2022
DOI: 10.1016/j.ejca.2022.07.009
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Continuous sunitinib schedule in advanced platinum refractory thymic epithelial neoplasms: A retrospective analysis from the ThYmic MalignanciEs (TYME) Italian collaborative group

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Cited by 10 publications
(8 citation statements)
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“…A recent study adopting a continuous oral administration also confirmed that the ORR of sunitinib was better in TC (41.7% vs. 14.3%), but the disease control rate was better in TM (100% vs. 75%), indicating that the response rate might be related to the tumor invasiveness. 58 In a phase II clinical study recruiting advanced or metastatic TC, 42 patients were treated with lovatinib, 16 patients had partial response, 24 patients had stable disease, the ORR was 38%, and the disease control rate was 95%. 59 Everolimus, a mammalian target of rapamycin (mTOR) inhibitor, has also achieved good efficacy in TET.…”
Section: Targeted Therapymentioning
confidence: 99%
“…A recent study adopting a continuous oral administration also confirmed that the ORR of sunitinib was better in TC (41.7% vs. 14.3%), but the disease control rate was better in TM (100% vs. 75%), indicating that the response rate might be related to the tumor invasiveness. 58 In a phase II clinical study recruiting advanced or metastatic TC, 42 patients were treated with lovatinib, 16 patients had partial response, 24 patients had stable disease, the ORR was 38%, and the disease control rate was 95%. 59 Everolimus, a mammalian target of rapamycin (mTOR) inhibitor, has also achieved good efficacy in TET.…”
Section: Targeted Therapymentioning
confidence: 99%
“…Although there are no further recognized standard lines of chemotherapy, interesting results have been reported in the literature regarding the combination of capecitabine plus gemcitabine (CAP-GEM) and the tyrosine kinase inhibitor sunitinib, while imatinib can be considered for thymic carcinoma with c-KIT mutation [ 20 , 21 , 22 , 23 ]. A recent retrospective analysis from the TYME Italian collaborative group examined data from 20 patients with platinum-resistant TETs receiving continuous daily dosing (CDD) of sunitinib at a dosage of 37.5 mg [ 24 ]. The authors concluded that the CDD schedule showed similar effectiveness but a better toxicity profile as compared with intermittent dosing historical data.…”
Section: Treatmentmentioning
confidence: 99%
“…Different trials have tested and proved the efficacy of sunitinib, an anti-angiogenic and multikinase inhibitor targeting VEGF receptors, in thymic carcinomas and thymomas refractory to first-line chemotherapy, reaching disease control in up to 91% of thymic carcinomas and 86% of thymomas. Given this evidence, sunitinib has now been introduced as a standard second-line treatment for patients with thymic carcinoma who have progressed after first-line chemotherapy ( Figure 3 ) [ 123 , 124 , 125 , 126 ]. Similarly, lenvatinib, another VEGFR/multikinase inhibitor, showed promising effects on advanced or metastatic thymic carcinomas, with presumably higher efficacy than sunitinib [ 127 ].…”
Section: Diagnostic and Therapeutic Approachesmentioning
confidence: 99%