Outcomes Of The Spanish Cohort Of Early Access To Pertuzumab And Trastuzumab Emtansine

Completed

• Conditions: Breast Neoplasms

• Registration Number: NCT03025711
• Lead Sponsor: BELEN RUIZ-ANTORAN

Brief Summary

The overall study objective is to evaluate the effectiveness and safety of Trastuzumab emtansine (T-DM1) and Pertuzumab under real-world disease conditions in the Spain, and specifically in patients treated under compassionate use or early access program

Detailed Description

This is a retrospective, non-interventional, non-comparative, observational cohort study / registry in the Spain. The study design will reflect real-life clinical management of patients with HER2-positive MBC. Type and frequency of actual patient visits and all evaluations will be done as for routine clinical practice.

The analysis of the efficacy and safety results obtained in patients receiving pertuzumab or TDM1 in those early access systems is of utmost importance. These real-world patients with advanced breast cancer may have different characteristics than those enrolled in clinical trials and clinicians must often extrapolate into therapeutic decisions not fully supported by a robust evidence.

Study Timeline

• Study First Submitted: 2017-01-11
• Study First Submitted QC: 2017-01-16
• Study First Posted: 2017-01-19
• Study Start: 2017-12-01
• Primary Completion: 2018-10-01
• Study Completion: 2020-01-31
• Status Verified: 2020-03
• Last Update Submitted: 2020-03-04
• Last Update Posted: 2020-03-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 220

Inclusion Criteria

• Adult patients (age ≥ 18 years at enrolment) with HER2-positive metastatic or locally recurrent unresectable breast cancer and who are treated with Trastuzumab emtansine (T-DM1) or Pertuzumab.
• Patients who initiate Trastuzumab emtansine (T-DM1) and Pertuzumab under Spanish compassionate use or early access program.

Exclusion Criteria

• Given the characteristics of the study there are no exclusion criteria.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Overall survival.	Through study completion (from date of start of treatment until the date of death from any cause, assessed up to 48 months).	The time between the date of start of treatment and the date of death. For subjects without documentation of death, OS will be censored on the last date the subject was known to be alive

Secondary Outcome Measures

Name	Time	Method
Time to treatment failure	Through study completion (from date of start of treatment until the date of treatment failure, assessed up to 48 months)
Time to change treatment	Through study completion (from date of start of treatment until the date of change treatment, assessed up to 48 months)
Time to next treatment	Through study completion (from date of start of treatment until the date of start other treatment, assessed up to 48 months)
Progression free survival.	Through study completion (from date of start of treatment until the date of first documented progression assessed up to 48 months)	The time from start of treatment to the date of the first documented tumour progression as determined by the clinician (may be based on clinical examination or radiographic or laboratory features).
Duration of response (DOR)	Through study completion, an average of 4 year	The time between the date of first confirmed response to the date of the first documented tumour progression, or death due to any cause, whichever occurs first. At the time of the analysis, several limitations should be taken into consideration for this retrospective study: DOR is only appraisable if measurable disease and DOR data availability in the medical records (ideally assessed with the RECIST criteria) could be incomplete.
Time to Objective Response	Through study completion (from date of start of treatment until the date of the first confirmed response, assessed up to 48 months)	The time from start of treatment to the date of the first confirmed response (evaluated for responders only)
Adverse events of special interest to anti HER2 Mab (AESI)	Through study completion, an average of 4 year	* AESIs regarding treatment with T-DM1: Hepatic disorder (specific analytical alteration); * AESIs regarding treatment with Pertuzumab: Interstitial Lung Disease
Best overall response rate	Through study completion, an average of 4 year	Response rate is defined as the proportion of patients with complete response (CR) or partial response (PR) based on their best overall response as written in the medical record
AEs of scientific interest	Through study completion, an average of 4 year	* An asymptomatic decline in LVEF requiring treatment or leading to discontinuation of study treatment (regarding treatment with T-DM1 and Pertuzumab); * Other AEs leading to treatment discontinuation
All suspected Grade 3/4/5 adverse reactions	Through study completion, an average of 4 year

Trial Locations

Locations (1)

Puerta de Hierro University Hospital; 🇪🇸 Madrid, Spain