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Evaluation of the Efficacy of Low-dose Acetylsalicylic Acid on Diarrhea Induced by Anti-cancer Targeted Therapies. (ASPIDIA)

Primary Purpose

Cancer

Status
Withdrawn
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Acetylsalicylic acid + loperamide
diosmectite + loperamide
Sponsored by
Centre Francois Baclesse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cancer

Eligibility Criteria

18 Months - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Aged at least 18 years old patient;
  • WHO 0 to 2;
  • Any solid tumor or hematologic malignancy requiring a tyrosine kinase inhibitor prescription in the absence of digestive disorders related to tumor disease;
  • Treatment with one of the following targeted therapies: Gefitinib, erlotinib, sunitinib, sorafenib, Axitinib, Pazopanib, Lapatinib, Imatinib, afatinib,vemurafenib and Dabrafenib;
  • Targeted therapy treatment whatever the processing line monotherapy, administered over a period of at least 15 days with continued dosing, with usual care recommendations;
  • Diarrhea grade 1-3 according to NCI criteria CTCAE.4, in the absence of complications signs with at least 2 doses of loperamide per day.

Exclusion Criteria:

  • Processing acetylsalicylic acid;
  • Allergy or against-indications to acetylsalicylic acid (including concomitant antiplatelet or anticoagulant considered as increasing the risk of bleeding by the investigator) acid;
  • Treatment with anti vitamin K or new oral anticoagulants;
  • Absolute in pursuit of targeted therapy contraindication;
  • Chronic diarrhea prior to clinical introduction of targeted therapy;
  • Diarrhoea unrelated to targeted therapy such as:

    • extended resection of esophagus, inflammatory bowel disease, etc ...
    • carcinoid syndrome;
    • occlusive syndrome;
  • Grade 3 diarrhea with signs of complications or grade 4
  • Patients with a history of grade 3 diarrhea with signs of complications or grade 4 during previous treatment with TKI;
  • Participation in other medical test;
  • Pregnant women / nursing;
  • Association with methotrexate at doses > 15 mg / d;
  • Patient Trust or deprived of liberty.

Sites / Locations

  • CHU
  • Centre François Baclesse
  • Centre Hospitalier public du Cotentin
  • Centre hospitalier
  • Centre Léon Bérard

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Acetylsalicylic acid + loperamide

diosmectite + loperamide

Arm Description

Acetylsalicylic acid + loperamide

Acetylsalicylic acid + loperamide

Outcomes

Primary Outcome Measures

Efficacy measured by the decrease in the intensity of diarrhea and / or anti-diarrheal consumption
Effectiveness of acetylsalicylic acid versus diosmectite

Secondary Outcome Measures

Toxicity
Diarrhea decrease 3 months after the introduction of acetylsalicylic acid or diosmectite; Proportion of patients with a decrease in the grade of diarrhea during the months following the introduction of acetylsalicylic acid or diosmectite. Rate and intensity of side effects associated with other targeted therapy.
TKI dose reduction
Proportion of patients requiring dose reduction of targeted therapy
Quality of life
Quality of life and its evolution by month using ladders FACIT-G and FACIT-D.
Safety measured by the proportion of adverse event
Safety of acetylsalicylic acid in patients with diarrhea in targeted therapy

Full Information

First Posted
November 19, 2014
Last Updated
December 7, 2015
Sponsor
Centre Francois Baclesse
Collaborators
Ligue contre le cancer, France, Canceropôle Nord Ouest
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1. Study Identification

Unique Protocol Identification Number
NCT02323516
Brief Title
Evaluation of the Efficacy of Low-dose Acetylsalicylic Acid on Diarrhea Induced by Anti-cancer Targeted Therapies.
Acronym
ASPIDIA
Official Title
Evaluation of the Efficacy of Low-dose Acetylsalicylic Acid on Diarrhea Induced by Anti-cancer Targeted Therapies.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Withdrawn
Study Start Date
December 2014 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Francois Baclesse
Collaborators
Ligue contre le cancer, France, Canceropôle Nord Ouest

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The mechanisms of action of the side effects associated with targeted therapies are still poorly understood. He was found in patients treated with gefitinib, increased levels of thromboxane B2 and P-selectin Thromboxane B2 is the result of the hydrolysis of thromboxane A2, which is itself obtained from Prostaglandin H2 under the action of the thromboxane synthetase. The thromboxane A2 is produced by platelets and the active pro-thrombotic properties as follows: stimulation of platelets and activation of other increased platelet aggregation. The selectins are cell adhesion proteins with a role in the adhesion phenomena. P-selectin is expressed by platelets and endothelial cells. The demonstration of increased plasma levels of thromboxane B2 and P-selectin leaves suggest a role of platelet activation in the occurrence of side effects associated with targeted therapies. Kanazawa's study was conducted in 39 Japanese patients, trying to assess the value of low-dose acetylsalicylic acid or 100mg per day, that is to say, anti-aggrégantes doses, the occurrence rash and diarrhea induced by gefitinib. In this study, the group of patients treated with acetylsalicylic acid presented a lower rate of side effects significantly, 58.3% versus 77.8%. The frequency of diarrhea was 18.5% (or 5 patients) in the standard group versus 0% in the group with acetylsalicylic acid. Similarly, it was found a reduction in the occurrence of skin rash, 33.3% or 4 patients in the acetylsalicylic acid group versus 74.1% s, 20 patients in the standard group. Finally, in this study, it was not revealed significant differences in terms of response to treatment with gefitinib (37% in the standard group versus 33% in the group treated with aspirin patient) It does not exist in our knowledge of prospective data evaluating the effect of acetylsalicylic acid on the reduction of side effects associated with targeted in a population of patients of Caucasian-type treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Acetylsalicylic acid + loperamide
Arm Type
Experimental
Arm Description
Acetylsalicylic acid + loperamide
Arm Title
diosmectite + loperamide
Arm Type
Active Comparator
Arm Description
Acetylsalicylic acid + loperamide
Intervention Type
Drug
Intervention Name(s)
Acetylsalicylic acid + loperamide
Intervention Description
In case of inefficiency in one month, according to predefined criteria, acetylsalicylic acid will be stopped and replaced by diosmectite.
Intervention Type
Drug
Intervention Name(s)
diosmectite + loperamide
Intervention Description
In case of inefficiency in one month, according to predefined criteria, diosmectite will be stopped and replaced by acetylsalicylic acid.
Primary Outcome Measure Information:
Title
Efficacy measured by the decrease in the intensity of diarrhea and / or anti-diarrheal consumption
Description
Effectiveness of acetylsalicylic acid versus diosmectite
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Toxicity
Description
Diarrhea decrease 3 months after the introduction of acetylsalicylic acid or diosmectite; Proportion of patients with a decrease in the grade of diarrhea during the months following the introduction of acetylsalicylic acid or diosmectite. Rate and intensity of side effects associated with other targeted therapy.
Time Frame
Three months
Title
TKI dose reduction
Description
Proportion of patients requiring dose reduction of targeted therapy
Time Frame
Three months
Title
Quality of life
Description
Quality of life and its evolution by month using ladders FACIT-G and FACIT-D.
Time Frame
Three months
Title
Safety measured by the proportion of adverse event
Description
Safety of acetylsalicylic acid in patients with diarrhea in targeted therapy
Time Frame
Months 1 to 3

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged at least 18 years old patient; WHO 0 to 2; Any solid tumor or hematologic malignancy requiring a tyrosine kinase inhibitor prescription in the absence of digestive disorders related to tumor disease; Treatment with one of the following targeted therapies: Gefitinib, erlotinib, sunitinib, sorafenib, Axitinib, Pazopanib, Lapatinib, Imatinib, afatinib,vemurafenib and Dabrafenib; Targeted therapy treatment whatever the processing line monotherapy, administered over a period of at least 15 days with continued dosing, with usual care recommendations; Diarrhea grade 1-3 according to NCI criteria CTCAE.4, in the absence of complications signs with at least 2 doses of loperamide per day. Exclusion Criteria: Processing acetylsalicylic acid; Allergy or against-indications to acetylsalicylic acid (including concomitant antiplatelet or anticoagulant considered as increasing the risk of bleeding by the investigator) acid; Treatment with anti vitamin K or new oral anticoagulants; Absolute in pursuit of targeted therapy contraindication; Chronic diarrhea prior to clinical introduction of targeted therapy; Diarrhoea unrelated to targeted therapy such as: extended resection of esophagus, inflammatory bowel disease, etc ... carcinoid syndrome; occlusive syndrome; Grade 3 diarrhea with signs of complications or grade 4 Patients with a history of grade 3 diarrhea with signs of complications or grade 4 during previous treatment with TKI; Participation in other medical test; Pregnant women / nursing; Association with methotrexate at doses > 15 mg / d; Patient Trust or deprived of liberty.
Facility Information:
Facility Name
CHU
City
Amiens
Country
France
Facility Name
Centre François Baclesse
City
Caen
ZIP/Postal Code
14076
Country
France
Facility Name
Centre Hospitalier public du Cotentin
City
Cherbourg
ZIP/Postal Code
50100
Country
France
Facility Name
Centre hospitalier
City
Compiegne
Country
France
Facility Name
Centre Léon Bérard
City
Lyon
Country
France

12. IPD Sharing Statement

Learn more about this trial

Evaluation of the Efficacy of Low-dose Acetylsalicylic Acid on Diarrhea Induced by Anti-cancer Targeted Therapies.

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