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Comparison · NCT02764541-58d6bf70

Arm C Endocrine With Palbociclib vs Arm D Endocrine Therapy Alone: Number of Participants With RCB Response in Arm C and Arm D During the Treatment Phase

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Arm C Endocrine With Palbociclib vs Arm D Endocrine Therapy Alone: Number of Participants With RCB Response in Arm C and Arm D During the Treatment Phase. Trial comparisons, record NCT02764541-58d6bf70. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02764541-58d6bf70

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.07810.0430.138wilson
Risk in group 20.050.01710.137wilson
Risk difference, group 1 minus group 20.0281-0.06570.0963newcombe hybrid score
Risk ratio, group 1 over group 21.560.4465.47log
Odds ratio, group 1 over group 21.610.4276.08log
Number needed to treat, for one more participant with the outcome on Arm C Endocrine With Palbociclib than on Arm D Endocrine Therapy Alone35.6from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Arm C Endocrine With PalbociclibEndocrine therapy in combination with Palbociclib are given in the treatment phase for 24 weeks.10128OG000
Group 2Arm D Endocrine Therapy AloneEndocrine therapy alone is given in the treatment phase for 24 weeks360OG001

Outcome

Type
SECONDARY
Title
Number of Participants With RCB Response in Arm C and Arm D During the Treatment Phase
Description
RCB response is defined as RCB-0 or RCB-I; RCB not response is defined as RCB-II or RCB-III Residual Cancer Burden (RCB) considers residual disease in the tumor bed and lymph nodes after NAC, generating a continuous score which is then grouped into four categories: RCB-0, RCB-I, RCB-II and RCB-III. Higher RCB group reflects more tumor burden remaining, thus worse outcome
Time frame
day 15 to 24 weeks
Population
Patients with treatment and surgery are included into the analysis population

Source ClinicalTrials.gov

Trial

Title
Palbociclib and Endocrine Therapy for LObular Breast Cancer Preoperative Study (PELOPS)
NCT number
NCT02764541
Phases
PHASE2
Conditions
Breast Cancer
Interventions
Letrozole, Tamoxifen, Palbociclib, Endocrine Therapy
Lead sponsor
Dana-Farber Cancer Institute
Results first posted
2023-08-31

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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