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The Identification of Novel Prognostic Markers in Melanoma

Novel Prognostic Markers in Melanoma: a Protocol for the Analysis of Paraffin-embedded Tumour Samples

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01002560
Enrollment
500
Registered
2009-10-27
Start date
2008-12-31
Completion date
2009-12-31
Last updated
2009-10-27

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

Conditions

Malignant Melanoma

Keywords

Melanoma, Novel Prognostic Markers

Brief summary

The purpose of this project is to analyze tumour tissue from a group of subjects with malignant melanoma, who have been treated at the Royal Marsden Hospital.

Detailed description

Background - The Royal Marsden Hospital and the Institute of Cancer Research constitute the largest comprehensive cancer centre in Europe. In addition to an in-house drug development program, phase I - phase III clinical trials of novel anti-cancer agents are hosted. In order to investigate the optimal use of novel molecularly targeted agents, access to clinical tumour samples is needed in order to determine which particular cancer type expresses a molecular signature that may indicate potential therapeutic utility. Understanding such signatures should accelerate the registration of new drugs for routine cancer therapy; offering the potential of selecting those patients with tumour types most likely to benefit from therapy. Furthermore, new insights into disease biology may be gained. Main research question/ objective - Are there features of primary melanoma or lymph node metastases that predict subsequent clinical outcome better than existing markers?

Interventions

None listed

Sponsors

Royal Marsden NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Diagnosis of melanoma * Adequate paraffin-embedded material available for analysis. * Adequate clinical follow-up information * Written informed consent where applicable

Exclusion criteria

* Inadequate paraffin-embedded material available * Inadequate clinical follow-up information.

Design outcomes

Primary

MeasureTime frame
Given that the nature of the research is qualitative, there is no primary outcome measure.

Countries

United Kingdom

Contacts

Primary ContactProfessor Martin Gore
martin.gore@rmh.nhs.uk02078082198

Outcome results

None listed

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