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Recruiting NCT07121998

Study of Acquired Resistance to Alkylator Chemotherapy in Endocrine Neoplasms

Observational Neuroendocrine (NE) Tumors Endocrine Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Core needle biopsy, Phlebotomy.
Who it may be relevant to
Registry conditions: Neuroendocrine (NE) Tumors, Endocrine Cancer. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Sweden
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Longitudinal Biomarker Study in Endocrine Neoplasms to Study Acquired Resistance to Alkylator Chemotherapy

Overview

It has been showed that alkylating chemotherapy, particularly the widely used agent temozolomide, may cause high tumor mutational burden (TMB) in certain tumors by causing inactivating mutations in the DNA mismatch repair (MMR) system. This can cause therapy resistance and tumor progression but may also predict response for immunotherapy. Hypermutation is very uncommon in neuroendocrine tumors. However, small studies indicate that around 30% of pancreatic tumors develop high TMB after alkylating chemotherapy. The aim of this study is therefore to study the occurrence and frequency of DNA hypermutation after alkylating chemotherapy in endocrine neoplasms and to investigate non-invasive methods that may capture the development of hypermutation (imaging, ctDNA etc.). This is a prospective multicenter study. 94 patients from Swedish endocrine cancer centers in Uppsala, Stockholm, Göteborg and Lund will be included and divided into two groups. Group A will include patients that are about to start treatment with alkylating chemotherapy. Blood samples for liquid biopsy will be collected at baseline and at follow-up and if the tumor progresses, tissue biopsy will be obtained from two different lesions and analyzed with GMS560. Group B will include patients experiencing tumor progression after having received alkylating chemotherapy at any point in their disease course before. At inclusion, both liquid and tissue biopsy will be obtained and analyzed as described above.

Interventions

  • Procedure Core needle biopsy
    Core needle biopsy of metastatic lesions
  • Procedure Phlebotomy
    Phlebotomy of peripheral vein

Primary outcome measures

  • Proportion of pancreatic neuroendocrine tumor patients with hypermutation and/or mismatch repair deficiency after treatment with alkylating chemotherapy [Time frame: Through study completion, an average of 2 years.]

Eligibility criteria

Inclusion criteria

  • Informed consent
  • Age ≥18 years
  • Histopathology confirmed endocrine neoplasm
  • Treatment with alkylating chemotherapy: Arm A; about to start alkylating chemotherapy, or Arm B; at disease progression or recurrence with previous alkylating chemotherapy treatment.

Exclusion criteria

  • If planned tissue biopsy: risk factors for biopsy-related complications accordingly to local investigator, including coagulation disorder
  • Long term treatment with anticoagulant that cannot be temporarily paused without unacceptable risk
  • Pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Sweden · 1 center
  • Akademiska Sjukhuset — Uppsala

Identifiers

NCT: NCT07121998 · V1.1

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗