TY - JOUR
T1 - Assessment of pegylated arginine deiminase and modified FOLFOX6 in patients with advanced hepatocellular carcinoma
T2 - Results of an international, single-arm, phase 2 study
AU - Harding, James J.
AU - Yang, Tsai Sheng
AU - Chen, Yen Yang
AU - Feng, Yin Hsun
AU - Yen, Chia Jui
AU - Ho, Ching Liang
AU - Huang, Wen Tsung
AU - El Dika, Imane
AU - Akce, Mehmet
AU - Tan, Benjamin
AU - Cohen, Stacey A.
AU - Meyer, Timothy
AU - Sarker, Debashis
AU - Lee, Dae Won
AU - Ryoo, Baek Yeol
AU - Lim, Ho Yeong
AU - Johnston, Amanda
AU - Bomalaski, John S.
AU - O’Reilly, Eileen M.
AU - Qin, Shukui
AU - Abou-Alfa, Ghassan K.
N1 - Funding Information:
James J. Harding reports grants from Bristol Myers Squibb; personal fees from Adaptimmune, Bristol Myers Squibb, Merck, Eli Lilly, Exelexis, Eisai, CytomX, Imvax, Zymeworks, and QED; and participates on an advisory board for Merck outside the submitted work. Mehmet Akce reports institutional research funding from Bristol Myers Squibb, Merck, Polaris Pharmaceuticals Inc, Xencor, GlaxoSmithKline, Eisai, RedHill Biopharma, Bellicum Pharmaceuticals, and Boehringer Ingelheim; and participation on advisory boards for Eisai, Exelixis, Ipsen, GlaxoSmithKline, and QED outside the submitted work. Benjamin Tan reports institutional research funding from Adaptimmune, Bristol Myers Squibb, Exelexis, TYME, Agios, AstraZeneca, and Zymeworks outside the submitted work. Stacey A. Cohen reports grants from Isofol and Sumitomo Dainippon and personal fees from Acrotech, Natera, and Kallyope outside the submitted work. Timothy Meyer reports personal fees from Ipsen, Roche, Bayer, Eisai, Adaptimmune, Boston Scientific, and AstraZeneca outside the submitted work. Ho Yeong Lim reports honoraria from Bayer, Ipsen, Eisai, and Bristol Myers Squibb; and participates on advisory boards for Ipsen, Eisai, Bristol Myers Squibb, MSD Pharmaceuticals, and Roche outside the submitted work. Amanda Johnston received a salary from Polaris Pharmaceuticals Inc during the conduct of the study and owns stock in the company. John S. Bomalaski is an employee of Polaris Pharmaceuticals Inc. Eileen M. O'Reilly reports grants from Genentech/Roche, Celgene/Bristol Myers Squibb, BioNTech, BioAtla, AstraZeneca, Arcus, Elicio, Parker Institute; personal fees from Sobi, Silenseed, Tyme, Seagen, Molecular Templates, Boehringer Ingelheim, BioNTech, Ipsen, Polaris Pharmaceuticals Inc, Merck, IDEAYA, Cend, AstraZeneca, Noxxon, BioSapien, Bayer (spouse), Genentech-Roche (spouse), Celgene-Bristol Myers Squibb (spouse), and Eisai (spouse); and participation on data safety monitoring boards for CytomX Therapeutics and Rafael Therapeutics outside the submitted work. Ghassan K. Abou-Alfa reports grants from Arcus, Agios, AstraZeneca, BioNTech, Bristol Myers Squibb, Celgene, Flatiron, Genentech/Roche, Genoscience, Incyte, Polaris Pharmaceuticals Inc, Puma, QED, Sillajen, and Yiviva; and personal fees from Adicet, Agios, AstraZeneca, Alnylam, Autem, Bayer, Beigene, Berry Genomics, Cend, Celgene, CytomX, Eisai, Eli Lilly, Exelixis, Flatiron, Genentech/Roche, Genoscience, Helio, Incyte, Ipsen, Legend Biotech, Loxo, Merck, MINA, Nerviano, QED, Redhill, Rafael, Silenseed, Sillajen, Sobi, Surface Oncology, Therabionics, Twoxar, Vector, and Yiviva outside the submitted work. The remaining authors made no disclosures. This study was funded by Polaris Pharmaceuticals, Inc, San Diego, California.
Funding Information:
James J. Harding reports grants from Bristol Myers Squibb; personal fees from Adaptimmune, Bristol Myers Squibb, Merck, Eli Lilly, Exelexis, Eisai, CytomX, Imvax, Zymeworks, and QED; and participates on an advisory board for Merck outside the submitted work. Mehmet Akce reports institutional research funding from Bristol Myers Squibb, Merck, Polaris Pharmaceuticals Inc, Xencor, GlaxoSmithKline, Eisai, RedHill Biopharma, Bellicum Pharmaceuticals, and Boehringer Ingelheim; and participation on advisory boards for Eisai, Exelixis, Ipsen, GlaxoSmithKline, and QED outside the submitted work. Benjamin Tan reports institutional research funding from Adaptimmune, Bristol Myers Squibb, Exelexis, TYME, Agios, AstraZeneca, and Zymeworks outside the submitted work. Stacey A. Cohen reports grants from Isofol and Sumitomo Dainippon and personal fees from Acrotech, Natera, and Kallyope outside the submitted work. Timothy Meyer reports personal fees from Ipsen, Roche, Bayer, Eisai, Adaptimmune, Boston Scientific, and AstraZeneca outside the submitted work. Ho Yeong Lim reports honoraria from Bayer, Ipsen, Eisai, and Bristol Myers Squibb; and participates on advisory boards for Ipsen, Eisai, Bristol Myers Squibb, MSD Pharmaceuticals, and Roche outside the submitted work. Amanda Johnston received a salary from Polaris Pharmaceuticals Inc during the conduct of the study and owns stock in the company. John S. Bomalaski is an employee of Polaris Pharmaceuticals Inc. Eileen M. O'Reilly reports grants from Genentech/Roche, Celgene/Bristol Myers Squibb, BioNTech, BioAtla, AstraZeneca, Arcus, Elicio, Parker Institute; personal fees from Sobi, Silenseed, Tyme, Seagen, Molecular Templates, Boehringer Ingelheim, BioNTech, Ipsen, Polaris Pharmaceuticals Inc, Merck, IDEAYA, Cend, AstraZeneca, Noxxon, BioSapien, Bayer (spouse), Genentech‐Roche (spouse), Celgene‐Bristol Myers Squibb (spouse), and Eisai (spouse); and participation on data safety monitoring boards for CytomX Therapeutics and Rafael Therapeutics outside the submitted work. Ghassan K. Abou‐Alfa reports grants from Arcus, Agios, AstraZeneca, BioNTech, Bristol Myers Squibb, Celgene, Flatiron, Genentech/Roche, Genoscience, Incyte, Polaris Pharmaceuticals Inc, Puma, QED, Sillajen, and Yiviva; and personal fees from Adicet, Agios, AstraZeneca, Alnylam, Autem, Bayer, Beigene, Berry Genomics, Cend, Celgene, CytomX, Eisai, Eli Lilly, Exelixis, Flatiron, Genentech/Roche, Genoscience, Helio, Incyte, Ipsen, Legend Biotech, Loxo, Merck, MINA, Nerviano, QED, Redhill, Rafael, Silenseed, Sillajen, Sobi, Surface Oncology, Therabionics, Twoxar, Vector, and Yiviva outside the submitted work. The remaining authors made no disclosures.
Funding Information:
This study was funded by Polaris Pharmaceuticals, Inc, San Diego, California.
Publisher Copyright:
© 2021 American Cancer Society
PY - 2021/12/15
Y1 - 2021/12/15
N2 - Background: Arginine starvation depletes the micronutrients required for DNA synthesis and interferes with both thymidylate synthetase activity and DNA repair pathways in preclinical models of hepatocellular carcinoma (HCC). Pegylated arginine deiminase (ADI-PEG 20), an arginine degrader, potentiates the cytotoxic activity of platinum and pyrimidine antimetabolites in HCC cellular and murine models. Methods: This was a global, multicenter, open-label, single-arm, phase 2 trial of ADI-PEG 20 and modified 5-fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) in patients who had HCC with Child-Pugh A cirrhosis and disease progression on ≥2 prior lines of treatment. The primary objective was the objective response rate assessed according to Response Evaluation Criteria in Solid Tumors, version 1.1. Secondary objectives were to estimate progression-free survival, overall survival, safety, and tolerability. Eligible patients were treated with mFOLFOX6 intravenously biweekly at standard doses and ADI-PEG-20 intramuscularly weekly at 36 mg/m2. Results: In total, 140 patients with advanced HCC were enrolled. The median patient age was 62 years (range, 30-85 years), 83% of patients were male, 76% were of Asian race, 56% had hepatitis B viremia, 10% had hepatitis C viremia, 100% had received ≥2 prior lines of systemic therapy, and 39% had received ≥3 prior lines of systemic therapy. The objective response rate was 9.3% (95% confidence interval [CI], 5.0%-15.4%), with a median response duration of 10.2 months (95% CI, 5.8 months to not reached). The median progression-free survival was 3.8 months (95% CI, 1.8-6.3 months), and the median overall survival was 14.5 months (95% CI, 13.6-20.9 months). The most common grade ≥3 treatment-related events were neutropenia (32.9%), white blood cell count decrease (20%), platelet count decrease (19.3%), and anemia (9.3%). Conclusions: Concurrent mFOLFOX6 plus ADI-PEG 20 exhibited limited antitumor activity in patients with treatment-refractory HCC. The study was terminated early, and no further evaluation of the combination will be pursued. Lay Summary: Arginine is an important nutrient for hepatocellular carcinoma (HCC). The depletion of arginine with pegylated arginine deiminase (ADI-PEG 20), an arginine degrader, appeared to make chemotherapy (FOLFOX) work better in animal models of HCC and in patients with HCC on an early phase clinical trial. To formally test this hypothesis in the clinical setting, a large, global, phase 2 clinical trial was conducted of ADI-PEG 20 and FOLFOX in the treatment of patients with refractory HCC. The study showed limited activity of ADI-PEG 20 and FOLFOX in advanced HCC and was stopped early.
AB - Background: Arginine starvation depletes the micronutrients required for DNA synthesis and interferes with both thymidylate synthetase activity and DNA repair pathways in preclinical models of hepatocellular carcinoma (HCC). Pegylated arginine deiminase (ADI-PEG 20), an arginine degrader, potentiates the cytotoxic activity of platinum and pyrimidine antimetabolites in HCC cellular and murine models. Methods: This was a global, multicenter, open-label, single-arm, phase 2 trial of ADI-PEG 20 and modified 5-fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) in patients who had HCC with Child-Pugh A cirrhosis and disease progression on ≥2 prior lines of treatment. The primary objective was the objective response rate assessed according to Response Evaluation Criteria in Solid Tumors, version 1.1. Secondary objectives were to estimate progression-free survival, overall survival, safety, and tolerability. Eligible patients were treated with mFOLFOX6 intravenously biweekly at standard doses and ADI-PEG-20 intramuscularly weekly at 36 mg/m2. Results: In total, 140 patients with advanced HCC were enrolled. The median patient age was 62 years (range, 30-85 years), 83% of patients were male, 76% were of Asian race, 56% had hepatitis B viremia, 10% had hepatitis C viremia, 100% had received ≥2 prior lines of systemic therapy, and 39% had received ≥3 prior lines of systemic therapy. The objective response rate was 9.3% (95% confidence interval [CI], 5.0%-15.4%), with a median response duration of 10.2 months (95% CI, 5.8 months to not reached). The median progression-free survival was 3.8 months (95% CI, 1.8-6.3 months), and the median overall survival was 14.5 months (95% CI, 13.6-20.9 months). The most common grade ≥3 treatment-related events were neutropenia (32.9%), white blood cell count decrease (20%), platelet count decrease (19.3%), and anemia (9.3%). Conclusions: Concurrent mFOLFOX6 plus ADI-PEG 20 exhibited limited antitumor activity in patients with treatment-refractory HCC. The study was terminated early, and no further evaluation of the combination will be pursued. Lay Summary: Arginine is an important nutrient for hepatocellular carcinoma (HCC). The depletion of arginine with pegylated arginine deiminase (ADI-PEG 20), an arginine degrader, appeared to make chemotherapy (FOLFOX) work better in animal models of HCC and in patients with HCC on an early phase clinical trial. To formally test this hypothesis in the clinical setting, a large, global, phase 2 clinical trial was conducted of ADI-PEG 20 and FOLFOX in the treatment of patients with refractory HCC. The study showed limited activity of ADI-PEG 20 and FOLFOX in advanced HCC and was stopped early.
KW - arginine
KW - fluorouracil, leucovorin, and oxaliplatin (FOLFOX)
KW - hepatocellular carcinoma
KW - pegylated arginine deiminase (ADI-PEG 20)
KW - phase 2
UR - http://www.scopus.com/inward/record.url?scp=85113175620&partnerID=8YFLogxK
U2 - 10.1002/cncr.33870
DO - 10.1002/cncr.33870
M3 - Article
C2 - 34415578
AN - SCOPUS:85113175620
SN - 0008-543X
VL - 127
SP - 4585
EP - 4593
JO - Cancer
JF - Cancer
IS - 24
ER -