Abstract 229TiP
Background
Precision oncology in the form of one actionable mutation targeted with a specific drug/drug combination benefits a minority of pts. This results in the majority having clinical grade next generation sequencing (cNGS) results that do not impact on treatment (tx) decisions. Polygenic analysis of such cNGS data to predict efficacious tx, via drug response prediction tools (DRPs), represents a potential solution. Several DRPs utilising artificial intelligence show early promise however the majority use gene expression or whole exome sequencing input data that is not available in the clinic. An exception is DruID (Drug IDentifier), a DRP trained using cell-line and pt data that is designed to perform with limited input data from cNGS panels, utilising domain-invariant representation learning and multi-task learning. Reported aberrations are analysed by DruID giving an output of anti-cancer agents ranked by a predicted efficacy score. In this single-centre phase II trial we aim to assess the efficacy of DruID recommended tx (DruID-Tx) in pts with refectory malignancies.
Trial design
Eligible pts have a histologically confirmed solid organ malignancy with progressive disease (PD) after ≥2 lines of tx and ECOG PS 0-2. Pts cNGS results are input into DruID to generate recommendations. Agents on a pre-defined panel of generic locally approved (HSA, Singapore) anti-cancer tx, with a predicted efficacy in the 4th quartile of DruID scores generated from a reference dataset can be considered. Specific DruID-Tx options will be omitted if a subject has received them in the prior 3 lines, with remaining options subjected to panel discussion by investigators. Pts with an available DruID-Tx after this selection criteria will undergo single agent tx until PD or unacceptable toxicity. Trial primary end point is objective response rate (ORR) with the hypothesis that DruID-Tx will give an ORR ≥25%. Using a Simon 2-stage optimal design, (80% power, one-sided α of 0.1) 13 pts will be enrolled to Stage I with a further 21 pts recruited in Stage II if ≥2 pts achieve response in Stage I. Secondary endpoints include clinical benefit rate, progression free and overall survival. Recruitment for Stage I is ongoing with 5/13 pts enrolled.
Clinical trial identification
NCT05719428.
Editorial acknowledgement
Legal entity responsible for the study
NUHS.
Funding
NCIS-N2CR.
Disclosure
R.J. Walsh: Financial Interests, Personal, Advisory Board: Pfizer, Novartis; Financial Interests, Personal, Speaker, Consultant, Advisor: AstraZeneca; Non-Financial Interests, Institutional, Local PI: BMS, Merck; Financial Interests, Institutional, Speaker, Consultant, Advisor: Merck. R. Sundar: Financial Interests, Personal, Advisory Board, Advisory Board, Invited Speaker: Bristol Myers Squibb, MSD; Financial Interests, Personal, Advisory Board: Merck, Bayer, Novartis, GSK, Pierre-Fabre, Tavotek, AstraZeneca, Daiichi Sankyo, BeiGene; Financial Interests, Personal, Advisory Board, Advisory Board, Invited Speaker, Travel: Eisai; Financial Interests, Personal, Advisory Board, Advisory Board, Invited Speaker, Travel for conferences. Funding declared is over several years (<10,000 Euro per year): Taiho; Financial Interests, Personal, Invited Speaker: Eli Lilly, BMS, Roche, Taiho, AstraZeneca, DKSH, Daiichi Sankyo, BeiGene, Astellas; Financial Interests, Personal, Advisory Board, Travel for conference and Advisory Board, funding declared is over several years, S.C. Lee: Financial Interests, Personal, Advisory Board, Advisory board, speaker invitations: Pfizer, Novartis, AstraZeneca, Roche, MSD; Financial Interests, Personal, Advisory Board, Advisory Board: Eli Lilly; Financial Interests, Personal, Advisory Board: Gilead; Financial Interests, Institutional, Research Grant: Pfizer, ACT Genomics, Eisai, Taiho, MSD, Karyopharm, ASLAN Pharmaceuticals, Adagene; Financial Interests, Institutional, Local PI: Roche, Novartis, Daiichi Sankyo, BMS, AstraZeneca; Financial Interests, Personal, Steering Committee Member: AstraZeneca. B. Goh: Financial Interests, Institutional, Invited Speaker: MSD; Financial Interests, Institutional, Advisory Board: Bayer Healthcare; Financial Interests, Personal, Other, Consultancy: Adagene pharmaceutical; Financial Interests, Institutional, Research Grant, Support for investigator initiated trial: MSD; Financial Interests, Institutional, Other, Pharmaceutical support for clinical trial: BMS; Financial Interests, Institutional, Other, Pharmaceutical support for investigator initiated clinical trial: Taiho pharmaceuticals; Financial Interests, Institutional, Coordinating PI: Adagene, Bayer; Financial Interests, Institutional, Local PI: Pfizer; Financial Interests, Institutional, Local PI, Conducting clinical trial: alx; Financial Interests, Institutional, Local PI, Pharmaceutical phase 1 trial: Novartis; Non-Financial Interests, Institutional, Other, Lead clinical trial platform of the Singapore Translational Cancer Consortium: Consortium for Clinical Research and Innovation Singapore; Non-Financial Interests, Member: ASCO. D.S. Tan: Financial Interests, Personal, Invited Speaker: AstraZeneca, MSD, Merck Serono, Roche, Eisai, GSK, Takeda; Financial Interests, Personal, Advisory Board: AstraZeneca, Bayer, MSD, Eisai, Roche, Genmab, GSK, Boehringer Ingelheim; Financial Interests, Personal, Stocks/Shares: Asian Microbiome Library (AMiLi); Financial Interests, Institutional, Research Grant: Roche, Bayer, Karyopharm Therapeutics, AstraZeneca; Financial Interests, Institutional, Coordinating PI: AstraZeneca, Bergen Bio; Financial Interests, Institutional, Local PI: Zeria Pharmaceutical Co Ltd, Bayer, Byondis B.V.; Non-Financial Interests, Leadership Role, Ex society president: Gynecologic Cancer Group Singapore; Non-Financial Interests, Member of Board of Directors: Gynaecologic Cancer Intergroup (GCIG); Non-Financial Interests, Leadership Role, Ex- Chair: Asia-Pacific Gynecologic Oncology Trials Group (APGOT); Non-Financial Interests, Institutional, Product Samples, Research Study: MSD, Eisai, AstraZeneca, Cyclacel Pharmaceuticals. A.D. Jeyasekharan: Financial Interests, Personal, Speaker, Consultant, Advisor: DKSH, Roche, Gilead Sciences, Turbine, AstraZeneca, Janssen, MSD; Financial Interests, Personal, Funding: AstraZeneca, Janssen. All other authors have declared no conflicts of interest.
Resources from the same session
836P - A prospective study to evaluate the prognostic implications and molecular mechanism of SLC40A1 gene in primary acute myeloid leukemia
Presenter: Harsh Goel
Session: Poster session 09
Resources:
Abstract
837P - Expression analysis, clinical significance and potential function of ALOX5AP in acute myeloid leukemia
Presenter: Harsh Goel
Session: Poster session 09
Resources:
Abstract
838P - Bayesian modeling in the survival analysis of patients with multiple myeloma with emphasis on missing data analysis
Presenter: Nelson Cruz Gutierrez
Session: Poster session 09
839P - Preliminary results from a phase II study of amulirafusp alfa (IMM0306) in patients with relapsed or refractory CD20-positive B-cell non-Hodgkin's lymphoma
Presenter: jianliang yang
Session: Poster session 09
840P - Orelabrutinib-based regimens in chronic lymphocytic leukemia with comorbidities: A real-world study
Presenter: Xun Lai
Session: Poster session 09
841P - Transforming the landscape of pediatric AML treatment: A cutting-edge SCT prognostic model
Presenter: Hua Yang
Session: Poster session 09
Resources:
Abstract
842P - Exploring the association of side-effects with depression in patients with chronic lymphocytic leukemia who have received treatment: An analysis of the lymphoma coalition’s 2022 global patient survey
Presenter: Natacha Bolanos Fernandez
Session: Poster session 09
843P - Challenges and insights in treating Langerhans cell histiocytosis: Persistent mutations and novel therapeutic approaches
Presenter: Marzieh NASHVI
Session: Poster session 09
844TiP - Orelabrutinib combined with rituximab for the treatment of elderly patients with newly diagnosed non-GCB diffuse large B-cell lymphoma (DLBCL) under the guidance of genetic subtype: A prospective, multicenter, single-arm, response-adaptive clinical study (Origin)
Presenter: Wanzhuo Xie
Session: Poster session 09
845TiP - CNS lymphoma imaging and molecular biomarkers study: CLIMB
Presenter: Panagiotis Ntellas
Session: Poster session 09