Key result
Monthly docetaxel yielded equivalent overall survival and dose duration time to three-weekly paclitaxel in cutaneous angiosarcoma, though severe adverse events were higher (40.0% vs 23.6%).
Why the study?
Cutaneous angiosarcoma treatment options are controversial, and while only paclitaxel is supported by high-level evidence, the real-world efficacy of docetaxel required evaluation.
Does docetaxel provide equivalent efficacy and safety to paclitaxel as maintenance chemoradiotherapy in Japanese patients with cutaneous angiosarcoma?
Cohort (n=90)
Yes
Does docetaxel provide equivalent efficacy and safety to paclitaxel as maintenance chemoradiotherapy in Japanese patients with cutaneous angiosarcoma?
Docetaxel is an effective and tolerable alternative to paclitaxel for maintenance therapy in cutaneous angiosarcoma, though it carries a higher risk of severe adverse events like interstitial pneumonia.
Early data support docetaxel chemoradiotherapy in CAS; leaves open randomized comparison with paclitaxel.
Cutaneous angiosarcoma (CAS) is rare and most previous studies of CAS have been small case series, and randomized, phase II studies of CAS are limited. Since treatment options for CAS are controversial, and because only paclitaxel should be recommended based on high-level evidence, it is important to evaluate the efficacy of another taxane-derived agents, docetaxel, in real-world practice. The efficacy and safety profiles of chemoradiotherapy using taxane-based agents, docetaxel and paclitaxel, were retrospectively examined in the maintenance setting in 90 Japanese CAS patients, including 35 docetaxel-treated cases and 55 paclitaxel-treated cases. Overall survival and dose duration time of the patient group treated with docetaxel was equivalent to that with paclitaxel, even in the cohorts with metastasis. Adverse events due to docetaxel and paclitaxel were observed in 77.1% and 69.1% of cases, respectively. The incidence ratio of total severe adverse events tended to be higher in the docetaxel-treated group (40.0%) than in the paclitaxel-treated group (23.6%). Peripheral neuropathy occurred only in the paclitaxel-treated group, whereas high-grade interstitial pneumonia developed only in the docetaxel-treated group. In addition, we also evaluate 19 patients selected other taxanes, 17 patients selected eribulin methylate, 11 patients pazopanib, and 2 patients selected nivolumab as second-line chemotherapy. The efficacy of a monthly docetaxel regimen is equivalent to a three-weekly paclitaxel regimen evaluated by Overall survival and DDT, even in the cohorts with metastasis, and it is a tolerable protocol for CAS as a maintenance therapy in the Japanese population.
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Fujimura et al. (2022) conducted a cohort in Cutaneous angiosarcoma (n=90). Docetaxel vs. Paclitaxel (three-weekly) was evaluated on Overall survival and dose duration time. Monthly docetaxel yielded equivalent overall survival and dose duration time to three-weekly paclitaxel in cutaneous angiosarcoma, though severe adverse events were higher (40.0% vs 23.6%).
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