First-in-human phase I/II study of NEOD001 in patients with light chain amyloidosis and persistent organ dysfunction / Morie A. Gertz, Heather Landau, Raymond L. Comenzo, David Seldin, Brendan Weiss, Jeffrey Zonder, Giampaolo Merlini, Stefan Schönland, Jackie Walling, Gene G. Kinney, Martin Koller, Dale B. Schenk, Spencer D. Guthrie, Michaela Liedtke
PURPOSE: Light chain (AL) amyloidosis is caused by the accumulation of misfolded proteins, which induces the dysfunction of vital organs. NEOD001 is a monoclonal antibody targeting these misfolded proteins. We report interim data from a phase I/II dose-escalation/expansion study of NEOD001 in patients with AL amyloidosis and persistent organ dysfunction (NCT01707264). - PATIENTS AND METHODS: Patients who had completed at least one previous anti-plasma cell-directed therapy, had partial hematologic response or better, and had persistent organ dysfunction received NEOD001 intravenously every 28 days. Dose levels of 0.5, 1, 2, 4, 8, 16, and 24 mg/kg were evaluated (3 + 3 study design). Primary objectives were to determine the maximum tolerated dose and the recommended dose for future studies and to evaluate safety/tolerability. Secondary and exploratory objectives included pharmacokinetics, immunogenicity, and organ responses on the basis of published consensus criteria. - RESULTS: Twenty-seven patients were enrolled in seven cohorts (dose-escalation component). No drug-related serious adverse events (AEs), discontinuations because of drug-related AEs, dose-limiting toxicities, or antidrug antibodies were reported. The most frequent AEs were fatigue, upper respiratory tract infection, cough, and dyspnea. Recommended dosing was 24 mg/kg. Pharmacokinetics support intravenous dosing every 28 days. Of 14 cardiac-evaluable patients, eight (57%) met the criteria for cardiac response and six (43%) had stable disease. Of 15 renal-evaluable patients, nine (60%) met the criteria for renal response and six (40%) had stable disease. - CONCLUSION: Monthly infusions of NEOD001 were safe and well tolerated. Recommended future dosing was 24 mg/kg. Organ response rates compared favorably with those reported previously for chemotherapy. A phase II expansion is ongoing. A global phase III study (NCT02312206) has been initiated. Antibody therapy targeting misfolded proteins is a potential new therapy for the management of AL amyloidosis..
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
February 8, 2016 2016 |
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| Erschienen: |
February 8, 2016 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:34 |
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| Enthalten in: |
Journal of clinical oncology - 34(2016), 10, Seite 1097-1103 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Gertz, Morie A. [VerfasserIn] |
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| Anmerkungen: |
Gesehen am 04.06.2020 |
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| Umfang: |
7 |
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| doi: |
10.1200/JCO.2015.63.6530 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| 245 | 1 | 0 | |a First-in-human phase I/II study of NEOD001 in patients with light chain amyloidosis and persistent organ dysfunction |c Morie A. Gertz, Heather Landau, Raymond L. Comenzo, David Seldin, Brendan Weiss, Jeffrey Zonder, Giampaolo Merlini, Stefan Schönland, Jackie Walling, Gene G. Kinney, Martin Koller, Dale B. Schenk, Spencer D. Guthrie, Michaela Liedtke |
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| 520 | |a PURPOSE: Light chain (AL) amyloidosis is caused by the accumulation of misfolded proteins, which induces the dysfunction of vital organs. NEOD001 is a monoclonal antibody targeting these misfolded proteins. We report interim data from a phase I/II dose-escalation/expansion study of NEOD001 in patients with AL amyloidosis and persistent organ dysfunction (NCT01707264). - PATIENTS AND METHODS: Patients who had completed at least one previous anti-plasma cell-directed therapy, had partial hematologic response or better, and had persistent organ dysfunction received NEOD001 intravenously every 28 days. Dose levels of 0.5, 1, 2, 4, 8, 16, and 24 mg/kg were evaluated (3 + 3 study design). Primary objectives were to determine the maximum tolerated dose and the recommended dose for future studies and to evaluate safety/tolerability. Secondary and exploratory objectives included pharmacokinetics, immunogenicity, and organ responses on the basis of published consensus criteria. - RESULTS: Twenty-seven patients were enrolled in seven cohorts (dose-escalation component). No drug-related serious adverse events (AEs), discontinuations because of drug-related AEs, dose-limiting toxicities, or antidrug antibodies were reported. The most frequent AEs were fatigue, upper respiratory tract infection, cough, and dyspnea. Recommended dosing was 24 mg/kg. Pharmacokinetics support intravenous dosing every 28 days. Of 14 cardiac-evaluable patients, eight (57%) met the criteria for cardiac response and six (43%) had stable disease. Of 15 renal-evaluable patients, nine (60%) met the criteria for renal response and six (40%) had stable disease. - CONCLUSION: Monthly infusions of NEOD001 were safe and well tolerated. Recommended future dosing was 24 mg/kg. Organ response rates compared favorably with those reported previously for chemotherapy. A phase II expansion is ongoing. A global phase III study (NCT02312206) has been initiated. Antibody therapy targeting misfolded proteins is a potential new therapy for the management of AL amyloidosis. | ||
| 650 | 4 | |a Adult | |
| 650 | 4 | |a Aged | |
| 650 | 4 | |a Amyloidosis | |
| 650 | 4 | |a Antibodies, Monoclonal, Humanized | |
| 650 | 4 | |a Cough | |
| 650 | 4 | |a Dose-Response Relationship, Drug | |
| 650 | 4 | |a Drug Administration Schedule | |
| 650 | 4 | |a Dyspnea | |
| 650 | 4 | |a Fatigue | |
| 650 | 4 | |a Female | |
| 650 | 4 | |a Heart | |
| 650 | 4 | |a Humans | |
| 650 | 4 | |a Immunoglobulin Light Chains | |
| 650 | 4 | |a Kidney | |
| 650 | 4 | |a Male | |
| 650 | 4 | |a Maximum Tolerated Dose | |
| 650 | 4 | |a Middle Aged | |
| 650 | 4 | |a Multiple Organ Failure | |
| 650 | 4 | |a Plasma Cells | |
| 650 | 4 | |a Respiratory Tract Infections | |
| 650 | 4 | |a Treatment Outcome | |
| 700 | 1 | |a Landau, Heather |e verfasserin |4 aut | |
| 700 | 1 | |a Comenzo, Raymond L. |e verfasserin |4 aut | |
| 700 | 1 | |a Seldin, David |e verfasserin |4 aut | |
| 700 | 1 | |a Weiss, Brendan |e verfasserin |4 aut | |
| 700 | 1 | |a Zonder, Jeffrey |e verfasserin |4 aut | |
| 700 | 1 | |a Merlini, Giampaolo |e verfasserin |4 aut | |
| 700 | 1 | |a Schönland, Stefan |d 1969- |e verfasserin |0 (DE-588)122405226 |0 (DE-627)705896137 |0 (DE-576)293255792 |4 aut | |
| 700 | 1 | |a Walling, Jackie |e verfasserin |4 aut | |
| 700 | 1 | |a Kinney, Gene G. |e verfasserin |4 aut | |
| 700 | 1 | |a Koller, Martin |e verfasserin |4 aut | |
| 700 | 1 | |a Schenk, Dale B. |e verfasserin |4 aut | |
| 700 | 1 | |a Guthrie, Spencer D. |e verfasserin |4 aut | |
| 700 | 1 | |a Liedtke, Michaela |e verfasserin |4 aut | |
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