OSL oncosil medical ltd

Research

  1. 923 Posts.
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    I think the below is the first time we've been at ASCO for anything

    It's from their LinkedIn site. Spanish experience

    The data is showing reasonably consistent outcomes.

    I don;t know how they can report OS times when half the cohort was still alive at the end of followup.

    I hope TRIPP and Pancosil complete soon, but followup up will take some time

    Background:


    Phosphorous 32 microparticle (32P) brachytherapy delivered by echoendoscopy (EUS) represents an innovative therapy in pancreatic cancer (PC). Our aim is to evaluate efficacy and safety outcomes for Spanish patients in real clinical practice.


    Methods:


    After being assessed by a multidisciplinary committee and meeting eligibility criteria (Table 1), patients signed consent to receive intratumoural 32P by EUS within the international observational registry OSPREY (March 2022-January 2025). Complications associated with intratumoural 32P injection via EUS, associated adverse events (AEs) and preliminary efficacy results (progression-free survival [PFS] and overall survival [OS]) were analysed.


    Results:


    Twenty-five patients (16 females and 9 males; age 67 years [range 48, 80]; 20 ECOG 1 and 5 ECOG 0) with unresectable locally advanced PC (16 in head, 4 in uncinate and 5 in body; tumour size 31.5 mm [range 12, 60]) were included. Seven patients (28%) had received a previous treatment. 23 patients (92%) received gemcitabine-based chemotherapy concomitant with intratumoural 32P (17 gemcitabine plus nabpaclitaxel; 6 gemcitabine monotherapy), 1 patient FOLFIRINOX and 1 patient did not receive concomitant chemotherapy. Two patients had AEs related to 32P injection by EUS: G2 asthenia and G1 abdominal pain, respectively. Seventeen patients (68%) had chemotherapy-related AEs, with 3 cases of G3 neutropenia and 1 of G3 thombopenia; 14 had G1-2 toxicities: neutropenia (3), thrombopenia (4), neurotoxicity (4), anaemia (2), asthenia (3), hyporexia (1), nausea (1), diarrhea (1) and constipation (1) . Four (16%) patients underwent surgery after intratumoural treatment. With a median follow-up of 17.2 months after injection, 14 patients (56%) have progressed, 13 distantly and 7 also locoregionally; 1 patient progressed only locally. The median PFS since 32P injection is 8.4 months (95% CI 4.3, 17.0). 12 patients are alive at the end of follow-up (48%) with a median OS since 32P injection of 13.8 months (95% CI 9.4, 26,9].


    Conclusions:


    The experience of Spanish centres suggests that intratumoural 32P associated with gemcitabine-based chemotherapy is safe and achieve long survival. Our ongoing prospective registry will allow evaluation of the oncological outcomes of this therapy at longer follow-up times.
 
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