Evidence map›Paper›PMID 24252799›Full record

Trial reportHuman vaccines & immunotherapeutics2014

Significant clinical response of progressive recurrent ovarian clear cell carcinoma to glypican-3-derived peptide vaccine therapy: two case reports.

Shiro Suzuki, Kiyosumi Shibata, Fumitaka Kikkawa, Tetsuya Nakatsura

Open access · hybridAbstract readCase ReportsClinical Trial, Phase II
In one paragraph

Trial report in Human vaccines & immunotherapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  7. Review
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  11. [Progress on biotherapy of hepatocellular carcinoma].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2015
    Article
  12. Review
  13. Article
  14. Immunotherapy for ovarian cancer.Current treatment options in oncology · 2015
    Review
  15. Glypican 3 overexpression in primary and metastatic Wilms tumors.Virchows Archiv : an international journal of pathology · 2015
    Article
  16. Article
  17. Review
  18. Article
  19. 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

4 authors at 3 institutions in 1 country.

Shiro SuzukiDepartment of Obstetrics and Gynecology; Nagoya University Graduate School of Medicine; Showa-ku, Nagoya Japan.
Kiyosumi ShibataDepartment of Obstetrics and Gynecology; Nagoya University Graduate School of Medicine; Showa-ku, Nagoya Japan.
Fumitaka KikkawaDepartment of Obstetrics and Gynecology; Nagoya University Graduate School of Medicine; Showa-ku, Nagoya Japan.
Tetsuya NakatsuraDivision of Cancer Immunotherapy; Exploratory Oncology Research and Clinical Trial Center; National Cancer Center; Kashiwa, Chiba Japan.
Nagoya University · JPChiba Cancer Center · JPNational Cancer Center Hospital East · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carcinoembryonic antigen glypican-3 (GPC3) is expressed by>40% of ovarian clear cell carcinoma (CCC) and is a promising immunotherapeutic target. We previously reported the safety of and immunological and clinical responses to a GPC3-derived peptide vaccine in a phase I clinical trial of patients with advanced hepatocellular carcinoma (HCC). Although the efficacy of the GPC3-derived peptide vaccine against HCC patients was evaluated, other GPC3-positive cancer patients have not yet been investigated. Therefore, we conducted a phase II trial to evaluate the clinical outcome of ovarian CCC patients treated with a GPC3-derived peptide vaccine. The GPC3 peptide was administered at a dose of 3 mg per body. Patients received an intradermal injection of the GPC3 peptide emulsified with incomplete Freund's adjuvant. Vaccinations were performed biweekly from the first until the 6th injection and were then repeated at 6-week intervals after the 7th injection. Treatment continued until disease progression. We herein present two patients with chemotherapy-refractory ovarian CCC who achieved a significant clinical response in an ongoing trial of a GPC3 peptide vaccine. Case 1, a 42-year-old patient with advanced recurrent ovarian CCC with liver and retroperitoneal lymph node metastases, received the HLA-A24-restricted GPC3 peptide vaccine. Contrast-enhanced CT at week 10 revealed a partial response (PR) using RECIST criteria. Case 2 was a 67-year-old female with multiple lymph node metastases. She was injected with the HLA-A2-restricted GPC3 peptide vaccine. According to RECIST, PR was achieved at week 37. The stabilization of their diseases over one year provided us with the first clinical evidence to demonstrate that GPC3 peptide-based immunotherapy may significantly prolong the overall survival of patients with refractory ovarian CCC.

Indexed as

Adjuvants, ImmunologicAdultAgedCarcinomaFemaleFreund's AdjuvantGlypicansHumansImmunotherapyInjections, IntradermalOvarian NeoplasmsRecurrenceTreatment OutcomeVaccines, SubunitAdjuvants, ImmunologicFreund's AdjuvantGlypicansGPC3 protein, humanVaccines, Subunitclinical responseGlypican-3ovarian clear cell carcinomapeptide vaccinerefractory disease

Identifiers

PMID24252799
PMCPMC4185885
OpenAlexW2028763729

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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.