A phase II trial of doxorubicin and gemcitabine in renal cell carcinoma with sarcomatoid features: ECOG 8802

Medical Oncology - Tập 29 - Trang 761-767 - 2011
Naomi B. Haas1, Xinyi Lin2, Judith Manola3, Michael Pins4, Glenn Liu5, David McDermott6, David Nanus7, Elisabeth Heath8, George Wilding5, Janice Dutcher9
1Abramson Cancer Center, Philadelphia, USA
2Department of Biostatistics, Harvard School of Public Health, Boston, USA
3Dana-Farber Cancer Institute, Boston, USA
4Advocate Lutheran General Hospital, University of Illinois Chicago College of Medicine, Park Ridge, USA
5University of Wisconsin Carbone Cancer Center, Madison, USA
6Beth Israel Deaconess Medical Center, Boston, USA
7New York Presbyterian Hospital, New York, USA
8Karmanos Cancer Center Institute, Detroit, USA
9Division of Hematology/Oncology, St. Luke’s Roosevelt Hospital Center, Continuum Cancer Centers, New York, USA

Tóm tắt

Sarcomatoid features can arise in renal cell carcinoma of any subtype and are associated with a poor prognosis. Doxorubicin and gemcitabine in a limited series showed activity in aggressive renal tumors and we wished to formally assess the combination in patients with renal cell carcinoma specifically containing sarcomatoid features. The Eastern Cooperative Oncology Group (ECOG) conducted a phase II trial of doxorubicin 50 mg/m2 IV push and gemcitabine 1,500 mg/m2 IV over 30 min every 2 weeks in 39 patients with locally advanced or metastatic renal cell carcinoma with sarcomatoid features. Ten patients (26%) had grade 3 toxicity, and four patients (11%) had grade 4 toxicities. Although most toxicity was from myelosuppression, one patient died on study from cardiac dysfunction after a cumulative dose of 450 mg/m2 doxorubicin. Six (16%) patients experienced responses (5 partial responses and 1 complete response), and ten (26%) patients had stable disease. In addition, another patient had an unconfirmed partial response and an additional patient experienced over 50% decrease in her tumor burden after an initial progression. The median overall survival was 8.8 months, and the median progression-free survival was 3.5 months. We conclude that the combination of doxorubicin and gemcitabine, inactive in patients with mostly clear cell histology, demonstrated responses in patients with RCC with sarcomatoid features. We acknowledge the toxicity of this combination but note that limited treatment options exist for this aggressive histology. Only through prospective multicenter trials with comprehensive central pathology review will better treatment options be identified.

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