Neoplasms

Skin and Connective Tissue Diseases

All Conditions

Digestive System Diseases

Breast Neoplasms

Gastrointestinal Neoplasms

Digestive System Neoplasms

Gastrointestinal Diseases

Antineoplastic Agents

All Drugs and Chemicals

Irinotecan

Paclitaxel

Docetaxel

Azacitidine

Albumin-Bound Paclitaxel

Tubulin Modulators

Antimitotic Agents

Topoisomerase I Inhibitors

Enzyme Inhibitors

Antimetabolites

Participants will undergo two study stages: QPOP drug selection and CURATE.AI-guided dosing modulation. In the QPOP drug selection stage, participants will undergo a baseline biopsy for organoid generation and subsequently receive treatment as per SOC. During this time, QPOP will identify optimal drug combinations for the participant based on ex vivo experiments on the participant's organoid. Participants who are identified via QPOP to potentially benefit from azacitidine in combination therapy (azacitidine + docetaxel, azacitidine + paclitaxel or azacitidine + irinotecan) will move on to the CURATE.AI-guided dosing modulation stage with treatment with azacitidine. Azacitidine treatment will begin once disease progression after SOC treatment is determined based on CT scans. Only azacitidine dose in the selected azacitidine combination will be modulated by CURATE.AI

QPOP is a mechanism-agnostic platform for optimizing drug selection. QPOP uses a quadratic equation to describe the patient-specific drug-drug interaction space based solely on experimentally derived drug-response data on individual patient's tissue sample, from which optimal drug combinations can be identified. Drug selection via QPOP allows for identification of an optimal combination therapy without the need for exhaustive testing of every combination. The first stage of the trial aims to generate a personalised QPOP drugs list for each participant based on experimentally derived data from ex vivo testing in the participant's tissue sample. Optimal drugs from a pre-specified drug pool will be recommended by the QPOP team.

QPOP

CURATE.AI - a small data, AI-derived technology platform based on this discovery - allows personalised guidance of an individual's dose modulations based only on that individual's data. Additionally, CURATE.AI is mechanism-independent, and dynamically adapts to changes experienced by the participant, providing dynamic dose optimisation throughout the duration of the participant's treatment.

The second stage of the trial aims to obtain a personalised CURATE.AI profile for each participant, based on their phenotypic response to a set of drug doses from the drug combinations with azacitidine identified and recommended by the QPOP team. The doses will be recommended by the CURATE.AI team, when relevant to the clinical decision-making process. Once an actionable profile is obtained, dose recommendations are based on the profile and aimed to treat the participant.

The maximum period of involvement with this study when azacitidine may be adjusted by CURATE.AI is 18 months.

CURATE.AI

Azacitidine subcutaneous injection Day 1, 2 and Day 8, 9 + 30 mg/m2 docetaxel intravenously Day 1 and 8

Each chemotherapy cycle will be 21 days.

Azacitidine + docetaxel

Azacitidine subcutaneous injection Day 1, 2 and Day 8, 9 + 80 mg/m2 paclitaxel intravenously Day 1 and 8

Each chemotherapy cycle will be 21 days.

Azacitidine + paclitaxel

Azacitidine intravenously subcutaneous injection Day 1, 2 and Day 8, 9 + 100 mg/m2 irinotecan intravenously Day 1 and 8.

Each chemotherapy cycle will be 21 days.

Azacitidine + irinotecan

Wei Peng Yong

Cheng Ean Chee

Raghav Sundar

Hon Lyn Tan

Jingshan Ho

Gloria Chan

Joan Choo

Soo Chin Lee

Boon Cher Goh

Ross Soo

David Tan

Andrea Wong

Joline Lim

Robert Walsh

Jia Li Low

This pilot feasibility study aims to set the foundation to investigate the applicability of QPOP drug selection followed by CURATE.AI-guided dose optimisation of the selected azacitidine combination therapy for solid tumours using CURATE.AI within the current clinical setting.

QPOP will identify drug interactions towards optimal efficacy and cytotoxicity from the pre-specified drug pool based on ex vivo experimental data from the individual participant's tissue sample model. With these drug interactions, QPOP will identify the optimal drugs for the specific participant whose biopsy provided the cells for the ex vivo experimentation. Subsequently, CURATE.AI will be used to guide dosing for the selected combination therapy for that participant.

Individualised CURATE.AI profiles will be generated based on each participant's response to a set of drug doses. Subsequently, the personalised CURATE.AI profile will be used to recommend the efficacy-driven dose. CURATE.AI will operate only within the safety range for each drug pre-specified for each participant.

This pilot feasibility study will inform the investigators on the logistical and scientific feasibility of performing a large-scale randomised controlled trial (RCT) with the selected azacitidine combination therapy regimens and response markers. A secondary objective is to collect toxicity and efficacy data using established and exploratory response markers within and in-between cycles as exploratory outcomes.

Several drug combinations and modulation in drug dosing are given to promote cancer cell elimination in cancer patients. While advances in omics tools have led to greater understanding of the complexity of diseases such as cancer, they have also led to the understanding that large networks of molecular interactions contribute to both disease progression and therapeutic resistance. The rational design of drug combinations is a challenge because complex molecular networks contribute to feedback mechanisms of drug resistance and compensatory oncogenic drivers that limit the efficacy of targeted inhibitors. This challenge is compounded by the vast number of available drugs to identify optimal drug combinations from.

In addition to the complexities in identifying optimal drug combinations, optimal dosing remains a challenge as drug synergy is both dose, time- and patient- dependent. The final drug concentration in the body must fall within a narrow range that maximises cancer elimination while minimizing toxic side effects. The complexity of this task increases significantly with the number of drugs given in combination due to increasing parameters and stochastic behaviour of a biological system. Currently, the established approach is to select maximum tolerated doses (MTD) - the highest drug doses that do not cause unacceptable side effects. Treatment efficacy does not guide dose selection. Combined with limited personalisation, this dosing strategy often results in sub-optimal outcomes of the treatment.

In this pilot feasibility study, participants will undergo QPOP drug selection, a stage of CURATE.AI profile generation, and a stage of CURATE.AI profile-based, efficacy-driven drug dosing.

As there are no prior clinical trial cohorts using CURATE.AI in participants with solid tumours and there are existing data for breast and gastric cancer for input into QPOP, this feasibility pilot study will focus on the practicality and feasibility of using QPOP and CURATE.AI in this clinical context.

At the end of the participation of the first 10 patients, an interim analysis will be conducted using the data generated from these participants, which will include formal power and statistical sample size calculations. Based on these outcomes, the investigators will consider cohort expansion or an RCT. Specifically, the interim analysis will aid the decisions on whether to proceed with future RCTs; their design (superiority, equivalence or non-inferiority); logistical and practical aspects of running a large-scale RCT; patient population selection for the RCT; and potential applicability of CURATE.AI in a wider range of systemic therapy regimens, response markers and/or expansion of the current cohort to elicit further data on secondary endpoints and/or new randomized cohorts.

Although not standard of care treatment for breast and gastric cancer, azacitidine combination therapy is chosen by the investigators as azacitidine combination therapy as azacitidine is a potent DNA methyltransferase inhibitor (DNMT) that can increase the sensitivity of a range of metastatic or advanced solid tumours, such as breast and gastric cancer, to treatment with docetaxel, paclitaxel, or irinotecan after developing resistance. Studies have also demonstrated the possibility of low dose treatment with chemotherapeutic agents when given together with azacitidine. However, cytotoxicity of azacitidine increases with dose and exposure time, which highlights the need to rapidly identify the optimal azacitidine-containing drug combinations and for personalised dose modulation during treatment. As such, QPOP drug selection and CURATE.AI dose modulation pipeline is in the ideal position to optimise treatment with azacitidine in combination with docetaxel, paclitaxel, or irinotecan via a personalised manner to maximise efficacy while minimising toxicities.

Participants will undergo QPOP drugs selection optimisation, and those participants who are identified via QPOP to potentially benefit from azacitidine in combination with docetaxel, paclitaxel, or irinotecan will transition to the CURATE.AI stage of the trial after treatment fails. Participants who have undergone QPOP drug selection (e.g. under QGAIN (2019/00924) or NGAIN trial (2021/00009)) are allowed to enrol for the CURATE.AI modulation period of this study at the approval of the Principal Investigator and Sponsor.

CURATE.AI will facilitate personalised treatment to each of the participants by recommending optimal doses in a dynamic fashion. In this phase, only azacitidine dose in the selected azacitidine combination will be modulated by CURATE.AI. Criteria for recruitment allow a high variability in the participant population to reflect a true variability in the cases faced in the clinical practice.

10 participants diagnosed with breast or gastric cancer undergoing or planned for treatment will be enrolled. The participants will undergo QPOP drug selection optimisation, and those participants who are identified via QPOP to potentially benefit from azacitidine in combination with docetaxel, paclitaxel or irinotecan will transition to the CURATE.AI dose modulation phase of the trial. Only azacitidine dose in the selected azacitidine combination will be modulated by CURATE.AI

Optimizing and Personalising Azacitidine Combination Therapy for Treating Solid Tumours QPOP and CURATE.AI

Optimizing and Personalising Azacitidine Combination Therapy for Treating Solid Tumours Using the Quadratic Phenotypic Optimization Platform (QPOP) and an Artificial Intelligence-based Platform (CURATE.AI)

Data collection and explorative analysis of response marker in higher frequency serial measurements after modulated dosing in relation to standard frequency readings and other efficacy measures, e.g RECIST criteria

Data collection and explorative analysis of ctDNA as:

1. a response marker in serial measurements at given clinical context and after modulated dosing;
2. potential input for CURATE.AI.

A decision on whether we "successfully apply" the QPOP drug selection requires expert judgement and cannot be made based on a purely numerical process. The expert panel will consider the following factors with careful regard for the individual circumstances of each participant:

1. The goodness-of-fit of the QPOP derived equation is acceptable to allow for a reliable list of effective drug combinations;
2. The drugs list is generated sufficiently early for the participant to potentially benefit

A decision on whether we "successfully apply" the CURATE.AI profile requires expert judgement and cannot be made based on a purely numerical process. The expert panel will consider the following factors with careful regard for the individual circumstances of each participant:

1. Error/variance (biological/analytical) is sufficiently small to allow accurate predictions;
2. Profile can be generated sufficiently early for the participant to potentially benefit;
3. Dose-dependent relationship is observed;
4. Profile is actionable (i.e. fulfils the co-investigator's pre-specified safety requirements);
5. Systemic changes in the participant which require profile recalibration are rare or readily assimilated into the CURATE.AI algorithm.

percentage of participants in whom the CURATE.AI-guided cumulative dose is substantially (≥10%) different from the projected SOC cumulative dose, which is defined as the maximum dose of the modulated drug\*, azacitidine, multiplied by the number of completed chemotherapy cycles.

\* The maximum dose of the modulated drug azacitidine is 120mg/m2 once daily given on days 1-2 and days 8-9, every 21 days, in combination with weekly docetaxel, paclitaxel or irinotecan for two weeks followed by one week of rest.

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization	Link
Optimizing and Personalising Azacitidine Combination Therapy for Treating Solid Tumours QPOP and CURATE.AI	NCT05381038	Solid Tumor Gastrointestina... Breast Cancer	QPOP CURATE.AI Azacitidine + d... Azacitidine + p... Azacitidine + i...	21 Years - 99 Years	National University Hospital, Singapore
Optimizing and Personalising Azacitidine Combination Therapy for Treating Solid Tumours QPOP and CURATE.AI	NCT05381038	Solid Tumor Gastrointestina... Breast Cancer	QPOP CURATE.AI Azacitidine + d... Azacitidine + p... Azacitidine + i...	21 Years - 99 Years	National University Hospital, Singapore

Spots Global Cancer Trial Database for azacitidine + docetaxel