Serial Tumour Biopsies and Blood Biomarkers in Melanoma
Molecular Characterisation of Serial Tumour Samples and Their Correlation With Circulating Biomarkers and Other Biospecimens Taken During the Clinical Course of Patients Receiving Treatment for Malignant Melanoma.
Recent advances in understanding how cancer develops and spreads have led to effective new treatments and improved outcomes for patients with melanoma. However, we know that these new treatments do not work for all patients: some do not respond to them and some initially respond but then develop resistance. The overall aim of this study will be to collect tumour biopsies, biomarkers present in the blood, and other biological specimens which can be used to try to understand why resistance to anti-cancer treatment occurs, and to develop predictive biomarkers of this resistance in patients with locally advanced and metastatic malignant melanoma.
The study will be open to NHS patients aged 16 and over, who have been diagnosed with advanced melanoma, and who will be receiving treatment for their disease as part of their routine care. Patients will be asked to provide samples from tumour biopsies before, during and after treatment. We will also ask for blood samples to look at biomarkers in the blood and see how these correspond with tumour samples, which will further help us to understand treatment response. Biomarkers are substances in the body that can be measured and help indicate how a disease is developing. It is hoped that soon we will be able to monitor cancer by analysing a patient's blood samples, thus reducing the need for biopsies. As blood tests could be taken more frequently, signs that patients are becoming resistant to treatments could be picked up sooner.
As well as monitoring biomarkers, we would also like to understand what happens to the healthy cells surrounding the tumour during treatment. This will improve our understanding of how cells adapt and respond to treatments, and may eventually lead to the discovery of new biomarkers to help predict which patients will develop resistance to certain treatments.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
This will be a prospective study recruiting patients who have been diagnosed wth advanced melanoma.
Participants will be asked to give informed consent before any samples are collected.
Participants will be asked to donate tissue and other biospecimens (see list below) that are surplus to clinical requirements if a participant is undergoing any of the following as part of their routine care:
- lymph node dissection
- sentinel lymph node biopsy as part of their normal care
- resection of metastatic skin lesions or visceral disease
- medical treatment for Stage IV disease Biospecimens include urine, stool, saliva, hair follicles, ascitic, pleural, pericardial or cerebrospinal fluid Collection of archival tumour tissue from previous biopsy/surgery that is surplus to clinical requirements will also be requested, where available.
Participants will be asked to consent to having easily accessible lesions biopsied or resected, which are not required for clinical reasons, but are for research purposes only. Participants can still be part of the study even if they do not agree to these extra, optional biopsies. Tissue samples from the surgical specimens and the original primaries will be examined to look for molecular markers to correlate with circulating tumour molecular markers.
Consent will be requested to grow cell lines from the donated tumour tissue and implant tumour tissue into mice to characterise the genetic changes seen in both CTCs and biopsies, in terms of resistance to targeted agents, in the lab setting. Consent to this part of the study will be optional.
A maximum of 50mls blood sample will be requested from participants before any intervention. Further blood samples (maximum of 50mls each time) will also be requested as follows:
- after surgery, on subsequent routine follow up at 3 months, and then 3 monthly thereafter (i.e. approximately 4 times in a year after the initial pre and post surgical specimens)
- at the time of disease recurrence
- If on treatment, then usually approximately 3 weeks after starting treatment, and then every 2 cycles of treatment
- at disease progression The samples will be tested for various circulating tumour biomarkers.
We will be asking a small group of patients, approx 20, to consent to weekly blood samples, for up to 8 weeks, for specific biomarker analyses.
Clinical data will be collected for each patient, looking at demographics, baseline haematology and biochemistry blood results, radiological extent of disease, time to disease progression, clinical and histological features of the primary. Patients will be followed up for approximately 10 years to assess their outcome.
Type d'étude
Inscription (Anticipé)
Contacts et emplacements
Coordonnées de l'étude
- Nom: Gupta, Dr
- Numéro de téléphone: 0161 446 3472
- E-mail: avinash.gupta@christie.nhs.uk
Sauvegarde des contacts de l'étude
- Nom: Valpione, Dr
- E-mail: sara.valpione@christie.nhs.uk
Lieux d'étude
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Manchester, Royaume-Uni, M20 4BX
- Recrutement
- The Christie
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Contact:
- Dr Gupta
- Numéro de téléphone: 0161 446 3472
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- Age of 16 years or more.
- Patients must have given written informed consent.
- Evidence of locally advanced or metastatic melanoma, i.e. stage III or IV disease.
- Accessible tumour that can be safely biopsied using radiological or surgical techniques (if consenting to part A).
- Full blood count and coagulation tests within acceptable parameters (if consenting to part A).
Exclusion Criteria:
- Inability to provide informed consent.
- History of significant bleeding disorder (patients on anticoagulation are eligible if the anticoagulation can be safely managed to allow fresh tumour biopsies and blood sampling).
- History of HIV, Hepatitis B/C or other transmissible human disease.
- Any conditions where research biopsies or blood sampling may increase risk of complications for the patient and/or investigator, including high risk groups such as intravenous drug users.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
|
Tous les participants
Tous les participants éligibles et consentants seront invités à donner du sang, des tissus et d'autres échantillons biologiques à des fins de recherche
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To collect tumour tissue
Autres noms:
To collect blood samples
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
The number of patients who consent to have additional samples taken for research purposes and the number of research samples collected.
Délai: Duration of study, 300 participants over 16 years
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This is primarily a sample collection study, where tissue will be used in future experiments to further understand mechanisms of disease resistance.
This study will however assess patients acceptability to enrol in a study, where biological samples are taken purely for research, and not part of routine care.
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Duration of study, 300 participants over 16 years
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Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Lorigan, Prof, University of Manchester
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Anticipé)
Achèvement de l'étude (Anticipé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- CFTSp157
- 18/NW/0515 (Autre identifiant: Preston NW REC)
- 132792 (Autre identifiant: IRAS)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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