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CompletedNCT02553954SkinAgeUpdated Mar 18, 2026

Molecular Mechanisms of Senescence Predisposing to Cancer : Exploratory Analysis on Healthy Tissues (SkinAge).

An interventional study of Collection of healthy skin tissue in Sarcoma, sponsored by Centre Oscar Lambret. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-18.

Sponsored by Centre Oscar Lambret · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 11 months after the study started (first participant enrolled Oct 2014, registered Sep 2015).
Phase
Not applicable
Study type
Interventional
Enrollment
58
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

Epidemiological data show that the incidence of carcinoma, the most common cancer, is strongly linked to the age. Non Melanoma Skin Carcinomas (NMSCs) (the most frequent cancers in the elderly population) derive from keratinocytes of the basal layer of the epidermis, from differentiated keratinocytes of the more superficial layers or from stem cells of hair follicles. Unlike NMSCs, soft-tissue sarcomas, including those deriving from dermal fibroblasts, are very rare (less than 1% of all cancers). Our overall purpose is to decipher the molecular pathways activated during the aging of these tissues that may explain why they have a so different propensity to undergo a malignant transformation. Given that senescent cells accumulate in the dermis and epidermis with age, we will constitute two groups : "young skin" that we arbitrarily limit to the range ≥ 18 and ≤ 40 and "aged skin" ≥ 55.

Thus the main objective of our study is to search within 2 age groups (≥ 18 and ≤ 40 years and ≥ 55 years) the expression of senescence markers on healthy skin tissue.

Read the detailed description
  • Information and obtaining informed consent.
  • Collection of clinical data.
  • Collection of two samples of healthy skin tissue, without disfigurement, during an intervention under general anesthesia for the treatment of a sarcoma.
  • Freezing samples of healthy skin tissue in liquid nitrogen within 10 minutes after collection.
  • Transfer of the samples to the laboratory of anatomopathology.
  • Preparation of the healthy skin samples by the laboratory of anatomopathology.
  • Transfer of the conditioned samples to the Institut de Biologie de Lille for analysis.
  • Control of the aesthetic appearance during the postoperative consultation.
  • Destruction of the samples at the end of analysis.
02

Conditions studied

  • Sarcoma

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Keywords

  • Mechanisms of Senescence
  • Senescence markers
03

In context

Sarcoma

1,667 studies on the registry are indexed under Sarcoma; 393 are open to participants now.

This study's enrollment of 58 is above the median of 40 across 1,283 interventional studies indexed under Sarcoma.

Browse Sarcoma studies →

Lead sponsor

Centre Oscar Lambret is the lead sponsor of 127 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patient with an operable sarcoma
  • Requiring a surgical operation under general anesthesia at the Oscar Lambret Centre
  • Age ≥ 18 ans, belonging to one of the two following age groups : [ ≥ 18 and ≤ 40 years] and [ ≥ 55 years]
  • Patient having a social security scheme
  • Patient having signed an informed consent form for the study

Exclusion criteria

Exclusion Criteria:

  • Patient aged under 18 or between 41 and 54
  • Location of the tumor on the face, neck or neckline
  • Patient with a skin tumor
  • Tumor-induced cutaneous fistula making suspect a tumor invasion of the skin
  • Patient with a chronic skin disease
  • Collection in an area already treated by surgery, radiotherapy or brachytherapy
  • Pregnant or breastfeeding women
  • Patient under guardianship or tutorship
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
58 participants (actual)

Study arms

  • Experimental
    Collection of healthy skin tissue

    Collection of healthy skin tissue

    Procedure: Collection of healthy skin tissue

Interventions

  • ProcedureCollection of healthy skin tissue

    Collection of two samples of healthy skin tissue, without disfigurement, during an intervention under general anesthesia for the treatment of a benign or malignant tumor.

06

What researchers measure

Primary outcomes

  1. Expression of senescence markers in healthy skin tissues collected for the two age groups.

    Time frame: Baseline

Secondary outcomes

  1. Research of emerging cells in the skin tissue of the subjects of the two age groups via the expression of the Protease-Activated Receptor-1 (PAR-1).

    Time frame: Baseline

  2. Presence of different types of DNA damage (single and double strand breaks) in the keratinocytes and fibroblasts of the skin tissues of the two age groups.

    Time frame: Baseline

  3. Morbidity

    Postoperative complications up to 30 days after surgery according to the Clavien-Dindo classification (2009), according to the NCI-CTCAE v4.0 beyond this deadline.

    Time frame: Baseline

07

Study locations

1 site
  • Centre Oscar Lambret
    Lille, 59020, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02553954
Lead sponsor
Centre Oscar Lambret
Collaborators
Institut de Biologie de Lille
Responsible party
Sponsor
First posted
Sep 18, 2015
Start date
Oct 7, 2014
Primary completion
Apr 16, 2019
Completion
Apr 2020
Last update
Mar 18, 2026

Study contacts

Nicolas PENEL, MD
study chair · Centre Oscar Lambret
Olivier PLUQUET
study director · Institut de Biologie de Lille

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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