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Hyperthermic Intraperitoneal Chemotherapy (HIPEC) : Predictive Marker and Mechanism

Primary Purpose

Peritoneal Carcinomatosis

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
peripheral venous blood samples
Sponsored by
Centre Hospitalier Universitaire de Nice
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Peritoneal Carcinomatosis focused on measuring intra peritonal chemo hyperthermia, peritoneal carcinomatosis, ovarian cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Females over 18 years.
  • Indication of Hyperthermic Intra Peritoneal Chemotherapy (HIPEC) for peritoneal carcinomatosis from ovarian origin
  • Obtaining written informed consent and signed for participation in the study and conservation of samples taken.
  • Affiliation to a social security scheme.

Non-inclusion criteria

  • Major patients protected by law or deprived of liberty.
  • Patients pregnant women in labor or breastfeeding.
  • Refusal of participation
  • Another cause of peritoneal carcinomatosis

Exclusion Criteria:

  • consent withdrawn

Sites / Locations

  • Digestive department - Archet hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Patient with HIPEC

Patient without HIPEC

Arm Description

Outcomes

Primary Outcome Measures

Changes in serum levels of HSP90 and 70 on peripheral venous samples.
Changes in serum levels of HSP90 and 70 postoperatively HIPEC (Day 1, day 3 and day 5 postoperative) compared to basal levels measured preoperatively on peripheral venous samples. Patients who had HIPEC will be compared with patients overturned on early intervention

Secondary Outcome Measures

Full Information

First Posted
June 14, 2016
Last Updated
August 30, 2019
Sponsor
Centre Hospitalier Universitaire de Nice
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1. Study Identification

Unique Protocol Identification Number
NCT02803515
Brief Title
Hyperthermic Intraperitoneal Chemotherapy (HIPEC) : Predictive Marker and Mechanism
Official Title
HSP90 as a Predictive Marker of the Response to Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in the Treatment of Peritoneal Carcinomatosis From Ovarian Origin.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Terminated
Study Start Date
January 16, 2017 (Actual)
Primary Completion Date
July 2, 2017 (Actual)
Study Completion Date
July 2, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nice

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Peritoneal carcinomatosis (PC) is the stage III of the FIGO ovarian cancer staging. It corresponds to an advanced stage with a relative 5 year survival rate of 52%. The multimodal treatment approach combines neoadjuvant chemotherapy, cytoreductive surgery of macroscopic lesions, and hyperthermic intraperitoneal chemotherapy (HIPEC). It has significantly improved survival rate in patients with ovarian PC and decreased recurrence and mortality rate by 21%. The efficacy of HIPEC is based on chemotherapy potentiated by the hyperthermia (43°). However, the cellular mechanisms involved are not fully understood, but they include cell death pathways and heat shock proteins (Hsp70 and Hsp90). RICCI et al. showed, based on pre-clinical models, that the efficacy of HIPEC was partly due to the overexpression and exposure of HSP90 on the cell surface leaded to an anti-cancer immune response. The aims of this study are to validate these findings in tissue samples of patients with ovarian PC. We will constitute a bank of isolated tumor samples before and after HIPEC and measure postoperative HSP90 serum levels in order to establish if they are predictive of a response. HSPs expression on the cancer cell surface will be determined by flow cytometry. Forty-four patients will be included. Elucidating the underlying mechanisms of HIPEC will broaden therapeutic possibilities including the use of new immunotherapy. The multimodal approach could improve the efficacy of HIPEC with a minimal systemic toxicity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peritoneal Carcinomatosis
Keywords
intra peritonal chemo hyperthermia, peritoneal carcinomatosis, ovarian cancer

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patient with HIPEC
Arm Type
Experimental
Arm Title
Patient without HIPEC
Arm Type
Sham Comparator
Intervention Type
Biological
Intervention Name(s)
peripheral venous blood samples
Intervention Description
peripheral venous blood samples measured preoperatively and postoperatively HIPEC (Day 1, day 3 and day 5 postoperative)
Primary Outcome Measure Information:
Title
Changes in serum levels of HSP90 and 70 on peripheral venous samples.
Description
Changes in serum levels of HSP90 and 70 postoperatively HIPEC (Day 1, day 3 and day 5 postoperative) compared to basal levels measured preoperatively on peripheral venous samples. Patients who had HIPEC will be compared with patients overturned on early intervention
Time Frame
basal levels (preoperatively), postoperatively HIPEC (Day 1, day 3 and day 5 postoperative)

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Females over 18 years. Indication of Hyperthermic Intra Peritoneal Chemotherapy (HIPEC) for peritoneal carcinomatosis from ovarian origin Obtaining written informed consent and signed for participation in the study and conservation of samples taken. Affiliation to a social security scheme. Non-inclusion criteria Major patients protected by law or deprived of liberty. Patients pregnant women in labor or breastfeeding. Refusal of participation Another cause of peritoneal carcinomatosis Exclusion Criteria: consent withdrawn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Marc BEREDER, MD
Organizational Affiliation
Centre Hospitalier Universitaire de Nice
Official's Role
Principal Investigator
Facility Information:
Facility Name
Digestive department - Archet hospital
City
Nice
ZIP/Postal Code
06000
Country
France

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Hyperthermic Intraperitoneal Chemotherapy (HIPEC) : Predictive Marker and Mechanism

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