Journal of Clinical Oncology, Vol 22, No 10 (May 15), 2004: pp. 1815-1822
© 2004 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2004.11.120
Pegylated Arginine Deiminase Treatment of Patients With Unresectable Hepatocellular Carcinoma: Results From Phase I/II Studies
Francesco Izzo,
Paolo Marra,
Gerardo Beneduce,
Giuseppe Castello,
Paolo Vallone,
Vincenzo De Rosa,
Franco Cremona,
C. Mark Ensor,
Frederick W. Holtsberg,
John S. Bomalaski,
Mike A. Clark,
Chaan Ng,
Steven A. Curley
From the Pascale National Cancer Institute, Naples, Italy; Phoenix Pharmacologics Inc, and University of Kentucky, Lexington, KY; and M.D. Anderson Cancer Center, University of Texas, Houston, TX.
Address reprint requests to Steven Curley, MD, Department of Surgical Oncology, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Blvd, Box 444, Houston, TX 77030; e-mail: scurley{at}mdanderson.org
PURPOSE: Recently, we reported that a large number of human hepatocellular cancer (HCC) cell lines were auxotrophic for arginine. Here we report the results obtained with the amino aciddegrading enzyme arginine deiminase (ADI) conjugated to polyethylene glycol (ADI-SS PEG 20,000 mw) as a means of lowering plasma arginine to treat HCC. The study was a cohort dose-escalation phase I/II study.
PATIENTS AND METHODS: Pharmacodynamic studies indicated an ADI-SS PEG 20,000 mw dose level of 160 U/m2 was sufficient to lower plasma arginine from a resting level of approximately 130 µmol/L to below the level of detection (< 2 µmol/L) for more than 7 days, a dose later defined as the optimal biologic dose. All patients were to receive three cycles at the optimum biologic dose.
RESULTS: This therapy was well tolerated, even in patients who had no detectable plasma arginine for 3 continuous months of therapy. Of the 19 patients enrolled, two had a complete response, seven had a partial response, seven had stable disease, and three had progressive disease. The median survival for the 19 patients enrolled on this study was 410 days, with four patients still alive at present (> 680 days).
CONCLUSION: Elimination of all detectable plasma arginine in patients with HCC was well tolerated and seemed to be effective in the treatment of some patients with HCC. Further testing of ADI-SS PEG 20,000 mw in a larger population of individuals with HCC as well as other human tumors auxotrophic for arginine is warranted.
Phoenix Pharmacologics provides support for a research nurse to F.I.
Authors' disclosures of potential conflicts of interest are found at the end of this article.

CiteULike Complore Connotea Del.icio.us Digg Facebook Reddit Technorati Twitter What's this?
This article has been cited by other articles:

|
 |

|
 |
 
R. H. Kim, J. M. Coates, T. L. Bowles, G. P. McNerney, J. Sutcliffe, J. U. Jung, R. Gandour-Edwards, F. Y.S. Chuang, R. J. Bold, and H.-J. Kung
Arginine Deiminase as a Novel Therapy for Prostate Cancer Induces Autophagy and Caspase-Independent Apoptosis
Cancer Res.,
January 15, 2009;
69(2):
700 - 708.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. D. Roberts, J. S. Isenberg, L. A. Ridnour, and D. A. Wink
Nitric Oxide and Its Gatekeeper Thrombospondin-1 in Tumor Angiogenesis
Clin. Cancer Res.,
February 1, 2007;
13(3):
795 - 798.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. N.-M. Cheng, T.-L. Lam, W.-M. Lam, S.-M. Tsui, A. W.-M. Cheng, W.-H. Lo, and Y.-C. Leung
Pegylated Recombinant Human Arginase (rhArg-peg5,000mw) Inhibits the In vitro and In vivo Proliferation of Human Hepatocellular Carcinoma through Arginine Depletion
Cancer Res.,
January 1, 2007;
67(1):
309 - 317.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. Cherukuri, C. J. Gannon, T. K. Leeuw, H. K. Schmidt, R. E. Smalley, S. A. Curley, and R. B. Weisman
Mammalian pharmacokinetics of carbon nanotubes using intrinsic near-infrared fluorescence
PNAS,
December 12, 2006;
103(50):
18882 - 18886.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. W. Szlosarek, A. Klabatsa, A. Pallaska, M. Sheaff, P. Smith, T. Crook, M. J. Grimshaw, J. P. Steele, R. M. Rudd, F. R. Balkwill, et al.
In vivo Loss of Expression of Argininosuccinate Synthetase in Malignant Pleural Mesothelioma Is a Biomarker for Susceptibility to Arginine Depletion
Clin. Cancer Res.,
December 1, 2006;
12(23):
7126 - 7131.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. X. Zhu
Systemic Therapy of Advanced Hepatocellular Carcinoma: How Hopeful Should We Be?
Oncologist,
July 1, 2006;
11(7):
790 - 800.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. X. Zhu, L. S. Blaszkowsky, D. P. Ryan, J. W. Clark, A. Muzikansky, K. Horgan, S. Sheehan, K. E. Hale, P. C. Enzinger, P. Bhargava, et al.
Phase II Study of Gemcitabine and Oxaliplatin in Combination With Bevacizumab in Patients With Advanced Hepatocellular Carcinoma
J. Clin. Oncol.,
April 20, 2006;
24(12):
1898 - 1903.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. A. Ascierto, S. Scala, G. Castello, A. Daponte, E. Simeone, A. Ottaiano, G. Beneduce, V. De Rosa, F. Izzo, M. T. Melucci, et al.
Pegylated Arginine Deiminase Treatment of Patients With Metastatic Melanoma: Results From Phase I and II Studies
J. Clin. Oncol.,
October 20, 2005;
23(30):
7660 - 7668.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|