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NCT Number: NCT05178693

Lutathera and ASTX727 in Neuroendocrine Tumours

Patients entered into the study will receive ASTX727 orally for 5 days, prior to receiving Lutathera treatment on Day 8, to determine whether pre-treatment with ASTX727 results in re-expression of somatostatin receptor-2 in patients with metastatic neuroendocrine tumours. The study will use [68Ga]-DOTA-TATE PET to image epigenetic modification of the receptor locus.

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Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Hammersmith Hospital

London, London, City of, W12 0HS, United Kingdom

Location status: Recruiting

Location contact

Rohini Sharma, MD

CONTACT

[email protected]

02075942807

About this study

Patients with neuroendocrine tumours (NET) who are found to be eligible will receive up to 4 doses of Lutathera on this trial. All participants will receive ASTX727 orally (cedazuridine 100mg + 35mg decitabine) Days 0-5 prior to receiving Lutathera Day 8 +/- 2days. Each cycle will be repeated every 2 months for 4 cycles unless unacceptable toxicity, progression of disease or withdrawal of patients' consent. Restaging will occur after 2 cycles of Lutathera and at the end of treatment. Patients will be followed 3 monthly until disease progression, death or withdrawal of patients' consent.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Be willing and able to provide written informed consent for the trial.
  • Be aged 18 or over at the day of signing consent
  • Histologic or cytologic confirmed diagnosis of neuroendocrine tumour
  • Have archival tissue block available or willing to have fresh tissue biopsy if blocks not available
  • Have disease that can be readily biopsied by ultrasound guidance (n=5)
  • Ki67 < 55% (only patients with well differentiated grade 1-3 NETs will be included in the study as patients with poorly differentiated grade 3 NETs have a prognosis of less than 6 months)
  • Progression or intolerance to first line therapy including somatostatin analogues
  • ECOG Performance status 0 - 2
  • No tumoural uptake on [68Ga]-DOTA-TATE or uptake less than background liver
  • Measurable disease based on RECIST 1.1. Lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions
  • Adequate organ function as outlined in the protocol
  • Women of childbearing potential must be willing to use a highly effective method of contraception as outlined in the protocol for the course of the study through 6 months after the last dose of Investigational Medicinal Product (IMP).

Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the subjects

  • Sexually active males must agree to use an adequate method of contraception as outlined in the protocol starting with the first dose of IMP through 6 months after the last dose of study therapy. Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the subject

Exclusion criteria

  • Previous treatment with either study medication and/or known hypersensitivity to the study medication
  • Serious concurrent medical illness, including serious active infection
  • History of organ transplant
  • Has a known history of Human Immunodeficiency Virus (HIV). Note: No HIV testing is required unless mandated by local health authority.
  • Has a known history of active Bacillus Tuberculosis (TB).
  • Has known active CNS metastases and/or carcinomatous meningitis. Participants with previously treated brain metastases may participate provided they are radiologically stable, i.e. without evidence of progression for at least 4 weeks by repeat imaging (note that the repeat imaging should be performed during study screening), clinically stable and without requirement of steroid treatment for at least 14 days prior to first dose of study treatment.
  • Bleeding or thrombotic disorders or subjects at risk for severe haemorrhage
  • Is currently participating and receiving therapy or has participated or is participating in a study of an IMP or used an investigational device within 4 weeks of the first dose of IMP.
  • Has a known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer.
  • Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating Principal Investigator (PI).
  • Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
  • Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the screening visit through to 6 months after the last dose of IMP.
  • Has received a live vaccine within 30 days of first dose of ASTX727 administration. Note: Seasonal influenza vaccines for injection are generally inactivated flu vaccines and are allowed; however intranasal influenza vaccines (e.g., Flu-Mist®) are live attenuated vaccines, and are not allowed.
  • Has received prior radiotherapy within 2 weeks of start of study treatment. Participants must have recovered from all radiation-related toxicities, not require corticosteroids, and not have had radiation pneumonitis. A 1-week washout is permitted for palliative radiation (≤2 weeks of radiotherapy) to non-CNS disease and stereotactic radiotherapy to the CNS
  • Other clinically significant co-morbidities that could compromise the subject's participating in the study

Treatment and study plan

ASTX727

Drug

Cedazuridine 100mg + 35mg decitabine

Lutathera

Radiation

Peptide receptor radionuclide therapy (PRRT)

Other names: lutetium Lu 177 dotatate

Primary outcomes

  1. To determine whether pre-treatment with ASTX727 results in re-expression of SSTR2 in patients with metastatic NETs, using [68Ga]-DOTA-TATE to image epigenetic modification of the SSTR2 locus allowing subsequent treatment with Lutathera

    Time frame: Through study completion, an average of 1 year

    This outcome will be assessed using a specific PET scan

Secondary outcomes

  1. To assess tolerability of combination therapy

    Time frame: Through study completion, an average of 1 year

    This outcome will be assessed using CTCAE v5.0

  2. To assess response to treatment using conventional imaging

    Time frame: Through study completion, an average of 1 year

    This outcome will be assessed using standard of care CT scans

  3. To assess patients quality of life during treatment

    Time frame: Through study completion, an average of 1 year

    This will be assessed using standardised quality of life questionnaires, which will be given to the patients

  4. To assess progression free survival

    Time frame: Through study completion, an average of 1 year

    This will be the time until patients show progressive disease on their routine CT scans

Study contacts

Contact information is provided by the study sponsor or research team.

Rohini Sharma, Professor

CONTACT

[email protected]

02083833170

Sponsors and collaborators

Lead sponsor

Imperial College London

Other

Collaborators

  • Advanced Accelerator Applications

Registry information

Official study title

The Epigenetic Modification of Somatostatin Receptor-2 to Improve Therapeutic Outcome With Lutathera in Patients With Metastatic Neuroendocrine Tumours.

Acronym: LANTana

Important dates

Study start
2022
Primary completion
2026
Study completion
2029
First posted
Jan 5, 2022
Registry last updated
Nov 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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