Immune Checkpoint Blockade in Combination with Stereotactic Body Radiotherapy in Patients with Metastatic Pancreatic Ductal Adenocarcinoma

التفاصيل البيبلوغرافية
العنوان: Immune Checkpoint Blockade in Combination with Stereotactic Body Radiotherapy in Patients with Metastatic Pancreatic Ductal Adenocarcinoma
المؤلفون: Jeremy L. Davis, Bradford J. Wood, Elizabeth Gil Ramirez, Gagandeep Brar, Cecilia Monge Bonilla, Freddy E. Escorcia, Melissa Walker, Jennifer Jones, Tim F. Greten, Donna Mabry-Hrones, Austin G. Duffy, Deborah Citrin, David E. Kleiner, Seth M. Steinberg, Billel Gasmi, Jonathan M. Hernandez, Suzanne Fioravanti, Changqing Xie, Bernadette Redd
المصدر: Clinical cancer research : an official journal of the American Association for Cancer Research. 26(10)
سنة النشر: 2019
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Cancer Research, medicine.medical_specialty, Durvalumab, Pilot Projects, Antibodies, Monoclonal, Humanized, Radiosurgery, Gastroenterology, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Antineoplastic Combined Chemotherapy Protocols, medicine, Humans, Tissue Distribution, Adverse effect, Immune Checkpoint Inhibitors, Aged, Aged, 80 and over, business.industry, Antibodies, Monoclonal, Middle Aged, Prognosis, Confidence interval, Immune checkpoint, Blockade, Pancreatic Neoplasms, Survival Rate, 030104 developmental biology, Oncology, 030220 oncology & carcinogenesis, Lymphatic Metastasis, Cohort, Toxicity, Female, business, Tremelimumab, medicine.drug, Carcinoma, Pancreatic Ductal, Follow-Up Studies
الوصف: Purpose: The effectiveness of immune checkpoint inhibitors (ICI) is limited in pancreatic ductal adenocarcinoma (PDAC). We conducted a phase I study to evaluate the safety of ICI with stereotactic body radiation therapy (SBRT) in patients with metastatic PDAC. Patients and Methods: Patients enrolled must have received at least one line of prior systemic chemotherapy for metastatic disease. Cohorts A1 and A2 received durvalumab every 2 weeks plus either 8 Gy in one fraction of SBRT on day 1 or 25 Gy in five fractions on day −3 to +1. Cohorts B1 and B2 received durvalumab plus tremelimumab every 4 weeks and either 8 Gy in one fraction of SBRT on day 1 or 25 Gy in five fractions on day −3 to +1. ICIs were continued until unacceptable toxicity or disease progression. The primary objective was the safety and feasibility of treatment. Objective response was assessed in lesions not subjected to SBRT. Results: Fifty-nine patients were enrolled and 39 were evaluable for efficacy. No dose-limiting toxicities were seen. The most common adverse event was lymphopenia. Two patients achieved a partial response (one confirmed and the other unconfirmed). The overall response rate was 5.1%. Median PFS and OS was 1.7 months [95% confidence intervals (CI), 0.8–2.0 months] and 3.3 months (95% CI, 1.2–6.6 months) in cohort A1; 2.5 months (95% CI, 0.1–3.7 months) and 9.0 months (95% CI, 0.5–18.4 months) in A2; 0.9 months (95% CI, 0.7–2.1 months) and 2.1 months (95% CI, 1.1–4.3 months) in B1; and 2.3 months (95% CI, 1.9–3.4 months) and 4.2 months (95% CI, 2.9–9.3 months) in B2. Conclusions: The combination of ICI and SBRT has an acceptable safety profile and demonstrates a modest treatment benefit in patients with metastatic PDAC.
تدمد: 1557-3265
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4e6456ae1a28e453383372345b34396
https://pubmed.ncbi.nlm.nih.gov/33397682
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....b4e6456ae1a28e453383372345b34396
قاعدة البيانات: OpenAIRE