Biomarkers for Cancer Treatment

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospitals Coventry and Warwickshire NHS Trust

About this trial

Circulating biomarkers, such as miRNAs and proteomics, undergo identifiable and measurable changes during and following treatment for cancer, compared to pre-treatment baseline. Some of these changes may be associated either with known treatment parameters or predictive for cardiac or lung toxicity.

The aim is to identify and validate changes following treatment for cancer, compared to pre-treatment baseline, as well as differential miRNA expression in two-group comparisons (patients receiving radical RT/chemoRT for thoracic cancers versus IO-based complex SACT).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients (Age >18 years)

Histologically/Cytological confirmed solid tumour

Treated with radical RT or concurrent chemo-RT (Cohort 1) OR

Treated with chemo-IO or IO-IO combination (Cohort 2)

Disqualifiers

Contraindication for RT or chemotherapy (Cohort 1) OR

Contraindication for chemotherapy or IO (Cohort 2)

Use of chemotherapy or immunotherapy in the last 5 years. (Cohort 1) OR

Use of radical RT or chemo-RT within the thorax in the last 5 years. (Cohort 2)

Trial population

Patients on treatment for cancer at UHCW NHS Trust

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

48 Participants
are grouped into 2 trial groups
Group A: Patients treated with RT
Group B: Patients treated with SACT

Trial outcomes

Primary outcomes

1

Blood results

Identifying and validating changes in miRNA expression

Time frame
Baseline visit
2

Blood results

Identifying and validating changes in miRNA expression

Time frame
12 week follow-up visit

Secondary outcomes

1

Blood results

Identifying and validating changes in protein biomarker profiles

Time frame
Baseline visit
2

Blood results

Identifying and validating changes in protein biomarker profiles

Time frame
12 week follow-up visit

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.