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Implementation of Liquid Biopsies During Routine Clinical Care in Patients With Advanced Malignancies (LIQPLAT)

Not Applicable
Recruiting
Conditions
Advanced Solid Tumor
Interventions
Diagnostic Test: ctDNA measurement
Registration Number
NCT06367751
Lead Sponsor
University Hospital, Basel, Switzerland
Brief Summary

The goal of this study is to assess the implementation and feasibility of ctDNA measurements from blood samples obtained during routine clinical care of cancer patients in the University Hospital Basel.

Researchers will compare clinical and patient reported outcomes from the LIQPLAT study with patients who did not receive ctDNA measurements (external comparator from registry AO_2023-00091).

Blood samples will be drawn from the patients as part of routine care and ctDNA measurements will be performed on these samples.

Detailed Description

Liquid biopsies, in particular the analysis of circulating tumor DNA (ctDNA), have emerged as a promising tool for detecting and monitoring cancer. Measuring ctDNA in patients with solid malignancies may help to identify targetable alterations, measure disease burden, identify early mutations of resistance, tailor and deescalate cancer treatment, and predict patient prognosis. Although the adoption and application of ctDNA measurements for patients with solid tumors in routine clinical care is increasing, evidence supporting the integration of ctDNA into current practice is limited, especially for patients with advanced cancers.

This is a trial using routinely collected health care data from an ongoing registry (AO_2023-00091) in cancer patients with advanced solid malignancies receiving first line systemic anticancer treatment for advanced disease.

This trial will assess the feasibility and implementation of routine measurement of ctDNA and its association with clinical outcomes, including quality of life and survival. All patients will receive routine diagnostics, treatment and follow-up. All patients with a new cancer diagnosis will be assessed for eligibility based on the routinely collected information available in the registry. We will then randomly decide which eligible patients are invited to participate in the trial. If patients accept the invitation and intend to get a measurement of ctDNA, they have to provide written informed consent.

Results from ctDNA analyses will be discussed at the molecular tumor board, an established regular interdisciplinary meeting at the University Hospital Basel (part of routine care) to discuss patients with complex findings from tumor sequencing analyses. Treatment changes occurring during the trial duration will be at the discretion of treating physician and according to patient's preference as is routine standard of care.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
150
Inclusion Criteria
  • Patients with a proven solid malignant disease, i.e. with solid malignant tumors where no primary surgical resection is planned OR solid malignant tumors that are locally advanced and inoperable OR solid tumors that are metastatic
  • No prior treatment for advanced/metastatic disease
  • Indication for medical anti-cancer treatment (including combined chemoradiotherapy) as judged by the treating physician
  • Patient age 18 years and older
  • General research consent of the University Hospital Basel
Exclusion Criteria

● Patients with primary brain tumors

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Active ComparatorctDNA measurementPatients included in the ongoing registry AO_2023-00091. Patients will have ctDNA measurements being performed on blood samples collected as part of clinical routine.
Primary Outcome Measures
NameTimeMethod
Patients in whom actionable alterations were identified in ctDNA analysisbaseline, between month 2 and 3, between month 5 and 6, clinical event

Patients in whom actionable alterations were identified in ctDNA analysis. Calculated as the number of patients with actionable alterations over the total number of patients included, expressed as a percentage.

Clinical event is defined as suspicious or confirmed clinical or radiological disease progression or treatment discontinuation for any reason.

Turn-around time of ctDNA analysisbaseline, between month 2 and 3, between month 5 and 6, clinical event

Time from ctDNA request until issuing the first report. Expressed as hours.

Clinical event is defined as suspicious or confirmed clinical or radiological disease progression or treatment discontinuation for any reason.

Number and proportion of patients in whom ctDNA was detectable before starting medical anticancer treatment1 time assessment at baseline

Number and proportion of patients in whom ctDNA was detectable before starting medical anticancer treatment. Calculated as the number of patients with detectable ctDNA over the total number of patients included, expressed as a percentage.

ctDNA kineticsup to 24 months

Change in allelic frequency over time including relative changes from baseline.

Secondary Outcome Measures
NameTimeMethod
Survival rate 12 monthsMonth 12

Survival rate 12 months.

Time to next treatment lineup to 24 months

Time to next treatment line, expressed in days.

Survival rate 6 monthsMonth 6

Survival rate 6 months.

Unplanned hospital admissions and emergency room visitsup to 24 months

Number and proportion of unplanned hospital admissions and emergency room visits.

Number of patients being positive for ctDNA and suspicious Clonal Hematopoiesis of Indeterminate Potentialup to 24 months

Number of patients being positive for ctDNA and suspicious Clonal Hematopoiesis of Indeterminate Potential

Number of ctDNA analyses with a valid resultup to 24 months

Number of ctDNA analyses with a valid result - that is all ctDNA analyses conducted without any observed technical errors.

Number of ctDNA testing results that were successfully made available to the molecular tumor boardup to 24 months

Number of ctDNA testing results that were successfully made available to the molecular tumor board.

Progression free survivalup to 24 months

Progression free survival as determined by routine imaging (e.g. CT scan, MRI), tumor marker (e.g. PSA). Defined as time from date of informed consent until disease progression or death, whatever occurs first.

Quality of life and physical functionmonth 3, month 6, month 12

Global quality of life and physical function as measured by EORTC QLQ C30 and C15 (European Organisation for Research and Treatment of Cancer, Quality of Life Questionnaire). Calculation of the scores follows the validated formulas as issued by the EORTC. Scores range from 0% to 100% for all domains with higher values representing better outcome.

Overall survivalup to 24 months

Overall survival.

Trial Locations

Locations (1)

Department of Medical Oncology, University Hospital Basel

🇨🇭

Basel, Switzerland

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