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Using QPOP to Predict Treatment for Sarcomas and Melanomas

Q-SAM (Using QPOP to Predict Treatment for Sarcomas and Melanomas)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04986748
Enrollment
100
Registered
2021-08-03
Start date
2020-09-08
Completion date
2028-12-31
Last updated
2025-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Melanoma, Sarcoma

Keywords

Tumour-derived models, Organoids, Ex vivo drug testing, Personalised therapy, QPOP

Brief summary

This is a multi-cohort proof of concept study involving patients with sarcomas or melanomas. Patient models, both two- and three-dimensional, will be derived from tumour samples. These will then be used to evaluate drug sensitivities ex vivo. Enrolled patients will undergo resections or biopsies as part of standard-of-care, which will be used to generate patient models. Patients will receive standard-of-care systemic treatment. Patient models will also be subjected up to a 14-drug screening panel. The majority of drugs in the respective drug panels has been shown to have activity in the respective cancers and would be used in the standard-of-care setting by treating physicians.

Detailed description

Hypothesis: Ex vivo drug testing on patient-derived models using QPOP can identify drug sensitivities and combinations which may have clinical efficacy against sarcomas and melanomas. Specific aim 1: To derive patient models, both two- and three-dimensional, of sarcomas and melanomas Specific aim 2: To perform ex vivo drug testing on patient models of sarcoma and melanoma using QPOP Specific aim 3: To assess the efficacy of phenotype directed therapy using QPOP to assign treatment after progression on standard-of-care treatment in sarcoma and melanoma

Interventions

None listed

Sponsors

National Cancer Centre, Singapore
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of sarcoma or melanoma * At least 1 tumour lesion amenable to fresh biopsy or resection * Signed informed consent from patient or legal representative * Able to comply with study-related procedures

Exclusion criteria

* There are no specific

Design outcomes

Primary

MeasureTime frameDescription
Percentage of patients with successful model generation for each tumour subtype.8 years.Patients enrolled on study will undergo resection or biopsy of fresh tumour tissue to obtain cells for the generation of models.
Rates of radiological response from QPOP-directed treatment regimens.8 years.Complete and partial clinical response and stable disease.
Survival outcomes from QPOP-directed treatment regimens.8 years.Overall survival, progression-free survival.

Countries

Singapore

Contacts

Primary ContactValerie Shiwen Yang, BSc, MB BChir, PhD
valerie.yang.s.w@singhealth.com.sg+65 6436 8088

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026