diseases
  4. A stable body weight (±3 kg) for at least 6 months
  5. Those diagnosed with colorectal cancer by preoperative pathology or enteroscopy
  6. Patients undergoing laparoscopic radical colorectal cancer resection
  7. ASA grade I-III grade
  8. Initial patients have not received any treatment for bowel cancer except neoadjuvant chemotherapy
  9. Patients with confirmed and feasible radical resection of colorectal cancer
  10. No evidence of distant metastasis before surgery
  11. Willing to participate in the research of the subject and agree to follow up regularly

Exclusion Criteria:

  1. Patients with relapsed colorectal cancer who are going to undergo surgery and re-excision
  2. accompanied by other malignant tumors
  3. Severe malnourished patients
  4. History of systemic metabolism such as diabetes
  5. Before surgery, have received other treatments for colorectal cancer (such as local excision, etc.) in addition to neoadjuvant chemotherapy
  6. Have a history of immunotherapy before surgery
  7. Combined with basic diseases of serious heart, lung, brain, kidney and other important organs
  8. Combined with severe primary diseases such as severe immune system or hematopoietic system
  9. The tumor burden cannot be cured, and there is distant metastasis. Those who intend to undergo palliative surgery
  10. People with gastroesophageal reflux disease, difficulty swallowing, intestinal obstruction, or difficulty in airway management
  11. People who refuse to participate in the study or cannot receive long-term follow-up

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
PLACEBO_COMPARATOR: Normal Fasting
The patient starts fasting 8 hours before the operation,and does not take any solid or liquid foods and nutrients during the fasting process.The fasting period does not strictly limit the consumption of pure water,After surgery 8 hours,the patients was allowed to feeding.
Normal Fasting hours before CRC surgery for 8 hours and feeding 8 hours after surgery; Prolong fasting hours before CRC surgery for 24 hours and feeding 24 hours after surgery.
EXPERIMENTAL: Prolong Fasting
The patient starts fasting 24 hours before the operation, and does not take any solid or liquid foods and nutrients during the fasting process. The fasting period does not strictly limit the consumption of pure water.After surgery 24 hours,the patients was allowed to feeding.
Normal Fasting hours before CRC surgery for 8 hours and feeding 8 hours after surgery; Prolong fasting hours before CRC surgery for 24 hours and feeding 24 hours after surgery.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Disease-free Survival
Time Frame: During 2 years after surgery
Defined and calculated as the time from the date of surgery to the first time of colon cancer recurrence or metastasis or cancer-related death
During 2 years after surgery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postoperative pain score and side effects of patient-controlled analgesia
Time Frame: During the first 48 hours after surgery
Assessed with visual analogue score ( 0 is no pain and 10 is the most severe pain)
During the first 48 hours after surgery
Incidence of delirium
Time Frame: During the first 1 week after surgery
Assessed for delirium using the 3D-CAM instrument
During the first 1 week after surgery
Return of bowel function
Time Frame: During the first 30 days after surgery
Measured by the time of first flatus
During the first 30 days after surgery
Overall Survival
Time Frame: During 2 years after surgery
Defined and calculated as the time from the date of surgery to the first time of Colon cancer recurrence or metastasis or cancer-related death
During 2 years after surgery
Length of stay in hospital after surgery and total costs after surgery
Time Frame: During the first 30 days after surgery
Length of stay in hospital after surgery and total costs after surgery
During the first 30 days after surgery
Neutrophil to Lymphocyte Ratio,LMR,SII
Time Frame: During the first24、48 and 72 hours after surgery
Neutrophil to Lymphocyte Ratio,Lymphocyte to Monocyte ratio,Symstem Imflammatory Index
During the first24、48 and 72 hours after surgery
Serum CA19-9 、CA125、CEA、CA72-4、CA242、AFP、CA15-3、CA50 levels
Time Frame: During 2 years after surgery
Tumor Biomaker Level
During 2 years after surgery
Recovery Parameter
Time Frame: During the first24、48 and 72 hours after surgery
Q40 scale score
During the first24、48 and 72 hours after surgery
T Lymphocyte cell count
Time Frame: During the first24、48 and 72 hours after surgery
T lymphocyte cell count before fasting and after fasting
During the first24、48 and 72 hours after surgery
T Lymphocyte cell DNA damage
Time Frame: During the first24、48 and 72 hours after surgery
T lymphocyte cell count before fasting and after fasting
During the first24、48 and 72 hours after surgery
IL-1β,IL-2,IL-4,IL-5,IL-6,IL-8,IL-10,IL-17A,IL-17F,TNF-α,TNF-β,
Time Frame: During the first24、48 and 72 hours after surgery
Inflammatory factor level
During the first24、48 and 72 hours after surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 1, 2020

Primary Completion (ANTICIPATED)

September 30, 2022

Study Completion (ANTICIPATED)

September 30, 2023

Study Registration Dates

First Submitted

April 8, 2020

First Submitted That Met QC Criteria

April 10, 2020

First Posted (ACTUAL)

April 15, 2020

Study Record Updates

Last Update Posted (ACTUAL)

August 11, 2020

Last Update Submitted That Met QC Criteria

August 9, 2020

Last Verified

August 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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