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CPCT-05 Biopsy Protocol Patient Selection

Protocol to Obtain Tumor Biopsies From Patients With Locally Advanced (Incurable) or Metastatic Cancer to Improve Selection for Clinical Trials. (CPCT - 05 Biopsy Protocol Patient Selection)

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01904916
Enrollment
195
Registered
2013-07-22
Start date
2014-01-31
Completion date
2017-03-31
Last updated
2018-03-09

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

Conditions

Metastatic Disease, Solid Tumors

Brief summary

Our knowledge on the genetic mutations in cancer is rapidly expanding and we are increasingly testing drugs in mainly metastatic cancer patient populations with rare mutations. Successful examples of this new strategy are ALK inhibitors in ALK translocated NSCLC (less than 5% frequency) and EGFR inhibitors in EGFR mutant NSCLC (approximately 5% frequency). Selecting molecularly stratified patient populations for studies benefits the patient as it increases the odds of obtaining benefit from experimental treatment, especially in early clinical trials. Moreover it increases the speed and efficacy of drug development as signs of efficacy are picked up in earlier phases. Therefore, broad screening of molecular lesions in the tumors of patients that are being considered for participation in trials is crucial. This pre-selection increases our ability to perform several trials in parallel and thus include more patients in more meaningful trials. With the still dismal prognosis of patients with metastatic cancer, increasing the accrual rate to pivotal trials in selected patient populations is a key factor in improving prognosis. The advent of Next Generation Sequencing (NGS) platforms enables us to probe a limited number of cancer related genes within 2-4 weeks. We have extensively piloted this approach and are now able to deliver clinically meaningful turn-around-times. This development enables us to use this technology to enrich clinical trials using targeted therapies for patients with specific mutations. We will obtain tumor biopsies of a metastatic or locally advanced lesion and a peripheral blood sample from all patients included in the trial; the biopsies to obtain information on the tumor related genetic mutations (mutational profile) and the blood samples to assess each patient's germline DNA background variation. As patients will be asked to undergo an invasive procedure it is important to address the potential safety issues. Review of the literature and our own experience show that tumor biopsies can be performed with only minor complications and acceptable risks. We will recruit patients with metastatic or locally advanced solid tumors from patients that can potentially be included in clinical trials.

Interventions

Sponsors

The Netherlands Cancer Institute
CollaboratorOTHER
Erasmus Medical Center
CollaboratorOTHER
P.O. Witteveen
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Locally advanced (incurable) or metastatic cancer from a histological or cytological proven solid tumor * Indication for systemic treatment with anti-cancer agents (with no treatment options with curative intent) * Measurable locally advanced (incurable) or metastatic lesion(s), according to RECIST 1.1 criteria. * Safe biopsy of a metastatic or locally advanced lesion possible * No contraindications for lidocaine (or its derivatives) and/or midazolam and/or phentanyl * Adequate organ function * WHO performance status 0-2 * Age \> 18 yr * Expected adequacy to follow up * Written informed consent

Exclusion criteria

• If one or more of the above mentioned inclusion criteria is not met

Design outcomes

Primary

MeasureTime frame
Percentage of screened patients allocated to trials based upon outcome of genetic screening effort.1 year

Secondary

MeasureTime frame
Number and nature of (serious) adverse events of the performed histological biopsies.2 days after each biopsy procedure
Number of samples stored for future related research.1 year
Number of samples with an adequate microRNA, (phospho)proteomic profiles and organoid cultures that allows biomarker discovery efforts. These profiles will be deposited in the CPCT database.1 year

Countries

Netherlands

Outcome results

None listed

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