Evidence map›Paper›PMID 23078230›Full record

Trial reportCancer science2013

Immunotherapeutic benefit of α-interferon (IFNα) in survivin2B-derived peptide vaccination for advanced pancreatic cancer patients.

Hidekazu Kameshima, Tetsuhiro Tsuruma, Goro Kutomi, Hiroaki Shima, Yuji Iwayama, Yasutoshi Kimura, Masahumi Imamura, Toshihiko Torigoe, Akari Takahashi, Yoshihiko Hirohashi and 5 more

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Cancer science, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 2 pooled it
4.2field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 2 syntheses or guidelines pooled it, 78 citations in OpenAlex.

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  10. Tumor vaccines: Toward multidimensional anti-tumor therapies.Human vaccines & immunotherapeutics · 2023
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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

15 authors at 1 institution in 1 country.

Hidekazu KameshimaDepartment of Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Tetsuhiro Tsuruma
Goro Kutomi
Hiroaki Shima
Yuji Iwayama
Yasutoshi Kimura
Masahumi Imamura
Toshihiko Torigoe
Akari Takahashi
Yoshihiko Hirohashi
Yasuaki Tamura
Tomohide Tsukahara
Takayuki Kanaseki
Noriyuki Sato
Koichi Hirata
Sapporo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Survivin, a member of the inhibitor of apoptosis protein (IAP) family containing a single baculovirus IAP repeat domain, is highly expressed in cancerous tissues but not in normal counterparts. Our group identified an HLA-A24-restricted antigenic peptide, survivin-2B80-88 (AYACNTSTL), that is recognized by CD8 + CTLs and functions as an immunogenic molecule in patients with cancers of various histological origins such as colon, breast, lung, oral, and urogenital malignancies. Subsequent clinical trials with this epitope peptide alone resulted in clinical and immunological responses. However, these were not strong enough for routine clinical use as a therapeutic cancer vaccine, and our previous study of colon cancer patients indicated that treatment with a vaccination protocol of survivin-2B80-88 plus incomplete Freund's adjuvant (IFA) and α-interferon (IFNα) conferred overt clinical improvement and enhanced the immunological responses of patients. In the current study, we further investigated whether this vaccination protocol could efficiently provide not only improved immune responses but also better clinical outcomes for advanced pancreatic cancers. Tetramer and enzyme-linked immunosorbent spot analysis data indicated that more than 50% of the patients had positive clinical and immunological responses. In contrast, assessment of treatment with IFNα only to another group of cancer patients resulted in no obvious increase in the frequency of survivin-2B80-88 peptide-specific CTLs. Taken together, our data clearly indicate that a vaccination protocol of survivin-2B80-88 plus IFA and IFNα is very effective and useful in immunotherapy for this type of poor-prognosis neoplasm. This trial was registered with the UMIN Clinical Trials Registry, no. UMIN000000905.

Indexed as

AgedAged, 80 and overCancer VaccinesColonic NeoplasmsFemaleHLA-A24 AntigenHumansImmunotherapyInhibitor of Apoptosis ProteinsInterferon-alphaMaleMiddle AgedPancreatic NeoplasmsSurvivinT-Lymphocytes, CytotoxicTreatment OutcomeBIRC5 protein, humanCancer VaccinesHLA-A24 AntigenInhibitor of Apoptosis ProteinsInterferon-alphaSurvivinVaccines, Subunit

Identifiers

PMID23078230
PMCPMC7657125
OpenAlexW2096740579

What OpenQuestion holds

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Registered trials

None linked

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.