Evidence map›Paper›PMID 32729929›Full record

Trial reportJAMA oncology2020

Evaluation of Combination Nivolumab and Ipilimumab Immunotherapy in Patients With Advanced Biliary Tract Cancers: Subgroup Analysis of a Phase 2 Nonrandomized Clinical Trial.

Oliver Klein, Damien Kee, Adnan Nagrial, Ben Markman, Craig Underhill, Michael Michael, Louise Jackett, Caroline Lum, Andreas Behren, Jodie Palmer and 3 more

2 registry-linked trialsOpen access · bronzeAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in JAMA oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 132 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
132citing papers in PubMed, 8 pooled it
32.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02923934 phase2completednot on this map

A Phase II Clinical Trial Evaluating Ipilimumab and Nivolumab in Combination for the Treatment of Rare Gastrointestinal, Neuro-Endocrine and Gynaecological Cancers

TypeinterventionalSponsorOlivia Newton-John Cancer Research InstituteRan2017 to 2023Enrolled120ConditionsGastrointestinal Cancer, Neuroendocrine Tumours, Malignant Female Reproductive System NeoplasmArmsIpilimumab, Nivolumab
NCT06662877 phase2 / phase3not yet recruitingnot on this mapstarted 2024, after this paper: background citation

Anlotinib Plus Nab-Paclitaxels and S-1 Versus FOLFOX for Patients with Advanced Biliary Tract Cancer As Second-Line Treatment: a Phase 2/3, Multi-centric Double-stage Randomized Controlled Trial

TypeinterventionalSponsorSun Yat-sen UniversityRan2024 to 2029Enrolled206ConditionsBiliary Tract Cancer, Second Line Treatment, Chemotherapy, Tyrosine Kinase InhibitorArmsAlbumin-bound Paclitaxel + Tegafur Gimeracil Oteracil (S-1) + Anlotinib, Oxaliplatin + Leucovorin + Fluorouracil (FOLFOX regimen)
3 · Its place in the literature

Who cites it

132 citing papers in PubMed, 8 syntheses or guidelines pooled it, 224 citations in OpenAlex.

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  16. A Phase II Trial of Pembrolizumab plus Granulocyte-Macrophage Colony-Stimulating Factor in Advanced Biliary Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  17. Advances in Immunotherapy for Intrahepatic Cholangiocarcinoma.International journal of molecular sciences · 2026
    Review
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72 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 8 institutions in 1 country.

Oliver KleinDepartment of Medical Oncology, Austin Health, Melbourne, Australia.
Damien KeeDepartment of Medical Oncology, Austin Health, Melbourne, Australia.
Adnan NagrialBlacktown Hospital and the University of Sydney, Sydney, Australia.
Ben MarkmanDepartment of Medical Oncology, Monash Health, Melbourne, Australia.
Craig UnderhillAlbury-Wodonga Regional Cancer Centre, Albury-Wodonga, Australia.
Michael MichaelDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.
Louise JackettDepartment of Anatomical Pathology, Austin Health, Melbourne, Australia.
Caroline LumDepartment of Medical Oncology, Monash Health, Melbourne, Australia.
Andreas BehrenOlivia Newton-John Cancer Research Institute, Melbourne, Australia.
Jodie PalmerOlivia Newton-John Cancer Research Institute, Melbourne, Australia.
Niall C TebbuttDepartment of Medical Oncology, Austin Health, Melbourne, Australia.
Matteo S CarlinoBlacktown Hospital and the University of Sydney, Sydney, Australia.
Jonathan CebonDepartment of Medical Oncology, Austin Health, Melbourne, Australia.
Austin Health · AULa Trobe University · AUThe University of Sydney · AUAlbury Wodonga Health · AUMonash Health · AUMonash University · AUOlivia Newton-John Cancer Wellness & Research Centre · AUPeter MacCallum Cancer Centre · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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: To evaluate the efficacy and safety of combination immunotherapy with nivolumab and ipilimumab in patients with advanced biliary tract cancers. Design, Setting, and Participants: 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. Interventions: 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. Results: 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.

Indexed as

AdultAgedAged, 80 and overAntibodies, MonoclonalBiliary Tract NeoplasmsDisease ProgressionFemaleHumansImmunotherapyIpilimumabMaleMicrosatellite InstabilityMiddle AgedNivolumabProgrammed Cell Death 1 ReceptorProgression-Free SurvivalAntibodies, MonoclonalIpilimumabNivolumabProgrammed Cell Death 1 Receptor

Identifiers

PMID32729929
PMCPMC7393585
OpenAlexW3046384500

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.