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Association details:
Biomarker:BRCA wild-type
Cancer:Ovarian Cancer
Drug:bortezomib (Proteasome inhibitor)
Direction:Sensitive
Evidence:
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

A Phase II Trial to Evaluate the Efficacy of Bortezomib and Liposomal Doxorubicin in Patients With BRCA Wild-type Platinum-resistant Recurrent Ovarian Cancer (KGOG 3044/EBLIN)

Published date:
06/23/2022
Excerpt:
...we conducted a phase II multicenter study evaluated the efficacy and safety of bortezomib plus pegylated liposomal doxorubicin (PLD) in patients with BRCA wild-type platinum-resistant recurrent ovarian cancer (NCT03509246)....The combination of bortezomib and PLD was well tolerated....The overall confirmed ORR was 8.7% (2/23); partial response was observed in two patients. Disease control was achieved in 69.6% (16/23) patients (Table IV). Tumor shrinkage was noted in 9 (39.1%) of 23 patients who had at least one post-baseline efficacy assessment (Figure 2). The mean best percentage change of the target lesion size from the baseline was –0.6% (SD 19.1). The median duration of response was 10.5 months...the median PFS was 2.9 months, and median OS was 19.0 months (Figure 3).
Secondary therapy:
pegylated liposomal doxorubicin
DOI:
10.21873/invivo.12917
Trial ID: