Molecular profiling holds promise to speed up drug development in rare tumours
Findings from several studies highlight the increasing utility of this approach to identify druggable genetic alterations
Findings from several studies highlight the increasing utility of this approach to identify druggable genetic alterations
Most, but not all, patients on chemotherapy or immunotherapy for solid tumours had an adequate immune response after two doses of mRNA-1273 vaccination, with no new safety concerns
In the NeoTRIPaPDL1 study, combining information from biomarker analysis at baseline and during treatment was informative on clinical benefit
A Japanese study reports discrepancies among centres, highlighting the need for better strategies to improve the quality of treatment recommendations
Rare tumours have been neglected for decades, with lack of funding, lack of research and lack of visibility. It is encouraging to see how this is changing and how research in rare tumours is not only taking place, but also being highlighted in Presidential Symposium 3 at this year’s ESMO Congress.
Results show it may help to define more homogeneous subgroups of patients with grade II–III glioma for more timely and effective cancer care
Phase I/II trials also show these compounds have more convenient dosing and are well tolerated in both the early and advanced settings
Studies also suggest hope for TKI inhibitor combinations in patients with symptomatic brain metastases
An exploratory analysis from the IMpower010 trial adds support to the use of post-chemotherapy adjuvant immunotherapy for selected early stage non-small-cell lung cancer
Data from SECOMBIT provide useful insights to the optimal sequence of immune checkpoint inhibitor therapy and targeted treatment combinations for patients with BRAF-mutated, advanced melanoma
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