Non-interventional Study to Assess the Effectiveness and Safety of Ribociclib in the Adjuvant Therapy of Hormone Receptor Positive (HR+) HER2-negative Stage II and III Breast Cancer in Real Clinical Practice in Russia

Status: Recruiting
Location: See all (12) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

This prospective, observational, multicenter study aims at evaluating the efficacy of adjuvant ribociclib in combination with hormone therapy (aromatase inhibitor ± GnRH aginost) in various subgroups of patients with HR+HER2- stage II-III breast cancer in real clinical practice in Russia. Subgroup division will be based on the tumor grade, lymph node involvement, and the response to test hormone therapy. The study will consist of two cohorts: a prospective one with patients receiving adjuvant therapy with ribociclib combined with Aromatase inhibitors (AI), and a retrospective one with patients receiving adjuvant therapy with AI alone. Thus, both primary data collection and secondary use of data will be organized.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:

⁃ Patients from the prospective cohort of the study must meet all of the following criteria:

• Signed and dated Informed Consent Form (ICF) not later than 28 days after the initiation of adjuvant therapy with ribociclib in combination with aromatase inhibitors (±GnRH agonists).

• Age ≥18 years at the time of signing the ICF.

• Histologically verified HR+ HER2-negative stage II-III breast cancer, for which radical treatment was carried out.

• The adjuvant hormone therapy with aromatase inhibitors (±GnRH agonists) may be started not earlier than 12 months before initiation of therapy with ribociclib.

• ECOG performance status 0-1

⁃ Patients from the retrospective cohort of the study must meet all of the following criteria:

• Age ≥18 years at the initiation of hormone therapy.

• Histologically verified HR+ HER2-negative stage II-III breast cancer, for which radical treatment was carried out.

• Initiation of adjuvant hormone monotherapy with aromatase inhibitors (±GnRH agonists) in the index period from July 1, 2019 to July 1, 2020.

• Presence of the necessary information in the source documentation.

Locations
Other Locations
Russian Federation
Novartis Investigative Site
RECRUITING
Barnaul
Novartis Investigative Site
RECRUITING
Irkutsk
Novartis Investigative Site
RECRUITING
Izhevsk
Novartis Investigative Site
RECRUITING
Kaluga
Novartis Investigative Site
RECRUITING
Khimky
Novartis Investigative Site
RECRUITING
Krasnoyarsk
Novartis Investigative Site
RECRUITING
Saint Petersburg
Novartis Investigative Site
RECRUITING
Saransk
Novartis Investigative Site
RECRUITING
Surgut
Novartis Investigative Site
RECRUITING
Tver'
Novartis Investigative Site
RECRUITING
Yaroslavl
Novartis Investigative Site
RECRUITING
Yuzhno-sakhalinsk
Contact Information
Primary
Novartis Pharmaceuticals
novartis.email@novartis.com
+41613241111
Backup
Novartis Pharmaceuticals
Time Frame
Start Date: 2025-12-03
Estimated Completion Date: 2032-12-31
Participants
Target number of participants: 2766
Treatments
Ribociclib+AI
Patients with HR+ HER2- stage II-III breast cancer receiving adjuvant ribociclib plus AI (aromatase inhibitor)
Monotherapy AI
Patients with HR+ HER2- stage II-III breast cancer receiving adjuvant AI (aromatase inhibitor) monotherapy
Related Therapeutic Areas
Sponsors
Leads: Novartis Pharmaceuticals

This content was sourced from clinicaltrials.gov