Pencil Beam Scanning Proton Beam Chemoradiation Therapy With 5-Fluorouracil and Mitomycin-C for Definitive Treatment of Carcinoma of the Anal Canal: A Multi-institutional Pilot Feasibility Study.
Aged
Anal Canal
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Anus Neoplasms
/ pathology
Carcinoma, Squamous Cell
/ pathology
Chemoradiotherapy
/ adverse effects
Colostomy
Feasibility Studies
Female
Fluorouracil
/ administration & dosage
Follow-Up Studies
Humans
Kaplan-Meier Estimate
Male
Middle Aged
Mitomycin
/ administration & dosage
Pilot Projects
Progression-Free Survival
Prospective Studies
Proton Therapy
/ adverse effects
Radiodermatitis
/ pathology
Radiotherapy Dosage
Journal
International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616
Informations de publication
Date de publication:
01 09 2019
01 09 2019
Historique:
received:
27
11
2018
revised:
19
04
2019
accepted:
26
04
2019
pubmed:
28
5
2019
medline:
17
1
2020
entrez:
26
5
2019
Statut:
ppublish
Résumé
Definitive chemoradiation with concurrent 5-fluorouracil (5-FU)/mitomycin C (MMC) is an effective treatment for localized anal cancer, but it is associated with significant acute long-term treatment-related toxicity. Pencil beam scanning proton beam (PBS-PT) radiation therapy may potentially reduce this toxicity. This is a multi-institutional pilot study evaluating the feasibility of definitive concurrent chemoradiation with PBS-PT in combination with 5-FU and MMC for carcinoma of the anal canal. Patients were enrolled on a National Cancer Institute-sponsored, prospective, multi-institutional, single-arm pilot study (NCT01858025). Key eligibility criteria included Eastern Cooperative Oncology Group 0 to 2, age ≥18 years, histologically confirmed invasive squamous cell carcinoma of the anal canal, and clinically staged T1-4, N0-3 disease. Patients were treated with PBS-PT per Radiation Therapy Oncology Group 0529 dose schema and concurrent 5-FU/MMC on day 1 and 29. The primary objective of this study was to determine feasibility of PBS-PT with concurrent 5-FU/MMC, defined as grade 3+ dermatologic toxicity less than 48% (reported grade 3+ dermatologic toxicity from Radiation Therapy Oncology Group 98-11). Secondary objectives were to determine the rates of overall grade 3+ toxicities, clinical complete response rate, and disease outcomes. Between February 2014 and April 2017, we enrolled 25 patients into our study, all of whom were analyzed. Twenty-three patients (92%) completed treatment per protocol, and 2 patients died on treatment. Median time to completion of treatment was 42 days (range, 38-49). The grade 3+ radiation dermatitis rate was 24%. Median follow-up is 27 months (range, 21-50) among the 21 patients still alive. The overall rate of clinical complete response was 88%. The 2-year local failure, colostomy-free survival, progression-free survival, and overall survival are 12%, 72%, 80%, and 84%, respectively. In our prospective, multi-institutional pilot study of PBS-PT with concurrent 5-FU/MMC, PBS-PT was found to be feasible. A phase 2 study of proton beam radiation therapy is currently underway.
Identifiants
pubmed: 31128146
pii: S0360-3016(19)30747-3
doi: 10.1016/j.ijrobp.2019.04.040
pii:
doi:
Substances chimiques
Mitomycin
50SG953SK6
Fluorouracil
U3P01618RT
Banques de données
ClinicalTrials.gov
['NCT01858025']
Types de publication
Journal Article
Multicenter Study
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
90-95Subventions
Organisme : NCI NIH HHS
ID : C06 CA059267
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA006516
Pays : United States
Informations de copyright
Copyright © 2019. Published by Elsevier Inc.