CHOSA Oncology

CEO Peter Buhl comments: "I am very proud and happy to present these excellent results, which demonstrate our ability to identify and select patients who will benefit from treatment with our cancer drug, LiPlaCis®. LiPlaCis is a new formulation of cisplatin, and our tumor gene test, used to predict the individuals who will respond positively to the platinum-based drug, has shown clear efficacy in heavily treated breast cancer patients. This further supports previous data indicating that the test is also highly effective in identifying lung cancer patients who will benefit from cisplatin."

This metastatic breast cancer group, which has received several other treatments in the past, presents a major challenge as they may have developed 'treatment resistance'. Many times, physicians would like to choose cisplatin treatment, but opt ​​out of this as it has a strong side effect profile. Results from this prospective and predictive study show that DRP can facilitate the decision-making process for the doctor when cisplatin treatment may be relevant. With the help of DRP, the doctor has a better basis for decision-making, it is cheaper for healthcare to provide the right treatment at the right time, and above all a benefit for the patient.

Data from the current study is pointing towards a new treatment opportunity for 20% of heavily pretreated breast cancer patients with metastatic disease. In the study the patients had received a median of 6,6 therapies for their disease before they received LiPlaCis, and they were otherwise out of treatment options. We believe that a progression free survival advantage increase of 250 % in the sensitive 20% provides a potential break-through designation and a route for LiPlaCis approval.   

The current data also point to other opportunities. We believe that similarly it is very likely that there is a large or small fraction of patients with early lung and breast cancer who may benefit from precision use of cisplatin.

Here below are the results in summary - more details can be found at the ASCO website (please follow link below) and will be presented at a poster session at the ASCO conference on June 3^rd, 2023.

37 metastatic breast cancer patients had received a median of 7 previous treatment lines before treating with LiPlaCis. A DRP score >80% (DRP80+) discriminated well between responders and non-responders to liposomal cisplatin. All 4 partial remissions in the study were in the DRP80+ group, and other key efficacy endpoints were in favor of the DRP80+ vs the lower scores (DRP80-).

DRP® is proprietary to and a registered trademark of Allarity Therapeutics (Nasdaq:ALLR). These data are from a clinical study previously run by Allarity (formerly Oncology Venture). CHOSA Oncology AB has licensed worldwide rights to LiPlaCis® and its DRP® companion diagnostic (together referred to as iCIP™) from Allarity Therapeutics Inc.  

Link to ASCO website for electronic abstracts: https://meetings.asco.org/abstracts-presentations/226582

Abstract number and title: 3130; Predictive biomarker for cisplatin in prospective phase 2 of liposomal cisplatin in metastatic breast cancer
Session: Developmental Therapeutics-Molecularly Targeted Agents and Tumor Biology
Poster Board: 328
Date and time: Saturday 3 June 2023; 8:00-11:00 CDT
Presenter: Peter Buhl Jensen