Results of the JRS-I LRA0401 and LRB0402 Japan Rhabdomyosarcoma Study Group trials for low-risk embryonal rhabdomyosarcoma.

Central pathology review system Embryonal rhabdomyosarcoma Low risk Nationwide group study Risk-adopted therapy

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:
23 Aug 2024
Historique:
received: 04 01 2024
accepted: 04 08 2024
medline: 23 8 2024
pubmed: 23 8 2024
entrez: 23 8 2024
Statut: aheadofprint

Résumé

Failure-free survival (FFS) rates of low-risk patients with rhabdomyosarcoma improved in Intergroup Rhabdomyosarcoma Study IV after the escalation of cyclophosphamide total dose to 26.4 g/m Subgroup-A patients received eight cycles (24 weeks) of vincristine, actinomycin D, and 1.2 g/m In subgroup A (n = 12), the 3-year FFS rate was 83% (95% confidence interval [CI], 48-96), and the 3-year overall survival (OS) rate was 100%. Only one isolated local recurrence was observed (8.3%). There were no unexpected grade-4 toxicities and no deaths. In subgroup B (n = 16), the 3-year FFS and OS rates were 88% (95% CI, 59-97) and 94% (95% CI, 63-99), respectively. There were no unexpected grade 4 toxicities and no deaths. Shorter duration therapy using vincristine, actinomycin D, and lower dose cyclophosphamide with or without radiotherapy for patients with low-risk subgroup A rhabdomyosarcoma (JRS-I LRA0401 protocol) and moderate reduction of cyclophosphamide dose for patients with low-risk subgroup B rhabdomyosarcoma (JRS-I LRB0402 protocol) did not compromise FFS.

Sections du résumé

BACKGROUND BACKGROUND
Failure-free survival (FFS) rates of low-risk patients with rhabdomyosarcoma improved in Intergroup Rhabdomyosarcoma Study IV after the escalation of cyclophosphamide total dose to 26.4 g/m
METHODS METHODS
Subgroup-A patients received eight cycles (24 weeks) of vincristine, actinomycin D, and 1.2 g/m
RESULTS RESULTS
In subgroup A (n = 12), the 3-year FFS rate was 83% (95% confidence interval [CI], 48-96), and the 3-year overall survival (OS) rate was 100%. Only one isolated local recurrence was observed (8.3%). There were no unexpected grade-4 toxicities and no deaths. In subgroup B (n = 16), the 3-year FFS and OS rates were 88% (95% CI, 59-97) and 94% (95% CI, 63-99), respectively. There were no unexpected grade 4 toxicities and no deaths.
CONCLUSIONS CONCLUSIONS
Shorter duration therapy using vincristine, actinomycin D, and lower dose cyclophosphamide with or without radiotherapy for patients with low-risk subgroup A rhabdomyosarcoma (JRS-I LRA0401 protocol) and moderate reduction of cyclophosphamide dose for patients with low-risk subgroup B rhabdomyosarcoma (JRS-I LRB0402 protocol) did not compromise FFS.

Identifiants

pubmed: 39177879
doi: 10.1007/s10147-024-02608-x
pii: 10.1007/s10147-024-02608-x
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Japan Agency for Medical Research and Development
ID : JP19ck0106333
Organisme : Japan Agency for Medical Research and Development
ID : JP20ck0106610

Informations de copyright

© 2024. The Author(s) under exclusive licence to Japan Society of Clinical Oncology.

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Auteurs

Hajime Hosoi (H)

Department of Pediatrics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine (KPUM), Kyoto, Japan. hhosoi@koto.kpu-m.ac.jp.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan. hhosoi@koto.kpu-m.ac.jp.
Department of Nursing, Doshisha Women's College of Liberal Arts, Kyoto, Japan. hhosoi@koto.kpu-m.ac.jp.

Mitsuru Miyachi (M)

Department of Pediatrics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine (KPUM), Kyoto, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Satoshi Teramukai (S)

Department of Biostatistics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.
Department of Clinical Trial Design and Management, Translational Research Center, Kyoto University Hospital, Kyoto, Japan.

Satomi Sakabayashi (S)

Department of Biostatistics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.

Kunihiko Tsuchiya (K)

Department of Pediatrics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine (KPUM), Kyoto, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Yasumichi Kuwahara (Y)

Department of Pediatrics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine (KPUM), Kyoto, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Rie Onodera (R)

Translational Research Informatics Center, Kobe, Japan.
Department of Clinical Trial Design and Management, Translational Research Center, Kyoto University Hospital, Kyoto, Japan.
Health and Medical Innovation, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.

Kotone Matsuyama (K)

Translational Research Informatics Center, Kobe, Japan.
Department of Health Policy and Management, Nippon Medical School, Tokyo, Japan.

Isao Yokota (I)

Department of Biostatistics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Department of Biostatistics, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Hiroshi Hojo (H)

Department of Diagnostic Pathology, School of Medicine, Fukushima Medical University, Fukushima, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Hajime Okita (H)

Division of Diagnostic Pathology, Keio University School of Medicine, Tokyo, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Jun-Ichi Hata (JI)

Experimental Medicine and Life Science, Kanagawa, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Minori Hamasaki (M)

Department of Pathology, Shizuoka Children's Hospital, Shizuoka, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Masazumi Tsuneyoshi (M)

Department of Anatomic Pathology, Pathological Sciences, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.
Department of Diagnostic Pathology, Fukuoka Sanno Hospital, Fukuoka, Japan.

Yoshinao Oda (Y)

Department of Anatomic Pathology, Pathological Sciences, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Atsuko Nakazawa (A)

Department of Pathology, Saitama Children's Medical Center, Saitama, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Miho Kato (M)

Childhood Cancer Center, National Center for Child Health and Development, Tokyo, Japan.

Tetsuya Takimoto (T)

Childhood Cancer Center, National Center for Child Health and Development, Tokyo, Japan.

Keizo Horibe (K)

Clinical Research Center, NHO Nagoya Medical Center, Aichi, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Jun-Ichi Hara (JI)

Department of Pediatric Hematology/Oncology, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Sachiyo Suita (S)

Department of Pediatric Surgery, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Ryoji Hanada (R)

Department of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Hidekazu Masaki (H)

Department of Radiology, National Center for Child Health and Development (NCCHD), Tokyo, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Miwako Nozaki (M)

Department of Radiology, Dokkyo Medical University Saitama Medical Center, Saitama, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Hitoshi Ikeda (H)

Department of Pediatric Surgery, Dokkyo Medical University Saitama Medical Center, Saitama, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Seiji Kishimoto (S)

Department of Otolaryngology, Head and Neck Surgery, Kameda Medical Center, Chiba, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Michio Kaneko (M)

Department of Pediatric Surgery, Institute of Clinical Medicine, University of Tsukuba, Ibaraki, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Akira Kawai (A)

Department of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Yasuhide Morikawa (Y)

Department of Pediatric Surgery, International University of Health and Welfare Hospital, Tokyo, Japan.
Japan Rhabdomyosarcoma Study Group (JRSG), Tokyo, Japan.

Classifications MeSH