Evidence map›Paper›PMID 35116396›Full record

ArticleTranslational cancer research2021

Phase 1 dose-escalation study of apatinib and irinotecan in esophageal squamous cell carcinoma patients.

Jun Jia, Jing Yu, Zhiwei Sun, Ying Yang, Chuanling Liu, Yanjie Xiao, Xiaodong Zhang

Open access · diamondAbstract read
In one paragraph

Article in Translational cancer research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 37% of its field
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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. 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

7 authors at 3 institutions in 2 countries.

Jun Jia *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), the VIP-II Gastrointestinal Cancer Division of the Medical Department, Peking University Cancer Hospital & Institute, Beijing, China.
Jing Yu *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), the VIP-II Gastrointestinal Cancer Division of the Medical Department, Peking University Cancer Hospital & Institute, Beijing, China.
Zhiwei SunKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), the VIP-II Gastrointestinal Cancer Division of the Medical Department, Peking University Cancer Hospital & Institute, Beijing, China.
Ying YangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), the VIP-II Gastrointestinal Cancer Division of the Medical Department, Peking University Cancer Hospital & Institute, Beijing, China.
Chuanling LiuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), the VIP-II Gastrointestinal Cancer Division of the Medical Department, Peking University Cancer Hospital & Institute, Beijing, China.
Yanjie XiaoKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), the VIP-II Gastrointestinal Cancer Division of the Medical Department, Peking University Cancer Hospital & Institute, Beijing, China.
Xiaodong ZhangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), the VIP-II Gastrointestinal Cancer Division of the Medical Department, Peking University Cancer Hospital & Institute, Beijing, China.
Ministry of Education · ETPeking University Cancer Hospital · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApatinib, an inhibitor of vascular endothelial growth factor receptor (VEGFR), has been used to treat esophagogastric adenocarcinoma. However, the dosage of apatinib varies greatly in clinical practice, and its safety in esophageal squamous cell carcinoma (ESCC) patients is unclear. Therefore, we initiated a phase 1 dose-escalation trial to identify the maximum tolerated dose (MTD) of apatinib when combined with irinotecan in ESCC.

methodsThe trial had a standard 3+3 design. The dosage of irinotecan was fixed at 150 mg/m

resultsTwelve patients were enrolled. Three DLTs occurred, comprising a grade 3 perianal abscess and a grade 3 case of kaliopenia in the level 3 cohort, and a grade 4 leukopenia in the level 2 cohort. Based on these DLTs, the MTD of apatinib was 500 mg daily. The most common AEs were leukopenia (91.7%), fatigue (91.7%), anemia (66.7%), and diarrhea (58.3%). One case of grade 2 hematochezia and one case of grade 2 subclavian vein thrombosis were observed. In the nine evaluable cases, the disease control rate (DCR) was 66.7% (6/9). The median progression-free and overall survival (OS) times were 3.6±1.2 and 6.6±3.4 months, respectively.

conclusionsThis phase 1 dose-escalation trial showed that, when combined with irinotecan, a daily dose of 500 mg apatinib was the optimum dose to treat ESCC.

Indexed as

Apatinibesophageal squamous cell carcinoma (ESCC)maximum tolerated dose (MTD)

Identifiers

PMID35116396
PMCPMC8798775
OpenAlexW3133791009

What OpenQuestion 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 OpenQuestion graph.