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Title: | KEYNOTE-051: An update on the phase 2 results of pembrolizumab (pembro) in pediatric patients (pts) with advanced melanoma or a PD-L1-positive advanced, relapsed or refractory solid tumor or lymphoma | Authors: | Geoerger, B. Kang, H. J. Yalon-Oren, M. Marshall, L. V. Vezina, C. Pappo, A. S. Laetsch, T. W. Petrilli, A. S. Ebinger, M. Toporski, J. Glade-Bender, J. Nicholls, W. Fox, E. DuBois, S. G. Macy, M. Cohn, S. L. Pathiraja, K. Diede, S. J. Ebbinghaus, S. Pinto, N. R. |
Issue Date: | 2018 | Source: | 36, (15), 2018 | Journal: | Journal of Clinical Oncology | Abstract: | Background: In the phase 1 portion of KEYNOTE-051 (NCT02332668), the 2-mg/kg-Q3W dose of pembro was identified as the pediatric recommended phase 2 dose. We provide an update on the safety and efficacy of this dose by tumor type in the ongoing phase 2 trial. Methods: Pts aged 6 mo to < 18 y with advanced melanoma or a PD-L1-positive, advanced relapsed/refractory solid tumor or lymphoma and measurable disease per RECIST v1.1 received pembro 2 mg/kg Q3W until confirmed disease progression per irRECIST by investigator review, intolerable toxicity, or pt/investigator decision to discontinue. Key efficacy end points were ORR and PFS per RECIST v1.1 by investigator and OS (data cutoff Oct 10, 2017). Results: 689 of 748 prescreened pts had PD-L1-evaluable tumors. Of these, 229 (33.2%) were PD-L1-positive; 125 pts (median age, 13 y [range, 1-17]) were enrolled and treated (10 Hodgkin lymphoma [HL]; 115 other tumors). Median follow-up was 5.7 mo (range, 0.2-29). Primary diagnoses were other non-central nervous system (CNS) solid tumors (46%), sarcoma (19%), CNS tumors (26%), and lymphoma (9%). Seven (6%) pts experienced grade 3-5 treatmentrelated AEs; of these, 2 (1.6%) discontinued (1 due to increased aspartate aminotransferase; 1 with renal medullary carcinoma died of treatment-related pulmonary edema). No major untoward effects on the developing immune system were observed. One pt (10.0%) with HL achieved CR and 5 (50%) achieved PR. Six (5.2%) pts with other tumors achieved prolonged PR (2 adrenocortical carcinoma and 1 each epithelioid sarcoma, mesothelioma, malignant ganglioglioma, and lymphoepithelial carcinoma). ORR was 60.0% (95% CI, 26.2-87.8) in pts with HL and 5.2% (95% CI, 1.9-11.0) in pts with all other tumor types. Median PFS was 12.2 mo in HL and 1.9 mo in any other tumor type; 12-mo PFS was 56.3% and 8.3%, respectively. Four (40.0%) pts with HL and 19 (16.5%) with any other tumor type survived ≥12 months. Conclusions: Pembro was well tolerated and showed response in HL and in a few rare tumor types, which warrants further study. Enrollment in KEYNOTE-051 is ongoing.L6259752152019-01-22 | DOI: | 10.1200/JCO.2018.36.15_suppl.10525 | Resources: | https://www.embase.com/search/results?subaction=viewrecord&id=L625975215&from=exporthttp://dx.doi.org/10.1200/JCO.2018.36.15_suppl.10525 | | Keywords: | mesothelioma;response evaluation criteria in solid tumors;pediatric patient;aspartate aminotransferaseendogenous compound;pembrolizumab;programmed death 1 ligand 1;adolescent;adrenal cortex carcinoma;advanced cancer;cancer patient;cancer recurrence;cancer resistance;cancer survival;central nervous system tumor;child;conference abstract;controlled study;disease exacerbation;drug efficacy;drug safety;drug therapy;epithelioid sarcoma;female;follow up;ganglioneuroma;Hodgkin disease;human;immune system;kidney;lung edema;lymphoepithelioma;major clinical study;male;medullary carcinoma;melanoma | Type: | Article |
Appears in Sites: | Children's Health Queensland Publications |
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