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NCT02744053 · ClinicalTrials.gov registry record · Early Phase 1

DCE-MRI and MBI in Assessing Tumor Response to Chemotherapy in Patients With Triple Negative Breast Cancer

A Early Phase 1 study of HER2/Neu Negative and Triple-Negative Breast Carcinoma, sponsored by M.D. Anderson Cancer Center.

Active
Registry status
Early Phase 1
Development phase
96
Enrollment target
6
Study locations

NCT02744053: Active Early Phase 1 study of HER2/Neu Negative and Triple-Negative Breast Carcinoma, sponsored by M.D. Anderson Cancer Center.

NCT02744053 is a Early Phase 1 study of HER2/Neu Negative and Triple-Negative Breast Carcinoma that is active but no longer recruiting, run by M.D. Anderson Cancer Center. The registered enrollment target is 96 participants, below the 164-participant average among 28 other HER2/Neu Negative trials with a reported enrollment target (41% lower). The trial reports 6 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02744053, a Early Phase 1 study of HER2/Neu Negative and Triple-Negative Breast Carcinoma, is active but no longer recruiting, sponsored by M.D. Anderson Cancer Center.

ACTIVE NOT RECRUITING
Registry status
Early Phase 1
Development phase
96 participants
Enrollment target
6
Study locations

Study Summary

This early phase I trial studies how well dynamic contrast enhanced molecular resonance imaging (DCE-MRI) and technetium-Tc99m sestamibi molecular breast imaging (MBI) work in assessing tumor response to chemotherapy in patients with triple negative breast cancer (TNBC) who are undergoing chemotherapy. Investigational imaging scans such as MBI and DCE-MRI may help researchers predict which patients may respond to treatment.

Primary Outcome

The ability to assess and predict response will be compared among the imaging modalities and with standard pathological evaluation. These volume changes will be correlated with residual cancer burden (RCB) status after surgery and will be used to classify patients into predicted responder or non-responder categories. Predictive accuracies among the imaging modalities will be compared using paired ROC curve analyses.

Interventions

  • OTHER Laboratory Biomarker Analysis
  • RADIATION Scintimammography
  • PROCEDURE Dynamic Contrast-Enhanced Magnetic Resonance Imaging
  • DRUG Technetium Tc-99m Sestamibi

Study Locations (6)

Texas

  • Memorial Hermann Memorial City Medical Center - Houston
  • M D Anderson Cancer Center - Houston
  • MD Anderson in Katy - Houston
  • MD Anderson League City - Nassau Bay
  • MD Anderson in Sugar Land - Sugar Land
  • MD Anderson in The Woodlands - The Woodlands

Trial Details

FieldValue
Enrollment Target 96 participants
Start Date 2016-11-07
Est. Completion 2026-04-30
Phase Early Phase 1
M.D. Anderson Cancer Center

2,692 total trials

What the registry record for NCT02744053 still lists

NCT02744053 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 96 participants, a relatively small participant target, below the 164-participant average among 28 other HER2/Neu Negative trials with a reported enrollment target (41% lower).

The record links to 4 conditions, with HER2/Neu Negative appearing as the primary indexed condition, and to 4 interventions - of which Laboratory Biomarker Analysis is the first listed.

NCT02744053 lists 6 locations in 1 state (Texas).

Frequently Asked Questions

What is clinical trial NCT02744053 about?

NCT02744053 is a clinical study titled "DCE-MRI and MBI in Assessing Tumor Response to Chemotherapy in Patients With Triple Negative Breast Cancer". This early phase I trial studies how well dynamic contrast enhanced molecular resonance imaging (DCE-MRI) and technetium-Tc99m sestamibi molecular breast imaging (MBI) work in assessing tumor response to chemotherapy in patients with triple negative breast cancer (TNBC) who are undergoing chemothera...

What is the current status of trial NCT02744053?

This trial is currently active not recruiting. It is a Early Phase 1 study. The enrollment target is 96 participants. The study started on 2016-11-07. Estimated completion is 2026-04-30.

What conditions does trial NCT02744053 study?

This clinical trial studies the following conditions: HER2/Neu Negative, Triple-Negative Breast Carcinoma, Estrogen Receptor Negative, Progesterone Receptor Negative.

What interventions are being tested in trial NCT02744053?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Scintimammography (RADIATION), Dynamic Contrast-Enhanced Magnetic Resonance Imaging (PROCEDURE), Technetium Tc-99m Sestamibi (DRUG).

Who is sponsoring clinical trial NCT02744053?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02744053 being conducted?

This trial has 6 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for HER2/Neu Negative

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02744053's enrollment target sits among peer trials

96 11th of 28 higher than 18 of 28 other HER2/Neu Negative trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other HER2/Neu Negative trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02744053, the US trial registry maintained by the National Library of Medicine. NCT02744053 (small enrollment · multi site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.