MEDIOLA is a phase I/II basket trial of olaparib and durvalumab. In a study cohort of the MEDIOLA study, the combination of olaparib and durvalumab showed promising anti-tumor activity in HER2-negative gBRCA-mutated breast cancer.
Source:
Lancet Oncol.
In a phase 3 study (eXalt3), ensartinib showed longer mPFS and higher intracranial ORR compared with crizotinib. The results indicated ensartinib can be a new first-line treatment option for patients with ALK+ NSCLC.
Source:
IASLC WCLC 2020
In a phase I study, the anti-tumor activity of vorasidenib (VOR; AG-881) was demonstrated in mutated IDH1/2 low-grade glioma.
Source:
J Clin Oncol
In a phase 2 study, futibatinib showed anti-tumor efficacy in chemotherapy-treated intrahepatic cholangiocarcinoma with FGFR2 fusion
Source:
J Clin Oncol
In phase 3 PADA-1 study, HR+ breast cancer patients with an ESR1 mutation showed worse outcomes in response to the 1st-line combination therapy of AI and palbociclib. Moreover, the reduction of plasma ESR1 mutation ctDNA level in the early stage of treatm
Source:
J Clin Oncol
MET amplification is one of the driver genetic alterations in advanced NSCLC. In a phase II study, the anti-tumor activity of capmatinib was demonstrated in treatment-na?ve and pretreated patients with MET-amplified advanced NSCLC.
Source:
J Clin Oncol
The immunotherapy-related biomarkers other than PD-L1, MSI-H/dMMR or TMB are still under development. A study analyzed the immunotherapy clinical outcome in cancer patients with LRP1B mutations. The results indicated the LRP1B pathogenic mutations were as
Source:
J Clin Oncol
Recently, phase 2 TBCRC 048 study results were published at the 2020 ASCO Virtual Scientific Program. This study aimed to investigate the activities of olaparib in metastatic breast cancer patients who have a homologous recombination repair gene mutation.
Source:
J Clin Oncol
Cancer immunotherapy has been hailed as the most promising treatment against cancer in recent decades, but what exactly is immunotherapy? Is Immunotherapy right for me?
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Merck is proficient in the mechanism of immunotherapy, and after Keytruda's first approval in 2017 with MSI-H as biomarker regardless of where in the body cancer started, the same approval came in June 2020 with TMB-H, showing prospects in immunotherapy.
Source:
Fierce Pharma