Evidence map›Paper›PMID 41545814›Full record

ArticleEsophagus : official journal of the Japan Esophageal Society2026

Treatment resistance factors associated with Talaporfin sodium photodynamic therapy for local control after chemoradiotherapy for esophageal cancer.

Masashi Tamaoki, Akira Yokoyama, Chikatoshi Katada, Kenshiro Hirohashi, Yosuke Mitani, Yusuke Amanuma, Takahiro Horimatsu, Hirokazu Higuchi, Natsuko Yamahigashi, Motoo Nomura and 9 more

Abstract read
In one paragraph

Article in Esophagus : official journal of the Japan Esophageal Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

19 authors.

Masashi TamaokiDepartment of Medical Oncology, Kyoto University Graduate School of Medicine, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.
Akira YokoyamaDepartment of Medical Oncology, Kyoto University Graduate School of Medicine, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.
Chikatoshi KatadaDepartment of Medical Oncology, Kyoto University Graduate School of Medicine, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.
Kenshiro HirohashiDepartment of Medical Oncology, Kyoto University Graduate School of Medicine, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.
Yosuke MitaniDepartment of Medical Oncology, Kyoto University Graduate School of Medicine, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.
Yusuke AmanumaDepartment of Medical Oncology, Kyoto University Graduate School of Medicine, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.
Takahiro HorimatsuDepartment of Medical Oncology, Kyoto University Graduate School of Medicine, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.
Hirokazu HiguchiDepartment of Medical Equipment, Kyoto University Hospital, Kyoto, Japan.
Natsuko YamahigashiDepartment of Medical Equipment, Kyoto University Hospital, Kyoto, Japan.
Motoo NomuraDepartment of Medical Oncology, Kyoto University Graduate School of Medicine, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.
Hiroyuki InooDepartment of Radiation Oncology and Image-Applied Therapy, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Katsuyuki SakanakaDepartment of Radiation Oncology and Image-Applied Therapy, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Mitsuhiro NikaidoDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Takahiro ShimizuDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Yo KishimotoDepartment of Otolaryngology-Head and Neck Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Shigeru TsunodaDepartment of Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Kazutaka ObamaDepartment of Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Shinya OhashiDepartment of Medical Oncology, Kyoto University Graduate School of Medicine, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.
Manabu MutoDepartment of Medical Oncology, Kyoto University Graduate School of Medicine, 54 Kawahara-Cho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan. mmuto@kuhp.kyoto-u.ac.jp.ORCID 0000-0002-3127-8203

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTalaporfin sodium photodynamic therapy (Talaporfin-PDT) shows a high local complete response (L-CR) rate for local failure after chemoradiotherapy in esophageal cancer; however, some patients do not achieve L-CR. We investigated the treatment resistance factors associated with Talaporfin-PDT for local control.

methodsThis study included 55 consecutive patients with ycT1-2 esophageal cancer who received Talaporfin-PDT. We investigated the L-CR rate, cumulative survival rate according to local effect, and treatment resistance factors associated with Talaporfin-PDT for local control using a multivariate logistic regression model.

resultsThe L-CR rate was 65.5% (95% confidence interval [CI]: 52.3-76.6). During the median follow-up of 17.8 months (range, 1.7-69.3), the 1-year overall survival (OS), progression-free survival (PFS), and disease-specific survival (DSS) rates were significantly higher in patients who achieved L-CR than in those who did not: 97.0% vs. 75.6% (P = 0.008), 64.6% vs. 0% (P < 0.001), and 97.0% vs. 85.7% (P = 0.005), respectively. In the multivariate logistic regression model, esophageal stenosis before Talaporfin-PDT was an independent predictor of local failure after Talaporfin-PDT (odds ratio: 5.626, 95% CI: 1.051-30.124, P = 0.044). The 1-year OS and DSS rates were significantly lower in patients with stenosis before Talaporfin-PDT than in those without: 75.0% vs. 92.4% (P = 0.015) and 85.7% vs. 94.6% (P = 0.015), respectively.

conclusionsEsophageal stenosis before Talaporfin-PDT was associated with resistance to local control and poor survival. The indications for the use of Talaporfin-PDT in patients with stenosis should be considered carefully.

Indexed as

ChemoradiotherapyEsophageal NeoplasmsPhotochemotherapyPorphyrinsAgedAged, 80 and overFemaleFollow-Up StudiesHumansMaleMiddle AgedPhotosensitizing AgentsRetrospective StudiesSurvival RateTreatment OutcomePhotosensitizing AgentsPorphyrinsTalaporfinChemoradiotherapyEsophageal cancerEsophageal stenosisLocal neoplasm recurrencePhotodynamic therapy

Identifiers

PMID41545814
PMCPMC13038797

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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.