Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/29052
Title: Evaluation of Combination Nivolumab and Ipilimumab Immunotherapy in Patients with Advanced Biliary Tract Cancers: Subgroup Analysis of a Phase 2 Nonrandomized Clinical Trial.
Authors: Palmer J.;Lum C.;Behren A.;Tebbutt N.C.;Cebon J.;Carlino M.S.;Klein O.;Kee D.;Nagrial A.;Markman B.;Underhill C.;Michael M.;Jackett L.
Institution: (Klein, Kee, Tebbutt, Cebon) Department of Medical Oncology, Austin Health, Melbourne, Australia (Klein, Behren, Palmer, Cebon) Olivia Newton-John Cancer Research Institute, Melbourne, Australia (Kee, Michael) Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia (Nagrial, Carlino) Blacktown Hospital and the University of Sydney, Sydney, Australia (Markman, Lum) Department of Medical Oncology, Monash Health, Melbourne, Australia (Markman) Monash University, Melbourne, Australia (Underhill) Albury-Wodonga Regional Cancer Centre, Albury-Wodonga, Australia (Jackett) Department of Anatomical Pathology, Austin Health, Melbourne, Australia (Behren, Palmer, Cebon) School of Cancer Medicine, La Trobe University, Australia (Tebbutt) Department of Surgery, University of Melbourne, Melbourne, Australia
Issue Date: 23-Oct-2020
Copyright year: 2020
Publisher: American Medical Association (E-mail: shirley.martin@ama-assn.org)
Place of publication: United States
Publication information: JAMA Oncology. 6 (9) (pp 1405-1409), 2020. Date of Publication: September 2020.
Journal: JAMA Oncology
Abstract: Importance: Biliary tract cancers represent a rare group of malignant conditions with very limited treatment options. Patients with advanced disease have a poor outcome with current therapies. Objective(s): To evaluate the efficacy and safety of combination immunotherapy with nivolumab and ipilimumab in patients with advanced biliary tract cancers. Design, Setting, and Participant(s): The CA209-538 prospective multicenter phase 2 nonrandomized clinical trial included patients with advanced rare cancers including patients with biliary tract cancers. This subgroup analysis evaluated 39 patients from CA209-538 with biliary tract cancers who were enrolled from December 2017 to December 2019. Most of the patients (n = 33) had experienced disease progression after 1 or more lines of therapy and had tumor tissue available for biomarker research. Intervention(s): Patients received treatment with nivolumab at a dose of 3 mg/kg and ipilimumab at 1 mg/kg every 3 weeks for 4 doses, followed by nivolumab 3 mg/kg every 2 weeks and continued for up to 96 weeks until disease progression or the development of unacceptable toxic events. Main Outcomes and Measures: The primary end point was disease control rate (complete remission, partial remission, or stable disease) as assessed by RECIST 1.1. Result(s): Among the 39 patients included in this subgroup analysis of a phase 2 clinical trial (20 men, 19 women; mean [range] age, 65 [37-81] years), the objective response rate was 23% (n = 9) with a disease control rate of 44% (n = 17); all responders had received prior chemotherapy, and none had a microsatellite unstable tumor. Responses were exclusively observed in patients with intrahepatic cholangiocarcinoma and gallbladder carcinoma. The median duration of response was not reached (range, 2.5 to =23 months). The median progression-free survival was 2.9 months (95% CI, 2.2-4.6 months), and overall survival was 5.7 months (95% CI, 2.7-11.9 months). Immune-related toxic events were reported in 49% of patients (n = 19), with 15% (n = 6) experiencing grade 3 or 4 events. Conclusions and Relevance: This subgroup analysis of a phase 2 clinical trial found that combination immunotherapy with nivolumab and ipilimumab was associated with substantial positive outcomes patients with advanced biliary tract cancers. This treatment compares favorably to single-agent anti-programmed cell death protein 1 (anti-PD-1) therapy and warrants further investigation. Ongoing translational research is focused on identifying biomarkers that can predict treatment response. Trial Registration: ClinicalTrials.gov Identifier: NCT02923934.Copyright © 2020 American Medical Association. All rights reserved.
DOI: http://monash.idm.oclc.org/login?url=http://acs.hcn.com.au/?acc=36265&url=http://dx.doi.org/10.1001/jamaoncol.2020.2814
PubMed URL: 32729929 [http://www.ncbi.nlm.nih.gov/pubmed/?term=32729929]
ISSN: 2374-2437
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/29052
Type: Article
Subjects: cancer patient
*nivolumab/iv [Intravenous Drug Administration]
*nivolumab/pd [Pharmacology]
*nivolumab/pv [Special Situation for Pharmacovigilance]
triacylglycerol lipase/ec [Endogenous Compound]
abdominal pain/si [Side Effect]
abnormally high substrate concentration in blood/si [Side Effect]
adrenal insufficiency/si [Side Effect]
adult
advanced cancer/dt [Drug Therapy]
aged
anemia/si [Side Effect]
antineoplastic activity
article
*bile duct carcinoma/dt [Drug Therapy]
*cancer combination chemotherapy
cancer control
cancer immunotherapy
cancer regression
cancer survival
cancer tissue
clinical article
cohort analysis
colitis/si [Side Effect]
controlled study
decreased appetite/si [Side Effect]
diarrhea/si [Side Effect]
drug efficacy
drug eruption/si [Side Effect]
drug fatality/si [Side Effect]
drug fever/si [Side Effect]
drug safety
drug screening
drug withdrawal
endocrine disease/si [Side Effect]
fatigue/si [Side Effect]
female
*gallbladder carcinoma/dt [Drug Therapy]
hepatitis/si [Side Effect]
human
human tissue
hyperthyroidism/si [Side Effect]
hypertransaminasemia/si [Side Effect]
hypophosphatemia/si [Side Effect]
hypothyroidism/si [Side Effect]
immunopathology/si [Side Effect]
injection site reaction/si [Side Effect]
kidney failure/si [Side Effect]
lymphocytopenia/si [Side Effect]
maintenance therapy
male
microsatellite instability
monotherapy
multicenter study
nausea/si [Side Effect]
outcome assessment
overall survival
phase 2 clinical trial
pneumonia/si [Side Effect]
progression free survival
prospective study
pruritus/si [Side Effect]
response evaluation criteria in solid tumors
treatment duration
treatment response
triacylglycerol lipase blood level
very elderly
*ipilimumab/ae [Adverse Drug Reaction]
*ipilimumab/ct [Clinical Trial]
*ipilimumab/cb [Drug Combination]
*ipilimumab/dt [Drug Therapy]
*ipilimumab/iv [Intravenous Drug Administration]
*ipilimumab/pd [Pharmacology]
*ipilimumab/pv [Special Situation for Pharmacovigilance]
*nivolumab/ae [Adverse Drug Reaction]
*nivolumab/ct [Clinical Trial]
*nivolumab/dt [Drug Therapy]
cancer control
cancer immunotherapy
cancer patient
cancer regression
cancer survival
cancer tissue
clinical article
cohort analysis
colitis / side effect
controlled study
decreased appetite / side effect
diarrhea / side effect
drug efficacy
drug eruption / side effect
drug fatality / side effect
drug fever / side effect
drug safety
drug screening
drug withdrawal
endocrine disease / side effect
fatigue / side effect
female
*gallbladder carcinoma / *drug therapy
hepatitis / side effect
human
human tissue
hyperthyroidism / side effect
hypertransaminasemia / side effect
hypophosphatemia / side effect
hypothyroidism / side effect
immunopathology / side effect
injection site reaction / side effect
kidney failure / side effect
lymphocytopenia / side effect
maintenance therapy
male
microsatellite instability
monotherapy
multicenter study
nausea / side effect
outcome assessment
overall survival
phase 2 clinical trial
pneumonia / side effect
progression free survival
pruritus / side effect
response evaluation criteria in solid tumors
treatment duration
treatment response
triacylglycerol lipase blood level
very elderly
adrenal insufficiency / side effect
abnormally high substrate concentration in blood / side effect
abdominal pain / side effect
prospective study
adult
advanced cancer / drug therapy
aged
anemia / side effect
antineoplastic activity
Article
*bile duct carcinoma / *drug therapy
*cancer combination chemotherapy
Type of Clinical Study or Trial: Observational study (cohort, case-control, cross sectional or survey)
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