A phase II study of adaptive two-step intensity-modulated radiation therapy (IMRT) with chemotherapy for loco-regionally advanced nasopharyngeal cancer (JCOG1015).


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
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

1250-1259

Subventions

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

Auteurs

Yasumasa Nishimura (Y)

Department of Radiation Oncology, Kindai University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka, 589-8511, Japan. ynishi@med.kindai.ac.jp.

Satoshi Ishikura (S)

Department of Radiology, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya, Aichi, 467-8601, Japan.

Taro Shibata (T)

JCOG Data Center/Operations Office, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.

Takeshi Kodaira (T)

Department of Radiation Oncology, Aichi Cancer Center Hospital, 1-1 Kanoko-den, Chikusa-ku, Nagoya, Aichi, 464-8681, Japan.

Yoshinori Ito (Y)

Department of Radiation Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.

Kazuhiko Tsuchiya (K)

Department of Radiation Oncology, Hokkaido University Hospital, Kita14 Nishi 5, Kita-ku, Sapporo, Hokkaido, 060-8648, Japan.

Yuji Murakami (Y)

Department of Radiation Oncology, Hiroshima University Hospital, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8551, Japan.

Jun-Ichi Saitoh (JI)

Department of Radiation Oncology, Gunma University, 3-39-22, Showa-machi, Maebashi, Gunma, 371-8511, Japan.

Tetsuo Akimoto (T)

Department of Radiation Oncology, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba, 277-8577, Japan.

Kensei Nakata (K)

Department of Radiology, Sapporo Medical University, S1W17, Chuo-ku, Sapporo, Hokkaido, 060-8556, Japan.

Michio Yoshimura (M)

Department of Radiation Oncology and Image-Applied Therapy, Kyoto University, 54 Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.

Teruki Teshima (T)

Department of Radiation Oncology, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-ku, Osaka, 541-8567, Japan.

Takashi Toshiyasu (T)

Department of Radiation Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, 3-8-31 Ariake, Koto-ku, Tokyo, 135-8550, Japan.

Yosuke Ota (Y)

Department of Radiation Oncology, Hyogo Cancer Center, 13-70 Kitaouji, , Akashi, Hyogo, 673-8558, Japan.

Kazuki Ishikawa (K)

Department of Radiation Oncology, Kindai University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka, 589-8511, Japan.

Hidetoshi Shimizu (H)

Department of Radiation Oncology, Aichi Cancer Center Hospital, 1-1 Kanoko-den, Chikusa-ku, Nagoya, Aichi, 464-8681, Japan.

Toshiyuki Minemura (T)

Center for Cancer Control and Information Services, National Cancer Center, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.

Kenichi Nakamura (K)

JCOG Data Center/Operations Office, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.

Masahiro Hiraoka (M)

Department of Radiation Oncology, Japanese Red Cross Wakayama Medical Center, 4-20 Komatsubara-Dori, Wakayama, 640-8558, Japan.

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