Evidence map›Paper›PMID 23829867›Full record

Trial reportCancer science2013

Phase II study of personalized peptide vaccination for refractory bone and soft tissue sarcoma patients.

Ryuji Takahashi, Yukinao Ishibashi, Koji Hiraoka, Satoko Matsueda, Kouichirou Kawano, Akihiko Kawahara, Masayoshi Kage, Koichi Ohshima, Ryuya Yamanaka, Shigeki Shichijo and 3 more

Open access · greenAbstract readClinical Trial, Phase II
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 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 44 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Immunotherapy and Biomarkers in Sarcoma.Current treatment options in oncology · 2022
    Review
  10. Article
  11. Review
  12. Review
  13. Immunotherapy in soft-tissue sarcoma.Current oncology (Toronto, Ont.) · 2020
    Review
  14. Article
  15. Review
  16. Review
  17. Immunotherapies in sarcoma: Updates and future perspectives.World journal of clinical oncology · 2017
    Review
  18. Article
  19. Article
  20. Review
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

13 authors at 1 institution in 1 country.

Ryuji TakahashiDepartment of Surgery, Kurume University School of Medicine, Kurume, Japan.
Yukinao Ishibashi
Koji Hiraoka
Satoko Matsueda
Kouichirou Kawano
Akihiko Kawahara
Masayoshi Kage
Koichi Ohshima
Ryuya Yamanaka
Shigeki Shichijo
Kazuo Shirouzu
Kyogo Itoh
Tetsuro Sasada
Kurume University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Refractory bone and soft tissue sarcomas are challenging diseases to treat because of their robustness to chemotherapy. Although cancer vaccines have the potential to become an attractive treatment modality, their progress has been hampered by the presence of many subtypes of sarcomas and different human leukocyte antigen (HLA)-types. We investigated whether personalized peptide vaccination (PPV) would be feasible for the vast majority of sarcoma patients. Twenty refractory bone and soft tissue sarcoma patients with nine different subtypes and 11 different HLA-class IA phenotypes were enrolled in this study. A maximum of four HLA-matched peptides showing higher peptide-specific IgG responses in pre-vaccination plasma were selected from 31 pooled peptide candidates applicable for the HLA-A2, -A3, -A11, -A24, -A26, -A31, and -A33 types, and were subcutaneously administered weekly for 6 weeks and bi-weekly thereafter. Measurement of peptide-specific CTL and IgG responses along with other laboratory analyses were conducted before and after vaccination. No patients were excluded by either sarcoma subtypes or different HLA-types. No severe adverse events associated with PPV were observed in any patients. Peptide-specific immunological boosting was observed in the post-vaccination samples from the majority of patients. Tumor reduction of the lung metastasis and a long stable disease was observed in each case, and the median overall survival time of the 20 cases was 9.6 months. Taken together, PPV could be feasible for the vast majority of refractory sarcoma patients because of the safety and higher rates of immunological responses regardless of the presence of different sarcoma subtypes and various HLA-types.

Indexed as

Immunotherapy, ActiveAdultAgedAntigens, NeoplasmAntineoplastic Combined Chemotherapy ProtocolsBone NeoplasmsCancer VaccinesCombined Modality TherapyCytokinesFemaleGastrointestinal DiseasesHematologic DiseasesHLA AntigensHumansImmunoglobulin GKaplan-Meier EstimateAntigens, NeoplasmCancer VaccinesCytokinesHLA AntigensImmunoglobulin GVaccines, Subunit

Identifiers

PMID23829867
PMCPMC7656559
OpenAlexW2057624250

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.