Phase 2 trial of sunitinib and gemcitabine in patients with sarcomatoid and/or poor‐risk metastatic renal cell carcinoma. Issue 19 (8th June 2015)

• Record Type: Journal Article
• Authors: Michaelson, M. Dror; McKay, Rana R.; Werner, Lillian; Atkins, Michael B.; Van Allen, Eliezer M.; Olivier, Kara M.; Song, Jiaxi; Signoretti, Sabina; McDermott, David F.; Choueiri, Toni K.
• Is Part Of: Cancer. Volume 121:Issue 19(2015)
• Page Start: 3435
• Page End: 3443
• Publication Date: 2015-06-08
• Subjects: Cancer -- Periodicals; Cancer -- Cytopathology -- Periodicals; 616.99405
• DOI: 10.1002/cncr.29503
• Languages: English
• ISSNs: 0008-543X

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="cncr29503-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>Sarcomatoid renal cell carcinoma (RCC) is associated with an aggressive biology and a poor prognosis. Poor‐risk RCC is defined by clinical prognostic factors and demonstrates similarly aggressive behavior. No standard treatment exists for patients with sarcomatoid RCC, and treatment options for patients with poor‐risk disease are of limited benefit. The objective of this study was to investigate the efficacy of antiangiogenic therapy in combination with cytotoxic chemotherapy in clinically aggressive RCC.</p> </sec> <sec id="cncr29503-sec-0002" sec-type="section"> <title>METHODS</title> <p>This was a phase 2, single‐arm trial of sunitinib and gemcitabine in patients with sarcomatoid or poor‐risk RCC. The primary endpoint was the objective response rate (ORR). Secondary endpoints included the time to progression (TTP), overall survival (OS), safety, and biomarker correlatives.</p> </sec> <sec id="cncr29503-sec-0003" sec-type="section"> <title>RESULTS</title> <p>Overall, 39 patients had sarcomatoid RCC, and 33 had poor‐risk RCC. The ORR was 26% for patients with sarcomatoid RCC and 24% for patients with poor‐risk RCC. The median TTP and OS for patients with sarcomatoid RCC were 5 and 10 months, respectively. For patients with poor‐risk disease, the median TTP and OS were 5.5 and 15 months, respectively. Patients whose tumors had >10% sarcomatoid histology had a higher clinical benefit rate (ORR plus stable disease) than those with ≤10% sarcomatoid histology (<italic>P</italic> = .04). The most common grade 3 or higher treatment‐related adverse events included neutropenia (n = 20), anemia (n = 10), and fatigue (n = 7).</p> </sec> <sec id="cncr29503-sec-0004" sec-type="section"> <title>CONCLUSIONS</title> <p>These results suggest that antiangiogenic therapy and cytotoxic chemotherapy are an active and well‐tolerated combination for patients with aggressive RCC. The combination may be more efficacious than either therapy alone and is currently under further investigation. <bold><italic>Cancer</italic> 2015;121:3435–43.</bold> © <italic>2015 American Cancer Society</italic>.</p> </sec> </abstract>