<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Siebert N</submitter><funding>Cancer Research UK</funding><funding>Deutsche Kinderkrebsstiftung</funding><pagination>387</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6210332</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(10)</volume><pubmed_abstract>GD₂-directed immunotherapies improve survival of high-risk neuroblastoma (NB) patients (pts). Treatment with chimeric anti-GD₂ antibodies (Ab), such as ch14.18, can induce development of human anti-chimeric Ab (HACA). Here, we report HACA effects on ch14.18/CHO pharmacokinetics, pharmacodynamics and pain intensity in pts treated by long-term infusion (LTI) of ch14.18/CHO combined with IL-2. 124 pts received up to 5 cycles of ch14.18/CHO 10 days (d) infusion (10 mg/m²/d; d8⁻18) combined with s.c. IL-2 (6 × 10⁶ IU/m²/d; d1⁻5, d8⁻12). HACA, treatment toxicity, ch14.18/CHO levels, Ab-dependent cellular- (ADCC) and complement-dependent cytotoxicity (CDC) were assessed using respective validated assays. HACA-negative pts showed a steadily decreased pain in cycle 1 (74% pts without morphine by d5</pubmed_abstract><journal>Cancers</journal><pubmed_title>Impact of HACA on Immunomodulation and Treatment Toxicity Following ch14.18/CHO Long-Term Infusion with Interleukin-2: Results from a SIOPEN Phase 2 Trial.</pubmed_title><pmcid>PMC6210332</pmcid><funding_grant_id>14042</funding_grant_id><funding_grant_id>DKS 2014.05 A/B</funding_grant_id><pubmed_authors>Ehlert K</pubmed_authors><pubmed_authors>Ash S</pubmed_authors><pubmed_authors>Siebert N</pubmed_authors><pubmed_authors>Castel V</pubmed_authors><pubmed_authors>Manzitti C</pubmed_authors><pubmed_authors>Klingebiel T</pubmed_authors><pubmed_authors>Beck J</pubmed_authors><pubmed_authors>Garaventa A</pubmed_authors><pubmed_authors>Troschke-Meurer S</pubmed_authors><pubmed_authors>Gray J</pubmed_authors><pubmed_authors>Lode HN</pubmed_authors><pubmed_authors>Marx M</pubmed_authors><pubmed_authors>Ladenstein R</pubmed_authors><pubmed_authors>Zumpe M</pubmed_authors><pubmed_authors>Valteau-Couanet D</pubmed_authors><pubmed_authors>Loibner H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of HACA on Immunomodulation and Treatment Toxicity Following ch14.18/CHO Long-Term Infusion with Interleukin-2: Results from a SIOPEN Phase 2 Trial.</name><description>GD₂-directed immunotherapies improve survival of high-risk neuroblastoma (NB) patients (pts). Treatment with chimeric anti-GD₂ antibodies (Ab), such as ch14.18, can induce development of human anti-chimeric Ab (HACA). Here, we report HACA effects on ch14.18/CHO pharmacokinetics, pharmacodynamics and pain intensity in pts treated by long-term infusion (LTI) of ch14.18/CHO combined with IL-2. 124 pts received up to 5 cycles of ch14.18/CHO 10 days (d) infusion (10 mg/m²/d; d8⁻18) combined with s.c. IL-2 (6 × 10⁶ IU/m²/d; d1⁻5, d8⁻12). HACA, treatment toxicity, ch14.18/CHO levels, Ab-dependent cellular- (ADCC) and complement-dependent cytotoxicity (CDC) were assessed using respective validated assays. HACA-negative pts showed a steadily decreased pain in cycle 1 (74% pts without morphine by d5</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Oct</publication><modification>2025-04-04T22:21:43.673Z</modification><creation>2019-03-27T00:05:45Z</creation></dates><accession>S-EPMC6210332</accession><cross_references><pubmed>30336605</pubmed><doi>10.3390/cancers10100387</doi></cross_references></HashMap>