NCT02224781 · OUTCOME

Response Rate (Arm A vs Arm D)

Dabrafenib and Trametinib Followed by Ipilimumab and Nivolumab or Ipilimumab and Nivolumab Followed by Dabrafenib and Trametinib in Treating Patients With Stage III-IV BRAFV600 Melanoma · Source last updated 2026-08-28

This outcome was registered, but no numerical results were posted in the captured record.

Measure: Not reported
Unit: Not reported
Interval / dispersion: Not reported
Time frame: assessed at baseline and then every 12 weeks from start of treatment if patient is < 2 years from study entry (or < 2 years from crossover), then every 6 months until 5 years from study entry

What was measured

Response was assessed based on the revised Response Evaluation Criteria in Solid Tumors (RECIST) guideline (version 1.1). Response rate was defined as proportion of patients with complete response or partial response. Response rates were compared using Fisher exact test in arms A vs D.

Groups in this outcome

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Reported measurements

No numerical measurement classes were posted for this outcome. Missing is not zero.

Complete source fields

denom Units Selected: Participants
description: Response was assessed based on the revised Response Evaluation Criteria in Solid Tumors (RECIST) guideline (version 1.1). Response rate was defined as proportion of patients with complete response or partial response. Response rates were compared using Fisher exact test in arms A vs D.
reporting Status: NOT_POSTED
time Frame: assessed at baseline and then every 12 weeks from start of treatment if patient is < 2 years from study entry (or < 2 years from crossover), then every 6 months until 5 years from study entry
title: Response Rate (Arm A vs Arm D)
type: SECONDARY

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Preserved source evidence · Not medical advice