PMID- 22321067 OWN - NLM STAT- MEDLINE DCOM- 20120516 LR - 20211021 IS - 1349-7006 (Electronic) IS - 1347-9032 (Print) IS - 1347-9032 (Linking) VI - 103 IP - 4 DP - 2012 Apr TI - Immunological evaluation of personalized peptide vaccination in refractory small cell lung cancer. PG - 638-44 LID - 10.1111/j.1349-7006.2012.02202.x [doi] AB - Since the prognosis of small cell lung cancer (SCLC) remains poor, development of new therapeutic approaches, including immunotherapies, would be desirable. In the current study, to evaluate immunological responses in refractory SCLC patients, we conducted a small scale phase II clinical trial of personalized peptide vaccination (PPV), in which vaccine antigens are selected based on pre-existing host immunity. Ten refractory SCLC patients, who had failed to respond to chemo- and/or chemoradiotherapies (median number of regimens, 2.5; median duration, 20.5 months), were enrolled. A maximum of four human leukocyte antigen (HLA)-matched peptides showing higher antigen-specific humoral responses were subcutaneously administered (weekly for six consecutive weeks and then bi-weekly thereafter). PPV was terminated before the 3rd administration in four patients because of rapid disease progression, whereas the remaining six patients completed at least one cycle (six times) of vaccinations. Peptide-specific immunological boosting was observed in all of the six patients at the end of the first cycle of vaccinations, with their survival time of 25, 24.5 (alive), 10 (alive), 9.5, 6.5, and 6 months. Number of previous chemotherapy regimens and frequency of CD3(+) CD26(+) cells in peripheral blood were potentially prognostic in the vaccinated patients (hazard ratio [HR] = 2.540, 95% confidence interval [CI] = 1.188-5.431, P = 0.016; HR = 0.941, 95% CI = 0.878-1.008, P = 0.084; respectively). Based on the feasible immune responses in refractory SCLC patients who received at least one cycle (six times) of vaccinations, PPV could be recommended for a next stage of larger-scale, prospective clinical trials. CI - (c) 2012 Japanese Cancer Association. FAU - Terazaki, Yasuhiro AU - Terazaki Y AD - Department of Surgery, Kurume University School of Medicine, Kurume, Japan. FAU - Yoshiyama, Koichi AU - Yoshiyama K FAU - Matsueda, Satoko AU - Matsueda S FAU - Watanabe, Noriko AU - Watanabe N FAU - Kawahara, Akihiko AU - Kawahara A FAU - Naito, Yoshiki AU - Naito Y FAU - Suekane, Shigetaka AU - Suekane S FAU - Komatsu, Nobukazu AU - Komatsu N FAU - Ioji, Tetsuya AU - Ioji T FAU - Yamada, Akira AU - Yamada A FAU - Mine, Takashi AU - Mine T FAU - Terasaki, Mizuhiko AU - Terasaki M FAU - Itoh, Kyogo AU - Itoh K FAU - Takamori, Shinzo AU - Takamori S FAU - Sasada, Tetsuro AU - Sasada T LA - eng PT - Clinical Trial, Phase II PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20120213 PL - England TA - Cancer Sci JT - Cancer science JID - 101168776 RN - 0 (CD3 Complex) RN - 0 (Cancer Vaccines) RN - 0 (Vaccines, Subunit) RN - EC 3.4.14.5 (Dipeptidyl Peptidase 4) SB - IM MH - Aged MH - CD3 Complex MH - Cancer Vaccines/adverse effects/*immunology/therapeutic use MH - Dipeptidyl Peptidase 4 MH - Humans MH - Lung Neoplasms/*therapy MH - Lymphocyte Subsets/immunology MH - Lymphocytes, Tumor-Infiltrating/immunology MH - Male MH - Middle Aged MH - Small Cell Lung Carcinoma/*therapy MH - Vaccines, Subunit/*immunology/therapeutic use PMC - PMC7659229 EDAT- 2012/02/11 06:00 MHDA- 2012/05/17 06:00 PMCR- 2012/04/01 CRDT- 2012/02/11 06:00 PHST- 2011/09/02 00:00 [received] PHST- 2011/12/16 00:00 [revised] PHST- 2011/12/25 00:00 [accepted] PHST- 2012/02/11 06:00 [entrez] PHST- 2012/02/11 06:00 [pubmed] PHST- 2012/05/17 06:00 [medline] PHST- 2012/04/01 00:00 [pmc-release] AID - CAS2202 [pii] AID - 10.1111/j.1349-7006.2012.02202.x [doi] PST - ppublish SO - Cancer Sci. 2012 Apr;103(4):638-44. doi: 10.1111/j.1349-7006.2012.02202.x. Epub 2012 Feb 13.