Real-world experience of everolimus as second-line treatment in metastatic renal cell cancer after failure of pazopanib

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3108243 22 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Real-world experience of everolimus as second-line treatment in metastatic renal cell cancer after failure of pazopanib
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Aim: We aimed to provide real-life data on the outcomes of metastatic renal cell carcinoma (mRCC) patients treated with everolimus as second-line treatment after failure of first-line pazopanib. Patients and methods: Data from the medical charts of mRCC patients from 8 centers in Greece and Spain were ed. All patients had received or were continuing to receive second-line everolimus treatment after failure of first-line treatment with pazopanib. No other previous therapies were allowed. The primary end point was the determination of progression-free survival (PFS). Results: In total, 31 patients were enrolled. Of these, 26% had performance status (PS).0, 88% were of intermediate/poor Memorial Sloan-Kettering Cancer Center (MSKCC) risk group, and only 61% had undergone prior nephrectomy. Median PFS was 3.48 months (95% CI: 2.37-5.06 months). Median overall survival (OS) from everolimus initiation was 8.9 months (95% CI: 6.47-13.14 months). Median OS from pazopanib initiation was 14.78 months (95% CI: 10.54-19.08 months). Furthermore, 32% of patients temporarily discontinued everolimus due to adverse events (AEs), and 22% of patients discontinued everolimus permanently due to toxicity. Most common toxicities were anemia (29%), stomatitis (26%), pneumonitis (19%), and fatigue (10%). Moreover, 14 AEs (27%) were graded as 3 or 4 and were reported by 13 patients (42%). Conclusion: This study provides data exclusively on the sequence pazopanib-everolimus in mRCC. Everolimus has a favorable safety profile and is active. The short PFS and OS could be attributed to the fact that the pazopanib-everolimus sequence was mainly offered to patients with adverse prognostic features, resulting in a modest increase in the combined OS of our population. © 2017 Koutsoukos et al.
Έτος δημοσίευσης:
2017
Συγγραφείς:
Koutsoukos, K.
Bamias, A.
Tzannis, K.
Montaño, M.E.
Bozionelou, V.
Christodoulou, C.
Stefanou, D.
Kalofonos, H.
Duran, I.
Papazisis, K.
Περιοδικό:
OncoTargets and therapy
Εκδότης:
Dove Medical Press Ltd
Τόμος:
10
Σελίδες:
4885-4893
Λέξεις-κλειδιά:
everolimus; gamma glutamyltransferase; pazopanib, acute kidney failure; adult; aged; alopecia; anemia; arthralgia; Article; bleeding; bone pain; cancer prognosis; clinical article; diarrhea; drug fatality; drug safety; drug withdrawal; edema; experience; fatigue; female; fever; Greece; human; hypercalcemia; hyperlipidemia; intermediate risk population; kidney metastasis; loss of appetite; lung embolism; male; medical record review; mucosa inflammation; nephrectomy; overall survival; pleura effusion; pneumonia; progression free survival; proteinuria; rash; retrospective study; Spain; stomach hemorrhage; stomatitis; tooth pain; treatment failure; treatment outcome; unspecified side effect; very elderly
Επίσημο URL (Εκδότης):
DOI:
10.2147/OTT.S141260
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