AI Article Synopsis

  • - OBP-301 (Telomelysin) is a modified adenovirus designed to enhance cancer treatment by sensitizing oesophageal cancer cells to radiation therapy while also being regulated by a specific promoter to control its replication.
  • - A phase I study involved 13 elderly cancer patients who were unfit for traditional surgery or chemotherapy and received OBP-301 injections alongside a 6-week radiation treatment, resulting in significant tumor responses.
  • - The results showed a high objective response rate of 91.7%, with 8 patients achieving complete tumor response and evidence of immune system activation, indicating this approach is both feasible and beneficial for these patients.

Article Abstract

Purpose: OBP-301 (Telomelysin) is an attenuated type-5 adenovirus that contains the human telomerase reverse transcriptase promoter to regulate viral replication. OBP-301 sensitises human cancer cells to ionising radiation by inhibiting DNA repair, and radiation enhances coxsackievirus and adenovirus receptor-mediated OBP-301 infection on the contrary. We assessed OBP-301 with radiotherapy in oesophageal cancer patients unfit for standard chemoradiation treatments.

Methods: A phase I dose-escalation study of OBP-301 with radiotherapy was conducted in 13 histologically confirmed oesophageal cancer patients deemed unfit to undergo surgery or chemotherapy. Study treatment consisted of OBP-301 administration by intratumoural needle injection using a flexible endoscope on days 1, 18 and 32. Radiotherapy was administered concurrently over 6 weeks, beginning on day 4, to a total of 60 Gy.

Results: Of the 13 patients, 7, 3 and 3 patients were treated with 10, 10 and 10 virus particles, respectively. Study group comprised 10 males and 3 females, with a median age of 82 years (range, 53-91 years). All patients developed a transient, self-limited lymphopenia. Distribution studies revealed transient virus shedding in the plasma. Eight patients had local complete response (CR); all of them exhibited no pathologically viable malignant cells in biopsy specimens, and 3 patients had a partial response. The objective response rate was 91.7%. The clinical CR rate was 83.3% in stage I and 60.0% in stage II/III. Histopathological examination revealed massive infiltration of CD8 cells and increased PD-L1 expression.

Conclusion: Multiple courses of endoscopic intratumoural OBP-301 injection with radiotherapy are feasible and provide clinical benefits in patients with oesophageal cancer unfit for standard treatments.

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Source
http://dx.doi.org/10.1016/j.ejca.2021.04.043DOI Listing

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