Impact of depatuxizumab mafodotin on health-related quality of life and neurological functioning in the phase II EORTC 1410/INTELLANCE 2 trial for EGFR-amplified recurrent glioblastoma

In the EORTC 1410/INTELLANCE 2 randomised, phase II study (NCT02343406), with the antibody–drug conjugate depatuxizumab mafodotin (Depatux-M, ABT-414) in patients with recurrent EGFR-amplified glioblastoma, the primary end-point (overall survival) was not met, and the drug had ocular dose-limiting t...

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Veröffentlicht in:European journal of cancer (1990) 2021-04, Vol.147, p.1-12
Hauptverfasser: Clement, Paul M.J., Dirven, Linda, Eoli, Marica, Sepulveda-Sanchez, Juan M., Walenkamp, Annemiek M.E., Frenel, Jean S., Franceschi, Enrico, Weller, Michael, Chinot, Olivier, De Vos, Filip Y.F.L., Whenham, Nicolas, Sanghera, Paul, Looman, Jim, Kundu, Madan G., Peter de Geus, Jan, Nuyens, Sarah, Spruyt, Maarten, Gorlia, Thierry, Coens, Corneel, Golfinopoulos, Vassilis, Reijneveld, Jaap C., van den Bent, Martin J.
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container_title European journal of cancer (1990)
container_volume 147
creator Clement, Paul M.J.
Dirven, Linda
Eoli, Marica
Sepulveda-Sanchez, Juan M.
Walenkamp, Annemiek M.E.
Frenel, Jean S.
Franceschi, Enrico
Weller, Michael
Chinot, Olivier
De Vos, Filip Y.F.L.
Whenham, Nicolas
Sanghera, Paul
Looman, Jim
Kundu, Madan G.
Peter de Geus, Jan
Nuyens, Sarah
Spruyt, Maarten
Gorlia, Thierry
Coens, Corneel
Golfinopoulos, Vassilis
Reijneveld, Jaap C.
van den Bent, Martin J.
description In the EORTC 1410/INTELLANCE 2 randomised, phase II study (NCT02343406), with the antibody–drug conjugate depatuxizumab mafodotin (Depatux-M, ABT-414) in patients with recurrent EGFR-amplified glioblastoma, the primary end-point (overall survival) was not met, and the drug had ocular dose-limiting toxicity. This study reports results from the prespecified health-related quality of life (HRQoL) and neurological deterioration-free survival (NDFS) exploratory analysis. Patients (n = 260) were randomised 1:1:1 to receive either Depatux-M 1.25 mg/kg or 1.0 mg/kg intravenously every 2 weeks with oral temozolomide (TMZ) 150 mg/m2, Depatux-M alone, or TMZ or oral lomustine (CCNU) 110 mg/m2 (TMZ/CCNU). HRQoL outcomes were recorded using the EORTC core Quality of Life QLQ-C30, and brain cancer-specific QLQ-BN20 questionnaires. Questionnaires were completed at baseline, weeks 8 and 16, and month 6, and changes from baseline to each time point were calculated. NDFS was defined as time to first deterioration in World Health Organisation performance status. Compliance with HRQoL was 88.1% at baseline and decreased to 37.9% at month 6. Differences from baseline between Depatux-M arms and TMZ/CCNU in global health/QoL status throughout treatment did not reach clinical relevance (≥10 points). Self-reported visual disorders deteriorated to a clinically relevant extent with Depatux-M arms versus TMZ/CCNU at all timepoints (mean differences range: 24.6–35.1 points). Changes from baseline for other HRQoL scales and NDFS were generally similar between treatment arms. Depatux-M had no impact on HRQoL and NDFS in patients with EGFR-amplified recurrent glioblastoma, except for more visual disorders, an expected side-effect of the study drug. NCT02343406. •Clinically relevant increases in self-reported visual disorders with Depatux-M.•Similar health-related quality of life scores between Depatux-M and standard care.•Neurological deterioration-free survival was similar between treatments.
doi_str_mv 10.1016/j.ejca.2021.01.010
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This study reports results from the prespecified health-related quality of life (HRQoL) and neurological deterioration-free survival (NDFS) exploratory analysis. Patients (n = 260) were randomised 1:1:1 to receive either Depatux-M 1.25 mg/kg or 1.0 mg/kg intravenously every 2 weeks with oral temozolomide (TMZ) 150 mg/m2, Depatux-M alone, or TMZ or oral lomustine (CCNU) 110 mg/m2 (TMZ/CCNU). HRQoL outcomes were recorded using the EORTC core Quality of Life QLQ-C30, and brain cancer-specific QLQ-BN20 questionnaires. Questionnaires were completed at baseline, weeks 8 and 16, and month 6, and changes from baseline to each time point were calculated. NDFS was defined as time to first deterioration in World Health Organisation performance status. Compliance with HRQoL was 88.1% at baseline and decreased to 37.9% at month 6. Differences from baseline between Depatux-M arms and TMZ/CCNU in global health/QoL status throughout treatment did not reach clinical relevance (≥10 points). Self-reported visual disorders deteriorated to a clinically relevant extent with Depatux-M arms versus TMZ/CCNU at all timepoints (mean differences range: 24.6–35.1 points). Changes from baseline for other HRQoL scales and NDFS were generally similar between treatment arms. Depatux-M had no impact on HRQoL and NDFS in patients with EGFR-amplified recurrent glioblastoma, except for more visual disorders, an expected side-effect of the study drug. NCT02343406. •Clinically relevant increases in self-reported visual disorders with Depatux-M.•Similar health-related quality of life scores between Depatux-M and standard care.•Neurological deterioration-free survival was similar between treatments.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/j.ejca.2021.01.010</identifier><identifier>PMID: 33601293</identifier><language>eng</language><publisher>London: Elsevier Ltd</publisher><subject>Amplification ; Antibodies ; Brain cancer ; Depatuxizumab mafodotin ; Deterioration ; Disorders ; Epidermal growth factor receptors ; Glioblastoma ; Global health ; Life Sciences ; Life Sciences &amp; Biomedicine ; Lomustine ; Oncology ; Patient-reported outcomes ; Patients ; Phase II ; Public health ; Quality of life ; Questionnaires ; Randomised ; Science &amp; Technology ; Side effects ; Survival ; Temozolomide ; Toxicity ; Vision ; Visual disorders</subject><ispartof>European journal of cancer (1990), 2021-04, Vol.147, p.1-12</ispartof><rights>2021 Elsevier Ltd</rights><rights>Copyright © 2021 Elsevier Ltd. 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Self-reported visual disorders deteriorated to a clinically relevant extent with Depatux-M arms versus TMZ/CCNU at all timepoints (mean differences range: 24.6–35.1 points). Changes from baseline for other HRQoL scales and NDFS were generally similar between treatment arms. Depatux-M had no impact on HRQoL and NDFS in patients with EGFR-amplified recurrent glioblastoma, except for more visual disorders, an expected side-effect of the study drug. 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This study reports results from the prespecified health-related quality of life (HRQoL) and neurological deterioration-free survival (NDFS) exploratory analysis. Patients (n = 260) were randomised 1:1:1 to receive either Depatux-M 1.25 mg/kg or 1.0 mg/kg intravenously every 2 weeks with oral temozolomide (TMZ) 150 mg/m2, Depatux-M alone, or TMZ or oral lomustine (CCNU) 110 mg/m2 (TMZ/CCNU). HRQoL outcomes were recorded using the EORTC core Quality of Life QLQ-C30, and brain cancer-specific QLQ-BN20 questionnaires. Questionnaires were completed at baseline, weeks 8 and 16, and month 6, and changes from baseline to each time point were calculated. NDFS was defined as time to first deterioration in World Health Organisation performance status. Compliance with HRQoL was 88.1% at baseline and decreased to 37.9% at month 6. Differences from baseline between Depatux-M arms and TMZ/CCNU in global health/QoL status throughout treatment did not reach clinical relevance (≥10 points). Self-reported visual disorders deteriorated to a clinically relevant extent with Depatux-M arms versus TMZ/CCNU at all timepoints (mean differences range: 24.6–35.1 points). Changes from baseline for other HRQoL scales and NDFS were generally similar between treatment arms. Depatux-M had no impact on HRQoL and NDFS in patients with EGFR-amplified recurrent glioblastoma, except for more visual disorders, an expected side-effect of the study drug. NCT02343406. •Clinically relevant increases in self-reported visual disorders with Depatux-M.•Similar health-related quality of life scores between Depatux-M and standard care.•Neurological deterioration-free survival was similar between treatments.</abstract><cop>London</cop><pub>Elsevier Ltd</pub><pmid>33601293</pmid><doi>10.1016/j.ejca.2021.01.010</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-9157-9895</orcidid><orcidid>https://orcid.org/0000-0001-9332-4677</orcidid><orcidid>https://orcid.org/0000-0002-1748-174X</orcidid><orcidid>https://orcid.org/0000-0003-4744-9377</orcidid><orcidid>https://orcid.org/0000-0001-6616-5762</orcidid><orcidid>https://orcid.org/0000-0001-5710-5127</orcidid><oa>free_for_read</oa></addata></record>
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source Web of Science - Science Citation Index Expanded - 2021<img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" />; Access via ScienceDirect (Elsevier)
subjects Amplification
Antibodies
Brain cancer
Depatuxizumab mafodotin
Deterioration
Disorders
Epidermal growth factor receptors
Glioblastoma
Global health
Life Sciences
Life Sciences & Biomedicine
Lomustine
Oncology
Patient-reported outcomes
Patients
Phase II
Public health
Quality of life
Questionnaires
Randomised
Science & Technology
Side effects
Survival
Temozolomide
Toxicity
Vision
Visual disorders
title Impact of depatuxizumab mafodotin on health-related quality of life and neurological functioning in the phase II EORTC 1410/INTELLANCE 2 trial for EGFR-amplified recurrent glioblastoma
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