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Evaluation in the Treatment of Neuropathic Pain Post Breast Surgery (CAPTRANE)

Primary Purpose

Breast Cancer Patient

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Capsaicin
Pregabalin
Sponsored by
Institut Cancerologie de l'Ouest
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Cancer Patient focused on measuring Breast cancer patient, Surgery, Inter Costobrachial Neuralgia

Eligibility Criteria

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

Inclusion Criteria:

  • Male or female who had first breast cancer surgery, regardless of the type of surgery
  • Age ≥ 18 years
  • Healthy, non-irritated skin on painful areas to treat
  • During the inclusion visit to M4 post surgery, neuropathic pain of the breast and / or axillary area corresponding to inter-brachial neuralgia with a DN4≥4 score.
  • Obtaining the signed written consent of the patient
  • Major patient affiliated to a social security scheme

Exclusion Criteria:

  • Contraindications specific to the treatments studied : capsaicine and pregabalin
  • Diabetic patient
  • Previous treatment with capsaicin or pregabalin
  • Opioid treatment> 80 mg / day (oral morphine equivalent) in progress- Topical treatment of pain between surgery and inclusion visit
  • Uncontrolled hypertension (systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 90 mmHg) or recent history (<3 months) of cardiovascular events (stroke, heart attack, pulmonary embolism)
  • Creatinine clearance (CLcr) <60mL / min according to the Cockcroft-Gault formula
  • Pregnant woman, likely to be pregnant or breastfeeding
  • Persons deprived of their liberty or guardianship (including curators),
  • Impossibility of submitting to the medical follow-up of the test for geographical, social or psychological reasons

Sites / Locations

  • Institut de Cancerologie de L'Ouest
  • Chu Grenoble
  • Chd Vendee
  • Centre Oscar Lambret
  • Hopital Saint Vincent de Paul
  • Centre Leon Berard
  • CHU NICE
  • Institut Jean Godinot
  • Institut Curie
  • Iuct Oncopole
  • Ch Valenciennes

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Arm CAPSAICINE topical

Arm PREGABALINE

Arm Description

Application of capsaicin patches at 8% on the painful area 1 to 2 patches will be administered during the consultation. If necessary, a second application will be realized 3 months later.

Pregabalin tablets will be initiated at a dose of 50 mg / day taken in 2 doses Depending on the tolerance, the dose will be increased to 100 mg / day and then to 150 mg / day to reach a maximum dose of 600 mg / day. An interval of 3 to 7 days must be observed between each dose increase.

Outcomes

Primary Outcome Measures

To show the noninferiority of early early medical treatment by topical treatment with capsaicin compared to oral treatment of pregabalin on the evolution of neuropathic pain after 2 months in patients who have undergone surgical excision of breast cancer
The 11-point numerical scale (0-10) is collected at 2 months.

Secondary Outcome Measures

To compare the efficacy of an early medical treatment with capsaicin topical treatment compared to oral treatment pregabalin on the evolution of neuropathic pain in patients who had undergone excision surgical breast cancer after 6 months of treatment
The 11-point numerical scale of pain is also collected at the end of treatment
To compare the functional change and quality of life perceived by patients after 2 and 6 months of treatment between the two arms: Questionnaire PGIC (patients' global impression of change)
Questionnaire PGIC is administered to M4, M6 and at the end of treatment to measure the functional changes and quality of life changes experienced by the patient in the 2 treatment arms.
To compare the functional change and quality of life perceived by patients after 2 and 6 months of treatment between the two arms
Questionnaire QLQ-C30 (quality of life questionnaire) is administered to M4, M6 and at the end of treatment to measure the functional changes and quality of life changes experienced by the patient in the 2 treatment arms.
To compare the functional change and quality of life perceived by patients after 2 and 6 months of treatment between the two arms
Questionnaire EQ-5D is administered to M4, M6 and at the end of treatment to measure the functional changes and quality of life changes experienced by the patient in the 2 treatment arms.
Regression of the painful area after 2 and 6 months of treatment between the two arms.
The painful area is measured from pain mapping at baseline, and after 2 months and 6 months of treatment. It is measured by the area delimited by the contours of the painful surface (centralized reading).
Tolerance of each type of treatment by collecting side effects in each treatment arm.
The tolerance of the treatments will be measured by the number of patients having at least one adverse event of grade ≥ 2 according to the classification CTCAE v5.0.
Proportion of patients for whom only 1 application has been sufficient.
In the capsaicin arm, the number of total patches received by the patient during the 6 months will also be counted
Impact of peri-surgical anxiety and depression on the development of neuropathic pain after surgery for breast cancer
The HAD (Hospital anxiety and despression scale) questionnaire will be collected during the screening visit
The incidence of NICBs 4 months after surgery for breast cancer
The incidence of NICBs will be measured by the number of patients included in the study (DN4 +) compared to the number of patients screened before surgery
The evolution of the weight between the two arms after 6 months of treatment.
The weight is collected after 6 months of treatment

Full Information

First Posted
November 5, 2018
Last Updated
July 31, 2023
Sponsor
Institut Cancerologie de l'Ouest
Collaborators
Grünenthal GmbH
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1. Study Identification

Unique Protocol Identification Number
NCT03794388
Brief Title
Evaluation in the Treatment of Neuropathic Pain Post Breast Surgery
Acronym
CAPTRANE
Official Title
Multicentric, Open, Randomized Study Comparing Topical Treatment by Patch of Capsaicin to 8% (Qutenza) to Pregabalin Oral in the Early Treatment of Neuropathic Pain After Primary Surgery for Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
March 19, 2019 (Actual)
Primary Completion Date
November 18, 2022 (Actual)
Study Completion Date
November 18, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut Cancerologie de l'Ouest
Collaborators
Grünenthal GmbH

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
Breast cancer is the most common cancer in women in Europe. Therefore, breast cancer has become a chronic disease and patients need to learn to live with it as well as with the adverse effects related to the disease itself or to the therapies used. As noted in the third "Plan cancer", pain is a major criterion in the quality of life of patients treated for breast cancer. Neuropathic pain was defined in 2011 by the international Association for the Study of Pain (I.A.S.P.) as the direct result of a lesion or disease affecting the somato-sensory system. Surgical treatment is often the first treatment of breast cancer. It can be conservative by performing a partial mastectomy (lumpectomy or quadrantectomy) or non-preservative by total mastectomy. Intercostobrachial neuralgia (NICB) or Post mastectomy painful Syndrome (MPRR) was first described by Wood in 1978 as "chronic pain beginning immediately or early after a mastectomy" Or a lumpectomy affecting the anterior thorax, armpit and/or arm in its upper half. These post-surgical pains are related to a lesion of the nerves in the breast area. In particular, the intercostobrachial nerve can be severed, stretched or crushed during surgery. Post-operative neuropathic pain in patients with breast cancer is underdiagnosed either by general practitioner or in a specialized environment. The diagnosis of neuropathic pain is performed during examination and clinical examination. Several scales allow to detect neuropathic pain but only the DN4 is recognized to be the most specific and sensitive scale. Patients do not always express this pain. They do not always reconcile with the surgery. Either because the pain occurs a long time after the surgery, or they find it normal to get hurt. These diagnostic difficulties cause a delay in setting up a suitable analgesic treatment. However, neuropathic pain responds poorly to common analgesics. Diagnosis, evaluation and early management of neuropathic pain are a priority in order to avoid their chronicization, to improve the quality of life of patients with breast cancer and to enable them to return to work quickly. We therefore assume that the diagnosis of early neuropathic pain at 2 months of surgery associated with initiation of appropriate topical treatment without the systemic effects of conventional oral treatments, would reduce the incidence of Chronic neuropathic pain 6 months after surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer Patient
Keywords
Breast cancer patient, Surgery, Inter Costobrachial Neuralgia

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Multicenter, open, randomized study
Masking
None (Open Label)
Allocation
Randomized
Enrollment
140 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm CAPSAICINE topical
Arm Type
Experimental
Arm Description
Application of capsaicin patches at 8% on the painful area 1 to 2 patches will be administered during the consultation. If necessary, a second application will be realized 3 months later.
Arm Title
Arm PREGABALINE
Arm Type
Active Comparator
Arm Description
Pregabalin tablets will be initiated at a dose of 50 mg / day taken in 2 doses Depending on the tolerance, the dose will be increased to 100 mg / day and then to 150 mg / day to reach a maximum dose of 600 mg / day. An interval of 3 to 7 days must be observed between each dose increase.
Intervention Type
Drug
Intervention Name(s)
Capsaicin
Other Intervention Name(s)
qutenza EU/1/09/524/001
Intervention Description
Application of capsaicin patches at 8% on painful area
Intervention Type
Drug
Intervention Name(s)
Pregabalin
Other Intervention Name(s)
Lyrica
Intervention Description
Taking Pregabalin tablets
Primary Outcome Measure Information:
Title
To show the noninferiority of early early medical treatment by topical treatment with capsaicin compared to oral treatment of pregabalin on the evolution of neuropathic pain after 2 months in patients who have undergone surgical excision of breast cancer
Description
The 11-point numerical scale (0-10) is collected at 2 months.
Time Frame
2 months
Secondary Outcome Measure Information:
Title
To compare the efficacy of an early medical treatment with capsaicin topical treatment compared to oral treatment pregabalin on the evolution of neuropathic pain in patients who had undergone excision surgical breast cancer after 6 months of treatment
Description
The 11-point numerical scale of pain is also collected at the end of treatment
Time Frame
6 months
Title
To compare the functional change and quality of life perceived by patients after 2 and 6 months of treatment between the two arms: Questionnaire PGIC (patients' global impression of change)
Description
Questionnaire PGIC is administered to M4, M6 and at the end of treatment to measure the functional changes and quality of life changes experienced by the patient in the 2 treatment arms.
Time Frame
6 months
Title
To compare the functional change and quality of life perceived by patients after 2 and 6 months of treatment between the two arms
Description
Questionnaire QLQ-C30 (quality of life questionnaire) is administered to M4, M6 and at the end of treatment to measure the functional changes and quality of life changes experienced by the patient in the 2 treatment arms.
Time Frame
6 months
Title
To compare the functional change and quality of life perceived by patients after 2 and 6 months of treatment between the two arms
Description
Questionnaire EQ-5D is administered to M4, M6 and at the end of treatment to measure the functional changes and quality of life changes experienced by the patient in the 2 treatment arms.
Time Frame
6 months
Title
Regression of the painful area after 2 and 6 months of treatment between the two arms.
Description
The painful area is measured from pain mapping at baseline, and after 2 months and 6 months of treatment. It is measured by the area delimited by the contours of the painful surface (centralized reading).
Time Frame
6 months
Title
Tolerance of each type of treatment by collecting side effects in each treatment arm.
Description
The tolerance of the treatments will be measured by the number of patients having at least one adverse event of grade ≥ 2 according to the classification CTCAE v5.0.
Time Frame
6 months
Title
Proportion of patients for whom only 1 application has been sufficient.
Description
In the capsaicin arm, the number of total patches received by the patient during the 6 months will also be counted
Time Frame
6 months
Title
Impact of peri-surgical anxiety and depression on the development of neuropathic pain after surgery for breast cancer
Description
The HAD (Hospital anxiety and despression scale) questionnaire will be collected during the screening visit
Time Frame
49 months
Title
The incidence of NICBs 4 months after surgery for breast cancer
Description
The incidence of NICBs will be measured by the number of patients included in the study (DN4 +) compared to the number of patients screened before surgery
Time Frame
4 months
Title
The evolution of the weight between the two arms after 6 months of treatment.
Description
The weight is collected after 6 months of treatment
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female who had first breast cancer surgery, regardless of the type of surgery Age ≥ 18 years Healthy, non-irritated skin on painful areas to treat During the inclusion visit to M4 post surgery, neuropathic pain of the breast and / or axillary area corresponding to inter-brachial neuralgia with a DN4≥4 score. Obtaining the signed written consent of the patient Major patient affiliated to a social security scheme Exclusion Criteria: Contraindications specific to the treatments studied : capsaicine and pregabalin Diabetic patient Previous treatment with capsaicin or pregabalin Opioid treatment> 80 mg / day (oral morphine equivalent) in progress- Topical treatment of pain between surgery and inclusion visit Uncontrolled hypertension (systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 90 mmHg) or recent history (<3 months) of cardiovascular events (stroke, heart attack, pulmonary embolism) Creatinine clearance (CLcr) <60mL / min according to the Cockcroft-Gault formula Pregnant woman, likely to be pregnant or breastfeeding Persons deprived of their liberty or guardianship (including curators), Impossibility of submitting to the medical follow-up of the test for geographical, social or psychological reasons
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
DENIS DUPOIRON, MD
Organizational Affiliation
Institut de Cancérologie de l'Ouest
Official's Role
Study Director
Facility Information:
Facility Name
Institut de Cancerologie de L'Ouest
City
Angers
ZIP/Postal Code
49000
Country
France
Facility Name
Chu Grenoble
City
Grenoble
ZIP/Postal Code
38700
Country
France
Facility Name
Chd Vendee
City
La Roche-sur-Yon
ZIP/Postal Code
85025
Country
France
Facility Name
Centre Oscar Lambret
City
Lille
ZIP/Postal Code
59020
Country
France
Facility Name
Hopital Saint Vincent de Paul
City
Lille
ZIP/Postal Code
59020
Country
France
Facility Name
Centre Leon Berard
City
Lyon
ZIP/Postal Code
69008
Country
France
Facility Name
CHU NICE
City
Nice
ZIP/Postal Code
06003
Country
France
Facility Name
Institut Jean Godinot
City
Reims
ZIP/Postal Code
51100
Country
France
Facility Name
Institut Curie
City
Saint-Cloud
ZIP/Postal Code
92210
Country
France
Facility Name
Iuct Oncopole
City
Toulouse
ZIP/Postal Code
31052
Country
France
Facility Name
Ch Valenciennes
City
Valenciennes
ZIP/Postal Code
53322
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Evaluation in the Treatment of Neuropathic Pain Post Breast Surgery

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