2016
DOI: 10.1016/s0959-8049(16)33041-6
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Exploratory biomarker analysis of first-line cobimetinib (C) + paclitaxel (P) in patients (pts) with advanced triple-negative breast cancer (TNBC) from the phase 2 COLET study

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“…Again, the addition of cobimetinib to first-line paclitaxel did not demonstrate significant improvement in mPFS 85 . Interestingly, the biomarker explorative analysis showed a potential immunomodulatory effect of cobimetinib in increasing the immune infiltration within TME 86 . Consistently, the part 2 of COLET study was designed to test the combination of cobimetinib, nab-paclitaxel and atezolizumab, with preliminary signs of activity in the PD-L1-positive population 87 .…”
Section: Introductionmentioning
confidence: 99%
“…Again, the addition of cobimetinib to first-line paclitaxel did not demonstrate significant improvement in mPFS 85 . Interestingly, the biomarker explorative analysis showed a potential immunomodulatory effect of cobimetinib in increasing the immune infiltration within TME 86 . Consistently, the part 2 of COLET study was designed to test the combination of cobimetinib, nab-paclitaxel and atezolizumab, with preliminary signs of activity in the PD-L1-positive population 87 .…”
Section: Introductionmentioning
confidence: 99%
“…63 In the phase 2 COLET trial, the MEK inhibitor cobimetinib was added to first-line paclitaxel for the treatment of patients with mTNBC but did not improve PFS. 64 However, an exploratory biomarker analysis suggested that cobimetinib increased immune infiltration within the tumor microenvironment 65 and, as such, a second part of the COLET trial began enrolling patients to be treated with a triplet of atezolizumab 840 mg IV on day 1 and 15, cobimetinib 60 mg PO on days 3-23, and paclitaxel IV 80 mg/m 2 (cohort 2) or nab-paclitaxel IV 100 mg/m 2 (cohort 3) on days 1, 8, and 15 of 28-day cycles. Data for 62 evaluable patients are presented in Table 1.…”
Section: Icis Plus Mek Inhibitorsmentioning
confidence: 99%