Abstract 1943P
Background
RLPS and RLMS are not sensitive to conventional chemotherapy. We evaluated the efficacy and safety of eribulin plus anlotinib and camrelizumab for RLMS and RLPS.
Methods
Patients (pts) with advanced/metastatic RLPS or RLMS treated with eribulin plus anlotinib and camrelizumab (Q3W) at Peking University Cancer Hospital Sarcoma Center were included in this retrospective analysis. Response (RECIST v1.1) was evaluated every 3 treatment cycles. Adverse event severity was graded per CTCAE v5.0.
Results
From December 17, 2020 to November 18, 2022, 60 pts (27 male; 33 female) were included. 22 pts had RLMS; RLPS subtypes were well-differentiated (n=9), de-differentiated (n=24), and myxoid (MLPS; n=5). Eribulin was given to 21 pts (35%) at 0.7–1.1 mg/m2, and 39 (65%) at 1.1–1.4 mg/m2.5 pts (RLMS, n=2; RLPS, n=3) were excluded from efficacy analyses due to drug intolerance and the COVID-19 pandemic. After a median of 5 cycles (range, 2–21), a partial response was observed in 15 pts (27.3%), stable disease in 27 (49.1%) and progressive disease in 13 (23.6%). The objective response rate (ORR) and disease control rate (DCR) were 27.3% and 76.4%, respectively. ORR and DCR in pts with RLMS were 42.1% and 84.2%, respectively; in pts with RLPS, they were 19.4% and 72.2%, respectively. After a median follow up of 11.3 months (mo), 10 pts had complete resection, 2 of whom had pathological complete response (1 with RLMS and 1 with MLPS); 3 other pts had locoregional recurrence after surgery. Median progression-free survival (mPFS) for the remaining 45 pts was 5.8 mo; mPFS for RLPS and RLMS subgroups were 5.5 and 6.2 mo, respectively. Any-grade treatment-related AEs (TRAEs) occurred in 51/60 pts (85.0%), with 22 (36.7%) experiencing grade ≥3 TRAEs. The most common TRAEs were neutropenia (58.3%), proteinuria (23.3%) and anorexia (23.3%). Due to AEs, 15 pts (25.0%) discontinued treatment and 6 (16.7%) reduced their eribulin dose.
Conclusions
Eribulin plus anlotinib and camrelizumab demonstrated clinically meaningful efficacy and a manageable safety profile in pts with advanced or metastatic RLPS or RLMS, especially in those with RLMS.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1982P - Transcriptomic analysis and tumor microenvironment (TME) classification reveals unique immune biology in HIV patients with Kaposi sarcoma (KS)
Presenter: Jihua Yang
Session: Poster session 15
1983P - Palliative spatially fractionated stereotactic radiation therapy (Lattice) for large sarcoma
Presenter: Gabriela Studer
Session: Poster session 15
1984P - Sex differences in anticancer treatment delivery and toxicity in patients with sarcoma in a reference center
Presenter: Ilaria Tortorelli
Session: Poster session 15
1985P - Expert sarcoma care is the need of the hour: Diagnostic and management challenges at a tertiary-care centre in India
Presenter: Ghazal Tansir
Session: Poster session 15
1986P - Impact of SARS-CoV-2 vaccines and recent chemotherapy on COVID-19 morbidity and mortality in patients with soft tissue sarcoma: An analysis from the OnCovid registry
Presenter: Alessandro Mazzocca
Session: Poster session 15
1987TiP - Pembrolizumab in combination with eftilagimod alpha and radiotherapy in neoadjuvant treatment of patients with soft tissue sarcomas: EFTISARC-NEO trial
Presenter: Katarzyna Kozak
Session: Poster session 15
2213P - Impact of the diagnosis-to-treatment interval on the survival of patients with papillary thyroid cancer
Presenter: Tingting Wei
Session: Poster session 15
2214P - Identification of prognosis-associated genes in locally advanced well-differentiated thyroid cancer using TCGA cohort analysis
Presenter: Ah Ra Jung
Session: Poster session 15
2216P - Clinicopathologic and genetic characteristics of patients of different ages with diffuse sclerosing variant papillary thyroid carcinoma
Presenter: Soo Young Kim
Session: Poster session 15
2220P - MOLTHY project (TTCC-2020-02): A Spanish observational study for MOLecular characterization of THYroid carcinoma
Presenter: Neus Baste Rotllan
Session: Poster session 15