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Caelyx as Primary Treatment for Patients With Breast Cancer and a History of Heart Disease and/or Age Over 65 Years (CAPRICE)

Primary Purpose

Breast Cancer

Status
Completed
Phase
Phase 2
Locations
Spain
Study Type
Interventional
Intervention
Liposomal pegylated doxorubicine
Sponsored by
SOLTI Breast Cancer Research Group
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring Breast, Cancer, Anthracyclines, Cardiopathy

Eligibility Criteria

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

Inclusion Criteria:

  • Histologically confirmed invasive breast cancer (tumor > 2 cm).
  • Estrogen receptor-negative or -weakly positive tumors (less than 50% of cells), as evaluated using IHC.
  • Risk factors for developing anthracycline-induced cardiomyopathy.

Exclusion Criteria:

  • Severe heart failure (NYHA Class III or IV) .
  • Metastatic disease.
  • LVEF < 45%.
  • Pregnant or breast-feeding patients.

Sites / Locations

  • Institut Català d'Oncologia
  • Hospital Son Llàtzer
  • Hospital Universitario Sant Joan de Reus
  • Hospital de la Santa Creu i Sant Pau
  • Hospital Universitari Vall d'Hebron
  • Hospital Universitari Arnau de Vilanova
  • Hospital Universitario 12 de Octubre
  • Hospital Universitario Morales Meseguer

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

Primary chemotherapy regimen consisting of four cycles of pegylated-liposomal doxorubicine at 35 mg/m² IV plus CPM 600 mg/m² on Day 1 every 4 weeks followed by paclitaxel 80 mg/m²/week for 12 weeks before surgery.

Outcomes

Primary Outcome Measures

Pathological complete response (pCR). pCR is defined as the absence of invasive cancer in the surgical breast specimen. This definition includes evidence of carcinoma in situ only.

Secondary Outcome Measures

Clinical response rate (complete plus partial responses). Clinical response will be assessed by imaging using the WHO criteria.
Breast-conserving surgery: tumorectomy or quadrantectomy with or without lymphadenectomy versus mastectomy.
Axillary node involvement after primary chemotherapy.
Left ventricular ejection fraction measured by echocardiography or MUGA.
Cardiac sign/symptom questionnaire.
Relapse-free survival at 5 years after surgery and overall survival at 5 years after study entry.

Full Information

First Posted
November 26, 2007
Last Updated
October 11, 2017
Sponsor
SOLTI Breast Cancer Research Group
Collaborators
Schering-Plough
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1. Study Identification

Unique Protocol Identification Number
NCT00563953
Brief Title
Caelyx as Primary Treatment for Patients With Breast Cancer and a History of Heart Disease and/or Age Over 65 Years
Acronym
CAPRICE
Official Title
A Phase II, Open-Label, Multicenter Clinical Trial of Pegylated Liposomal Doxorubicin (Caelyx®) as Primary Treatment for Patients With Breast Cancer and a History of Heart Disease or Age Over 65 Years.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
September 2007 (undefined)
Primary Completion Date
February 2011 (Actual)
Study Completion Date
August 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
SOLTI Breast Cancer Research Group
Collaborators
Schering-Plough

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a multicenter study of a primary chemotherapy regimen in breast cancer patients at risk of developing cardiotoxicity. The aim of the study is to evaluate the response rate at surgery.
Detailed Description
This is a phase II, uncontrolled, open label, multicenter study of a primary chemotherapy regimen consisting of four cycles of liposomal pegylated doxorubicine 35 mg/m² IV plus cyclophosphamide 600 mg/m² on Day 1 every 4 weeks followed by paclitaxel 80 mg/m²/week for 12 weeks before surgery in breast cancer patients at risk of developing anthracycline-induced cardiotoxicity. Surgery (tumorectomy, quadrantectomy, or mastectomy plus lymphadenectomy) will be performed 2 to 5 weeks after the last primary chemotherapy infusion. Patients with > 10% of hormone receptor-positive cells will receive appropriate hormone therapy according to menopausal status. Patients treated with breast-conserving surgery will receive radiation therapy to the mammary gland. Patients with T4 tumors or significant axillary involvement (≥ ypN2) will receive radiation therapy to the breast or chest wall and to the lymph node chains.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
Breast, Cancer, Anthracyclines, Cardiopathy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Primary chemotherapy regimen consisting of four cycles of pegylated-liposomal doxorubicine at 35 mg/m² IV plus CPM 600 mg/m² on Day 1 every 4 weeks followed by paclitaxel 80 mg/m²/week for 12 weeks before surgery.
Intervention Type
Drug
Intervention Name(s)
Liposomal pegylated doxorubicine
Other Intervention Name(s)
Caelyx
Intervention Description
Four cycles of liposomal pegylated doxorubicine at 35 mg/m² IV combined with cyclophosphamide at 600 mg/m² on Day 1 every 4 weeks, and followed by paclitaxel 80 mg/m²/week for 12 weeks before surgery.
Primary Outcome Measure Information:
Title
Pathological complete response (pCR). pCR is defined as the absence of invasive cancer in the surgical breast specimen. This definition includes evidence of carcinoma in situ only.
Time Frame
At surgery.
Secondary Outcome Measure Information:
Title
Clinical response rate (complete plus partial responses). Clinical response will be assessed by imaging using the WHO criteria.
Time Frame
Before and after treatment with paclitaxel.
Title
Breast-conserving surgery: tumorectomy or quadrantectomy with or without lymphadenectomy versus mastectomy.
Time Frame
At surgery.
Title
Axillary node involvement after primary chemotherapy.
Time Frame
At surgery.
Title
Left ventricular ejection fraction measured by echocardiography or MUGA.
Time Frame
At baseline, every 2 doxorubicine cycles and before surgery.
Title
Cardiac sign/symptom questionnaire.
Time Frame
At baseline, every 2 doxorubicine cycles and before surgery.
Title
Relapse-free survival at 5 years after surgery and overall survival at 5 years after study entry.
Time Frame
Until 5 years after surgery.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed invasive breast cancer (tumor > 2 cm). Estrogen receptor-negative or -weakly positive tumors (less than 50% of cells), as evaluated using IHC. Risk factors for developing anthracycline-induced cardiomyopathy. Exclusion Criteria: Severe heart failure (NYHA Class III or IV) . Metastatic disease. LVEF < 45%. Pregnant or breast-feeding patients.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Miguel Gil, MD
Organizational Affiliation
Institut Català d'Oncologia
Official's Role
Study Chair
Facility Information:
Facility Name
Institut Català d'Oncologia
City
L'Hospitalet de Llobregat
State/Province
Barcelona
ZIP/Postal Code
08907
Country
Spain
Facility Name
Hospital Son Llàtzer
City
Palma de Mallorca
State/Province
Illes Balears
ZIP/Postal Code
07198
Country
Spain
Facility Name
Hospital Universitario Sant Joan de Reus
City
Reus
State/Province
Tarragona
ZIP/Postal Code
42301
Country
Spain
Facility Name
Hospital de la Santa Creu i Sant Pau
City
Barcelona
ZIP/Postal Code
08025
Country
Spain
Facility Name
Hospital Universitari Vall d'Hebron
City
Barcelona
ZIP/Postal Code
08035
Country
Spain
Facility Name
Hospital Universitari Arnau de Vilanova
City
Lleida
ZIP/Postal Code
25198
Country
Spain
Facility Name
Hospital Universitario 12 de Octubre
City
Madrid
ZIP/Postal Code
28041
Country
Spain
Facility Name
Hospital Universitario Morales Meseguer
City
Murcia
ZIP/Postal Code
30008
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
25981896
Citation
Gil-Gil MJ, Bellet M, Morales S, Ojeda B, Manso L, Mesia C, Garcia-Martinez E, Martinez-Janez N, Mele M, Llombart A, Pernas S, Villagrasa P, Blasco C, Baselga J. Pegylated liposomal doxorubicin plus cyclophosphamide followed by paclitaxel as primary chemotherapy in elderly or cardiotoxicity-prone patients with high-risk breast cancer: results of the phase II CAPRICE study. Breast Cancer Res Treat. 2015 Jun;151(3):597-606. doi: 10.1007/s10549-015-3415-2. Epub 2015 May 16.
Results Reference
background
Citation
Gil MJ, Bellet MC, Llombart, Ojeda B, Manso L, Mesia C, Morales S, García-Martinez H, Martínez N, Melé M, Fernández-Ortega A, Baselga J. Pegylated Liposomal Doxorubicin (PLD) as Primary Treatment in Estrogen Receptor (ER) and HER2 Poor Breast Cancer and Risk of Developing Cardiotoxicity or Elderly Patients (pt). Results from the Phase II CAPRICE Study. Cancer Research 71(24 Suppl.): 403s, 2011.(CTRC-AACR San Antonio Breast Cancer Symposium)
Results Reference
result
PubMed Identifier
34307126
Citation
Gil-Gil MJ, Bellet M, Bergamino M, Morales S, Barnadas A, Manso L, Saura C, Fernandez-Ortega A, Garcia-Martinez E, Martinez-Janez N, Mele M, Villagrasa P, Celiz P, Perez Martin X, Ciruelos E, Pernas S. Long-Term Cardiac Safety and Survival Outcomes of Neoadjuvant Pegylated Liposomal Doxorubicin in Elderly Patients or Prone to Cardiotoxicity and Triple Negative Breast Cancer. Final Results of the Multicentre Phase II CAPRICE Study. Front Oncol. 2021 Jul 9;11:645026. doi: 10.3389/fonc.2021.645026. eCollection 2021.
Results Reference
derived

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Caelyx as Primary Treatment for Patients With Breast Cancer and a History of Heart Disease and/or Age Over 65 Years

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