EMA Accepts Marketing Authorization Application for Decitabine and Cedazuridine in Adult AML
August 24th 2022Adult patients with acute myeloid leukemia who are not eligible for treatment with standard induction chemotherapy may benefit from treatment with decitabine and cedazuridine, the marketing authorization application for which was accepted by the European Medicines Agency.
Laser Interstitial Thermal Therapy Appears to be a Promising Option in New, Recurrent Glioblastoma
August 23rd 2022Results from a multicenter study showed similar median overall survival results with laser interstitial thermal therapy compared with other tumor resection studies that used radiation and chemotherapy followed by laser ablation in patients with IDH wild-type glioblastoma.
Adjuvant Canakinumab Misses DFS End Point in R0 Resected Stage II-IIIA NSCLC
August 21st 2022In an update to the phase 3 CANOPY-A trial, investigators reported that canakinumab did not significantly improve disease-free survival over placebo in patients with completely resected non–small cell lung cancer.
TP53 Gain-of-Function Status Linked With Outcomes Based on Sidedness in Metastatic CRC
August 18th 2022Investigators found that patients with non–gain-of-function TP53-mutant right-sided metastatic colorectal cancer and gain-of-function TP53-mutant left-sided tumors had poorer survival vs their counterparts.
Supplemental BLA Accepted by FDA for Polatuzumab Vedotin/R-CHP Combo for Previously Untreated DLBCL
August 17th 2022Patients with previously untreated diffuse large B-cell lymphoma may benefit from treatment with polatuzumab vedotin-piiq plus rituximab, cyclophosphamide, doxorubicin, and prednisone, for which a supplemental biologics license application was accepted by the FDA.
FDA Gives Priority Review to Olaparib and Abiraterone for mCRPC Regardless of HRR Status
August 16th 2022Based on data showing that patients with metastatic castration-resistant prostate cancer may achieve benefit following treatment with olaparib plus abiraterone and prednisone or prednisolone regardless of homologous recombination repair mutational status, the FDA gave the combination priority review.