ConductScience.org, home

Comparison · NCT04770272-deaths

Arm A vs Arm B: deaths from any cause

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

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

Download JSON
Cite this record

ConductScience Library. Arm A vs Arm B: deaths from any cause. Trial comparisons, record NCT04770272-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04770272-deaths

On this page

Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.005560.0009810.0308wilson
Risk in group 2000.021wilson
Risk difference, group 1 minus group 20.00556-0.01590.0308newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harm, for one more death from any cause on Arm A than on Arm B180from 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.
1180EG000
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.
0179EG001

Harm

What it counts
Total, all-cause mortality
Time frame
AEs were recorded until 30 days after the last dose of study treatment or until initiation of new anticancer therapy, whichever occured first; SAEs were reported until 90 days after the last dose of study treatment or until initiation of new anticancer therapy. Therefore, AEs were usually reported for 29 - 30 weeks for participants in Arm A and 27 - 28 weeks for participants in Arm B. Data for survival analyses (OS, PFS) were assessed from randomization up to 24 months.

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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT04770272-deaths