84P Exploring BET inhibitors as promising agents for solitary fibrous tumor

9.0 (1.0 -21.6) for TKI.Eight pts (15%) had fertility preservation.Median follow-up was 9.6 months [95%CI: 6.6;11.9].Partial response and stable disease (SD) were observed in 28 (52%) and 21 pts (39%).Five pts (9%) had progressive disease (PD), with majority of extra-abdominal tumors and CTNNB1 mutations (4/5).38 pts (73%) had pain relief and 33 pts (77%) were able to reduce or interrupt analgesic TTT.Among pts with SD, 50% were less painful.The 1-y PFS rate was 77.5% [64.1%;93.8%]and 73.4% of pts [59.0%;91.4%]were without TTT change after 1 year.The most common side effects were diarrhea (51%), fatigue (45%) and cutaneous rash (27%).Ovarian dysfunction was reported for 9 pts.13 pts had dose reduction (24%).At the time of analysis, 34 pts (62%) are continuing Ni, 21 (38%) discontinued Ni because of PD (N5), toxicity (N8) or personal decision (N8).Conclusions: DeNi study confirms the clinical benefit of Ni with pain improvement even without tumor shrinkage.Questions remain such as TTT duration and first-line use.

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Publication Details

Journal
ESMO Open
Published
2025-03-01
DOI
https://doi.org/10.1016/j.esmoop.2025.104397
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
0.00

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article

84P Exploring BET inhibitors as promising agents for solitary fibrous tumor

John T. Nguyen, David S. Moura, José L. Mondaza-Hernández, Heather N. Hayenga et al.
ESMO Open
Protein Degradation and Inhibitors
article

84P Exploring BET inhibitors as promising agents for solitary fibrous tumor

John T. Nguyen, David S. Moura, José L. Mondaza-Hernández, Heather N. Hayenga, Javier Martín‐Broto, Leonidas Bleris, José I. López, Yanjun Li, Pablo Romero
article en

Abstract

9.0 (1.0 -21.6) for TKI.Eight pts (15%) had fertility preservation.Median follow-up was 9.6 months [95%CI: 6.6;11.9].Partial response and stable disease (SD) were observed in 28 (52%) and 21 pts (39%).Five pts (9%) had progressive disease (PD), with majority of extra-abdominal tumors and CTNNB1 mutations (4/5).38 pts (73%) had pain relief and 33 pts (77%) were able to reduce or interrupt analgesic TTT.Among pts with SD, 50% were less painful.The 1-y PFS rate was 77.5% [64.1%;93.8%]and 73.4% of pts [59.0%;91.4%]were without TTT change after 1 year.The most common side effects were diarrhea (51%), fatigue (45%) and cutaneous rash (27%).Ovarian dysfunction was reported for 9 pts.13 pts had dose reduction (24%).At the time of analysis, 34 pts (62%) are continuing Ni, 21 (38%) discontinued Ni because of PD (N5), toxicity (N8) or personal decision (N8).Conclusions: DeNi study confirms the clinical benefit of Ni with pain improvement even without tumor shrinkage.Questions remain such as TTT duration and first-line use.

ESMO OpenVol. 10
Hospital Universitario Fundación Jiménez Díaz (ES), University of North Texas at Dallas (US)
National Institutes of Health
Zero hunger
Openalex Percentile: Top 95%
Protein Degradation and Inhibitors
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