A controlled trial of intratumoral ONYX-015, a selectively-replicating adenovirus, in combination with cisplatin and 5-fluorouracil in patients with recurrent head and neck cancer

被引:904
作者
Khuri, FR
Nemunaitis, J
Ganly, I
Arseneau, J
Tannock, IF
Romel, L
Gore, M
Ironside, J
MacDougall, RH
Heise, C
Randlev, B
Gillenwater, AM
Bruso, P
Kaye, SB
Hong, WK
Kirn, DH
机构
[1] Univ Texas, MD Anderson Canc Ctr, Div Canc Med, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Div Surg, Houston, TX 77030 USA
[3] US Oncol, Dallas, TX USA
[4] Univ Glasgow, Beatson Oncol Inst, Glasgow, Lanark, Scotland
[5] Royal Marsden Hosp, London SW3 6JJ, England
[6] Western Gen Hosp, Edinburgh EH4 2XU, Midlothian, Scotland
[7] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
[8] ONYX Pharmaceut, Richmond, CA USA
[9] Imperial Canc Res Fund, London WC2A 3PX, England
关键词
D O I
10.1038/78638
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
ONYX-015 is an adenovirus with the E1B 55-kDa gene deleted, engineered to selectively replicate in and lyse p53-deficient cancer cells while sparing normal cells. Although ONYX-015 and chemotherapy have demonstrated anti-tumoral activity in patients with recurrent head and neck cancer, disease recurs rapidly with either therapy alone. We undertook a phase II trial of a combination of intratumoral ONYX-015 injection with cisplatin and 5-fluorouracil in patients with recurrent squamous cell cancer of the head and neck. There were substantial objective responses, including a high proportion of complete responses. By 6 months, none of the responding tumors had progressed, whereas all non-injected tumors treated with chemotherapy alone had progressed. The toxic effects that occurred were acceptable. Tumor biopsies obtained after treatment showed tumor-selective viral replication and necrosis induction.
引用
收藏
页码:879 / 885
页数:7
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