Combined immune checkpoint inhibition with durvalumab and tremelimumab with and without radiofrequency ablation in patients with advanced biliary tract carcinoma

Author:

Monge Cecilia1ORCID,Xie Changqing1,Myojin Yuta1,Coffman‐D'Annibale Kelley L.1ORCID,Hrones Donna1,Brar Gagandeep1,Wang Sophie1,Budhu Anuradha23,Figg William D.4,Cam Maggie5,Finney Richard5,Levy Elliot B.6,Kleiner David E.7,Steinberg Seth M.8,Wang Xin Wei23ORCID,Redd Bernadette9,Wood Bradford J.5,Greten Tim F.13ORCID

Affiliation:

1. Gastrointestinal Malignancies Section, Thoracic and GI Malignancies Branch, Center for Cancer Research, National Cancer Institute National Institutes of Health Bethesda Maryland USA

2. Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute National Institutes of Health Bethesda Maryland USA

3. Liver Cancer Program, Center for Cancer Research, National Cancer Institute National Institutes of Health Bethesda Maryland USA

4. Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute National Institutes of Health Bethesda Maryland USA

5. Center for Collaborative Bioinformatics, Center for Cancer Research, National Cancer Institute National Institutes of Health Bethesda Maryland USA

6. Center for Interventional Oncology, Center for Cancer Research, National Cancer Institute National Institutes of Health Bethesda Maryland USA

7. Laboratory of Pathology, Center for Cancer Research, National Cancer Institute National Institutes of Health Bethesda Maryland USA

8. Biostatistics and Data Management Section, Center for Cancer Research, National Cancer Institute National Institutes of Health Bethesda Maryland USA

9. Radiology and Imaging Sciences, Center for Cancer Research, National Cancer Institute National Institutes of Health Bethesda Maryland USA

Abstract

AbstractBackgroundCurrent standard of care for advanced biliary tract cancer (BTC) is gemcitabine, cisplatin plus anti‐PD1/PD‐L1, but response rates are modest. The purpose of this study was to explore the efficacy and safety of durvalumab (anti‐PD‐L1) and tremelimumab (anti‐CTLA‐4), with and without an interventional radiology (IR) procedure in advanced BTC.MethodsEligible patients with advanced BTC who had received or refused at least one prior line of systemic therapy were treated with tremelimumab and durvalumab for four combined doses followed by monthly durvalumab alone with and without an IR procedure until the progression of disease or unacceptable toxicity. Objective response was assessed through CT or MRI by Response Evaluation Criteria in Solid Tumors (RECIST, version 1.1) every 8 weeks. Adverse events (AEs) were recorded and managed. The primary endpoint was 6‐month progression‐free survival (PFS).ResultsTwenty‐three patients with advanced BTC were enrolled; 17 patients were assigned to treatment with durvalumab and tremelimumab (Durva/Treme); and 6 patients were treated with the combination of durvalumab, tremelimumab plus IR procedure (Durva/Treme + IR). The best clinical responses in the Durva/Treme arm were partial response (n = 1), stable disease (n = 5), progressive disease (n = 5), and in the Durva/Treme + IR arm: partial response (n = 0), stable disease (n = 3), progressive disease (n = 3). The median PFS was 2.2 months (95% CI: 1.3–3.1 months) in the Durva/Treme arm and 2.9 months (95% CI: 1.9–4.7 months) in the Durva/Treme + IR arm (p = 0.27). The median OS was 5.1 months (95% CI: 2.5–6.9 months) in the Durva/Treme arm and 5.8 months (95% CI: 2.9–40.1 months) in the Durva/Treme + IR arm (p = 0.31). The majority of AEs were grades 1–2.ConclusionDurva/Treme and Durva/Treme + IR showed similar efficacy. With a manageable safety profile. Larger studies are needed to fully characterize the efficacy of Durva/Treme ± IR in advanced BTC.

Funder

National Institutes of Health

Cholangiocarcinoma Foundation

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

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