Key result
Apatinib treatment in patients with metastatic alveolar soft part sarcoma yielded a 100% objective response rate and a median progression-free survival of 18.53 months.
Why the study?
Advanced or metastatic alveolar soft part sarcoma is chemo-resistant, but tyrosine kinase inhibitors have shown benefit, prompting evaluation of the efficacy and safety of the VEGFR-2 inhibitor apatinib.
Does apatinib improve tumor response and survival in patients with metastatic alveolar soft part sarcoma?
Observational (n=6)
No
Does apatinib improve tumor response and survival in patients with metastatic alveolar soft part sarcoma?
Apatinib demonstrated a 100% objective response rate and a median progression-free survival of 18.53 months in a small case series of patients with metastatic alveolar soft part sarcoma.
Hypothesis-generating for apatinib in metastatic alveolar soft part sarcoma; prospective trials needed before clinical adoption.
Background: Evidence suggests that advanced or metastatic alveolar soft part sarcoma (ASPS) with high metastatic potential is chemo-resistant. However, the benefits of tyrosine kinase inhibitors have been demonstrated for the treatment of ASPS. Purpose: This study aimed to investigate the efficacy and safety of apatinib, aspecific VEGFR-2 inhibitor, in ASPS patients. This retrospective analysis involved six patients with metastatic ASPS not amenable to curative treatment. Patients and methods: Apatinib was administered at a dose of 500mg per day. Tumor responses were assessed according to the Response Evaluation Criteria in Solid Tumors (RECIST 1.1) guidelines. Survival analysis was performed using the Kaplan–Meier test, and a safety profile was recorded. Results: The mean age of patients was 26.5 (range, 17–32) years. The median progression-free survival (PFS) was 18.53 months (95% CI, 12.23-NE). However, median overall survival (OS) has not been reached. Twenty-four month PFS and OS rates were 50.0% and 100.0%, respectively. One patient achieved a complete response, and the remaining patients achieved partial responses, with an objective response rate of 100%. Median follow-up was 20.6 (range, 12.43–34.13) months. The most common adverse events included gastrointestinal discomfort (4/6[66.7%]), hair hypopigmentation (4/6[66.7%]) and hand-foot skin reaction (3/6[50.0%]). Conclusion: Apatinib shows beneficial activity in metastatic ASPS patients, and further studies are warranted with more cases and longer follow-up periods to fully characterize clinical efficacy and safety of apatinib in ASPS.
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Wang et al. (2019) conducted an observational in Metastatic alveolar soft part sarcoma (n=6). Apatinib was evaluated on Progression-free survival (PFS) (95% CI 12.23-NE). Apatinib treatment in patients with metastatic alveolar soft part sarcoma yielded a 100% objective response rate and a median progression-free survival of 18.53 months.
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