Evidence map›Paper›PMID 42665401›Full record

ArticleIn vivo (Athens, Greece)

Efficacy of S-1 Monotherapy for Salivary Duct Carcinoma With

Hirotaka Suto, Miyuki Kawamura, Mitsunori Morita, Hideki Sakai, Takuma Onoe, Kyoko Ikeuchi, Naoko Maeda, Koji Matsumoto

Abstract readCase Reports
In one paragraph

Article in In vivo (Athens, Greece). 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

8 authors.

Hirotaka SutoDepartment of Medical Oncology, Hyogo Cancer Center, Akashi, Japan; hirotaka.suto@hyogo-cc.jp.
Miyuki KawamuraDepartment of Medical Oncology, Hyogo Cancer Center, Akashi, Japan.
Mitsunori MoritaDepartment of Medical Oncology, Hyogo Cancer Center, Akashi, Japan.
Hideki SakaiDepartment of Medical Oncology, Hyogo Cancer Center, Akashi, Japan.
Takuma OnoeDepartment of Medical Oncology, Hyogo Cancer Center, Akashi, Japan.
Kyoko IkeuchiDepartment of Medical Oncology, Hyogo Cancer Center, Akashi, Japan.
Naoko MaedaDepartment of Diagnostic Pathology, Hyogo Cancer Center, Akashi, Japan.
Koji MatsumotoDepartment of Medical Oncology, Hyogo Cancer Center, Akashi, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimSalivary duct carcinoma (SDC) is a rare, highly aggressive subtype of salivary gland carcinoma, commonly characterized by overexpression of erb-b2 receptor tyrosine kinase 2 [ERBB2, commonly known as human epidermal growth factor receptor 2 (HER2)] and androgen receptor positivity. Anti-HER2 therapy, platinum-based chemotherapy, and androgen-deprivation therapy (ADT) are commonly provided as standard systemic treatments for advanced SDC; however, effective therapeutic options after failure of these treatments remain limited. The clinical efficacy of S-1 monotherapy in SDC and its predictive biomarkers are not well established. Herein, we present a case in which S-1 monotherapy showed efficacy in a case of SDC after resistance to anti-HER2 therapy, platinum-based chemotherapy, and ADT. CASE REPORT: The patient was a 70-year-old man diagnosed with HER2-positive and androgen receptor-positive SDC of the submandibular gland, who presented with multiple lung metastases. He initially received trastuzumab plus docetaxel as first-line therapy, followed by platinum-based chemotherapy and ADT, but experienced disease progression after each treatment. Comprehensive genomic profiling revealed amplifications of

conclusionS-1 monotherapy may represent a treatment option for patients with advanced SDC refractory to anti-HER2 therapy, platinum-based chemotherapy, and ADT, particularly in cases harboring

Indexed as

Carcinoma, DuctalGene AmplificationOxonic AcidProto-Oncogene Proteins c-mycSalivary DuctsSalivary Gland NeoplasmsTegafurAgedDrug CombinationsErb-b2 Receptor Tyrosine KinasesHumansMaleProto-Oncogene MasTreatment OutcomeDrug CombinationsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesMAS1 protein, humanOxonic AcidProto-Oncogene MasProto-Oncogene Proteins c-mycS 1 (combination)Tegafurandrogen receptorhuman epidermal growth factor receptor 2MYC amplificationS-1Salivary duct carcinoma

Identifiers

PMID42665401
PMCPMC13531109

What Socratic holds

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Registered trials

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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 Socratic graph.