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Hyperthermic Intraperitoneal Chemotherapy for Advanced Gastric Cancer With Peritoneal Metastatis

Primary Purpose

Stage IV Gastric Cancer With Metastasis, Hyperthermic Intraperitoneal Chemotherapy, Exploratory Behavior

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Hyperthermic Intraperitoneal Chemotherapy
Without Hyperthermic Intraperitoneal Chemotherapy
Sponsored by
Guangdong Provincial Hospital of Traditional Chinese Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stage IV Gastric Cancer With Metastasis focused on measuring peritoneal metastatis, Hyperthermic Intraperitoneal Chemotherapy, Advanced gastric adenocarcinoma

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Primary gastric adenocarcinoma diagnosed pathologically by endoscopic biopsy;
  • Laparoscopic exploration of patients with advanced gastric adenocarcinoma of peritoneal metastasis;
  • Eastern Cooperative Oncology Group (ECOG): 0 ot 1;
  • American Society of Anesthesiologists (ASA) score: I to Ⅲ;
  • Patient informed consent。

Exclusion Criteria:

  • Pregnancy or female in suckling period;
  • Severe mental illness;
  • Preoperative imaging or intraoperative exploration reveals distant blood, liver, lung, and brain metastases;
  • 5 years of history of other malignant diseases;
  • A history of unstable angina or myocardial infarction within 6 months;
  • History of cerebral infarction or cerebral hemorrhage within 6 months;
  • A history of sustained systemic corticosteroid treatment within 1 month;
  • Emergency operation due to complication (bleeding, perforation or obstruction) caused by primary tumor;
  • Pulmonary function test FEV1 <predicted value 50%。

Sites / Locations

  • Guangdong Province Hospital of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

HIPEC and chemotherapy

Without HIPEC

Arm Description

Hyperthermic Intraperitoneal Chemotherapy and SOX(Tiggio+Oxaliplatin )

Without Hyperthermic Intraperitoneal Chemotherapy,Only SOX(Tiggio+Oxaliplatin )

Outcomes

Primary Outcome Measures

PFS
Progression-free survival

Secondary Outcome Measures

1-year survival
1-year overall survival rate
Ascites assessment
Ascites assessment during surgery
Median survival
Median Survival Time

Full Information

First Posted
June 14, 2018
Last Updated
July 20, 2018
Sponsor
Guangdong Provincial Hospital of Traditional Chinese Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT03604614
Brief Title
Hyperthermic Intraperitoneal Chemotherapy for Advanced Gastric Cancer With Peritoneal Metastatis
Official Title
A Randomized Controlled Clinical Trial of Hyperthermic Intraperitoneal Chemotherapy for Advanced Gastric Cancer With Peritoneal Metastatis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2017 (Actual)
Primary Completion Date
August 24, 2017 (Actual)
Study Completion Date
August 24, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Guangdong Provincial Hospital of Traditional Chinese Medicine

4. Oversight

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

5. Study Description

Brief Summary
The incidence rate of gastric cancer is high in Southeast Asia, so is the mortality rate.Due to the lack of specific performance, about 5%-20% of patients have found peritoneal metastases at the time of first diagnosis.At present, clinical studies on HIPEC in the treatment of patients with advanced gastric cancer peritoneal metastasis are almost related to abdominal perfusion after laparoscopic gastrectomy.Herein, we conduct a single-centre randomized controlled trial to explore the safety and feasibility of laparoscopic exploration combined with HIPEC in the treatment of advanced gastric cancer with peritoneal metastasis.
Detailed Description
Gastric cancer is one of the most common digestive tumors in the world.In China, advanced gastric cancer with severe local progression or distant metastasis is more common.Gastric cancer with peritoneal carcinomatosis has an extremely poor prognosis,with a median survival of less than 6 months.Hyperthermic Intraperitoneal Chemotherapy (HIPEC) is currently a treatment for malignant tumors in the abdominal cavity and prevents tumor recurrence and metastasis.Studies have shown that hyperthermic intraperitoneal perfusion chemotherapy (HIPEC) has good clinical efficacy in the prevention and treatment of peritoneal metastasis of gastric cancer and its associated malignant ascites.Therefore,we conduct a single-centre randomized controlled trial to explore the safety and feasibility of HIPEC in the treatment of advanced gastric cancer with peritoneal metastasis. The metahnism of HIPEC is taking advantage of the difference in temperature sensitivity between cancer cells and normal cells. Perfusion of the abdominal cavity with a chemical fluid of the appropriate temperature can be performed. Suitable high temperatures can directly kill tumor cells.It is generally believed that the optimal temperature for the treatment of tumors is 42.5°C to 44°C.In this study,we set the temperature 43°C. Paclitaxel is a novel broad-spectrum antitumor drug,which has a unique anti-cancer mechanism.We use Paclitaxel as peritoneal hyperthermic perfusion chemotherapy drugs.The chemotherapy is SOX(Teggio and Oxaliplatin),.The primary endpoint is PFS. Secondary endpoints are one-year OS、canversion rate and ascites assessment. A phase III study PHOENIX-GC trial had finished enrollment,and the conclusion was the median OS 17.7 and 15.2 months respectively for IP and SP.The primary analysis did not show the statistical superiority of the IP regimen.The sensitivity analysis IP considering the imbalance of ascites, suggested clinical efficacy of IP PTX in gastric cancer with peritoneal metastasis. For this reason,we conduct a trial to explore the safety and feasibility of HIPEC in the treatment of advanced gastric cancer with peritoneal metastasis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stage IV Gastric Cancer With Metastasis, Hyperthermic Intraperitoneal Chemotherapy, Exploratory Behavior
Keywords
peritoneal metastatis, Hyperthermic Intraperitoneal Chemotherapy, Advanced gastric adenocarcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
56 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
HIPEC and chemotherapy
Arm Type
Experimental
Arm Description
Hyperthermic Intraperitoneal Chemotherapy and SOX(Tiggio+Oxaliplatin )
Arm Title
Without HIPEC
Arm Type
Sham Comparator
Arm Description
Without Hyperthermic Intraperitoneal Chemotherapy,Only SOX(Tiggio+Oxaliplatin )
Intervention Type
Drug
Intervention Name(s)
Hyperthermic Intraperitoneal Chemotherapy
Intervention Description
The investigators use Paclitaxel as peritoneal hyperthermic perfusion chemotherapy drugs,75mg/m2 for the first time,50mg/m2 for the second time and third time.The chemotherapy is SOX(Tiggio d1-d14 bid po and Oxaliplatin 130mg/m2 ivd d1 qd).The Tiggio dosage depends on the patient's body surface area, body surface area <1.25m2 40mg/time, 1.25-1.50m2 50mg/time, >1.50m2 60mg/time.
Intervention Type
Drug
Intervention Name(s)
Without Hyperthermic Intraperitoneal Chemotherapy
Intervention Description
The chemotherapy is SOX(Tiggio d1-d14 bid po and Oxaliplatin 130mg/m2 ivd d1 qd).The Tiggio dosage depends on the patient's body surface area, body surface area <1.25m2 40mg/time, 1.25-1.50m2 50mg/time, >1.50m2 60mg/time.
Primary Outcome Measure Information:
Title
PFS
Description
Progression-free survival
Time Frame
From date of randomization until the date of first documented progression or date of death for tumor cause, whichever came first, assessed 7 months
Secondary Outcome Measure Information:
Title
1-year survival
Description
1-year overall survival rate
Time Frame
one year
Title
Ascites assessment
Description
Ascites assessment during surgery
Time Frame
Intraoperative
Title
Median survival
Description
Median Survival Time
Time Frame
From date of randomization until only 50% of individuals living for tumor cause, assessed 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Primary gastric adenocarcinoma diagnosed pathologically by endoscopic biopsy; Laparoscopic exploration of patients with advanced gastric adenocarcinoma of peritoneal metastasis; Eastern Cooperative Oncology Group (ECOG): 0 ot 1; American Society of Anesthesiologists (ASA) score: I to Ⅲ; Patient informed consent。 Exclusion Criteria: Pregnancy or female in suckling period; Severe mental illness; Preoperative imaging or intraoperative exploration reveals distant blood, liver, lung, and brain metastases; 5 years of history of other malignant diseases; A history of unstable angina or myocardial infarction within 6 months; History of cerebral infarction or cerebral hemorrhage within 6 months; A history of sustained systemic corticosteroid treatment within 1 month; Emergency operation due to complication (bleeding, perforation or obstruction) caused by primary tumor; Pulmonary function test FEV1 <predicted value 50%。
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wei Wang, M.D., PH.D.
Phone
+86-13922255515
Email
wangwei16400@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wei Wang
Organizational Affiliation
Guangdong Provincial Hospital of Traditional Chinese Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wenjun Xiong
Organizational Affiliation
Guangdong Provincial Hospital of Traditional Chinese Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Guangdong Province Hospital of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510120
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wei Wang, M.D.,PH.D.
Phone
+86-13922255515
Email
wangwei16400@163.com
First Name & Middle Initial & Last Name & Degree
Wenjun Xiong, M.D.
Phone
+86-15920553177
Email
xiongwj1988@163.com
First Name & Middle Initial & Last Name & Degree
Wei Wang
First Name & Middle Initial & Last Name & Degree
Jin Wan
First Name & Middle Initial & Last Name & Degree
Wen jun Xiong
First Name & Middle Initial & Last Name & Degree
De chang Diao
First Name & Middle Initial & Last Name & Degree
Yan sheng Zheng
First Name & Middle Initial & Last Name & Degree
Hong ming Li
First Name & Middle Initial & Last Name & Degree
Yao bin He
First Name & Middle Initial & Last Name & Degree
Li jie Luo

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The data has not been published.

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Hyperthermic Intraperitoneal Chemotherapy for Advanced Gastric Cancer With Peritoneal Metastatis

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