Evidence map›Paper›PMID 32209994›Full record

ArticleCancers2020

Early Tumor Shrinkage as a Predictive Factor for Outcomes in Hepatocellular Carcinoma Patients Treated with Lenvatinib: A Multicenter Analysis.

Aya Takahashi, Michihisa Moriguchi, Yuya Seko, Toshihide Shima, Yasuhide Mitsumoto, Hidetaka Takashima, Hiroyuki Kimura, Hideki Fujii, Hiroki Ishikawa, Yo Takaharu and 16 more

Abstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Response Assessment of Primary Liver Tumors to Novel Therapies: an Imaging Perspective.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2023
    Review
  4. Article
  5. Article
  6. The prognostic role of early tumor shrinkage in patients with hepatocellular carcinoma undergoing immunotherapy.Cancer imaging : the official publication of the International Cancer Imaging Society · 2022
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Observational
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

26 authors.

Aya TakahashiDepartment of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Michihisa MoriguchiDepartment of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Yuya SekoDepartment of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Toshihide ShimaDepartment of Gastroenterology and Hepatology, Saiseikai Suita Hospital, Suita 564-0013, Japan.
Yasuhide MitsumotoDepartment of Gastroenterology and Hepatology, Saiseikai Suita Hospital, Suita 564-0013, Japan.
Hidetaka TakashimaDepartment of Gastroenterology, Osaka General Hospital of West Japan Railway Company, Osaka 545-0053, Japan.
Hiroyuki KimuraDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Kyoto 605-0981, Japan.
Hideki FujiiDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Kyoto 605-0981, Japan.
Hiroki IshikawaDepartment of Gastroenterology and Hepatology, Omihachiman Community Medical Center, Omihachiman 523-0082, Japan.
Yo TakaharuDepartment of Gastroenterology and Hepatology, Omihachiman Community Medical Center, Omihachiman 523-0082, Japan.
Hiroshi IshibaDepartment of Gastroenterology and Hepatology, North Medical Center of Kyoto Prefectural University of Medicine, Yosagun 629-2261, Japan.
Atsuhiro MoritaDepartment of Gastroenterology, Japanese Red Cross Kyoto Daini Hospital, Kyoto 602-8026, Japan.
Masayasu JoDepartment of Gastroenterology, Otsu City Hospital, Otsu 520-0804, Japan.
Yasuyuki NagaoDepartment of Gastroenterology, Matsushita Memorial Hospital, Moriguchi 570-8540, Japan.
Masahiro AraiDepartment of Gastroenterology, Kyoto Yamashiro General Medical Center, Kizugawa 619-0214, Japan.
Tasuku HaraDepartment of Gastroenterology, Fukuchiyama City Hospital, Fukuchiyama 620-8505, Japan.
Akira OkajimaDepartment of Gastroenterology, Koseikai Takeda Hospital, Kyoto 600-8558, Japan.
Akira MuramatsuDepartment of Gastroenterology, Akashi City Hospital, Akashi 673-8501, Japan.
Naomi YoshinamiDepartment of Gastroenterology, Kyoto City Hospital, Kyoto 604-8845, Japan.
Tomoki NakajimaDepartment of Gastroenterology, Saiseikai Kyoto Hospital, Kyoto 617-0814, Japan.
Hironori MitsuyoshiDepartment of Gastroenterology and Hepatology, Kyoto Chubu Medical Center, Kyoto 629-0197, Japan.
Atsushi UmemuraDepartment of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Taichiro NishikawaDepartment of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Kanji YamaguchiDepartment of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Takeshi OkanoueDepartment of Gastroenterology and Hepatology, Saiseikai Suita Hospital, Suita 564-0013, Japan.
Yoshito ItohDepartment of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.

Funding

Japan Agency for Medical Research and Development JP19fk0210040
6 · The paper itself

Abstract

We investigated the association between early tumor shrinkage (ETS) and treatment outcome in patients with hepatocellular carcinoma treated with lenvatinib (LEN). A retrospective analysis was performed in 104 patients. ETS was defined as tumor shrinkage at the first evaluation in the sum of target lesions' longest diameters from baseline according to the Response Evaluation Criteria in Solid Tumors (RECIST). The median overall survival (OS) was not reached, whereas the median progression-free survival (PFS) was 5.0 months. The receiver operating characteristic curve analysis in differentiating long-term responders (PFS ≥ 5.0 months) from short-term responders (PFS < 5.0 months) revealed an ETS cut-off value of 10%. ETS ≥ 10% was significantly correlated with better PFS and OS compared with ETS < 10%. Additionally, ETS ≥ 10% showed a better discrimination ability on prognosis compared with modified RECIST-based objective response at the first evaluation. Multivariate analysis confirmed ETS ≥ 10% as an independent predictor of better OS, as well as a Child-Pugh score of 5 and macrovascular invasion. In conclusion, ETS ≥ 10% was strongly associated with outcome in patients treated with LEN. This biomarker could allow earlier assessment of the treatment response and guide treatment decision-making for HCC.

Indexed as

early tumor shrinkagehepatocellular carcinomalenvatiniboverall survivalResponse Evaluation Criteria in Solid Tumors (RECIST)

Identifiers

PMID32209994
PMCPMC7140019

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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.