During this year’s BIOTECHNICA exhibition, the international biotech news magazine GEN - Genetic Engineering & Biotechnology News yesterday held an information event with subsequent panel discussion featuring the topic “TGF-ß – an important target in cancer diseases."
Followed by industry representatives and journalists, national and international clinical and research experts reported on the latest findings concerning the tumor factor Transforming Growth Factor beta (TGF-ß) and the status of drug development fighting this tumour-specific drug target.
John Sterling, Chief Editor of Genetic Engineering & Biotechnology News: “Growth factors, such as VEGF, PDGF, etc. have been known for more than 30 years and the TGF-ß growth factor is involved in several malignant pathways. But what about the development of therapeutics against this important oncological target? With this session we wanted to place TGF-ß into the spotlight of public perception and provide the opportunity to learn more about this fascinating protein family.” The session was led by Dr Hubert Heinrichs, Chief Medical Officer at Antisense Pharma GmbH.
Prof Peter ten Dijke, professor of molecular cell biology at Leiden University, The Netherlands opened the session by giving an introduction about TGF-β and its role in aggressive cancer diseases. Ten Dijke graduated in 1991 based on his research on the identification of the third isoform of TGF-β and since then he has become one of the international leading TGF-β experts. Currently his laboratory analyses the molecular mechanisms by which TGF-β family members elicit their cellular effects via (co)receptors and intracellular SMAD effectors, and how subverted TGF family signaling is involved in cancer, vascular and bone diseases.
“The secreted molecule TGF-β is involved in several cell communication pathways”, ten Dijke explained. “Subverted TGF-β signaling has been implicated in multiple diseases, including cancer, fibrosis and cardiovascular illnesses. TGF-β and cancer were linked from the beginning: Highly aggressive tumours produce huge amounts of TGF-β - which enhances migration and metastasis of tumour cells, mediates angiogenesis and is known as one of the strongest immunosuppressors.”
Then Dr Piotr Jachimczak, physician and senior scientific advisor at Antisense Pharma, informed about therapies targeting TGF-β. In his doctoral thesis 1992 he had already demonstrated for the first time that the targeted inhibition of mRNA encoding TGF-β2 by antisense oligodeoxynucleotides may reverse glioma-derived immunosuppression. The long-term goal of his translational research is to develop an anti-TGF-β strategy to treat advanced, late-stage cancer. “On a global scale, different approaches of anti-TGF-beta strategies in cancer are pursued," Jachimczak explained. “Different TGF-β inhibitors such as small molecules, monoclonal antibodies and various other technologies are under development. The phosphorothioate oligodeoxynucleotide trabedersen has so far been clinically most successful: it inhibits the production of isoform TGF-β2 by binding to its mRNA. It shows a very good safety and compatibility profile both when applied locally and systemically, and promising efficacy data in particular in the indications of malignant brain tumours, pancreatic cancer and malignant melanoma.
PD Dr Peter Hau, section leader of the NeuroOncology group, Department of Neurology at University of Regensburg confirmed the potential of trabedersen. According to his scientific interests that are glioma, brain tumor initiating cells, tumour metabolism, transforming growth factor beta (TGF-β) and antisense technologies, Dr. Hau served as principal investigator and national coordinator in several clinical trials of the EORTC and the German NeuroOncology Working Group (NOA).
He presented the results of the completed, randomized, active-controlled clinical Phase IIb study of trabedersen in high-grade glioma.
“A significantly higher tumor control rate of trabedersen treated patients with anaplastic astrocytoma was observed at 14 months when compared to patients who had received standard chemotherapy”, Dr Hau described one of the outcomes. “Similarly the overall response rate at 14 months was significantly higher and the two-year survival rate was clearly improved under trabedersen with 83.3% versus 41.7%. Importantly, these trabedersen effects were associated with a median overall survival benefit of 17.4 months versus standard chemotherapy.”
These results impressively show that TGF-β2 silencing is a promising approach in tumour therapy and could serve the high unmet medical need. The current situation for the treatment of malignant brain tumors is still insufficient: Despite surgical tumor resection, radio- and chemotherapy, the tumor recurs in almost all cases and most patients unfortunately die within less than a year after recurrence.
“Our current clinical results reinforce our impression of having found in trabedersen an agent which offers patients with aggressive cancer diseases an urgently required treatment option," Dr Hubert Heinrichs, CMO at Antisense Pharma and chairman of the session summed up. Reason enough for Antisense Pharma to look ahead optimistically. “Based on the Phase IIb data, we already started an international pivotal Phase III study in recurrent or refractory AA patients (SAPPHIRE). Also the evolving results in pancreatic cancer and malignant melanoma are very encouraging.”
At the end of the session, Gen’s Edition, John Sterling, made note of the positive results of Antisense Pharma’s study. “Antisense Pharma is an excellent example of how determined biotechnology companies can focus their R&D efforts to advance the development of innovative anti-cancer drugs.”
Antisense Pharma GmbH
