SwePub
Sök i LIBRIS databas

  Utökad sökning

id:"swepub:oai:DiVA.org:uu-390379"
 

Sökning: id:"swepub:oai:DiVA.org:uu-390379" > First-in-human stud...

First-in-human study with intratumoral administration of a CD40 agonistic antibody, ADC-1013, in advanced solid malignancies

Irenaeus, Sandra (författare)
Uppsala universitet,Experimentell och klinisk onkologi
Nielsen, Dorte (författare)
Herlev Gentofte Hosp, Dept Oncol, Herlev, Denmark
Ellmark, Peter (författare)
Medicon Village, Alligator Biosci AB, Lund, Sweden
visa fler...
Yachnin, Jeffrey (författare)
Karolinska Institutet
Deronic, Adnan (författare)
Medicon Village, Alligator Biosci AB, Lund, Sweden
Nilsson, Anneli (författare)
Medicon Village, Alligator Biosci AB, Lund, Sweden
Norlen, Per (författare)
Medicon Village, Alligator Biosci AB, Lund, Sweden
Veitonmaki, Niina (författare)
Medicon Village, Alligator Biosci AB, Lund, Sweden
Wennersten, Camilla S. (författare)
Medicon Village, Alligator Biosci AB, Lund, Sweden
Ullenhag, Gustav (författare)
Uppsala universitet,Experimentell och klinisk onkologi
visa färre...
 (creator_code:org_t)
2019-03-08
2019
Engelska.
Ingår i: International Journal of Cancer. - : WILEY. - 0020-7136 .- 1097-0215. ; 145:5, s. 1189-1199
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Agonistic CD40 antibodies activate dendritic cells and can expand and activate tumor-specific T cells. Our purpose was to assess the CD40 agonistic antibody ADC-1013 in the clinical setting including intratumoral administration since preclinical studies have indicated that intratumoral is better than intravenous administration. A Phase I, open label, multicenter study was conducted in patients with advanced solid tumors who had received established treatments. A modified 3 + 3 dose-escalation was applied (every other week dosing). Twenty-three patients were treated with ADC-1013 intratumorally (dosing from 22.5 mu g/kg up to 400 mu g/kg) or intravenously (dosing at 75 mu g/kg). The pharmacodynamic effects observed in the patients were further verified in an hCD40tg mouse model. Adverse events were mostly Common Terminology Criteria for Adverse Events (CTCAE) Grades 1 or 2 and transient. The serum concentration ADC-1013 and cytokine release (MCP-1, TNF alpha and IL-6) were more pronounced in patients receiving injections in deep metastases compared to patients receiving injections in superficial metastases. Treatment with ADC-1013 resulted in a marked decrease in B cell levels in peripheral blood after 24 h while remaining B cells significantly increased their expression of the cell surface activation marker CD86. Activation of antigen-presenting cells and subsequent activation of T cells were demonstrated in hCD40tg mice. Moreover, ADC-1013 treatment in this mouse model acted synergistically with a PD-1 inhibitor. The results from the first-in-human study of ADC-1013 indicate that intratumoral administration of ADC-1013 into superficial lesions is well tolerated at clinically relevant doses and associated with pharmacodynamic responses.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

agonistic antibody
CD40
phase I study
metastatic cancer

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy