Proteogenomic Characterization of Ovarian HGSC Implicates Mitotic Kinases, Replication Stress in Observed Chromosomal Instability.
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McDermott Jason E, Arshad Osama A, Petyuk Vladislav A, Fu Yi, Gritsenko Marina A, Clauss Therese R, Moore Ronald J, Schepmoes Athena A, Zhao Rui, Monroe Matthew E, Schnaubelt Michael, Tsai Chia-Feng, Payne Samuel H, Huang Chen, Wang Liang-Bo, Foltz Steven, Wyczalkowski Matthew, Wu Yige, Song Ehwang, Brewer Molly A, Thiagarajan Mathangi, Kinsinger Christopher R, Robles Ana I, Boja Emily S, Rodriguez Henry, Chan Daniel W, Zhang Bing, Zhang Zhen, Ding Li, Smith Richard D, Liu Tao, Rodland Karin D, Clinical Proteomic Tumor Analysis Consortium
Аннотация
METHOD: In a randomized clinical trial (clinicaltrials.gov: NCT02807480) with partial blinding in Tulsa, OK, 102 adults with GAD were allocated to manualized, 10-session EXP or BA between April 2016-April 2021. Primary analyses were intention-to-treat and included the 94 (46 EXP, 48 BA) participants who started treatment. The GAD-7 self-report scale was the primary outcome measure.
RESULTS: Similar GAD-7 declines were observed at post-treatment for EXP (d=-0.97 [95% CI -1.40 to -0.53]) and BA (d=-1.14 [95% CI -1.57 to -0.70]), and were maintained through 6-month follow-up (EXP: d=-2.13, BA: d=-1.98). Compared to EXP, BA yielded more rapid declines in anxiety and depression scores during therapy (d=0.75-0.77), as well as lower anxiety and depression scores (d=0.13-0.14) and greater participant-rated improvement (d=0.64) at post-treatment. Bayesian analyses indicated 74-99% probability of greater change in BA than EXP at post-treatment.
CONCLUSIONS: BA and EXP are both effective in treating GAD, and BA may confer greater benefit during treatment. Future research is warranted to inform personalized treatment approaches.