Evidence map›Paper›PMID 41749832›Full record

ArticleCancers2026

Randomized Controlled Trial to Relieve Pain of Chemotherapy-Induced Peripheral Neuropathy by Magnetic Field: SMILE Study.

Emi Kubo, Eriko Satomi, Toru Mukohara, Nozomu Fuse, Masashi Wakabayashi, Yuichiro Tsukada, Hiroto Ishiki, Shin Takayama, Yukihide Kanemitsu, Iwao Kishita and 6 more

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Emi KuboDepartment of Palliative Medicine, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.ORCID 0000-0001-9369-2824
Eriko SatomiDepartment of Palliative Medicine, National Cancer Center Hospital, Tsukiji 104-0045, Japan.ORCID 0000-0003-1516-2849
Toru MukoharaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Nozomu FuseClinical Research Support Office, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Masashi WakabayashiClinical Research Support Office, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Yuichiro TsukadaDepartment of Colorectal Surgery, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.ORCID 0000-0001-6261-0152
Hiroto IshikiDepartment of Palliative Medicine, National Cancer Center Hospital, Tsukiji 104-0045, Japan.ORCID 0000-0002-0800-2161
Shin TakayamaDepartment of Breast Surgery, National Cancer Center Hospital, Tsukiji 104-0045, Japan.ORCID 0000-0001-7210-0922
Yukihide KanemitsuDepartment of Colorectal Surgery, National Cancer Center Hospital, Tsukiji 104-0045, Japan.
Iwao KishitaPeace of Mind Co., Ltd., Kumamoto 861-5525, Japan.
Keiko KobayashiClinical Research Support Office, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Chiaki KuriharaClinical Research Support Office, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Nami HiranoClinical Research Support Office, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Takashi IkenoClinical Research Support Office, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.
Tomofumi MiuraDepartment of Palliative Medicine, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.ORCID 0000-0002-7031-7279
Akihiro SatoClinical Research Support Office, National Cancer Center Hospital East, Kashiwa 277-8577, Japan.

Funding

Japan Agency for Medical Research and Development hk0102079h0003Peace of Mind Co., Ltd. xxxx
6 · The paper itself

Abstract

BACKGROUND/

objectivesChemotherapy-induced peripheral neuropathy (CIPN) is a common side effect of taxanes and platinum-based agents, impairing quality of life. Duloxetine is the only drug with proven efficacy, but is often limited by tolerability. AT-04 is a portable alternating magnetic field device that activates descending pain modulatory systems and has shown safety in other pain settings. This investigator-initiated trial evaluated the efficacy and safety of AT-04 for persistent CIPN.

methodsWe conducted a randomized, double-blind, sham-controlled, multicenter phase II study. Patients with CIPN lasting ≥12 weeks after chemotherapy and pain NRS ≥ 4 were enrolled. Participants used AT-04 or sham devices twice daily for 12 weeks. The primary endpoint was the change in pain NRS on day 85. Secondary endpoints included tingling NRS, numbness NRS, CIPN20 subscales, and safety.

resultsTwenty-eight patients were randomized (14 per arm). No significant difference was observed in pain NRS on day 85 {AT-04: -1.74 ± 0.6 vs. sham device: -1.45 ± 0.6; one-sided

conclusionsAT-04 did not significantly reduce pain NRS but improved motor function in CIPN patients, especially in those >1 year after chemotherapy. AT-04 may be a promising non-pharmacological option; larger confirmatory trials are required.

Indexed as

breast cancerchemotherapy-induced peripheral neuropathyCIPNcolorectal cancermagnetic fieldoxaliplatinpaclitaxel

Identifiers

PMID41749832
PMCPMC12938895

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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.