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Massive study maps breast cancer care in england

NCT ID NCT07498413

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at medical records from over 218,000 adults in England with a common type of breast cancer (HR+/HER2-). Researchers tracked which treatments people received, how the disease progressed over time, and how healthcare resources were used. The goal was to understand real-world care patterns, not to test a new treatment.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

218,677 people

The number who actually took part.

Started

Jun 2023

Finished

Jul 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adults captured in the cancer registry with a diagnosis of HR+/HER2- early BC or metastatic BC between 01 April 2012 and 31 December 2022.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion criteria: * Patient with a registered diagnosis of International Classification of Diseases,10th Revision (ICD-10) code C50: malignant neoplasm of the breast, between 01 April 2012 and 31 December 2022. * Patient ≥18 years of age at diagnosis. * Patient with estrogen receptor-positive (ER+) or progesterone receptor-positive (PR+), i.e., hormone receptor positive (HR+) breast cancer * Patient with human epidermal growth factor receptor 2 negative (HER2-) breast cancer. Additional inclusion criteria for patients with metastatic BC were defined as: * Tumor stage IV at diagnosis or on subsequent treatment or * Tumor Node Metastases (TNM) staging indicative of M1 at diagnosis or on subsequent treatment or * Record with ICD-10 codes indicating secondary malignant neoplasm C77\* (excluding C771 and C773), C78\*, or C79\* or * Initiation of treatment specified for metastatic BC, defined as ribociclib or palbociclib from 01 January 2017 to the end of the study period or abemaciclib from 01 January 2017 to 31 May 2022 or * Record of treatment for distant/metastatic recurrence. An additional inclusion criterion for patients with early BC was: • No evidence of metastatic disease (defined above) before or up to 100 days after the first BC diagnosis date. Additional inclusion criteria for patients in the NATALEE Trial-aligned sub-cohort: * Patient with stage IIa BC at diagnosis (i.e., T0-1 N1 or T2 N0 with Grade 3 tumor), or * Stage IIb BC at diagnosis (i.e., T2 N1, T3 N0), or * Stage III BC at diagnosis. Exclusion criteria: * Patient's sex unknown. * Patient with ductal carcinoma in situ (DCIS), or lobular carcinoma in situ (LCIS). * Patient with a diagnosis of Second Edition of the International Classification of Diseases for Oncology (ICD-0-O2) code 0, 1, or 2 denoting non-malignant disease. * Patient with any indication of co-positive disease before or within 6 months after diagnosis (i.e., HR+ and HER2+) including: * treated with trastuzumab * treated with tyrosine kinase inhibitors (TKIs) * Any registered BC tumor or evidence of metastatic cancer prior to index date.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Novartis

    London, W12 7FQ, United Kingdom

More trials for these conditions

Other studies related to the condition(s) this trial covers.