A phase 1/1B trial of ADI-PEG 20 plus nab-paclitaxel and gemcitabine in patients with advanced pancreatic adenocarcinoma Journal Article


Authors: Lowery, M. A.; Yu, K. H.; Kelsen, D. P.; Harding, J. J.; Bomalaski, J. S.; Glassman, D. C.; Covington, C. M.; Brenner, R.; Hollywood, E.; Barba, A.; Johnston, A.; Liu, K. C. W.; Feng, X.; Capanu, M.; Abou-Alfa, G. K.; O'Reilly, E. M.
Article Title: A phase 1/1B trial of ADI-PEG 20 plus nab-paclitaxel and gemcitabine in patients with advanced pancreatic adenocarcinoma
Abstract: BACKGROUND: ADI-PEG 20 is a pegylated form of the arginine-depleting enzyme arginine deiminase. Normal cells synthesize arginine with the enzyme argininosuccinate synthetase (ASS1); ADI-PEG 20 selectively targets malignant cells, which lack ASS1. METHODS: A single-arm, nonrandomized, open-label, phase 1/1B, standard 3 + 3 dose escalation with an expansion cohort of 9 patients at the recommended phase 2 dose (RP2D) was conducted. Patients who had metastatic pancreatic cancer, up to 1 line of prior treatment (the dose-escalation cohort) or no prior treatment (the expansion cohort), and an Eastern Cooperative Oncology Group performance status of 0 to 1 were included. Patients received both gemcitabine (1000 mg/m2) and nab-paclitaxel (125 mg/m2) for 3 of 4 weeks and intramuscular ADI-PEG 20 at 18 mg/m2 weekly (cohort 1) or at 36 mg/m2 weekly (cohort 2 and the expansion cohort).The primary endpoint was to determine the maximum tolerated dose and RP2D of ADI-PEG 20 in combination with nab-paclitaxel and gemcitabine. RESULTS: Eighteen patients were enrolled. No dose-limiting toxicities (DLTs) were observed in cohort 1; cohort 2 was expanded to 6 patients because of 1 DLT occurrence (a grade 3 elevation in bilirubin, aspartate aminotransferase, and alanine aminotransferase). The most frequent adverse events (AEs) of any grade were neutropenia, thrombocytopenia, leukopenia, anemia, peripheral neuropathy, and fatigue; all 18 patients experienced grade 3/4 AEs. The most frequent grade 3/4 toxicities, regardless of the relation with any drugs, included neutropenia (12 patients or 67%), leukopenia (10 patients or 56%), anemia (8 patients or 44%), and lymphopenia (6 patients or 33%). The RP2D for ADI-PEG 20 was 36 mg/m2 weekly in combination with standard-dose gemcitabine and nab-paclitaxel. The overall response rate among patients treated at the RP2D in the first-line setting was 45.5% (5 of 11).The median progression-free survival time for these patients treated at the RP2D was 6.1 months (95% confidence interval, 5.3-11.2 months), and the median overall survival time was 11.3 months (95% confidence interval, 6.7 months to not reached). CONCLUSIONS: ADI-PEG 20 was well tolerated in combination with gemcitabine and nab-paclitaxel. Activity was observed in previously treated and untreated patients with advanced pancreatic cancer and in patients with ASS1-deficient and -proficient tumors. Cancer 2017;123:4556-4565. © 2017 American Cancer Society. © 2017 American Cancer Society
Keywords: adult; clinical article; aged; middle aged; survival rate; clinical trial; constipation; fatigue; neutropenia; ascites; diarrhea; drug dose reduction; drug safety; hypertension; hypophosphatemia; side effect; gemcitabine; paclitaxel; pancreatic neoplasms; cancer staging; follow up; follow-up studies; antineoplastic agent; neoplasm staging; adenocarcinoma; progression free survival; phase 2 clinical trial; anemia; leukopenia; nausea; neuropathy; thrombocytopenia; vomiting; antineoplastic combined chemotherapy protocols; cohort analysis; deep vein thrombosis; pathology; abdominal pain; alanine aminotransferase blood level; aspartate aminotransferase blood level; chill; coughing; drug dose escalation; dyspnea; fever; hyperglycemia; rash; alanine aminotransferase; alkaline phosphatase; aspartate aminotransferase; bilirubin; confusion; hyperkalemia; hypoalbuminemia; hypokalemia; hyponatremia; hypotension; maculopapular rash; survival time; depression; albumins; pancreas tumor; drug response; acne; peripheral edema; anxiety disorder; pancreas adenocarcinoma; open study; alkaline phosphatase blood level; pancreatic cancer; maximum tolerated dose; phase 1 clinical trial; deoxycytidine; alopecia; bilirubin blood level; cytopenia; injection site erythema; polyethylene glycols; albuminoid; hypocalcemia; cellulitis; abdominal distension; decreased appetite; nab-paclitaxel; macrogol derivative; hydrolases; 130-nm albumin-bound paclitaxel; hydrolase; argininosuccinate synthase; tumor immunogenicity; humans; prognosis; human; male; female; priority journal; article; pegargiminase; analogs and derivatives; adi-peg 20
Journal Title: Cancer
Volume: 123
Issue: 23
ISSN: 0008-543X
Publisher: Wiley Blackwell  
Date Published: 2017-12-01
Start Page: 4556
End Page: 4565
Language: English
DOI: 10.1002/cncr.30897
PUBMED: 28832976
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 2 January 2018 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. James Joseph Harding
    250 Harding
  2. Ghassan Abou-Alfa
    568 Abou-Alfa
  3. Marinela Capanu
    385 Capanu
  4. Maeve Aine Lowery
    133 Lowery
  5. Kenneth Ho-Ming Yu
    163 Yu
  6. Eileen O'Reilly
    780 O'Reilly
  7. David P Kelsen
    537 Kelsen
  8. Robin Beth Brenner
    11 Brenner