Assessment of pegylated arginine deiminase and modified FOLFOX6 in patients with advanced hepatocellular carcinoma: Results of an international, single-arm, phase 2 study.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
15 Dec 2021
Historique:
revised: 27 07 2021
received: 25 06 2021
accepted: 28 07 2021
pubmed: 21 8 2021
medline: 11 3 2022
entrez: 20 8 2021
Statut: ppublish

Résumé

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. 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/m 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%). 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. 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.

Sections du résumé

BACKGROUND 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 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/m
RESULTS 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 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 BACKGROUND
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.

Identifiants

pubmed: 34415578
doi: 10.1002/cncr.33870
doi:

Substances chimiques

Polyethylene Glycols 3WJQ0SDW1A
Hydrolases EC 3.-
ADI PEG20 EC 3.5.3.6
Leucovorin Q573I9DVLP
Fluorouracil U3P01618RT

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4585-4593

Subventions

Organisme : Cancer Research UK
ID : 26813
Pays : United Kingdom
Organisme : Polaris Pharmaceuticals

Informations de copyright

© 2021 American Cancer Society.

Références

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Auteurs

James J Harding (JJ)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Weill Cornell Medical College, New York, New York.

Tsai-Sheng Yang (TS)

Internal Medicine, Linkou Chang Gung Medical Foundation, Taoyuan City, Taiwan.

Yen-Yang Chen (YY)

College of Medicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung City, Taiwan.

Yin-Hsun Feng (YH)

Internal Medicine, Chi Mei Medical Center, Tainan City, Taiwan.

Chia-Jui Yen (CJ)

Department of Internal Medicine, National Cheng Kung University Hospital, Tainan, Taiwan.

Ching-Liang Ho (CL)

Division of Hematology, Department of Medicine, National Defense Medical Center, Tri-Service General Hospital, Taipei City, Taiwan.

Wen-Tsung Huang (WT)

Department of Medicine, Chi Mei Medical Center-Liouying, Tainan City, Taiwan.

Imane El Dika (I)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Weill Cornell Medical College, New York, New York.

Mehmet Akce (M)

Department of Hematology and Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia.

Benjamin Tan (B)

Department of Medicine, Washington University in St Louis, St Louis, Missouri.

Stacey A Cohen (SA)

Oncology, University of Washington, Seattle, Washington.

Timothy Meyer (T)

Oncology, Royal Free Hospital, London, United Kingdom.

Debashis Sarker (D)

Department of Medicine, Guys Hospital, London, United Kingdom.

Dae-Won Lee (DW)

Internal Medicine, Seoul National University Hospital, Seoul, Korea.

Baek-Yeol Ryoo (BY)

Department of Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Ho Yeong Lim (HY)

Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Seoul, Korea.

Amanda Johnston (A)

Polaris Pharmaceuticals, Inc, San Diego, California.

John S Bomalaski (JS)

Polaris Pharmaceuticals, Inc, San Diego, California.

Eileen M O'Reilly (EM)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Weill Cornell Medical College, New York, New York.

Shukui Qin (S)

Cancer Center, Bayi Hospital of Nanjing Chinese Medicine University, Nanjing, China.

Ghassan K Abou-Alfa (GK)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Weill Cornell Medical College, New York, New York.

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