Efficacy and Safety of Laser-Assisted Combination Chemotherapy: An Explorative Imaging-Guided Treatment With 5-Fluorouracil and Cisplatin for Basal Cell Carcinoma.

ablative fractional CO2 laser laser ablation mass spectrometry imaging optical coherence tomography physical enhancement reflectance confocal microscopy skin cancer topical drug delivery

Journal

Lasers in surgery and medicine
ISSN: 1096-9101
Titre abrégé: Lasers Surg Med
Pays: United States
ID NLM: 8007168

Informations de publication

Date de publication:
01 2021
Historique:
received: 06 07 2020
revised: 30 08 2020
accepted: 09 09 2020
pubmed: 23 9 2020
medline: 29 10 2021
entrez: 22 9 2020
Statut: ppublish

Résumé

Rising incidences of basal cell carcinoma (BCC) have increased the need for effective topical therapies. By enhancing cutaneous uptake of the chemotherapeutic agents, cisplatin and 5-fluorouracil (5-FU), laser-assisted delivery may provide a new combination treatment for BCC. Accordingly, this study aimed to evaluate tumor response, safety, and drug biodistribution in tumors and blood after topical laser-assisted 5-FU + CIS treatment in BCC patients. This open-label, proof-of-concept trial investigated laser-assisted combination cisplatin + 5-FU treatment in 20 patients with histologically verified, low-risk superficial or nodular BCCs on the face (<20 mm) or trunk/extremities (<50 mm). After tumor demarcation guided by optical coherence tomography (OCT), BCCs were exposed to ablative fractional CO Nineteen patients completed the trial, with 32% (6/19) receiving a single treatment and 68% (13/19) treated twice. At 3 months, clinical clearance was seen in 18/19 patients with a corresponding 94% (17/18) achieving histological clearance. Baseline tumor thickness and subtype did not influence treatment number or clearance rate (P ≥ 0.61). LSRs were well-tolerated and consisted of erythema, edema, and erosion, followed by crusting by day 14. Erythema declined gradually by month 3, with 94% of patients and 79% of physicians rating cosmesis as "good" or "excellent." Scarring or hyperpigmentation was noted in 50% and 56%, respectively, while pain and infection were not observed during the follow-up period. Although chemotherapy uptake was visualized extending to deep skin layers, no systemic exposure to cisplatin or 5-FU was detected in patient blood. Laser-assisted cisplatin + 5-FU shows potential as an effective and tolerable treatment option for low-risk BCC, particularly in instances where self-application is not possible or where in-office, non-surgical therapy is preferred. Lasers Surg. Med. © 2020 Wiley Periodicals LLC.

Sections du résumé

BACKGROUND AND OBJECTIVES
Rising incidences of basal cell carcinoma (BCC) have increased the need for effective topical therapies. By enhancing cutaneous uptake of the chemotherapeutic agents, cisplatin and 5-fluorouracil (5-FU), laser-assisted delivery may provide a new combination treatment for BCC. Accordingly, this study aimed to evaluate tumor response, safety, and drug biodistribution in tumors and blood after topical laser-assisted 5-FU + CIS treatment in BCC patients.
STUDY DESIGN/MATERIALS AND METHODS
This open-label, proof-of-concept trial investigated laser-assisted combination cisplatin + 5-FU treatment in 20 patients with histologically verified, low-risk superficial or nodular BCCs on the face (<20 mm) or trunk/extremities (<50 mm). After tumor demarcation guided by optical coherence tomography (OCT), BCCs were exposed to ablative fractional CO
RESULTS
Nineteen patients completed the trial, with 32% (6/19) receiving a single treatment and 68% (13/19) treated twice. At 3 months, clinical clearance was seen in 18/19 patients with a corresponding 94% (17/18) achieving histological clearance. Baseline tumor thickness and subtype did not influence treatment number or clearance rate (P ≥ 0.61). LSRs were well-tolerated and consisted of erythema, edema, and erosion, followed by crusting by day 14. Erythema declined gradually by month 3, with 94% of patients and 79% of physicians rating cosmesis as "good" or "excellent." Scarring or hyperpigmentation was noted in 50% and 56%, respectively, while pain and infection were not observed during the follow-up period. Although chemotherapy uptake was visualized extending to deep skin layers, no systemic exposure to cisplatin or 5-FU was detected in patient blood.
CONCLUSION
Laser-assisted cisplatin + 5-FU shows potential as an effective and tolerable treatment option for low-risk BCC, particularly in instances where self-application is not possible or where in-office, non-surgical therapy is preferred. Lasers Surg. Med. © 2020 Wiley Periodicals LLC.

Identifiants

pubmed: 32960987
doi: 10.1002/lsm.23323
doi:

Substances chimiques

Cisplatin Q20Q21Q62J
Fluorouracil U3P01618RT

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

119-128

Informations de copyright

© 2020 Wiley Periodicals LLC.

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Auteurs

Emily Wenande (E)

Department of Dermatology, Bispebjerg University Hospital, University of Copenhagen, Copenhagen NV, 2400, Denmark.
Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, 02114, USA.

Kristoffer Hendel (K)

Department of Dermatology, Bispebjerg University Hospital, University of Copenhagen, Copenhagen NV, 2400, Denmark.

Mette Mogensen (M)

Department of Dermatology, Bispebjerg University Hospital, University of Copenhagen, Copenhagen NV, 2400, Denmark.

Charlotte Bagger (C)

Department of Pharmacy, University of Copenhagen, Copenhagen NV, 2100, Denmark.

Nina L Mårtensson (NL)

Department of Pathology, Rigshospitalet, University of Copenhagen, Copenhagen NV, 2100, Denmark.

Daniel P Persson (DP)

Department of Plant and Environmental Sciences (PLEN), University of Copenhagen, Frederiksberg, 1871, Denmark.

Catharina M Lerche (CM)

Department of Dermatology, Bispebjerg University Hospital, University of Copenhagen, Copenhagen NV, 2400, Denmark.

Søren Husted (S)

Department of Plant and Environmental Sciences (PLEN), University of Copenhagen, Frederiksberg, 1871, Denmark.

Christian Janfelt (C)

Department of Pharmacy, University of Copenhagen, Copenhagen NV, 2100, Denmark.

Katrine Togsverd-Bo (K)

Department of Dermatology, Bispebjerg University Hospital, University of Copenhagen, Copenhagen NV, 2400, Denmark.

Richard R Anderson (RR)

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, 02114, USA.

Merete Haedersdal (M)

Department of Dermatology, Bispebjerg University Hospital, University of Copenhagen, Copenhagen NV, 2400, Denmark.
Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, 02114, USA.

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