2018
DOI: 10.1200/jco.2018.36.15_suppl.4030
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Margetuximab (M) plus pembrolizumab (P) in ERBB2-amplified PD-L1+ gastroesophageal adenocarcinoma (GEA) post trastuzumab (T).

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Cited by 14 publications
(16 citation statements)
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“…While these findings lay the groundwork for combination therapy, further studies will help to elucidate the mechanisms that underlie the immunomodulation of chemotherapeutic agents to optimize their potent effects with checkpoint inhibition. A number of studies have sought to evaluate the efficacy of checkpoint inhibitors in combination with chemotherapeutic agents or radiotherapy (43,(76)(77)(78). One phase II trial found the PD-L1 inhibitor LY3300054 (LY) alone or in combination with ramucirumab or merestinib in 38 patients with advanced, refractory solid tumors demonstrated antitumor activity with one partial response in each cohort (76).…”
Section: Discussionmentioning
confidence: 99%
“…While these findings lay the groundwork for combination therapy, further studies will help to elucidate the mechanisms that underlie the immunomodulation of chemotherapeutic agents to optimize their potent effects with checkpoint inhibition. A number of studies have sought to evaluate the efficacy of checkpoint inhibitors in combination with chemotherapeutic agents or radiotherapy (43,(76)(77)(78). One phase II trial found the PD-L1 inhibitor LY3300054 (LY) alone or in combination with ramucirumab or merestinib in 38 patients with advanced, refractory solid tumors demonstrated antitumor activity with one partial response in each cohort (76).…”
Section: Discussionmentioning
confidence: 99%
“…In terms of safety, an adverse reaction rate of grade 3 and above was 13%. No treatment-related deaths occurred (48).…”
Section: Icis and Anti-her-2 Targeted Therapymentioning
confidence: 93%
“…Notably, for patients with HER2 amplification and PD-L1 positivity by circulating tumor DNA (ctDNA) detection, ORR was 57% and DCR was 86%. Treatment-related adverse events (TRAEs, ≥ grade 3) occurred in 13% of the patients, and serious adverse events (SAEs) included autoimmune hepatitis (two cases) and pneumonitis (one case) [69] (Table 1).…”
Section: Combination With Other Targeted Agentsmentioning
confidence: 99%