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Comparison · NCT04770272-2eaa1910

Arm A vs Arm B: Event Free Survival (EFS)

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 A vs Arm B: Event Free Survival (EFS). Trial comparisons, record NCT04770272-2eaa1910. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04770272-2eaa1910

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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 10.1110.07310.165wilson
Risk in group 20.08940.05580.14wilson
Risk difference, group 1 minus group 20.0217-0.04180.0856newcombe hybrid score
Risk ratio, group 1 over group 21.240.6662.32log
Odds ratio, group 1 over group 21.270.6372.55log
Number needed to treat, for one more participant with the outcome on Arm A than on Arm B46from 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 A
2 weeks Atezolizumab monotherapy before biopsy, followed by a 12-week therapy with Paclitaxel + Carboplatin+ Atezolizumab every 3 weeks for 4 cycles. This will be followed by Epirubicin + Cyclophosphamide + Atezolizumab every 3 weeks for 4 cycles.~Atezolizumab 840 MG in 14 ML Injection: 840 mg Day 1 for two weeks~Atezolizumab 1200 MG in 20 ML Injection: 1200 mg Day 1 every 3 weeks for 8 cycles~Carboplatin: Dosing according to Area Under the Curve of 2 Intravenous weekly x 12 cycles~Paclitaxel: Paclitaxel 80 mg/m² IV weekly x 12 cycles~Epirubicin: 90 mg/m2, day 1 for 4 cycles (12 weeks)~Cyclophosphamide: 600 mg/m2, day 1 for 4 cycles (12 weeks)~Biopsy Arm A: 1st Biopsy two weeks after Baseline visit. 2nd Biopsy after two weeks of Carboplatin + Paclitaxel + Atezolizumab therapy. 3rd Biopsy with tumor size greater 10 mm in diameter.~Surgery: After completion of 27-28 weeks (Arm B) or 29-30 weeks (Arm A) of neoadjuvant treatment, surgery is planned for all patients.
20180OG000
Group 2Arm B
12-week therapy with Paclitaxel + Carboplatin + Atezolizumab every 3 weeks for 4 cycles. This will be followed by Epirubicin + Cyclophosphamide + Atezolizumab every 3 weeks for 4 cycles.~Atezolizumab 1200 MG in 20 ML Injection: 1200 mg Day 1 every 3 weeks for 8 cycles~Carboplatin: Dosing according to Area Under the Curve of 2 Intravenous weekly x 12 cycles~Paclitaxel: Paclitaxel 80 mg/m² IV weekly x 12 cycles~Epirubicin: 90 mg/m2, day 1 for 4 cycles (12 weeks)~Cyclophosphamide: 600 mg/m2, day 1 for 4 cycles (12 weeks)~Biopsy Arm B: 1st Biopsy after two weeks of Carboplatin + Paclitaxel + Atezolizumab therapy. 2nd Biopsy with tumor size greater 10mm in diameter.~Surgery: After completion of 27-28 weeks (Arm B) or 29-30 weeks (Arm A) of neoadjuvant treatment, surgery is planned for all patients.
16179OG001

Outcome

Type
SECONDARY
Title
Event Free Survival (EFS)
Description
Event free survival (EFS) defined as length of time after randomization till death from any cause, failure to achieve remission after induction therapy, relapse in any site, or second malignancy
Time frame
from randomization up to 24 months until date of death from any cause, failure to achieve remission after induction therapy, relapse in any site, or second malignancy
Population

Source ClinicalTrials.gov

Trial

Title
Study to Compare a Mono Atezolizumab Window Followed by a Atezolizumab - CTX Therapy With Atezolizumab - CTX Therapy
NCT number
NCT04770272
Phases
PHASE2
Conditions
Triple-negative Breast Cancer
Interventions
Atezolizumab 840 MG in 14 ML Injection, Atezolizumab 1200 MG in 20 ML Injection, Carboplatin, Paclitaxel, Epirubicin, Cyclophosphamide, Biopsy Arm A, Biopsy Arm B, Surgery
Lead sponsor
Palleos Healthcare GmbH
Results first posted
2026-01-12

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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