A phase II trial of perifosine, an oral alkylphospholipid, in recurrent or metastatic head and neck cancer

被引:90
作者
Argiris, Athanassios
Cohen, Ezra
Karrison, Theodore
Esparaz, Benjamin
Mauer, Ann
Ansari, Rafat
Wong, Stuart
Lu, Yi
Pins, Michael
Dancey, Janet
Vokes, Everett
机构
[1] Univ Pittsburgh, Div Hematol Oncol, Pittsburgh, PA 15232 USA
[2] Univ Chicago, Chicago, IL 60637 USA
[3] Phase II Network, Chicago, IL USA
[4] Decatur Mem Hosp, Decatur, GA USA
[5] No Indiana Canc Res Consortium, South Bend, IN USA
[6] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[7] Northwestern Univ, Chicago, IL 60611 USA
[8] NCI, Bethesda, MD 20892 USA
关键词
head and neck cancer; squarnous cell carcinoma; recurrent or metastatic; perifosine; alkylphospholipids; AKT;
D O I
10.4161/cbt.5.7.2874
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Novel, effective therapies are warranted in the management of recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN). Perifosine is an oral alkylphospholipid that inhibits AKT phosphorylation and has shown preclinical antitumor activity in head and neck cancer cell lines and xenografts. Patients And Methods: We conducted a phase II trial of perifosine in patients with incurable, recurrent or metastatic SCCHN. Previous therapy for recurrent or metastatic disease was limited to no more than one prior chemotherapy and one prior targeted/ biologic agent regimen. Patients had to have measurable disease, Eastern Cooperative Oncology Group performance status 0-2, and adequate laboratory parameters. Perifosine was given as a loading dose of 150 mg every 6 hours x 6 doses orally in the first two days, with antiemetic prophylaxis, followed by 100 mg/day orally without interruption. Administration via gastrostomy tube was allowed. Tumor response was assessed every two cycles (eight weeks). Biomarkers in pathways potentially affected by perifosine, including AKT, P-AKT, P38, p53 and p21 were measured on tumor tissue by immunohistochemistry by manual and automated methods. Results: Nineteen patients were enrolled. No objective responses were observed. One patient had stable disease as best response and 18 patients progressed at first evaluation. The median overall survival time was 5.5 months and the median progression-free survival time was 1.7 months. The most frequent toxicities were gastrointestinal (constipation, nausea, vomiting) and fatigue. One patient developed grade 4 anorexia. Although the sample size was small, a significant correlation was detected between high expression of P38 and AKT in baseline tumor tissue and better survival. Conclusions: Perifosine in the doses and schedule used lacks single-agent activity in SCCHN. Our data do not justify further investigation of perifosine as a single agent in SCCHN.
引用
收藏
页码:766 / 770
页数:5
相关论文
共 32 条
[1]   Persistent activation of the Akt pathway in head and neck squamous cell carcinoma: a potential target for UCN-01 [J].
Amornphimoltham, P ;
Sriuranpong, V ;
Patel, V ;
Benavides, F ;
Conti, CJ ;
Sauk, J ;
Sausville, EA ;
Molinolo, AA ;
Gutkind, JS .
CLINICAL CANCER RESEARCH, 2004, 10 (12) :4029-4037
[2]  
ARGIRIS A, 2005, P AN M AM SOC CLIN, pA5528
[3]  
BAILEY H, 2004, EJC SUPPL, V2, pA377
[4]   A CONFIDENCE-INTERVAL FOR THE MEDIAN SURVIVAL-TIME [J].
BROOKMEYER, R ;
CROWLEY, J .
BIOMETRICS, 1982, 38 (01) :29-41
[5]  
COX DR, 1972, J R STAT SOC B, V34, P187
[6]  
ERNST DS, 2005, PHASE II STUDY PERIF
[7]   RANDOMIZED COMPARISON OF CISPLATIN PLUS FLUOROURACIL AND CARBOPLATIN PLUS FLUOROURACIL VERSUS METHOTREXATE IN ADVANCED SQUAMOUS-CELL CARCINOMA OF THE HEAD AND NECK - A SOUTHWEST-ONCOLOGY-GROUP STUDY [J].
FORASTIERE, AA ;
METCH, B ;
SCHULLER, DE ;
ENSLEY, JF ;
HUTCHINS, LF ;
TRIOZZI, P ;
KISH, JA ;
MCCLURE, S ;
VONFELDT, E ;
WILLIAMSON, SK ;
VONHOFF, DD .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (08) :1245-1251
[8]  
FORASTIERE AA, 1993, MONOGR NATL CANC I, V15, P181
[9]   Randomized phase III evaluation of cisplatin plus fluorouracil versus cisplatin plus paclitaxel in advanced head and neck cancer (E1395): An intergroup trial of the eastern cooperative oncology group [J].
Gibson, MK ;
Li, Y ;
Murphy, B ;
Hussain, MHA ;
DeConti, RC ;
Ensley, J ;
Forastiere, AA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (15) :3562-3567
[10]  
Grizzle WE, 1998, METH MOLEC MED, V14, P143