Open-label study of pemetrexed alone or in combination with cisplatin for the treatment of patients with peritoneal mesothelioma:: Outcomes of an expanded access program

被引:146
作者
Jaenne, Pasi A.
Wozniak, Antoinette J.
Belani, Chandra P.
Keohan, Mary-Louise
Ross, Helen J.
Polikoff, Jonathan A.
Mintzer, David M.
Taylor, Loretta
Ashland, Joseph
Ye, Zhishen
Monberg, Matthew J.
Obasaju, Coleman K.
机构
[1] Dana Farber Canc Inst, Lowe Ctr Thorac Oncol, Boston, MA 02115 USA
[2] Wayne State Univ, Karmanos Canc Inst, Dept Internal Med, Detroit, MI USA
[3] Univ Pittsburgh, Inst Canc, Div Hematol Oncol, Pittsburgh, PA 15260 USA
[4] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[5] Earle A Chiles Res Inst, Robert W Franz Canc Res Ctr, Portland, OR USA
[6] Kaiser Hosp, Dept Hematol Oncol, San Diego, CA USA
[7] Penn Hosp, Hematol Oncol Sect, Philadelphia, PA 19107 USA
[8] Eli Lilly & Co, Lilly Res Labs, Indianapolis, IN 46285 USA
关键词
chemotherapy-naive disease; compassionate-use program; efficacy; toxicity;
D O I
10.3816/CLC.2005.n.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: To date, few large studies have been reported of patients with peritoneal mesothelioma, and treatment of this disease has been largely extrapolated from the treatment of pleural disease. Hence, it was considered important to study and report on this specific patient population. Before the regulatory approval of pemetrexed, an expanded access program (EAP) provided access to eligible patients with malignant pleural or peritoneal mesothelioma. PATIENTS AND METHODS: Patients received pemetrexed 500 mg/m(2) alone or in combination with cisplatin 75 mg/m(2) once every 21 days for >= 6 cycles. All patients received folic acid, vitamin B-12, and steroid prophylaxis. Serious adverse events (SAEs) were compiled in a pharmacovigilance database, which included all patients in the EAP with pleural or peritoneal mesothelioma. From June 12, 2002 to February 18, 2004, 1056 patients with malignant mesothelioma were enrolled and received >= 1 dose of treatment at 462 sites in the United States. Of these patients, 98 (9.3%) had peritoneal mesothelioma (57 previously treated, 38 chemotherapy-naive, and 3 with missing data). RESULTS: Response data were available for 73 patients (43 previously treated, 28 chemotherapy-naive, and 2 not classified), indicating response rates of 23.3% for previously treated patients (0 complete responses [CRs], 10 partial responses [PRs], 21 cases of stable disease [SDs], 12 cases of progressive disease [PDs]) and 25% for chemotherapy-naive patients (3 CRs, 4 PRs, 12 SDs, and 9 PDs). Median survival was 13.1 months for previously treated patients and has not been reached for chemotherapy-naive patients. The most commonly reported SAEs for the total EAP were dehydration (7.2%), nausea (5.2%), and vomiting (4.9%). CONCLUSION: Pemetrexed with or without cisplatin had a favorable safety profile, and the disease control rate (CR + PR + SD) of 71.2% in the subset of patients with peritoneal mesothelioma indicated activity in this patient population.
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页码:40 / 46
页数:7
相关论文
共 17 条
[1]  
DERACO M, 2004, P AN M AM SOC CLIN, V22, P888
[2]   Randomized phase III trial of pemetrexed versus docetaxel in patients with non-small-cell lung cancer previously treated with chemotherapy [J].
Hanna, N ;
Shepherd, FA ;
Fossella, FV ;
Pereira, JR ;
De Marinis, F ;
von Pawel, J ;
Gatzemeier, U ;
Tsao, TCY ;
Pless, M ;
Muller, T ;
Lim, HL ;
Desch, C ;
Szondy, K ;
Gervais, R ;
Shaharyar ;
Manegold, C ;
Paul, S ;
Paoletti, P ;
Einhorn, L ;
Bunn, PA .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (09) :1589-1597
[3]   Factors predictive of survival among 337 patients with mesothelioma treated between 1984 and 1994 by the Cancer and Leukemia Group B [J].
Herndon, JE ;
Green, MR ;
Chahinian, AP ;
Corson, JM ;
Suzuki, Y ;
Vogelzang, NJ .
CHEST, 1998, 113 (03) :723-731
[4]  
KARTHAUS M, 2004, P AN M AM SOC CLIN, V22, P663
[5]  
KEOHAN M, 2001, P AN M AM SOC CLIN, V20, pA361
[6]  
LABOW D, 2004, P AN M AM SOC CLIN, V22, P345
[7]  
Mendelsohn LG, 1999, SEMIN ONCOL, V26, P42
[8]   The European mesothelioma epidemic [J].
Peto, J ;
Decarli, A ;
La Vecchia, C ;
Levis, F ;
Negri, E .
BRITISH JOURNAL OF CANCER, 1999, 79 (3-4) :666-672
[9]  
Price B, 1997, AM J EPIDEMIOL, V145, P211, DOI 10.1093/oxfordjournals.aje.a009093
[10]  
Schultz RM, 1999, SEMIN ONCOL, V26, P68