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Effects of Preoperative Enteral Immunonutrition for Esophageal Cancer Patients Given Neoadjuvant Chemoradiotherapy (POINT)

Primary Purpose

Esophageal Neoplasms

Status
Recruiting
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Preoperative immunonutrition
Sponsored by
Hecheng Li M.D., Ph.D
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Esophageal Neoplasms focused on measuring Esophageal Neoplasms, Neoadjuvant Therapy, Enteral Nutrition, Nutrition Therapy

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologically confirmed esophageal cancer
  • Staging as cT2N0M0 with high-risk lesions (lymphovascular invasion, ≥3cm, poorly differentiated) / cT1b-2N+M0 / cT3-4aN0-3M0 with the need of neoadjuvant therapy before radical esophagectomy
  • Tolerance with oral intake (at least fluid diet)
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤2
  • Body Mass Index (BMI) ≥ 18.5 kg/m2 before recruitment
  • Patient's approval and written informed consent

Exclusion Criteria:

  • Expected survival time less than 6 months
  • Complete dysphagia
  • Pregnant or breast-feeding women
  • Unable to obey the interventions because of any reasons
  • Serious co-morbidities (cardiac, pulmonary, liver, kidney, brain, hematologic, endocrine and other diseases) in patients who cannot tolerate neoadjuvant therapy and/or surgery
  • History of previous thoracic or abdominal surgery
  • History of other malignant tumor (previous or current)

Sites / Locations

  • Fujian Medical University Union HospitalRecruiting
  • Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University School of MedicineRecruiting
  • Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of MedicineRecruiting
  • Shanghai Chest Hospital Affiliated to Shanghai Jiao Tong UniversityRecruiting
  • Zhongshan Hospital Affiliated to Fudan University
  • Shanghai East Hospital, Tongji University School of Medicine
  • Cancer Hospital of University of Chinese Academy of Sciences, Zhejiang Cancer HospitalRecruiting
  • Ningbo Medical Center Lihuili HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Interventional group

Control group

Arm Description

Patients receive omega-3 fatty-acid enriched enteral nutritional emulsion during the neoadjuvant chemoradiotherapy. Patients are meanwhile encouraged to intake 25-30kcal/kg through regular food.

Patients are encouraged to intake 25-30kcal/kg through regular food without supplemental nutritional support before esophagectomy.

Outcomes

Primary Outcome Measures

Rate of postoperative nutrition and immune-related complications
Rate of gastrointestinal complications (anastomotic leakage, gastrointestinal dysfunction), metabolic complications (electrolyte disturbances, liver or renal dysfunction) and infectious complications(wound infection, catheter-related infection, pneumonia, sepsis, or other infections requiring antibiotics).

Secondary Outcome Measures

Completion rate of neoadjuvant therapy and esophagectomy
Adverse events during neoadjuvant chemoradiotherapy
Pathological complete response rate (pCR)
Blood loss
Duration of surgery
Rate of surgery-related complications
Conversion to open surgery, recurrent nerve injury, cardiac and cerebrovascular accident
Length of hospital stay
Hospitalization costs
30-day and 90-day mortality
Weight loss
Change in PG-SGA score after surgery
Change in biochemical indicators after surgery
WBC, hemoglobin, albumin, CRP, TNF-α, interleukins, IgA, IgG, IgM, fasting blood-glucose
Score of EORTC QLQ-C30 and OES-18 scale
Quality of life
Long-term survival
Overall survival (OS) and progression-free survival (PFS)

Full Information

First Posted
August 7, 2020
Last Updated
May 16, 2022
Sponsor
Hecheng Li M.D., Ph.D
Collaborators
Shanghai Chest Hospital, Shanghai Zhongshan Hospital, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University, Ningbo Medical Center Lihuili Hospital, Zhejiang Cancer Hospital, Fujian Medical University Union Hospital, Shanghai East Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04513418
Brief Title
Effects of Preoperative Enteral Immunonutrition for Esophageal Cancer Patients Given Neoadjuvant Chemoradiotherapy
Acronym
POINT
Official Title
Effects of Preoperative Enteral Immunonutrition for Esophageal Cancer Patients Given Neoadjuvant Chemoradiotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 10, 2020 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Hecheng Li M.D., Ph.D
Collaborators
Shanghai Chest Hospital, Shanghai Zhongshan Hospital, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University, Ningbo Medical Center Lihuili Hospital, Zhejiang Cancer Hospital, Fujian Medical University Union Hospital, Shanghai East Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This randomized controlled trial will evaluate the effects of preoperative enteral immunonutrition in esophageal cancer patients undergoing neoadjuvant therapy. The purpose of this study is to determine whether preoperative immune-modulating diet before surgery can improve the rate of complications and other perioperative outcomes.
Detailed Description
Esophageal cancer ranks the fourth in mortality and the sixth in incidence among cancers in China according to the latest report of cancer epidemiology. Although the development of neoadjuvant therapy and radical esophagectomy have improved the prognosis of esophageal cancer patients, dysphagia and digestive tract reconstruction can cause malnutrition and infection-related complications. Postoperative enteral and parenteral nutrition have proved to be effective in improving outcomes after esophagectomy. However, whether to provide a preoperative nutritional support for patients with resectable esophageal cancer remains controversial. This prospective randomized controlled trial will evaluate the effects of preoperative enteral immunonutrition in esophageal cancer patients undergoing neoadjuvant therapy. The purpose of this study is to determine whether preoperative immune-modulating diet before surgery can improve the rate of complications and other perioperative outcomes. The sample size is estimated with the hypothesis that preoperative immunonutrition during the neoadjuvant therapy can reduce postoperative nutrition and immune-related complications after esophagectomy. According to the previously published articles, the required sample size of interventional and control arm (ratio=2:1) was calculated as 137 cases and 69 cases to detect the reduction in related complications from 50% to 30% based on a bilateral significance level (α) of 0.05 and a power of test (1-β) of 0.80. Considering an estimated drop rate of 15%, the minimum sample size of this study is 244 patients, 162 cases in the interventional group and 82 in the control group. After signing the informed consent, every eligible participant will be randomized into either group based on a computer-generated random number. Blinding will not be applied to patients and surgeons due to the difficulty in clinical practice but outcomes assessor will be masked.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Neoplasms
Keywords
Esophageal Neoplasms, Neoadjuvant Therapy, Enteral Nutrition, Nutrition Therapy

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
244 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Interventional group
Arm Type
Experimental
Arm Description
Patients receive omega-3 fatty-acid enriched enteral nutritional emulsion during the neoadjuvant chemoradiotherapy. Patients are meanwhile encouraged to intake 25-30kcal/kg through regular food.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Patients are encouraged to intake 25-30kcal/kg through regular food without supplemental nutritional support before esophagectomy.
Intervention Type
Dietary Supplement
Intervention Name(s)
Preoperative immunonutrition
Intervention Description
Preoperative immunonutrition includes an omega-3 fatty-acid enriched enteral nutritional emulsion given by oral intake, nasogastric feeding tube or jejunostomy 600ml per day, lasting for the whole period of neoadjuvant chemoradiation. Meanwhile, oral intake is encouraged to reach 25-30kcal/kg through regular food.
Primary Outcome Measure Information:
Title
Rate of postoperative nutrition and immune-related complications
Description
Rate of gastrointestinal complications (anastomotic leakage, gastrointestinal dysfunction), metabolic complications (electrolyte disturbances, liver or renal dysfunction) and infectious complications(wound infection, catheter-related infection, pneumonia, sepsis, or other infections requiring antibiotics).
Time Frame
Up to 30 days after surgery
Secondary Outcome Measure Information:
Title
Completion rate of neoadjuvant therapy and esophagectomy
Time Frame
2-3 months before surgery
Title
Adverse events during neoadjuvant chemoradiotherapy
Time Frame
2-3 months before surgery
Title
Pathological complete response rate (pCR)
Time Frame
2-3 months before surgery
Title
Blood loss
Time Frame
At operation day
Title
Duration of surgery
Time Frame
At operation day
Title
Rate of surgery-related complications
Description
Conversion to open surgery, recurrent nerve injury, cardiac and cerebrovascular accident
Time Frame
At operation day
Title
Length of hospital stay
Time Frame
Postoperative in-hospital stay
Title
Hospitalization costs
Time Frame
Postoperative in-hospital stay
Title
30-day and 90-day mortality
Time Frame
Up to 90 days after surgery
Title
Weight loss
Time Frame
From neoadjuvant chemoradiotherapy to 6 months after surgery
Title
Change in PG-SGA score after surgery
Time Frame
From neoadjuvant chemoradiotherapy to 6 months after surgery
Title
Change in biochemical indicators after surgery
Description
WBC, hemoglobin, albumin, CRP, TNF-α, interleukins, IgA, IgG, IgM, fasting blood-glucose
Time Frame
From neoadjuvant chemoradiotherapy to 6 months after surgery
Title
Score of EORTC QLQ-C30 and OES-18 scale
Description
Quality of life
Time Frame
1-year, 3-year, and 5-year after surgery
Title
Long-term survival
Description
Overall survival (OS) and progression-free survival (PFS)
Time Frame
1-year, 3-year, and 5-year after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed esophageal cancer Staging as cT2N0M0 with high-risk lesions (lymphovascular invasion, ≥3cm, poorly differentiated) / cT1b-2N+M0 / cT3-4aN0-3M0 with the need of neoadjuvant therapy before radical esophagectomy Tolerance with oral intake (at least fluid diet) Eastern Cooperative Oncology Group (ECOG) performance status ≤2 Body Mass Index (BMI) ≥ 18.5 kg/m2 before recruitment Patient's approval and written informed consent Exclusion Criteria: Expected survival time less than 6 months Complete dysphagia Pregnant or breast-feeding women Unable to obey the interventions because of any reasons Serious co-morbidities (cardiac, pulmonary, liver, kidney, brain, hematologic, endocrine and other diseases) in patients who cannot tolerate neoadjuvant therapy and/or surgery History of previous thoracic or abdominal surgery History of other malignant tumor (previous or current)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hecheng Li, PhD, MD
Phone
00862164370045
Ext
664566
Email
lihecheng2000@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yuqin Cao, MD
Phone
008613918933069
Email
caoyuqin314@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hecheng Li, PhD, MD
Organizational Affiliation
Ruijin Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fujian Medical University Union Hospital
City
Fuzhou
State/Province
Fujian
ZIP/Postal Code
350001
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chun Chen
Email
chenchun@163.com
Facility Name
Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200011
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mingsong Wang
Phone
00862123271699
Email
wangmingsong@xinhuamed.com.cn
Facility Name
Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200025
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dingpei Han, PhD, MD
Phone
00862164370045
Ext
666112
Email
dmhan1985@163.com
First Name & Middle Initial & Last Name & Degree
Su Yang, MD
Phone
00862164370045
Ext
666112
Email
ys19851021@sina.com
Facility Name
Shanghai Chest Hospital Affiliated to Shanghai Jiao Tong University
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200030
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhigang Li
Phone
00862122200000
Email
zhigang_li_sch@163.com
Facility Name
Zhongshan Hospital Affiliated to Fudan University
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200032
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lijie Tan
Phone
00862164041990
Email
tan.lijie@zs-hospital.sh.cn
Facility Name
Shanghai East Hospital, Tongji University School of Medicine
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200120
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jinyi Wang
Email
jinyi_wang@126.com
Facility Name
Cancer Hospital of University of Chinese Academy of Sciences, Zhejiang Cancer Hospital
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310022
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Qixun Chen
Email
chenqixun64@163.com
Facility Name
Ningbo Medical Center Lihuili Hospital
City
Ningbo
State/Province
Zhejiang
ZIP/Postal Code
315048
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Weiyu Shen
Phone
0086057487018701
Email
ningbomblhlswy@163.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35698100
Citation
Cao Y, Han D, Yang S, Shi Y, Zhao S, Jin Q, Li J, Li C, Zhang Y, Shen W, He J, Wang M, Ji G, Li Z, He Y, Chen Q, Wei W, Chen C, Gong X, Wang J, Tan L, Wang H, Li H. Effects of pre-operative enteral immunonutrition for esophageal cancer patients treated with neoadjuvant chemoradiotherapy: protocol for a multicenter randomized controlled trial (point trial, pre-operative immunonutrition therapy). BMC Cancer. 2022 Jun 13;22(1):650. doi: 10.1186/s12885-022-09721-y.
Results Reference
derived

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Effects of Preoperative Enteral Immunonutrition for Esophageal Cancer Patients Given Neoadjuvant Chemoradiotherapy

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