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TENERGY: multicenter phase II study of Atezolizumab monotherapy following definitive Chemoradiotherapy with 5-FU plus Cisplatin in patients with unresectable locally advanced esophageal squamous cell carcinoma
BMC Cancer volume 20, Article number: 336 (2020)
The standard treatment for patients with unresectable locally advanced esophageal squamous cell carcinoma (ESCC) is definitive chemoradiotherapy (CRT) using 5-FU plus cisplatin. However, complete response (CR) rates are low at 11–25%, resulting in 9–10 months of median overall survival (OS). An improved therapeutic efficacy by combining immunotherapy with radiation has been reported in patients with locally advanced non-small cell lung cancer. The results using ESCC cell lines suggest sequential treatment with anti-PD-L1 agents soon after completion of CRT is the most effective combination.
TENERGY trial is a multicenter, phase II, proof-of-concept study to assess the efficacy and safety of atezolizumab following definitive CRT in patients with locally advanced ESCC. The main inclusion criteria are unresectable locally advanced ESCC without distant metastasis, completion of 60 Gy of radiation plus two concomitant cycles of chemotherapy (cisplatin 70 mg/m2 on day 1 and 5-FU 700 mg/m2 on days 1–4, every 28 days), and adequate organ function. Within 6 weeks after CRT, participants will start taking 1200 mg of atezolizumab every three weeks and continue until 12 months or disease progression. The primary endpoint is the confirmed CR rate by the investigator’s assessment. Secondary endpoints include overall response rate, progression-free survival (PFS), OS, adverse events, and confirmed CR rate by central assessment. We will enroll 50 patients (40 with primary locally advanced ESCC and 10 with postoperative locoregionally recurrent ESCC). We will obtain biopsies from the primary site and will collect blood at 3 time points (before CRT, after CRT, and four weeks after the start of atezolizumab) for an exploratory biomarker study. We will analyze the phenotype of immune-competent cells, neoantigens, tumor mutational burden, PD-L1 status, and Human Leukocyte Antigen haplotyping.
The synergistic efficacies of the sequential combination of CRT and atezolizumab should improve the CR rate, resulting in survival improvement for patients with unresectable locally advanced ESCC. Because CRT is a standard treatment option for patients with early stage to locally advanced ESCC, the sequential combination of CRT and atezolizumab has the potential to change the standard ESCC treatments.
Carcinoma of the esophagus is an extremely devastating disease, especially when the disease invades adjacent structures such as aorta, vertebral bodies, or trachea (T4b), and becomes unresectable. According to the Comprehensive Registry of Esophageal Cancer in Japan, the incidence of T4b esophageal cancer accounts for approximately 6.7% of all patients with esophageal cancer (approximately 1500 patients per year) . The standard treatment for this population is definitive chemoradiotherapy (CRT) using 5-FU plus cisplatin. However, complete response (CR) rates are low at 11 to 25%, resulting in 9 to 10 months of median overall survival (OS) [2,3,4]. Although new strategies have been investigated , the treatment regimens have not changed since 1990s.
Immunotherapy with immune checkpoint inhibitors (ICIs) has revolutionized the treatment of advanced cancers, including that of esophageal cancer. Pembrolizumab, an anti-programmed death 1 (PD-1) antibody, significantly improved OS in patients with programmed death ligand 1 (PD-L1) combined positive score (CPS) ≥10 metastatic esophageal cancer . Subgroup analyses indicated higher efficacies of pembrolizumab for patients with esophageal squamous cell carcinoma (ESCC) than those for patients with adenocarcinoma, and the Food and Drug Administration (FDA) approved pembrolizumab for patients with metastatic ESCC whose tumors express PD-L1 CPS ≥10 after ≥1 prior line of systemic therapy. Subsequently, nivolumab, another anti-PD-1 antibody, showed significant OS improvement in patients with metastatic ESCC after ≥1 prior line of systemic therapy (regardless of PD-L1 status) .
ICIs combined with ionizing radiation are promising approaches due to their efficacies. Mechanisms facilitating the action of ICIs by radiation include increased tumor antigen release, activation of innate immune pathway, increased T-cell infiltration, augmented antigen presentation, and modulation of immunosuppressive cells [7, 8]. Indeed, in in vivo models, sequential combination of an anti-PD-1 antibody and radiation increased the proportion of tumor antigen complexes and major histocompatibility complex (MHC) molecules, enhanced lymph node cross-presentation, and increased T-cell tumor infiltration . The polyclonal T-cell response also mediated out-of-field (abscopal) effects following local radiotherapy . An abscopal effect from the combination of radiation and immunotherapy has also been reported in cases with different cancer types . Phase I trials showed a 10–13.5% response rate for liver or lung metastases outside the radiation field [12, 13]; thus, similar efficacies may be expected for micro metastatic lesions in patients with locally advanced cancer.
According to other studies, chemotherapy and radiotherapy may mediate the release of interferon gamma (IFN-γ) produced by CD8+ T cells resulting in PD-L1 upregulations in various tumor cells [8, 14]. Our preliminary studies using both ESCC cell lines and a radiation irradiation device used in the clinical practice also reported that 60 Gy of radiation upregulated only the expression of PD-L1 and MHC Class I without affecting the expression of PD-L2 (data not shown). As lymphocytes are radiation sensitive, we hypothesized that the sequential treatment with anti-PD-L1 agents soon after completion of CRT would enhance the treatment efficacies.
Among patients with unresectable locally advanced non-small cell lung cancer, 12 months of the anti-PD-L1 antibody durvalumab following platinum-based CRT significantly improved both PFS and OS irrespective of PD-L1 expression before CRT [15, 16]. Durvalumab also had a favorable effect on the frequency of new metastases, including on the incidence of new brain metastases. The safety profile of durvalumab was consistent with those of other immunotherapy-related trials, and included a relatively high but acceptable radiation or ICI-induced pneumonitis rate.
Based on this information, we have planned a phase II proof-of-concept (POC) clinical trial to evaluate the safety and efficacy of the anti-PD-L1 antibody atezolizumab following definitive CRT in patients with unresectable locally advanced ESCC.
Study design and treatment
The TENERGY trial is a multicenter, phase II POC study to assess the safety and efficacy of a sequential combination therapy with atezolizumab following 5-FU plus cisplatin-based chemoradiotherapy (60 Gy/30 fractions without prophylactic irradiation) in patients with unresectable locally advanced ESCC without distant metastasis. This study consists of two parts: we will enroll patients with primary locally advanced ESCC into the primary locally advanced ESCC part, and patients with locoregionally recurrent ESCC after surgical resection into the postoperative locoregionally recurrent ESCC part (Fig. 1).
Table 1 shows the inclusion and exclusion criteria for both parts. We will provide the intervention treatment to patients who meet all the inclusion criteria and do not meet any of the exclusion criteria. Although the CRT is not included in the protocol therapy, both chemotherapy and radiation will be stringently qualified based on the quality assurance and quality control program. We will initiate the study intervention treatment within 6 weeks after CRT completion. Patients will receive 1200 mg of atezolizumab every three weeks until 12 months (maximum of 17 doses), disease progression, patient withdrawal, investigator’s decision, pregnancy, or unacceptable toxicities (whichever comes first).
We are conducting this study in accordance with the guidelines for Good Clinical Practice of the International Council on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use, as well as with the ethical guidelines for medical and health research involving human subjects. All patients are required to sign written informed consents. We registered the study in the University Hospital Medical Information Network (Clinical trial information number: UMIN000034373).
Endpoints and assessments
The primary endpoint is the confirmed CR rate by an investigator’s assessment in the primary locally advanced ESCC part. The secondary endpoints are the confirmed CR rate by central assessment, the objective response rate (ORR) by the investigator’s assessment, the PFS, the OS, and the incidence of adverse events (AEs).
CR will be determined by both computed tomography (CT) scanning and endoscopy based on the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 with modifications and on the Japanese Classification of Esophageal Cancer (11th edition), respectively. The schedule for both CT scans and endoscopy examinations are every 4 weeks until CR, following the confirmation of CR after more than 4 weeks, and thereafter every 12 weeks. The modified RECIST defines both measurable and non-measurable lymph nodes as those ≥10 mm and 5–10 mm in their short axis, respectively, when assessed by CT scan. According to the Japanese Classification of Esophageal Cancer, we defined the primary lesion is as CR when conditions satisfy all of the following 4 factors: disappearance of endoscopic findings suggesting the presence of a tumor, negative endoscopic biopsy findings from the area of the primary tumor, evaluable entire esophagus using endoscopy, and no endoscopic findings of active esophagitis. We defined ORR as the proportion of patients who achieve CR or partial response (PR). We defined PFS as the period from registration to progression or death from any cause and will censor it on the last day the patient is alive without progression. OS is the period from registration to death from any cause, and we will censor it on the last day the patient is alive. We will assess AEs according to the Common Terminology Criteria for Adverse Events (CTCAE) version 4.0 before administration of the investigational drug on the administration day. In the postoperative locoregionally recurrent ESCC part, we will assess the same endpoints in an exploratory manner.
Target sample size and statistical analyses
The reported CR rates have ranged from 11 to 25%. In this study, we estimate a rate of 20% as the CR threshold. Therefore, we calculated the sample size of the primary locally advanced ESCC part at 38 with a CR of 40% deemed promising and one of 20% deemed unacceptable (one-sided α, 0.05; β, 0.2). Under this calculation, we are planning to include a maximum of 40 patients in the primary locally advanced ESCC part. We set the planned sample size of the postoperative locoregionally recurrent ESCC part at a maximum of 10 patients in an exploratory manner. We will calculate the confirmed CR by the investigator’s assessment and its 90% confidence interval using the exact binomial method. The results will be considered statistically significant with more than 13 confirmed CR cases in accordance with both the RECIST and the Japanese Classification of Esophageal Cancer in the primary locally advanced ESCC part (i.e., CR rate ≥ 34.2%). We will also determine the confirmed CR rate by central assessment, the ORR by the investigators’ assessment, the PFS, and the OS using appropriate statistical methods. Finally, we will also tabulate the incidence of AEs in the safety population.
Biomarker analyses and translational research
We will perform serial biopsies from the primary site and blood collections at 3 time points (before CRT, after CRT, and four weeks after the first atezolizumab dose). Using the collected samples, we will investigate biomarkers for efficacy or resistance to the sequential combination of CRT and atezolizumab. We will also analyze whole exome sequencing, neoantigens, microsatellite instability, tumor mutational burden, phenotype of immune-competent cells using both flowcytometry and immunohistochemistry, PD-L1 status, and Human Leukocyte Antigen haplotyping.
The TENERGY trial is the first phase II POC study to evaluate the efficacy and safety of sequential combination therapy with 1 year of atezolizumab following definitive CRT in patients with unresectable locally advanced ESCC. The synergistic efficacies of CRT plus ICIs combination should improve the confirmed CR rate, resulting in a prolonged survival. If the combination significantly improves the confirmed CR rate, we will plan a confirmatory phase III trial. Also, as the incidence of T4b esophageal cancer is estimated approximately at 1500 patients per year in Japan, we expect the Japanese Accelerated Approval Program will allow for earlier approval of drugs that treat serious conditions, and that fill an unmet medical need.
Moreover, because CRT is one of the standard treatment options for patients with early stage to locally advanced ESCC, the application of sequential combinations of CRT plus ICIs should be potentially expandable to patients with all ESCC stages and the results of our trial may guide standard ESCC treatment modifications.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Immune checkpoint inhibitors
Programmed death 1
Programmed death ligand 1
Combined positive score
Esophageal squamous cell carcinoma
Food and Drug Administration
Major histocompatibility complex
Objective response rate
Response Evaluation Criteria in Solid Tumors
Common Terminology Criteria for Adverse Events
Tachimori Y, Ozawa S, Numasaki H, Ishihara R, Matsubara H, Muro K, et al. Comprehensive registry of esophageal cancer in Japan, 2012. Esophagus. 2019;16:221–45.
Ishida K, Ando N, Yamamoto S, Ide H, Shinoda M. Phase II study of cisplatin and 5-fluorouracil with concurrent radiotherapy in advanced squamous cell carcinoma of the esophagus: a Japan esophageal oncology group (JEOG)/Japan clinical oncology group trial (JCOG9516). Jpn J Clin Oncol. 2004;34:615–9.
Ohtsu A, Boku N, Muro K, Chin K, Muto M, Yoshida S, et al. Definitive chemoradiotherapy for T4 and/or M1 lymph node squamous cell carcinoma of the esophagus. J Clin Oncol. 1999;17:2915–21.
Shinoda M, Ando N, Kato K, Ishikura S, Kato H, Tsubosa Y, et al. Randomized study of low-dose versus standard-dose chemoradiotherapy for unresectable esophageal squamous cell carcinoma (JCOG0303). Cancer Sci. 2015;106:407–12.
Kojima T, Muro K, Francois E, Hsu CH, Moriwaki T, Kim SB, et al. Pembrolizumab versus chemotherapy as second-line therapy for advanced esophageal cancer: phase III KEYNOTE-181 study. J Clin Oncol. 2019;37:2.
Kato K, Cho BC, Takahashi M, Okada M, Lin CY, Chin K, Kadowaki S, et al. Nivolumab versus chemotherapy in patients with advanced oesophageal squamous cell carcinoma refractory or intolerant to previous chemotherapy (ATTRACTION-3): a multicentre, randomised, open-label, phase 3 trial. Lancet Oncol. 2019;20(11):1506–17.
Deng L, Liang H, Burnette B, Beckett M, Darga T, Weichselbaum RR, et al. Irradiation and anti-PD-L1 treatment synergistically promote antitumor immunity in mice. J Clin Invest. 2014;124:687–95.
Dovedi SJ, Adlard AL, Lipowska-Bhalla G, McKenna C, Jones S, Cheadle EJ, et al. Acquired resistance to fractionated radiotherapy can be overcome by concurrent PD-L1 blockade. Cancer Res. 2014;74:5458–68.
Sharabi AB, Nirschl CJ, Kochel CM, Nirschl TR, Francica BJ, Velarde E, et al. Stereotactic radiation therapy augments antigen-specific PD-1-mediated antitumor immune responses via cross-presentation of tumor antigen. Cancer Immunol Res. 2015;3:345–55.
Park SS, Dong H, Liu X, Harrington SM, Krco CJ, Grams MP, et al. PD-1 restrains radiotherapy-induced abscopal effect. Cancer Immunol Res. 2015;3:610–9.
Postow MA, Callahan MK, Barker CA, Yamada Y, Yuan J, Kitano S, et al. Immunologic correlates of the abscopal effect in a patient with melanoma. N Engl J Med. 2012;366:925–31.
Tang C, Welsh JW, de Groot P, Massarelli E, Chang JY, Hess KR, et al. Ipilimumab with stereotactic ablative radiation therapy: phase I results and immunologic correlates from peripheral T cells. Clin Cancer Res. 2017;23:1388–96.
Luke JJ, Lemons JM, Karrison TG, Melotek JM, Zha Y, Al-Hallaq HA, et al. Safety and clinical activity of pembrolizumab and multisite stereotactic body radiotherapy in patients with advanced solid tumors. J Clin Oncol. 2018;36:1611–8.
Zhang P, Su DM, Liang M, Fu J. Chemopreventive agents induce programmed death-1-ligand 1 (PD-L1) surface expression in breast cancer cells and promote PD-L1-mediated T cell apoptosis. Mol Immunol. 2008;45:1470–6.
Antonia SJ, Villegas A, Daniel D, Vicente D, Murakami S, Hui R, et al. Durvalumab after chemoradiotherapy in stage III non-small-cell lung cancer. N Engl J Med. 2017;377:1919–29.
Antonia SJ, Villegas A, Daniel D, Vicente D, Murakami S, Hui R, et al. Overall survival with Durvalumab after chemoradiotherapy in stage III NSCLC. N Engl J Med. 2018;379:2342–50.
We would like to express special thanks to all participating patients, their families, and all participating investigators.
This investigator-initiated trial is supported by Japan Agency for Medical Research and Development (AMED) (Grant Number 18ck0106420h0001). Chugai Pharmaceutical provided the fund for translational research and the study drugs. Our study protocol was submitted to AMED and Chugai Pharmaceutical for peer-review and was approved. The funding bodies do not affect the design of the study, data collection, data analysis, interpretation of data, and writing the manuscript.
Ethics approval and consent to participate
We are conducting this study in accordance with the guidelines for Good Clinical Practice of the International Council on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use, as well as with the ethical guidelines for medical and health research involving human subjects. This study was approved by the ethics committees at each institution (National Cancer Center Institutional Review Board, Aichi Cancer Center Institutional Review Board, Saitama Cancer Center Review Board, Shizuoka Cancer Center Review Board, Cancer Institute Hospital of Japanese Foundation for Cancer Research Review Board). All patients are required to sign written informed consents.
Consent for publication
HB reports research funding from AstraZeneca and Sysmex, and honoraria from Taiho. DK reports receiving honoraria from Takeda, Chugai, Lilly, Merck Biopharma, Taiho, and Sysmex. TT reports no competing interests. HH reports paid consulting or advisory roles for Chugai, Merck Biopharma, Ono and MSD; honoraria from Chugai, Taiho, Merck Biopharma, Yakult, Lilly, Takeda, Bristol-Myers Squibb, Sanofi, Ono and MSD; and research funding from Astellas, AstraZeneca, Merck Biopharma, Takeda, Boehringer Ingelheim, Lilly, Ono, Sumitomo Dainippon, Daiichi Sankyo, Taiho, Chugai, MSD, Pfizer, Incyte, Beigene, LSK BioPharma and Eisai. SK reports research funding from Taiho, Lilly, and Ono, and honoraria from Taiho, Lilly, Ono, Bristol-Myers Squibb, Yakult, Chugai, Bayer, and Merck BioPharma. KK and KC reports no competing interests. KY, SK, and HH reports no competing interests. MN reports personal fees from MSD and AstraZeneca. HT, MW, and MF report no competing interests. YT reports honoraria from Ono, Bristol-Myers Squibb, Chugai, MSD, and AstraZeneca. NF and HN reports no competing interests. TK reports paid consulting or advisory roles for Bristol-Myers Squibb, honoraria from Oncolys BioPharma, and research funding from Ono, MSD, Oncolys BioPharma, Sihonogi, Chugai and Astellas Amgen BioPharma.
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Bando, H., Kotani, D., Tsushima, T. et al. TENERGY: multicenter phase II study of Atezolizumab monotherapy following definitive Chemoradiotherapy with 5-FU plus Cisplatin in patients with unresectable locally advanced esophageal squamous cell carcinoma. BMC Cancer 20, 336 (2020). https://doi.org/10.1186/s12885-020-06716-5
- Unresectable locally advanced
- Esophageal squamous cell carcinoma