A phase II study of adaptive two-step intensity-modulated radiation therapy (IMRT) with chemotherapy for loco-regionally advanced nasopharyngeal cancer (JCOG1015).
Adult
Aged
Antineoplastic Agents
/ administration & dosage
Chemotherapy, Adjuvant
Cisplatin
/ administration & dosage
Dose Fractionation, Radiation
Female
Humans
Male
Middle Aged
Nasopharyngeal Neoplasms
/ drug therapy
Radiation Injuries
/ etiology
Radiotherapy, Intensity-Modulated
/ adverse effects
Survival Analysis
Treatment Outcome
Xerostomia
/ etiology
Adaptive IMRT method
Intensity-modulated radiation therapy (IMRT)
Nasopharyngeal cancer
Xerostomia
Journal
International journal of clinical oncology
ISSN: 1437-7772
Titre abrégé: Int J Clin Oncol
Pays: Japan
ID NLM: 9616295
Informations de publication
Date de publication:
Jul 2020
Jul 2020
Historique:
received:
13
02
2020
accepted:
16
03
2020
pubmed:
30
3
2020
medline:
2
9
2020
entrez:
30
3
2020
Statut:
ppublish
Résumé
A phase II study of adaptive two-step intensity-modulated radiotherapy (IMRT) with chemotherapy for nasopharyngeal cancer (NPC) (JCOG1015) was conducted to evaluate the efficacy and safety. Patients aged 20-75 years with stages II-IVB NPC were enrolled. As adaptive two-step IMRT, computed tomography planning was performed twice before IMRT for the initial plan of 46 Gy/23 fractions and during treatment for the boost plan of 24 Gy/12 fractions with a total dose of 70 Gy. Chemotherapy (cisplatin 80 mg/m Between 2011 and 2014, 75 patients were enrolled from 12 institutions. The 3-year overall survival (OS) for the 75 patients was 88%, and the upper and lower limits of the 95% CI of 78%-94% were higher than the expected 3-year OS of 75% for the target population adjusted by the actual proportion of stage II:III:IV = 21%:44%:35%. The 3-year progression-free survival (PFS) and loco-regional PFS were 71% [59-80%] and 77% [66-85%], respectively. Although no grade 4-5 late toxicities were observed, 15 patients (20%) developed grade 3 late toxicities. Grade 2 xerostomia was noted in 26%, 12%, and 9% at 1, 2, and 3 years after starting IMRT, respectively. Adaptive two-step IMRT for NPC demonstrated an excellent 3-year OS with acceptable toxicities. This method may be one treatment option for locally advanced NPC.
Sections du résumé
BACKGROUND
BACKGROUND
A phase II study of adaptive two-step intensity-modulated radiotherapy (IMRT) with chemotherapy for nasopharyngeal cancer (NPC) (JCOG1015) was conducted to evaluate the efficacy and safety.
METHODS
METHODS
Patients aged 20-75 years with stages II-IVB NPC were enrolled. As adaptive two-step IMRT, computed tomography planning was performed twice before IMRT for the initial plan of 46 Gy/23 fractions and during treatment for the boost plan of 24 Gy/12 fractions with a total dose of 70 Gy. Chemotherapy (cisplatin 80 mg/m
RESULTS
RESULTS
Between 2011 and 2014, 75 patients were enrolled from 12 institutions. The 3-year overall survival (OS) for the 75 patients was 88%, and the upper and lower limits of the 95% CI of 78%-94% were higher than the expected 3-year OS of 75% for the target population adjusted by the actual proportion of stage II:III:IV = 21%:44%:35%. The 3-year progression-free survival (PFS) and loco-regional PFS were 71% [59-80%] and 77% [66-85%], respectively. Although no grade 4-5 late toxicities were observed, 15 patients (20%) developed grade 3 late toxicities. Grade 2 xerostomia was noted in 26%, 12%, and 9% at 1, 2, and 3 years after starting IMRT, respectively.
CONCLUSIONS
CONCLUSIONS
Adaptive two-step IMRT for NPC demonstrated an excellent 3-year OS with acceptable toxicities. This method may be one treatment option for locally advanced NPC.
Identifiants
pubmed: 32221802
doi: 10.1007/s10147-020-01665-2
pii: 10.1007/s10147-020-01665-2
doi:
Substances chimiques
Antineoplastic Agents
0
Cisplatin
Q20Q21Q62J
Types de publication
Clinical Trial, Phase II
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
1250-1259Subventions
Organisme : Health Sciences Research Grants for the Grant-in-Aid for Cancer Research
ID : H23-009
Organisme : the Japan Agency for Medical Research and Development
ID : JP16ck0106093
Organisme : the National Cancer Center Research and Development Funds
ID : 26-A-4
Organisme : the National Cancer Center Research and Development Funds
ID : 29-A-3