|
|
Blood, 15 September 2007, Vol. 110, No. 6, pp. 1762-1769.
Prepublished online as a Blood First Edition Paper on June 11, 2007; DOI 10.1182/blood-2007-03-081364.
Previous Article | Table of Contents | Next Article 
CLINICAL TRIALS AND OBSERVATIONS
A phase 1 clinical-laboratory study of clofarabine followed by cyclophosphamide for adults with refractory acute leukemias
Judith E. Karp1,
Rebecca M. Ricklis1,
Kumudha Balakrishnan2,
Janet Briel1,
Jacqueline Greer1,
Steven D. Gore1,
B. Douglas Smith1,
Michael A. McDevitt1,
Hetty Carraway1,
Mark J. Levis1, and
Varsha Gandhi2
1 Division of Hematologic Malignancies, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD;
2 Department of Experimental Therapeutics, University of Texas M. D. Anderson Cancer Center, Houston, TX
Clofarabine has shown impressive response rates in patients with acute leukemias. In vitro investigations with clofarabine in combination with cyclophosphamide in primary cells have demonstrated synergistic cytotoxicity and inhibition of DNA repair. Based on these clinical and laboratory observations, we designed a mechanism-based combination protocol with clofarabine and cyclophosphamide for patients with relapsed acute leukemias. Eighteen patients were treated with cyclophosphamide (200 mg/m2) alone on day 0 and with clofarabine plus cyclophosphamide on day 1. Clinical responses, toxicity, DNA damage measured as H2AX phosphorylation, and accumulation of clofarabine triphosphate (TP) were analyzed. At dose level 1 (20 mg/m2 clofarabine + cyclophosphamide, 6 patients) and dose level 0 (10 mg/m2 clofarabine + cyclophosphamide, 12 patients) overall response rates were 50% and 30%, respectively, with responses in 4 (67%) of 6 patients with refractory acute lymphoblastic leukemia. Dose-limiting toxicity occurred at dose level 1 with prolonged marrow aplasia. Four (22%) patients died from prolonged aplasia (1), fungal pneumonia (1), or multiorgan failure (2). In 12 of 13 patient samples, increased DNA damage ( H2AX) was observed with clofarabine and cyclophosphamide compared with cyclophosphamide alone. In conclusion, pharmacodynamic end points along with clinical results suggest usefulness of this combination strategy, whereas toxicity data suggest reduction in chemotherapeutic intensity. This clinical trial is registered with the National Cancer Institute's PDQ at www.clinicaltrials.gov as no. JHOC-J0561.

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

|
 |

|
 |
 
A. E. Perl, M. T. Kasner, D. E. Tsai, D. T. Vogl, A. W. Loren, S. J. Schuster, D. L. Porter, E. A. Stadtmauer, S. C. Goldstein, N. V. Frey, et al.
A Phase I Study of the Mammalian Target of Rapamycin Inhibitor Sirolimus and MEC Chemotherapy in Relapsed and Refractory Acute Myelogenous Leukemia
Clin. Cancer Res.,
November 1, 2009;
15(21):
6732 - 6739.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Vitale, S. Grammatico, S. Capria, C. Fiocchi, R. Foa, and G. Meloni
Advanced Philadelphia chromosome positive acute lymphoblastic leukemia patients relapsed after treatment with tyrosine-kinase inhibitors: successful response to clofarabine and cyclophosphamide
Haematologica,
October 1, 2009;
94(10):
1471 - 1473.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Jeha, B. Razzouk, M. Rytting, S. Rheingold, E. Albano, R. Kadota, L. Luchtman-Jones, L. Bomgaars, P. Gaynon, S. Goldman, et al.
Phase II Study of Clofarabine in Pediatric Patients With Refractory or Relapsed Acute Myeloid Leukemia
J. Clin. Oncol.,
September 10, 2009;
27(26):
4392 - 4397.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. E. Karp, K. Flatten, E. J. Feldman, J. M. Greer, D. A. Loegering, R. M. Ricklis, L. E. Morris, E. Ritchie, B. D. Smith, V. Ironside, et al.
Active oral regimen for elderly adults with newly diagnosed acute myelogenous leukemia: a preclinical and phase 1 trial of the farnesyltransferase inhibitor tipifarnib (R115777, Zarnestra) combined with etoposide
Blood,
May 14, 2009;
113(20):
4841 - 4852.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. Hochhauser, T. Meyer, V. J. Spanswick, J. Wu, P. H. Clingen, P. Loadman, M. Cobb, L. Gumbrell, R. H. Begent, J. A. Hartley, et al.
Phase I Study of Sequence-Selective Minor Groove DNA Binding Agent SJG-136 in Patients with Advanced Solid Tumors
Clin. Cancer Res.,
March 15, 2009;
15(6):
2140 - 2147.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|