Correlation between prior therapeutic dendritic cell vaccination and the outcome of patients with metastatic melanoma treated with ipilimumab

2009 ◽  
Vol 27 (15_suppl) ◽  
pp. e20006-e20006 ◽  
Author(s):  
L. Pierret ◽  
S. Wilgenhof ◽  
J. Corthals ◽  
T. Roelandt ◽  
K. Thielemans ◽  
...  

e20006 Background: Ipilimumab (Ipi) is an anti-cytotoxic T lymphocyte associated antigen 4 (CTLA4) IgG1 monoclonal antibody active against metastatic melanoma. Ipi acts by reinforcement of CTL-activation trough B7/CD28 receptor stimulation. A pre- existing anti-tumor CTL repertoire, induced by dendritic cell (DC) vaccination, could influence the therapeutic effect of Ipi. The influence of prior DC-vaccination on the outcome of melanoma patients (pts) treated with Ipi at a single center was analyzed to evaluate this hypothesis. Methods: Data were obtained from the medical files of pts treated at the UZ Brussel with Ipi in protocols CA184–022, -025, and the BMS Ipi medical need program. Ipi (0.3, 3 or 10 mg/kg) was administered iv q3 wks x4 q12 wks thereafter. Results: 20 pts (10M/10F; med age 51y, range 28–72) were identified. Prior therapy: autologous DC-vaccine loaded with melanoma associated antigens (14 pts) ± IFN-a2b (9/14 pts), cytotoxic agents (17 pts). Baseline characteristics: AJCC st IV melanoma (20 pts); baseline LDH > ULN (16 pts). Ipi dose: 0.3 mg/kg (4 pts), 3 mg/kg (2 pts), 10 mg/kg (14 pts). Serial LDH measurements were available for 17 pts; 4 types of LDH-response following Ipi administration were observed: increase (11 pts), decrease (1 pt), fluctuation (4 pts), stable (1 pt). Objective response according to mWHO or irWHO: 3 PR, 1 SD, 16 PD. One pt received 0.3 mg/kg of Ipi (CA184–022) and had SD but no LDH response; at PD she received DC-vaccine and subsequently 10 mg/kg Ipi (medical need program) resulting in a fluctuating LDH-response and regression of an orbita-metastasis. Increasing LDH values following Ipi were less often observed in pts with prior DC-vaccination (5/6 pts (83%) without prior DC-vaccination had increasing LDH-values vs 6/12 pts (50%) with prior vaccination). DC- vaccination also correlated with regression of metastases and disease control (3/15 pts (20%) who were vaccinated had a PR/SD vs 1/6 (17%) PR for those who had not received prior DC-vaccinations). Conclusions: These data represent a small sample size from a single institution; however, our results suggests a potential correlation between prior therapeutic DC vaccination and outcomes in advanced melanoma patients treated with ipilimumab. [Table: see text]

2020 ◽  
Vol 9 (1) ◽  
pp. 1738814
Author(s):  
Wouter W. van Willigen ◽  
Martine Bloemendal ◽  
Marye J. Boers-Sonderen ◽  
Jan Willem B. de Groot ◽  
Rutger H.T. Koornstra ◽  
...  

2012 ◽  
Vol 61 (10) ◽  
pp. 1791-1804 ◽  
Author(s):  
Eva Ellebaek ◽  
Lotte Engell-Noerregaard ◽  
Trine Zeeberg Iversen ◽  
Thomas Moerch Froesig ◽  
Shamaila Munir ◽  
...  

2009 ◽  
Vol 27 (15_suppl) ◽  
pp. 9042-9042
Author(s):  
L. Ridolfi ◽  
L. Fiammenghi ◽  
M. Petrini ◽  
A. M. Granato ◽  
V. Ancarani ◽  
...  

9042 Background: Dendritic cells (DCs) play a crucial role in the interplay between innate and adaptive immune response towards cancer. The combination of immunotherapies with standard treatments for cancer could represent a further chance for advanced melanoma patients. In the literature, higher response rates than those normally obtained have been reported after second-line chemotherapy in patients with non small cell lung cancer pre-treated with vaccines and in patients with follicular B-cell lymphoma vaccinated with an anti-idiotype vaccine whilst in remission. On the basis of this data, we reviewed and updated the clinical results of our dendritic cell based vaccine clinical trial in stage IV melanoma patients. Methods: From December 2002 to 2007, 24 pre-treated metastatic melanoma patients were vaccinated with mature DCs (mDCs) pulsed with autologous tumor lysate (ATL) and keyhole limpet hemocyanin (KLH) followed by a 5-day treatment with low-dose subcutaneous Interleukin-2. Results: We observed 2 complete response (CR), 2 mixed response (MR), 5 partial response (PR), 4 stable disease (SD) and 11 progressive disease (PD) (overall response (OS) 37.5%; clinical benefit 54.1%). All 13 responders had delayed-type hypersensitivity (DTH) positivity to KLH, of whom 10 also showed positivity to the lysate. Eleven (45.8%) of the 24 patients underwent further lines of treatment (5 chemotherapy [CT], 3 surgery [S], 4 biotherapy, 2 radiotherapy [RT] and 4 biochemotherapy [BioCT]) after stopping vaccination (8 due to progression and 3, in SD, because all of their lysate had been used). Of these 11 patients, 2 obtained CR (1 RT, 1 S), 5 PR (3 BioCT, 2 S) for an OR of 63.6%, 1 SD (BioCT) and 3 showed PD as the best response to subsequent therapies, with a median OS of 30 months (range 16–52). Of the 3 SD patients who were forced to stop vaccine treatment, 1 had CR following RT and 2 progressed. Conclusions: Metastatic melanoma responds poorly to standard therapy, in particular after first-line treatment. Vaccination could enhance clinical response to subsequent third- or fourth-line therapies, thus prolonging overall survival. No significant financial relationships to disclose.


Transfusion ◽  
2002 ◽  
Vol 42 (4) ◽  
pp. 428-432 ◽  
Author(s):  
Xuan Duc Nguyen ◽  
Hermann Eichler ◽  
Antje Sucker ◽  
Udo Hofmann ◽  
Dirk Schadendorf ◽  
...  

2016 ◽  
Vol 5 (8) ◽  
pp. e1201625 ◽  
Author(s):  
Steve Boudewijns ◽  
Rutger H. T. Koornstra ◽  
Harm Westdorp ◽  
Gerty Schreibelt ◽  
Alfons J. M. van den Eertwegh ◽  
...  

2010 ◽  
Vol 16 (20) ◽  
pp. 5067-5078 ◽  
Author(s):  
Joannes F.M. Jacobs ◽  
Cornelis J.A. Punt ◽  
W. Joost Lesterhuis ◽  
Roger P.M. Sutmuller ◽  
H. Mary-lène H. Brouwer ◽  
...  

2012 ◽  
Vol 28 (4) ◽  
pp. 1131-1138 ◽  
Author(s):  
CHIE OSHITA ◽  
MASAKO TAKIKAWA ◽  
AKIKO KUME ◽  
HARUO MIYATA ◽  
TADASHI ASHIZAWA ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document