Effectiveness of an N-acetylcysteine and Urea-based Cream in Prevention of Capecitabine-induced HAND-foot Syndrome in Breast Cancer Patients

Last updated: October 14, 2024
Sponsor: Centro di Riferimento Oncologico - Aviano
Overall Status: Active - Recruiting

Phase

N/A

Condition

Breast Cancer

Cancer

Treatment

DECLARAN cream

Clinical Study ID

NCT06639178
CRO-2023-28
  • Ages > 18
  • All Genders

Study Summary

Breast cancer (BC) is the most frequent tumour in women. To date, among the available treatments, the use of Capecitabine, an oral prodrug of fluorouracil, has been shown activity in different setting. In advanced disease, Capecitabine is often used as monotherapy in patients pretreated with anthracycline, taxane or both.

One of the most frequent toxicities reported by patients receiving capecitabine is hand-foot syndrome (HFS), with an incidence of grade 3 HFS of 28%. HFS, also known as palmar-plantar erythrodysesthesia syndrome, is initially characterized by palmoplantar numbness, tingling, or burning pain. These symptoms usually coincide with sharply demarcated erythema with or without edema, cracking, or desquamation. In advanced stages, blistering and ulceration may occur. Although HFS is not considered life threatening, it can be painful and interfere with daily activities, thusseriously compromising quality of life (QoL), therefore this toxicity is considered dose limiting.Moreover, consistent with the theory that Capecitabine and its metabolites induce an inflammatory effect, the use of COX-2 inhibitors is an emerging strategies, but more evidence are needed from largest study to confirm their efficacy.

Similarly, N-acetylcysteine (NAC), an antioxidant, mucolytic and nephroprotective agent, that affects pathways involved in inflammatory conditions and that has demonstrated to be effective in several dermatologic conditions, could be useful in the management of Capecitabine-induced HFS.

From this arises the present study that has the objective of evaluating the role of NAC plus urea-based cream in the prevention of Capecitabineinduced HFS in patient affected by breast cancer.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Women and men ≥18 years old

  • Patients with diagnosis of breast cancer with stage I-III radically operated withresidual disease post neoadjuvant treatment or stage IV

  • Patients candidated for capecitabine in a post-neoadjuvant or metastatic settingtreated with 2000-2500 mg/m2 d1-14 q21, or 1500 mg daily continuously (metronomicschedule)

  • Patients who provided written informed consent

Exclusion

Exclusion Criteria:

  • Patients previously treated with drugs that may have induced HFS

  • Assessed by the investigator to be unable or unwilling to comply with therequirements of the protocol

  • Pregnant, lactating, or breastfeeding, or intending to become pregnant during thestudy or within 60 days after the final dose of study treatmen

Study Design

Total Participants: 25
Treatment Group(s): 1
Primary Treatment: DECLARAN cream
Phase:
Study Start date:
August 01, 2024
Estimated Completion Date:
May 15, 2026

Study Description

Breast cancer (BC) is the most frequent tumour in women. To date, among the available treatments, the use of Capecitabine, an oral prodrug of fluorouracil, has been shown activity in different setting. In advanced disease, Capecitabine is often used as monotherapy in patients pretreated with anthracycline, taxane or both.

One of the most frequent toxicities reported by patients receiving capecitabine is hand-foot syndrome (HFS), with an incidence of grade 3 HFS of 28%. HFS, also known as palmar-plantar erythrodysesthesia syndrome, is initially characterized by palmoplantar numbness, tingling, or burning pain. These symptoms usually coincide with sharply demarcated erythema with or without edema, cracking, or desquamation. In advanced stages, blistering and ulceration may occur. Although HFS is not considered life threatening, it can be painful and interfere with daily activities, thusseriously compromising quality of life (QoL), therefore this toxicity is considered dose limiting.Moreover, consistent with the theory that Capecitabine and its metabolites induce an inflammatory effect, the use of COX-2 inhibitors is an emerging strategies, but more evidence are needed from largest study to confirm their efficacy.

Similarly, N-acetylcysteine (NAC), an antioxidant, mucolytic and nephroprotective agent, that affects pathways involved in inflammatory conditions and that has demonstrated to be effective in several dermatologic conditions, could be useful in the management of Capecitabine-induced HFS.

From this arises the present study that has the objective of evaluating the role of NAC plus urea-based cream in the prevention of Capecitabineinduced HFS in patient affected by breast cancer.

Connect with a study center

  • Centro di Riferimento Oncologico (CRO) di Aviano - IRCCS

    Aviano, Pordenone 33081
    Italy

    Active - Recruiting

  • Azienda Sanitaria Universitaria del Friuli Centrale (ASUFC)

    Udine, 33100
    Italy

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.