2020
DOI: 10.1016/s0140-6736(20)31953-x
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Neoadjuvant atezolizumab in combination with sequential nab-paclitaxel and anthracycline-based chemotherapy versus placebo and chemotherapy in patients with early-stage triple-negative breast cancer (IMpassion031): a randomised, double-blind, phase 3 trial

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Cited by 782 publications
(725 citation statements)
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References 28 publications
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“…35 Higher rate of pCR was observed with the addition of pembrolizumab (64.8% vs 51.2%, P < .001). Similarly, another phase 3 randomized study IMpassion 031 36 randomized stage II and III TNBC to atezolizumab + nab-paclitaxel followed by atezolizumab and AC, or placebo + nab-paclitaxel followed by AC. Pathological complete response was observed in 57.6% in the atezolizumab arm, versus 41.1% in the placebo arm ( P = .0044).…”
Section: Nac For Tnbc and Subgroup Classification Using Gene-expressimentioning
confidence: 99%
“…35 Higher rate of pCR was observed with the addition of pembrolizumab (64.8% vs 51.2%, P < .001). Similarly, another phase 3 randomized study IMpassion 031 36 randomized stage II and III TNBC to atezolizumab + nab-paclitaxel followed by atezolizumab and AC, or placebo + nab-paclitaxel followed by AC. Pathological complete response was observed in 57.6% in the atezolizumab arm, versus 41.1% in the placebo arm ( P = .0044).…”
Section: Nac For Tnbc and Subgroup Classification Using Gene-expressimentioning
confidence: 99%
“…This humble benefit did not lead to a better overall survival and was not recapitulated when using paclitaxel as concomitant chemotherapy nor consistently associated to any predictive biomarker other than PD-L1 (6). Findings seem to be more clinically meaningful in the neoadjuvant setting, in which an increased pathological complete response rate has been reported in patients receiving atezolizumab (58 vs 41% for total population, 69 vs 49% in PD-L1 positive tumors) (7). This body of evidence underscores the need of a better understanding of the tumorimmune interaction, escape mechanisms, and the role of the microenvironment when a high tumor burden exists.…”
Section: Introductionmentioning
confidence: 83%
“…The primary endpoint was pCR in the intention-to-treat population and in the PD-L1-positive population. There was a significant increase in the pCR rate in patients who received atezolizumab compared to patients who received placebo, regardless of PD-L1 expression [38].…”
Section: Efficacymentioning
confidence: 88%
“…Details on the efficacy and toxicity of the aforementioned schemes are depicted in Tables 1 and 2, respectively. More recently, the IMpassion031, a phase III, randomised, double-blind study, evaluating the use of immunotherapy in early-stage TNBC, met its primary endpoint [38]. Overall, 333 patients were randomised to receive neoadjuvant chemotherapy (nab-paclitaxel followed by doxorubicin and cyclophosphamide) combined with atezolizumab versus chemotherapy compared to placebo and chemotherapy, followed by maintenance therapy with atezolizumab.…”
Section: Efficacymentioning
confidence: 99%