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Immunisation of metastatic cancer patients with MAGE-3 protein combined with adjuvant SBAS-2 : A clinical report

Marchand, M (author)
Punt, CJA (author)
Aamdal, S (author)
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Escudier, B (author)
Kruit, WHJ (author)
Keilholz, U (author)
Håkansson, Leif (author)
Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Onkologi,Onkologiska kliniken US
van Baren, N (author)
Humblet, Y (author)
Mulders, P (author)
Avril, M-F (author)
Eggermont, AMM (author)
Scheibenbogen, C (author)
Uiters, J (author)
Wanders, J (author)
Delire, M (author)
Boon, T (author)
Stoter, G (author)
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 (creator_code:org_t)
2003
2003
English.
In: European Journal of Cancer. - 0959-8049 .- 1879-0852. ; 39:1, s. 70-77
  • Journal article (peer-reviewed)
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  • Fifty-seven patients with MAGE-3-positive measurable metastatic cancer, most of them with melanoma, were vaccinated with escalating doses of a recombinant MAGE-3 protein combined with a fixed dose of the immunological adjuvant SBAS-2, which contained MPL and QS21. The immunisation schedule included 4 intramuscular (i.m.) injections at 3-week intervals. Patients whose tumour stabilised or regressed after 4 vaccinations received 2 additional vaccinations at 6-week intervals. The vaccine was generally well tolerated. Among the 33 melanoma patients who were evaluable for tumour response, we observed 2 partial responses, 2 mixed responses and 1 stabilisation. Time to progression in these 5 patients varied from 4 to 29 months. In addition, a partial response lasting 10 months was observed in 1 of the 3 metastatic bladder cancer patients included. None of the tumour responses described above involved visceral metastases. Immunological responses to the vaccine will be reported separately. ⌐ 2002 Elsevier Science Ltd. All rights reserved.

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