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NCT Number: NCT05874492

Evaluation of the Medical Benefit of Spa Therapy on Fibrosis After Radiotherapy for Breast Cancer or UADT (Upper Aerodigestive Tract) Cancer

FIBROTHERME is a comparative, controlled, randomized, multicenter and simple blinded (investigator) trial.

The aim of this study is to evaluate the medical benefit in terms of quality of life on the dermatological sequelae of fibrosis 6 months after a dermatologically oriented spa therapy in patients with severe late reactions affecting the skin and/or soft tissues at least 6 months after radiotherapy for breast cancer or UADT (Upper Aerodigestive Tract) cancer.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Clinique Tivoli-Ducos, Bordeaux, France

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About this study

Radiation-induced fibrosis is an equivalent of an "orphan disease", in which oncologists have only recently shown interest, despite its prevalence. No study on the medical service provided by crenotherapy has been published in late radiation-induced fibrosis, which shares a common pathophysiology and medico-psycho-social sequelae with the sequelae of burns.

Chronic progressive dermatoses are part of the 12 main therapeutic orientations of medical thermalism. In particular, burn scars are a very current indication. Crenotherapy allows the attenuation, or even the disappearance of: pruritus and dysesthesia, local inflammation, hypertrophy and sclerosis and favours the recovery of chronic superficial erosions. Fibrous scars, even old ones, respond favourably to thermal treatments. The thermal treatment combines baths which have a sedative, muscle-relaxing effect and which favour joint mobilisation, sprays which have a decongestant effect and above all thread-like showers which are carried out by jets of thermal water under high pressure for several minutes.

The primary endpoint is the self-assessment by the patient of the dermatological quality of life by the DLQI score at 6 months after the end of the treatment compared between the intervention group (immediate treatment) and the control group (delayed treatment after 6 months).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years
  • In situ or invasive breast cancer or cancer of the upper aerodigestive tract
  • DLQI ≥ 6 (at least moderate effect on patient's life)
  • General status WHO 0-1
  • Radiotherapy completed at least 6 months ago (with no maximum post radiotherapy delay)
  • Unilateral breast radiotherapy for breast cancer patients
  • Skin or soft tissue toxicity (- modules: Skin atrophy, fibrosis of deep connective tissues, fibrosis of superficial soft tissues) CTCAE v4.0 grade ≥ 2
  • No inflammatory or infectious flare at inclusion
  • Female of childbearing potential: negative urine pregnancy test at inclusion
  • Patient informed and signed consent
  • Affiliation to a social security systeme or equivalent

Exclusion criteria

  • Progressive phase of cancer
  • Metastatic disease
  • Patient undergoing specific treatment for breast cancer (except adjuvant hormone therapy and/or adjuvant herceptin)
  • Bilateral breast/parietal radiotherapy
  • Breast prosthesis wearer for breast cancer patients
  • Patient with a tracheostomy for patients with head and neck cancer
  • Obvious skin ulceration in the site of interest
  • Contraindication to spa treatment (acute inflammatory disease, active infections, heart failure with NYHA stage > 1, chronic respiratory failure, labile hypertension, bullous disease)
  • Chronic progressive dermatological disease
  • Women who are pregnant or likely to become pregnant within 6 months or who are breastfeeding
  • Persons deprived of liberty or under guardianship

Treatment and study plan

Thermal cure with a primary dermatological indication

Other

The thermal treatment combines baths which have a sedative, muscle-relaxing effect and encourage joint mobilisation, sprays which have a decongestant effect and, above all, thread-like showers which are carried out by jets of thermal water under high pressure for several minutes plus educational workshops (relaxation, sophrology, hygiene...)

Primary outcomes

  1. Evaluation of the medical benefit in terms of quality of life on the dermatological sequelae of fibrosis after a dermatologically oriented spa treatment.

    Time frame: 6 months

    Self-assessment by the patient of the dermatological quality of life by the DLQI (Dermatology Life Quality Index) score at 6 months after the end of the treatment compared between the intervention group (immediate treatment) and the control group (delayed treatment after 6 months). The DLQI score is between 0 and 30 where a high score indicates a significant impairment of quality of life.

Secondary outcomes

  1. Generic quality of life

    Time frame: 6 months

    Evaluation of the medical benefit on generic quality of life. Patient self-assessment of generic quality of life using the EQ5D-3L. EQ-5D-3L is a standardized instrument developed by the EuroQol Group as a measure of health-related quality of life that can be used in a wide range of health conditions and treatments. The EQ5D has 6 items intended to measure general health. The index score is between -0.53 and 1 where a high value indicates a good quality of life. The perceived health status is between 0 and 100 where a high value indicates good health.

  2. Cancer quality of life

    Time frame: 6 months

    Evaluation of the medical benefit on quality of life in patients with breast cancer or Upper Aerodigestive Tract (UADT) Cancer. Patient self-assessment of quality of life using the EORTC (European Organisation for Research and Treatment of Cancer) QLQ C30 Score (Quality of Life of Cancer Patients). The EORTC QLQ-C30 has 15 domains. There is no total score. For each domain, the score is between 0 and 100 where a high score for overall health and functional dimensions represents a good quality of life; and a high score for symptomatic dimensions represents a high level of symptoms.

  3. Senological or Upper Aerodigestive Tract (UADT) Cancer quality of life

    Time frame: 6 months

    Evaluation of the medical benefit on the quality of senological life or Upper Aerodigestive Tract (UADT) Cancer. Patient self-assessment of breast quality of life using the specific QLQ-BR23 module (breast cancer-specific quality of life questionnaire).

    Patient self-assessment of Upper Aerodigestive Tract (UADT) Cancer quality of life using the specific QLQ-H&N43 module (Quality of life in patients with head and neck cancer).

  4. Sequelae self assessment

    Time frame: 6 months

    Evaluation of the medical benefit on the self-assessment of the impact of radio induced sequelae. Self-assessment by the patient with an evaluation of the severity of the radiation-induced sequelae via the Pro-CTCAE self-questionnaire (Item 1: dry mouth, Item 2: difficulty swallowing, Item 3: mouth/throat sores, Item 4: cracked corners of the mouth, Item 5: changes in voice quality, Item 6: hoarseness, Item 7: changes in taste (Items 1-7 specific to head and neck cancer), item 25: skin dryness, item 28: itching, item 36: skin reaction to radiation, item 37: skin darkening, item 48: general pain, item 53: fatigue, item 54: anxiety, item 56: sadness, item 72: breast swelling and tenderness (item 72 specific to breast cancer)).

  5. Lesions radiological assessment

    Time frame: 6 months

    Hetero-evaluation of the clinical and imaging efficacy of treatment on post-radiation lesions with CTCAE scale (Common Terminology Criteria for Adverse Events). There is no total score. For each domain, the rank is between 1 and 5 where a high score represents the death.

  6. Thickness radiological assessment

    Time frame: 6 months

    Hetero-evaluation of the clinical and imaging efficacy of treatment on post-radiation lesions of thickness. Imaging assessment with blinded measurement by an independent radiologist of comparative thickness by ultrasound: Dermal radiotoxicity for breast cancer can indeed be defined as the difference in dermal thickness between the 2 breasts (lesion area and mirror area of the contralateral breast). Cutaneous radiotoxicity in head and neck cancers will be assessed by comparing irradiated areas with unexposed control areas.

    Dermal thickness is defined as the distance between the input ultrasound signal and the signal at the dermal-hypodermal interface at 6 months.

  7. Volumetric aspect radiological assessment

    Time frame: 6 months

    Hetero-evaluation of the clinical and imaging efficacy of treatment on post-radiation lesions with HBCS (Harvard-Breast-Cosmesis-Scale). Evaluation of the cutaneous and volumetric aspect by an evaluation carried out by the practitioner with the Harvard-breast-cosmesis-scale (HBCS) score at 6 months. The HBCS score is assessed by a 4-point Likert scale where a high value indicates a high severity, 1 represents excellent breast shape or texture, 2 means good, 3 average and 4 poor with a severely deformed breast.

  8. Consumption of treatment

    Time frame: 6 months

    Comparison of the type of treatment between the 2 groups.

  9. Consumption of medical consultation

    Time frame: 6 months

    Comparison of the number of hospitalisations, consultations, physiotherapy, specific cosmetic consultations between the 2 groups.

  10. Adverse events

    Time frame: 6 months

    Comparison of the adverse events in the 2 groups. Description of adverse events between the 2 groups.

  11. Long-term cure quality of life benefice

    Time frame: 12 months

    Evaluation of the stability of the long-term effect for the immediate cure group. Evaluation of the maintenance of benefits at 12 months (stability of the long term effect) on the primary outcome and secondary outcomes. Self-assessment by the patient of the dermatological quality of life by the DLQI (Dermatology Life Quality Index).

  12. Treatment effect size

    Time frame: 12 months

    Evaluation of the effect size of the treatment for the delayed treatment group. Confirmation of the size of the effect of the treatment on the primary and main secondary endpoints between 6 and 12 months.

  13. Subgroup analysis of the primary outcome

    Time frame: 6 months

    Stratification based on the location of the treated site (following breast cancer or cancer of the upper aerodigestive tract). Stratification by center to test for a center effect.

Study contacts

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

Claire Eychenne

CONTACT

[email protected]

0476766413

Nans FUSTIER

CONTACT

[email protected]

0476765040

Sponsors and collaborators

Lead sponsor

Association Francaise pour la Recherche Thermale

Other

Collaborators

  • Floralis

Registry information

Official study title

Evaluation of the Medical Benefit of a Spa Therapy on the Evolutionary Genius of Late Sequelae Fibrosis After Radiotherapy for Breast Cancer or UADT (Upper Aerodigestive Tract) Cancer in Remission

Acronym: FIBROTHERME

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
May 25, 2023
Registry last updated
Apr 13, 2026

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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