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. 2009 Sep 16;59(2):183–193. doi: 10.1007/s00262-009-0757-9

Table 3.

Phase I clinical trial targeting survivin for advanced and recurrent breast cancer (15 patients)

Survivin 2B 80-88 (AYACNTSTL) peptide vaccine alone (ten patients)
Vaccination 0.1–1.0 mg of survivin-2B peptide every 2 weeks for a total of four times
Toxicities No adverse response
Surrogate marker response Eight patients showed increased level of tumor markers (CEA, CA15-3, NCC-ST-439, and ICTP are examined); level decreased slightly in one patient
Immunologic response Three patients (30%) showed increased peptide-specific CTL
Survivin 2B 80-88 (AYACNTSTL) peptide + IFA (four patients)
Vaccination 1.0 mg of survivin 2B peptide mixed with IFA every 2 weeks for a total of four times
Toxicities Two patients had induration; one patient had general malaise (grade 1); one patient had general malaise and fever
Surrogate marker response All patients showed increased level of tumor markers (CEA, CA15-3, NCC-ST-439, and ICTP are examined)
Immunologic response Four patients (100%) demonstrated increased peptide-specific CTL