Evidence map›Paper›PMID 42279429›Full record

ArticleCancers2026

Molecular Subtype-Associated Response to Cyclophosphamide-Epirubicin-Cisplatin Regimen in Recurrent or Metastatic Adenoid Cystic Carcinoma: A Retrospective Single-Center Study.

Wenbo Tang, Jiuli Zhou, Wei Zhao, Fengjuan Lin, Liqiong Xue, Ye Guo

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

6 authors.

Wenbo TangDepartment of Oncology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai 200123, China.
Jiuli ZhouDepartment of Oncology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai 200123, China.
Wei ZhaoDepartment of Oncology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai 200123, China.
Fengjuan LinDepartment of Oncology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai 200123, China.
Liqiong XueDepartment of Oncology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai 200123, China.
Ye GuoDepartment of Oncology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai 200123, China.ORCID 0000-0002-1813-9815

Funding

Science and Technology Project of Pudong Health Commission PW2023A-11The Top-level Clinical Discipline Project of Shanghai Pudong PWYgf2021-07
6 · The paper itself

Abstract

BACKGROUND/

objectivesRecurrent or metastatic adenoid cystic carcinoma (R/M ACC) has no standard systemic therapy. VEGFR-targeting tyrosine kinase inhibitors (TKIs) are commonly used first-line, though no international standard exists; cisplatin-based chemotherapy is an alternative. We retrospectively reviewed the cyclophosphamide-epirubicin-cisplatin (CEP) regimen to determine whether prior TKI exposure compromises subsequent chemotherapy efficacy.

methodsWe studied 31 patients given CEP for progressive R/M ACC (2018-2023). Tumor response was assessed by RECIST 1.1. Molecular subtype was determined by c-MYC/p63 immunohistochemistry (ACC-I, c-MYC-positive/p63-negative; ACC-II, p63-positive/c-MYC-low or negative). Multivariable models used Firth's penalized likelihood Cox regression. Next-generation sequencing (NGS) was available in 21 of 31 patients.

resultsThirty-one patients were enrolled (median age 48; 17 [54.8%] with prior TKI). At median follow-up of 22.6 months, the objective response rate (ORR) was 19.4%, disease control rate 71.0%, median progression-free survival (PFS) 5.3 months, and median overall survival (OS) 10.3 months. Prior TKI did not lower efficacy: ORR 17.6% vs. 21.4%, PFS hazard ratio 0.76 (

conclusionsCEP is active in R/M ACC, and prior TKI exposure did not appear to reduce efficacy. Higher response rates in ACC-I tumors and the apparent PIK3CA-related survival deficit are exploratory observations that need prospective testing before they can guide treatment.

Indexed as

ACC molecular subtypebone metastasiscyclophosphamide–epirubicin–cisplatinPIK3CA mutationrecurrent or metastatic adenoid cystic carcinomasalvage chemotherapytyrosine kinase inhibitor

Identifiers

PMID42279429
PMCPMC13256737

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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.