Phase I/II Study of Oncolytic Herpes Simplex Virus NV1020 in Patients with Extensively Pretreated Refractory Colorectal Cancer Metastatic to the Liver

被引:125
作者
Geevarghese, Sunil K. [2 ]
Geller, David A. [3 ]
de Haan, Hans A. [4 ]
Hoerer, Markus [5 ]
Knoll, Anette E. [5 ]
Mescheder, Axel [5 ]
Nemunaitis, John [6 ]
Reid, Tony R. [1 ]
Sze, Daniel Y. [7 ]
Tanabe, Kenneth K. [8 ]
Tawfik, Hoda [5 ]
机构
[1] Univ Calif San Diego, Div Hematol & Oncol, Dept Med, La Jolla, CA 92093 USA
[2] Vanderbilt Univ, Dept Hepatobiliary Surg & Liver Transplantat, Nashville, TN 37232 USA
[3] Univ Pittsburgh, Thomas E Starzl Transplantat Inst, S Pittsburgh, PA 15213 USA
[4] MediGene, Clin Res, San Diego, CA 92030 USA
[5] MediGene, D-82152 Martinsried, Germany
[6] Mary Crowley Med Res Ctr, Dallas, TX 75201 USA
[7] Stanford Univ, Med Ctr, Div Intervent Radiol, Stanford, CA 94305 USA
[8] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Ctr Canc,Div Surg Oncol, Boston, MA 02114 USA
关键词
VIRAL THERAPY; TYPE-1; G207; CELLS; CARCINOMA; COMBINATION; IRINOTECAN; MANAGEMENT; ADENOVIRUS; RESISTANT; EFFICACY;
D O I
10.1089/hum.2010.020
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This multicenter phase I/II study evaluated the safety, pharmacokinetics, and antitumor effects of repeated doses of NV1020, a genetically engineered oncolytic herpes simplex virus, in patients with advanced metastatic colorectal cancer (mCRC). Patients with liver-dominant mCRC received four fixed NV1020 doses via weekly hepatic artery infusion, followed by two or more cycles of conventional chemotherapy. Phase I included cohorts receiving 3x10(6), 1x10(7), 3x10(7), and 1x10(8) plaque-forming units (PFU)/dose to determine the optimal biological dose (OBD) for phase II. Blind independent computed tomography scan review was based on RECIST (response evaluation criteria in solid tumors) to assess hepatic tumor response. Phase I and II enrolled 13 and 19 patients, respectively. Patients experienced transient mild-moderate febrile reactions after each NV1020 infusion. Grade 3/4 virus-related toxicity was limited to transient lymphopenia in two patients. NV1020 shedding was not detected. Simultaneous cytokine and grade 1 coagulation perturbations were dose-limiting at 1x10(8) PFU/dose, considered the OBD. All 22 OBD patients had previously received 5-fluorouracil; most had received oxaliplatin or irinotecan (50% had both), many with at least one targeted agent. After NV1020 administration, 50% showed stable disease. The best overall tumor control rate after chemotherapy was 68% (1 partial response, 14 stable disease); this did not correlate with baseline variables or chemotherapy. Median time to progression was 6.4 months (95% confidence interval: 2, 8.9); median overall survival was 11.8 months (95% confidence interval: 8.3, 20.7). One-year survival was 47.2%. We conclude that NV1020 stabilizes liver metastases with minimal toxicity in mCRC. It may resensitize metastases to salvage chemotherapy and extend overall survival. A randomized phase II/III trial now appears justified.
引用
收藏
页码:1119 / 1128
页数:10
相关论文
共 49 条
[1]  
AKIIHIRO N, 2008, CURR GENE THER, V8, P208
[2]   Interleukin 12 secretion enhances antitumor efficacy of oncolytic herpes simplex viral therapy for colorectal cancer [J].
Bennett, JJ ;
Malhotra, S ;
Wong, RJ ;
Delman, K ;
Zager, J ;
St-Louis, M ;
Johnson, P ;
Fong, Y .
ANNALS OF SURGERY, 2001, 233 (06) :819-826
[3]   Treatment of hepatic metastases from colorectal cancer: Many doubts, some certainties [J].
Biasco, G. ;
Derenzini, E. ;
Grazi, GL. ;
Ercolani, G. ;
Ravaioli, M. ;
Pantaleo, M. A. ;
Brandi, G. .
CANCER TREATMENT REVIEWS, 2006, 32 (03) :214-228
[4]  
CADOZ M, 1992, 32 INT C ANT AG CHEM
[5]   The role of salvage treatment in advanced colorectal cancer [J].
Capdevila, Jaume ;
Javier Ramos, Francisco ;
Macarulla, Teresa ;
Elez, Elena ;
Tabernero, Josep .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2009, 71 (01) :53-61
[6]   Selective infection and cytolysis of human head and neck squamous cell carcinoma with sparing of normal mucosa by a cytotoxic herpes simplex virus type 1 (G207) [J].
Carew, JF ;
Kooby, DA ;
Halterman, MW ;
Federoff, HJ ;
Fong, YM .
HUMAN GENE THERAPY, 1999, 10 (10) :1599-1606
[7]  
Coukos George, 2003, Current Gene Therapy, V3, P113, DOI 10.2174/1566523034578401
[8]   Intravesical oncolytic viral therapy using attenuated, replication-competent herpes simplex viruses G207 and Nv1020 is effective in the treatment of bladder cancer in an orthotopic syngeneic model [J].
Cozzi, PJ ;
Malhotra, S ;
Mcauliffe, P ;
Kooby, DA ;
Federoff, HJ ;
Huryk, B ;
Johnson, P ;
Scardino, PT ;
Heston, WDW ;
Fong, Y .
FASEB JOURNAL, 2001, 15 (07) :1306-1308
[9]   Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer [J].
Cunningham, D ;
Humblet, Y ;
Siena, S ;
Khayat, D ;
Bleiberg, H ;
Santoro, A ;
Bets, D ;
Mueser, M ;
Harstrick, A ;
Verslype, C ;
Chau, I ;
Van Cutsem, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (04) :337-345
[10]   Effects of preexisting immunity on the response to herpes simplex-based oncolytic viral therapy [J].
Delman, KA ;
Bennett, JJ ;
Zager, JS ;
Burt, BM ;
McAuliffe, PF ;
Petrowsky, H ;
Kooby, DA ;
Hawkins, WG ;
Horsburgh, BC ;
Johnson, P ;
Fong, Y .
HUMAN GENE THERAPY, 2000, 11 (18) :2465-2472