| Literature DB >> 33742104 |
Apostolia Maria Tsimberidou1, David S Hong2, Siqing Fu2, Daniel D Karp2, Sarina Piha-Paul2, Merrill S Kies3, Vinod Ravi4, Vivek Subbiah2, Sunil M Patel5, Shi-Ming Tu6, Filip Janku2, John Heymach3, Amber Johnson7, Carrie Cartwright2, Li Zhao8, Jianhua Zhang8, Donald A Berry9, David J Vining10, Andrew Futreal8, Vincent A Miller11, Funda Meric-Bernstam2.
Abstract
Precision medicine is associated with favorable outcomes in selected patients with cancer. Herein, we report an interim analysis of IMPACT2, an ongoing randomized study evaluating genomic profiling and targeted agents in metastatic cancer. Patients with metastatic cancer underwent tumor genomic profiling (ClinialTrials.gov: NCT02152254), and 69 patients met the criteria for randomization. Tumor board and multidisciplinary review of molecular alterations optimized treatment selection. From 5/2014 to 4/2017, 320 patients (median age, 63 years; men, 47%) had tumor molecular aberrations, and 213 (66.56%) received anticancer therapy. The most frequently mutated genes were TP53 (42%), KRAS (16%), PIK3CA (12%), and CDKN2A (11%). The median OS was 10.9 months (95% CI, 8.8-12.9). OS was shorter in patients with higher tumor mutational burden. Independent factors associated with shorter OS were age ≥60 years, liver metastases, low albumin levels, high LDH levels, and KRAS and TP53 mutations. Outcomes for randomized patients will be reported after completion of the study.Entities:
Year: 2021 PMID: 33742104 PMCID: PMC7979841 DOI: 10.1038/s41698-021-00159-2
Source DB: PubMed Journal: NPJ Precis Oncol ISSN: 2397-768X