Abstract
dl1520 (also known as Onyx-015) is an E1B-deleted adenovirus designed to selectively lyse p53-deficient cancer cells. Clinical trials involving patients with recurrent squamous cell carcinoma of the head and neck have shown clinical efficacy, but no direct evidence as to the tumor or p53 selectivity of the virus was demonstrated. We wanted to determine whether dl1520 is selective for survival and replication within tumor tissue after direct injection and whether this is determined by p53 status of the tissues. We also wanted to ascertain whether the virus has any macroscopic effect on normal tissue. An open-label Phase II trial was devised in which a fixed dose of the virus was administered to 15 patients via a direct intertumoral injection before surgery for untreated oral squamous cell carcinoma. The agent was also delivered into an area of adjacent normal buccal mucosa. Specimens of the excised tumor and of biopsies of the injected normal tissue were assessed for viral presence and p53 status. We demonstrated that the virus replicates selectively in tumor as opposed to normal tissue after this direct injection. It was not possible to determine whether this selectivity was p53 related. It was found that dl1520 triggers an early rise in apoptosis levels in injected normal tissues. No adverse effects of viral injection were noted. This is the first report of injection of dl1520 into previously untreated squamous cell cancer. The data support the concept that dl1520 is replication deficient in normal, compared with cancerous, tissues and has potential as a selective anticancer agent against tumor tissues.
Highlights
Improved treatments for recurrent and metastatic cancer refractory to conventional therapies are urgently required
We demonstrated that the virus replicates selectively in tumor as opposed to normal tissue after this direct injection
It was found that dl1520 triggers an early rise in apoptosis levels in injected normal tissues
Summary
Improved treatments for recurrent and metastatic cancer refractory to conventional therapies are urgently required This is so in squamous carcinoma of the head and neck, in which the primary tumor can be treated effectively with surgery and radiotherapy when localized but which is very difficult to treat, once recurrent or metastatic lesions develop. The virus is E1B gene deleted and is designed to be cytolytic to cancer cells after viral replication but to cause little harm to normal tissues [2, 3]. This is proposed to be due to the selective replication of the virus leading to cytolysis in mutant p53-expressing cells [4]. When dl1520 has been tested in other tumor types, it again has given encouraging results (9 –12)
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More From: Clinical cancer research : an official journal of the American Association for Cancer Research
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