Ipilimumab administered to metastatic melanoma patients who progressed after dendritic cell vaccination

被引:18
作者
Boudewijns, Steve [1 ,2 ]
Koornstra, Rutger H. T. [1 ]
Westdorp, Harm [1 ,2 ]
Schreibelt, Gerty [2 ]
van den Eertwegh, Alfons J. M. [3 ]
Foppen, Marnix H. Geukes [4 ]
Haanen, John B. [4 ]
de Vries, I. Jolanda M. [1 ,2 ]
Figdor, Carl G. [2 ]
Bol, Kalijn F. [1 ,2 ]
Gerritsen, Winald R. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Med Oncol, Geert Grootepl,Zuid 10, NL-6525 GA Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Tumor Immunol, Nijmegen, Netherlands
[3] Vrije Univ Amsterdam Med Ctr, Canc Ctr Amsterdam, Dept Med Oncol, Amsterdam, Netherlands
[4] Netherlands Canc Inst, Dept Med Oncol, Amsterdam, Netherlands
关键词
Dendritic cell vaccination; immunotherapy; ipilimumab; melanoma; PRETREATED ADVANCED MELANOMA; LONG-TERM SURVIVAL; PHASE-II; T-CELLS; TUMOR MICROENVIRONMENT; ANTITUMOR RESPONSES; CANCER VACCINES; STAGE-III; COMBINATION; IMMUNOTHERAPY;
D O I
10.1080/2162402X.2016.1201625
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Ipilimumab has proven to be effective in metastatic melanoma patients. The purpose of this study was to determine the efficacy of ipilimumab in advanced melanoma patients who showed progressive disease upon experimental dendritic cell (DC) vaccination. Methods: Retrospective analysis of 48 stage IV melanoma patients treated with ipilimumab after progression upon DC vaccination earlier in their treatment. DC vaccination was given either as adjuvant treatment for stage III disease (n = 18) or for stage IV disease (n = 30). Ipilimumab (3 mg/kg) was administered every 3 weeks for up to 4 cycles. Results: Median time between progression upon DC vaccination and first gift of ipilimumab was 5.4 mo. Progression-free survival (PFS) rates for patients that received ipilimumab after adjuvant DC vaccination, and patients that received DC vaccination for stage IV melanoma, were 35% and 7% at 1 y and 35% and 3% at 2 y, while the median PFS was 2.9 mo and 3.1 mo, respectively. Median overall survival of patients pre-treated with adjuvant DC vaccination for stage III melanoma was not reached versus 8.0 mo (95% CI, 5.2-10.9) in the group pre-treated with DC vaccination for stage IV disease (HR of death, 0.36; p = 0.017). Grade 3 immune-related adverse events occurred in 19% of patients and one death (2%) was related to ipilimumab. Conclusions: Clinical responses to ipilimumab were found in a considerable number of advanced melanoma patients with progression after adjuvant DC vaccination for stage III disease, while the effect was very limited in patients who showed progression after DC vaccination for stage IV disease.
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页数:9
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