Evidence map›Paper›PMID 42832019›Full record

ArticleInternational journal of hematology2026

Post-hoc analysis of induction failure in pediatric LCH: the JLSG-02 and LCH-12 clinical trials.

Yukayo Terashita, Rintaro Ono, Kenichi Sakamoto, Kazuko Kudo, Ko Kudo, Yoko Shioda, Shinya Osone, Toshihiko Imamura, Shinsaku Imashuku, Akira Morimoto

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Article in International journal of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Yukayo TerashitaDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Rintaro OnoDepartment of Pediatrics, St. Luke's International Hospital, Tokyo, Japan.
Kenichi SakamotoDepartment of Pediatrics, Shinshu University School of Medicine, 3-1-1 Asahi, Nagano, Matsumoto, Japan. sakamoto-k@shinshu-u.ac.jp.ORCID http://orcid.org/0000-0003-1499-538X
Kazuko KudoDepartment of Pediatrics, Fujita Health University, Toyoake, Japan.
Ko KudoDepartment of Pediatrics, Hirosaki University School of Medicine, Hirosaki, Japan.
Yoko ShiodaChildren's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.
Shinya OsoneDepartment of Pediatrics, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Toshihiko ImamuraAnyoji Kid's Clinic, Ritto, Japan.
Shinsaku ImashukuDepartment of Laboratory Medicine, Uji-Tokushukai Medical Center, Uji, Japan.
Akira MorimotoDivision of Pediatrics, Showa Inan General Hospital, Komagane, Japan.

Funding

Japan Agency for Medical Research and Development JP20ck0106605Japan Agency for Medical Research and Development JP23ck0106852Japan Agency for Medical Research and Development JP26ck0106143
6 · The paper itself

Abstract

Treatment options for refractory multisystem Langerhans cell histiocytosis (LCH) were not well established prior to the era of targeted therapy. We evaluated the efficacy and safety of cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP)-like salvage regimen (Induction B) in patients with induction failure in a post-hoc analysis of the JLSG-02 (N = 147) and JPLSG LCH-12 (N = 107) studies of pediatric LCH. Of 254 patients, 41 were refractory (no response or progressive disease) following initial Induction A therapy (prednisolone, vincristine, and cytarabine). Among them, 35 patients who received Induction B therapy were analyzed. The overall response rate to Induction B was 66% (23/35). Sixteen patients (46%) achieved no active disease after Induction B followed by maintenance therapy; among them, six patients with risk organ involvement (RO+) relapsed. The 5-year overall survival was 100% in the RO- group and 84.6% (95% CI, 64.0-93.9%) in the RO+ group. Grade 3/4 hematological toxicities were frequent; however, no fatal adverse events were observed. Induction B demonstrated efficacy and an acceptable safety profile in pediatric refractory multisystem LCH. This therapy could be a salvage treatment option for patients with refractory disease when targeted therapy is not available.

Indexed as

Induction failureJLSG-02LCH-12Pediatric LCHSalvage therapy

Identifiers

PMID42832019

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.