pubmed-article:20128819 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20128819 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:20128819 | lifeskim:mentions | umls-concept:C0376358 | lld:lifeskim |
pubmed-article:20128819 | lifeskim:mentions | umls-concept:C0030956 | lld:lifeskim |
pubmed-article:20128819 | lifeskim:mentions | umls-concept:C0042196 | lld:lifeskim |
pubmed-article:20128819 | lifeskim:mentions | umls-concept:C0220825 | lld:lifeskim |
pubmed-article:20128819 | lifeskim:mentions | umls-concept:C0205470 | lld:lifeskim |
pubmed-article:20128819 | lifeskim:mentions | umls-concept:C1709510 | lld:lifeskim |
pubmed-article:20128819 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:20128819 | pubmed:dateCreated | 2010-3-31 | lld:pubmed |
pubmed-article:20128819 | pubmed:abstractText | We previously reported that personalized peptide vaccine (PPV) therapy in combination with leutenizing hormone-releasing hormone (LH-RH) analog and estramustine phosphate in certain cases is safe and capable of inducing both immune responses and clinical responses for metastatic castration-resistant prostate cancer (CRPC) patients. In the present study, PPV monotherapy was given to CRPC patients. Twenty-three patients with metastatic CRPC were treated with PPV without any additional treatment modalities, including LH-RH analogs. Samples were analyzed for peptide-specific cytotoxic T-lymphocyte (CTL) precursor analysis and peptide-reactive IgG. Toxicity and immunological and clinical responses were assessed on a three-monthly basis. Seventeen patients were available for immunological and clinical evaluation. The vaccines were well tolerated, with grade 3 erythema at injection sites in only one patient. Augmentation of CTL or IgG responses to at least one of the peptides was observed in six of 17 (35%) and 15 of 17 (88%) patients tested, respectively. Among 57 peptides used, 9 and 36 peptides induced CTL and IgG responses, respectively. Delayed-type hypersensitivity reaction was observed in eight of 17 patients. More than 30% prostate-specific antigen (PSA) decline was observed in four of 17 patients. Of these, one patient achieved a complete PSA response and another patient showed a partial PSA response with profound shrinking of lymph node metastases and prostate. The overall median survival time was 24 months (range, 5-37 months). These results suggest that PPV monotherapy appears to be safe and capable of inducing peptide-specific immune responses and clinical responses in CRPC patients. This trial was registered with University Hospital Medical Information Network (UMIN) number R000003339. | lld:pubmed |
pubmed-article:20128819 | pubmed:language | eng | lld:pubmed |
pubmed-article:20128819 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20128819 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:20128819 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20128819 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20128819 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20128819 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20128819 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20128819 | pubmed:month | Mar | lld:pubmed |
pubmed-article:20128819 | pubmed:issn | 1349-7006 | lld:pubmed |
pubmed-article:20128819 | pubmed:author | pubmed-author:YamadaAkiraA | lld:pubmed |
pubmed-article:20128819 | pubmed:author | pubmed-author:FujimotoKiyoh... | lld:pubmed |
pubmed-article:20128819 | pubmed:author | pubmed-author:HiraoYoshihik... | lld:pubmed |
pubmed-article:20128819 | pubmed:author | pubmed-author:ItohKyogoK | lld:pubmed |
pubmed-article:20128819 | pubmed:author | pubmed-author:MineTakashiT | lld:pubmed |
pubmed-article:20128819 | pubmed:author | pubmed-author:UemuraHirotsu... | lld:pubmed |
pubmed-article:20128819 | pubmed:author | pubmed-author:KomatsuNobuka... | lld:pubmed |
pubmed-article:20128819 | pubmed:author | pubmed-author:UejimaShigeya... | lld:pubmed |
pubmed-article:20128819 | pubmed:author | pubmed-author:de... | lld:pubmed |
pubmed-article:20128819 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20128819 | pubmed:volume | 101 | lld:pubmed |
pubmed-article:20128819 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20128819 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20128819 | pubmed:pagination | 601-8 | lld:pubmed |
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pubmed-article:20128819 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20128819 | pubmed:articleTitle | Immunological evaluation of personalized peptide vaccination monotherapy in patients with castration-resistant prostate cancer. | lld:pubmed |
pubmed-article:20128819 | pubmed:affiliation | Department of Urology, Kinki University School of Medicine, Osaka-Sayama, Osaka, Japan. huemura@med.kindai.ac.jp | lld:pubmed |
pubmed-article:20128819 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20128819 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |