Skip to main content
  • Study Protocol
  • Open access
  • Published:

A safety study of intraoperative radiation therapy following stereotactic body radiation therapy and multi-agent chemotherapy in the treatment of localized pancreatic adenocarcinoma: study protocol of a phase I trial



Localized pancreatic adenocarcinoma carries a poor prognosis even after aggressive therapy. Up to 40% of patients may develop locoregional disease as the first site of failure. As such, there may be a role for intensification of local therapy such as radiation therapy. Radiation dose escalation for pancreatic cancer is limited by proximity of the tumor to the duodenum. However, the duodenum is removed during Whipple procedure, allowing the opportunity to dose escalate with intraoperative radiation therapy (IORT). Although prior studies have shown potential benefit of IORT in pancreatic cancer, these studies did not utilize ablative doses (biologically effective dose [BED10] > 100 Gy). Furthermore, the optimal radiation target volume in this setting is unclear. There has been increased interest in a “Triangle Volume” (TV), bordered by the celiac axis, superior mesenteric artery, common hepatic artery, portal vein, and superior mesenteric vein. Dissection of this area, has been advocated for by surgeons from Heidelberg as it contains extra-pancreatic perineural and lymphatic tracts, which may harbor microscopic disease at risk of mediating local failure. Interestingly, a recent analysis from our institution indicated that nearly all local failures occur in the TV. Therefore, the purpose of this protocol is to evaluate the safety of delivering an ablative radiation dose to the TV with IORT following neoadjuvant chemotherapy and stereotactic body radiation therapy (SBRT).


Patients with non-metastatic pancreatic adenocarcinoma centered in the head or neck of the pancreas will be enrolled. Following treatment with multi-agent neoadjuvant chemotherapy, patients will undergo SBRT (40 Gy/5 fractions) followed by IORT (15 Gy/1 fraction) to the TV during the Whipple procedure. The primary objective is acute (< 90 days) toxicity after IORT measured by Clavien-Dindo classification. Secondary objectives include late (> 90 days) toxicity after IORT measured by Clavien-Dindo classification, overall survival, local progression-free survival, distant metastasis-free survival, and progression-free survival.


If the results show that delivering an ablative radiation dose to the TV with IORT after neoadjuvant chemotherapy and SBRT is safe and feasible, it warrants further investigation in a phase II trial to evaluate efficacy of this approach.

Trial Registration This study was registered at on 12/2/2021 (NCT05141513).


Pancreatic adenocarcinoma (PDAC) is the third most common cause of cancer related deaths in the United States, responsible for over 48,000 deaths each year [1]. At time of diagnosis, approximately 10% are resectable, 40% are borderline resectable (BRPC) or locally advanced (LAPC), and the remaining 50% are metastatic. Treatment of localized disease usually involves a combination of multi-agent chemotherapy, radiation therapy, and surgery [2]. Unfortunately, even with aggressive therapy, prognosis is poor with 5-year overall survival (OS) of less than 15% [3].

Improvements in chemotherapy and radiation therapy have increased the proportion of patients with non-metastatic disease who can undergo surgery [4, 5]. However, after surgery, while distant failure predominates, a not insignificant portion of patients (30–40%) develop local recurrence [6, 7]. In fact, one report demonstrated that 30% of all pancreatic cancer patients die from locally destructive disease [8]. This suggests that there may be a role for intensification of local therapies such as radiation. However, dose escalation of radiation therapy in this context is limited by proximity to gastrointestinal structures and in particularly the duodenum. Given that the duodenum is resected during Whipple surgery, intra-operative radiation therapy (IORT) provides a unique opportunity to intensify radiation delivery for pancreatic cancer and further escalate the radiation dose delivered beyond what is feasible with external beam radiation therapy alone, even with modern technologies such as stereotactic body radiation therapy (SBRT). Additionally, IORT allows for shielding of other normal organs, direct visualization of the target, and elimination of positional uncertainties.

Several studies have investigated the role of IORT for localized pancreatic cancer and have suggested that the addition of IORT may improve local control without additional acute or late toxicity [9,10,11]. Keane et al. evaluated a group of BRPC/LAPC who underwent neoadjuvant chemotherapy and chemoradiation, followed by surgical resection with or without IORT [10]. The addition of IORT led to improved median survival (35.1 vs 24.5 months, p = nss) with no differences in intraoperative blood loss, 90-day readmission rates, or post-operative complications between the two groups. A more recent study by Sekigami et al. showed that IORT after neoadjuvant chemotherapy and chemoradiation in BRPC/LAPC mitigates the poor prognosis of R1 resection when compared to no IORT. There was no difference in 90-day mortality rate or 30-day major complication rate (IORT: 17% vs no IORT: 22%, p = 0.477) [11].

Although the aforementioned retrospective reports suggest the efficacy and safety of IORT, there are few prospective studies [12]. Furthermore, prior studies have used conventional dose fractionation schemes, with a total radiation dose (external beam radiation therapy + IORT) less than what is considered ablative (Biologically effective dose [BED10] > 100 Gy). Additionally, many of these studies were performed prior to the incorporation of FOLFIRINOX chemotherapy, which has been shown to improve OS and disease-free survival. Finally, these studies limited IORT fields to the specific vascular margins at risk as opposed to a larger peri-pancreatic target encompassing perineural tracts and lymphovascular channels at risk of microscopic residual disease after resection, which may drive local failure in this population [13].

The optimal radiation volume in the treatment of localized pancreatic cancer is currently unknown. However, there is growing interest among surgeons in the dissection of the space between the celiac artery (CA), superior mesenteric artery (SMA), common hepatic artery (CHA), portal vein (PV), and superior mesenteric vein (SMV) [13, 14]. This region is thought contain extra-pancreatic perineural and lymphatic tracts, which can harbor microscopic disease, and therefore, mediate locoregional relapse. Surgeons from Heidelburg are proponents of the “Triangle Operation”, which involves extended dissection of this space [14]. In fact, our group previously performed an analysis in which the location of local failures was mapped [15], and this analysis showed that local failures are nearly universally located within this space, which we will hereto forward refer to as the “Triangle Volume (TV).”

As such, the goal of this protocol is to prospectively explore the safety and feasibility of implementing IORT in patients with localized pancreatic cancer undergoing surgical resection after pre-operative chemotherapy and SBRT, with the goal of safely reaching ablative radiation doses to the TV when combined with pre-operative SBRT. At the conclusion of this study, we will compare the safety outcomes to prior institutional data [16]. If deemed safe and feasible, we will plan to open a phase II trial to formally evaluate the efficacy of this approach with the goal of improving local control for this disease.



The primary objective is to evaluate acute post-operative toxicity (< 90 days) of IORT targeted to the TV in patients with non-metastatic pancreatic adenocarcinoma undergoing surgical resection after neoadjuvant multi-agent chemotherapy and SBRT.

The secondary objectives are as follows: 1.To evaluate late toxicity (> 90 days) of IORT targeted to the TV in patients with non-metastatic PDAC undergoing surgical resection after neoadjuvant multi-agent chemotherapy and SBRT, 2. Estimate median local progression-free survival (LPFS) from time of IORT, 3. Estimate median overall survival (OS) from time of IORT, 4. Estimate median distant metastasis-free survival (DMFS) from time of IORT and 5. Estimate median progression-free survival (PFS) from time of IORT.

Study design

This is a prospective, single institution, single arm safety study to evaluate the safety and feasibility of implementing IORT in patients with non-metastatic PDAC centered in the head or neck of the pancreas who have been treated with neoadjuvant chemotherapy and SBRT and who are undergoing Whipple procedure. All patients will be discussed in our institutional pancreatic multi-disciplinary clinic. Patients with localized PDAC will be considered for enrolling in the study. Patients will be formally enrolled after completion of chemotherapy and just prior to SBRT. This would allow us to assess treatment response with imaging and exclude patients who developed distant disease during chemotherapy. Table 1 shows the protocol calendar and Fig. 1 displays the protocol schema.

Table 1 Study calendar
Fig. 1
figure 1

Study protocol schema


This study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by the institutional review board (IRB) of Johns Hopkins University (IRB00294801). All subjects or an authorized representative, will be informed of the nature of the study and will provide written informed consent, approved by the IRB of Johns Hopkins University. All patients enrolled on this protocol will undergo discussions with health care providers regarding risks, benefits, and details of each intervention. This study has been registered at (NCT05141513).



All patients will be treated upfront multi-agent chemotherapy, with the exact regimen and duration at the discretion of the treating medical oncologist. During chemotherapy, patients will generally have pancreatic protocol imaging approximately every 2 months to assess treatment response.

Stereotactic body radiation therapy

After completion of chemotherapy, patients will be planned for SBRT to 40 Gy in 5 fractions. This dose and fractionation is recommended by the Australasian Gastrointestinal Trials and Trans-Tasman Radiation Oncology Group [17]. Prior to SBRT, all patients will have ultrasound guided endoscopic gold or platinum fiducial placement for the purpose of daily image guidance. At time of simulation, patients will be positioned supine with arms above head in a Vac-Lok (CIVCO Medical Solutions, Coralville, IA, USA) for immobilization. Thin-sliced computed tomography (CT) scans with intravenous contrast will be obtained for radiation treatment planning. Motion management with active breathing control (ABC, Elekta, Stockholm, Sweden) will be performed. Patients who cannot tolerate breath-hold will be treated under free-breathing conditions, with an internal target volume (ITV) generated from the peak inspiratory and expiratory phases from a 4-dimensional CT scan. The clinical target volume (CTV) and organs at risk will be contoured using Pinnacle treatment planning system (Phillips Radiation Oncology Systems, Fitchburg, WI). The CTV will include gross disease as well as the TV, which includes the space between the CA, SMA, CHA, PV, and SMV. The planning target volume (PTV) will be generated by adding a patient-specific margin to the CTV based on assessment of variability in fiducial positioning between multiple breath-hold scans acquired at simulation (usually on the order of 2-4 mm) followed by an additional 2 mm isotropic expansion. For free-breathing cases, the PTV will be generated by adding a 2 mm isotropic expansion to the iCTV. Daily image guidance with pre-treatment and intrafractional cone-beam CT scans will be performed to ensure proper setup. Patients will be aligned to spine and then shifted to align to fiducials.


Approximately 1–8 weeks after completion of SBRT, patients will have restaging imaging. The decision for surgical exploration will be at the discretion of the surgical oncologist. Surgery may take place anywhere from 2 and 10 weeks after completion of SBRT. Intraoperatively, a photo will be taken to document dissection of the TV.

Intraoperative radiation therapy

Intraoperative radiation therapy will be delivered with high-dose-rate (HDR) brachytherapy using a Freiburg flap applicator. This approach was chosen because the Freiburg flap can be placed to ensure proper contact with key vasculature that define the borders of the TV and the ability to space the applicator into the area at risk. A Freiburg flap that corresponds in size to the TV will be constructed. A radiation plan will be generated in conjunction with the medical physics team to optimally target the TV with 15 Gy, prescribed to the surface of the volume. Catheters will be threaded through the Freiburg Flap, secured in place, and numbered. The Freiburg Flap will then be positioned into the TV. Lead shields will be placed between the Freiburg Flap and normal organs at risk, including stomach, remaining small and large bowel, ureters, etc. The catheters will subsequently be connected to the afterloader system that houses the Ir-192 source. A “dummy” run will be performed to ensure no kinks in the system. The operative room will subsequently be cleared of personnel, and remote monitoring from the control room will be confirmed. A timeout will subsequently be performed, after which treatment will commence to deliver 15 Gy in 1 fraction. Upon completion of treatment, the room will be checked for any radio-activity, after which personnel can subsequently re-enter the room. At this point, surgical clips will be placed along the vessels that border the flap to confirm dosimetry on post-operative imaging. The Freiburg Flap and any lead will be removed. During the post-operative hospital stay, patients will undergo a CT Abdomen in the radiation oncology department to confirm dosimetry and ensure appropriate radiation coverage.

Rational for radiation dose

A total radiation dose of 109.5 Gy BED10 will be delivered, with SBRT in 40 Gy in 5 fractions (BED10 = 72 Gy) and IORT in 15 Gy in 1 fraction (BED10 = 37.5 Gy). This dose was chosen because BED10 > 100 Gy has been associated with excellent local control in both pancreatic cancer and other solid tumors [18,19,20]. Stereotactic body radiation therapy to 40 Gy in 5 fractions is recommended by the Australasian Gastrointestinal Trials and Trans-Tasman Radiation Oncology Group [17]. Intraoperative radiation therapy to 15 gy in 1 fraction is a commonly used dose for pancreatic cancer with a range of 12.5–20 Gy in 1 fraction [10,11,12].


Patients will follow-up in clinic every 3 months with imaging for the first 2 years post-surgery and then every 6 months with imaging for years 3–5 post-surgery. During each follow-up visit, patients will undergo a physical exam, assessment of performance status, and have routine blood work including cancer antigen 19–9. Additionally, chemotherapy-induced and radiation-induced toxicity will be assessed using the Common Terminology Criteria for Adverse Events (CTCAE) criteria (v5.0). Surgical- toxicity will be assessed using Clavien-Dindo classification. Toxicity will be evaluated at each follow-up visit. Disease progression and response will be assessed using Response Evaluation Criteria in Solid Tumors (RECIST) criteria (v1.1).

Inclusion criteria

Subjects must meet all of the following criteria to be eligible for participation in the study:

  1. 1.

    Age ≥ 18 years old

  2. 2.

    Resectable/BRPC/LAPC as defined by National Comprehensive Cancer Network guidelines [2] confirmed via CT, endoscopic ultrasound, or other imaging modalities.

  3. 3.

    Eastern Cooperative Oncology Group performance status 0–2

  4. 4.

    Subject or authorized representative, has been informed of the nature of the study and has provided written informed consent, approved by the appopriate Institutional Review Board of Johns Hopkins Hospital

  5. 5.

    Upfront treatment with multi-agent chemotherapy

  6. 6.

    Tumor location in the pancreatic head or neck that would be technically amenable to Whipple resection

  7. 7.

    Candidate for surgical exploration at Johns Hopkins Hospital

  8. 8.

    Candidate for SBRT at Johns Hopkins Hospital

Exclusion criteria

Sujects who meet any of the following criteria are not eligible for participation in the study:

  1. 1.

    Previous thoracic/abdominal radiation therapy

  2. 2.

    Unable to receive SBRT at Johns Hopkins Hospital

  3. 3.

    Duodenal invasion detected on imaging which would exclude candidacy for SBRT

  4. 4.

    Tumor located in pancreatic body or tail

  5. 5.

    Medical or technical contraindications to a Whipple procedure

  6. 6.

    Evidence of disease not localized to the pancreas

  7. 7.

    Any arterial reconstruction during surgery

  8. 8.

    Currently enrolled in another investigational drug or device trial that clinically interferes with this study

  9. 9.

    Unable to comply with study requirements or follow-up schedule

  10. 10.

    Women of child bearing potential or sexually active fertile men with partners who are women of child bearing potenital who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study

Statistical analysis and sample size

Descriptive statistics will be utilized to record patient demographic, disease, and treatment characteristics including age, sex, race, disease extent, chemotherapy, radiation therapy, and type of surgery. Time to event outcomes such as OS, LPFS, DMFS, and PFS will be analyzed using Kaplan–Meier method. Our institution’s data and experience suggest that 15% of patients will not be surgically explored due to development of radiographic metastatic disease or too locally extensive disease after SBRT. An additional 15% will require unexpected arterial reconstruction (exclusion criteria). Therefore, 25 patients will be enrolled with the expectation that 20/25 patients will undergo surgical exploration and IORT. A sample size of 20 patients was chosen because this will enable safety evaluation using a closely monitored Bayesian stopping rule and is also recommended by the literature [21, 22]. There will not be any interim data analysis. Data analysis will occur once the study has been completed.

Study endpoints

Primary endpoint: post-operative complications in first 90 days following IORT will be recorded as a binary variable (≥ Clavien-Dindo grade IIIa or < Clavien-Dindo grade IIIa). Clavien-Dindo classification is displayed in Table 2 [23].

Table 2 Clavien-Dindo classification

Secondary endpoints are as follows: 1. Post-operative complications after 90 days following IORT will be recorded as a binary variable (≥ Clavien-Dindo grade IIIa or < Clavien-Dindo grade IIIa), 2.Local progression-free will be recorded as time from IORT to first occurrence of locoregional or last known negative imaging. Locoregional failure will include disease recurrence occurring within the surgical bed, extra-pancreatic perineural tracts, regional nodal basins, or the triangle volume, 3. Overall survival will be recorded as the time from IORT to death or last known clinic follow-up, 4. Distant metastasis-free survival will be measured from time of IORT to the development of distant progression or last known negative imaging. 5. Progression-free survival will be measured as the interval from the end of IORT to the time of the first radiographic evidence of any failure, death, or last known negative imaging.

Safety stopping rules

To minimize the risks of IORT, safety will be monitored by a Bayesian stopping rule for the rate of adverse events of interest. Previous experience demonstrated that the incidence of 90-day Clavien-Dindo Grade ≥ IIIa is 25% [23]. Safety will be monitored continuously for 20 patients through day 90.

Adverse events (AE) will be monitored continuously for all patients. A Bayesian safety monitoring rule will be used to evaluate the rate of the AE of interest continuously, from the 3rd evaluable patient, and will suspend accrual at any point if there is sufficient evidence of excessive toxicity. Specifically, the Bayesian toxicity monitoring rule will suspend accrual anytime if the posterior probability of AE of interest being larger than 40%, is 70% or higher. We assume a priori that the experimental regimens has an average risk of 25% and there is a 25% chance that the risk will be 40% or higher. Table 3 summarizes the continuous stopping rule for the 20 evaluable patients for each regimen. For example, if 2 patients out of the first 3 evaluable patients experience adverse events of interest, we will stop accrual. Furthermore, to cautiously assess the toxicity profiles of experimental regimens in the event that accrual is relatively “fast” comparing to the safety assessment duration, the accruals of each cohort will be suspended when 6 eligible patients have been accrued to allow the continuous safety evaluations to be done among the first 6 evaluable patients before further accruals. The accrual would resume only if the Bayesian stopping rule utilized is not met. At any time if the stopping criterion is met, accrual to the trial will be temporarily suspended and the principle investigators and study team will review the toxicity data and recommend either modification or termination of the trial.

Table 3 Stopping rule for safety

Table 4 summarizes the operating characteristics based on 5,000 simulations with 20 evaluable patients in terms of how frequent the study would stop based on the stopping rule under different hypothetical toxicity rates, as well as the average sample sizes.

Table 4 Operating characteristics of the stopping rule for safety


Although distant progression is most common after primary resection of pancreatic cancer, locoregional relapse can be common, with up to 40% patients developing locoregional disease as the first site of failure [24, 25]. Uncontrolled locoregional progression can negatively impact morbidity and mortality outcomes [26]. Cardillo et al. demonstrated that the uncontrolled locoregional disease was the most common cause of hospitalization in pancreatic cancer patients [26]. Therefore, intensification of local therapy, such as dose-escalated radiation, is warranted. Dose escalation in pancreatic cancer is limited by proximity of the tumor to the duodenum. However, the duodenum is removed during Whipple procedure, allowing opportunity for dose escalation using IORT.

There is debate regarding the appropriate treatment volumes for localized pancreatic cancer in the pre-operative and/or definitive setting. While consensus guidelines recommend treatment of gross disease alone, others suggest that treatment of elective nodal regions in addition to gross disease may provide benefit [27,28,29,30]. Surgeons from Heidelberg have advocated for extended dissection of the space between the CA, SMA, CHA, PV, and SMV, termed the “Triangle Operation” [14]. This region, which we call the “Triangle volume”, is thought to contain extrapancreatic perineural tracts and lymphatic channels, which may harbor microscopic disease and mediate locoregional relapse [13]. In fact, a recent analysis from our institution [15] demonstrated that nearly all local failures occur within this TV.

This protocol will evaluate the safety and feasibility of delivering an ablative dose of radiation to the TV using IORT (15 Gy/1 fraction) after neoadjuvant chemotherapy and SBRT (40 Gy/5 fractions) in patients undergoing Whipple procedure. A total BED10 of 109.5 Gy will be delivered to the TV. If the results show that dose escalation with IORT is safe and feasible, it warrants further investigation in a phase II setting to evaluate efficacy of this approach.

Availability of data and materials

Not applicable.



Pancreatic adenocarcinoma


Borderline resectable pancreatic cancer


Locally advanced pancreatic cancer:


Intraoperative radiation therapy


Stereotactic body radiation therapy

BED10 :

Biologically effective dose


Celiac axis


Superior mesenteric artery


Common hepatic artery


Portal vein


Superior mesenteric vein


Triangle volume


Overall survival


Local progression-free survival


Distant metastasis-free survival


Progression-free survival


Institutional review board


Computed tomography


Internal target volume


Clinical target volume


Planning target volume




Common terminology criteria for adverse events


Response evaluation criteria in solid tumors


Adverse events


  1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2020. CA Cancer J Clin. 2020;70:7–30.

    Article  PubMed  Google Scholar 

  2. National comprehensive cancer network. Pancreatic adenocarcinoma. version 2.2021) Accessed 1/22/2022

  3. Rawla P, Sunkara T, Gaduputi V. Epidemiology of pancreatic cancer: global trends, etiology and risk factors. World J Oncol. 2019;10:10–27.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Gemenetzis G, Groot VP, Blair AB, et al. Survival in locally advanced pancreatic cancer after neoadjuvant therapy and surgical resection. Ann Surg. 2019;270:340–7.

    Article  PubMed  Google Scholar 

  5. Javed AA, Wright MJ, Siddique A, et al. Outcome of patients with borderline resectable pancreatic cancer in the contemporary Era of neoadjuvant chemotherapy. J Gastrointest Surg. 2019;23:112–21.

    Article  PubMed  Google Scholar 

  6. Van den Broeck A, Sergeant G, Ectors N, et al. Patterns of recurrence after curative resection of pancreatic ductal adenocarcinoma. Eur J Surg Oncol. 2009;35:600–4.

    Article  PubMed  Google Scholar 

  7. Hishinuma S, Ogata Y, Tomikawa M, et al. Patterns of recurrence after curative resection of pancreatic cancer, based on autopsy findings. J Gastrointest Surg. 2006;10:511–8.

    Article  PubMed  Google Scholar 

  8. Iacobuzio-Donahue CA, Fu B, Yachida S, et al. DPC4 gene status of the primary carcinoma correlates with patterns of failure in patients with pancreatic cancer. J Clin Oncol. 2009;27:1806–13.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Showalter TN, Rao AS, Rani Anne P, et al. Does intraoperative radiation therapy improve local tumor control in patients undergoing pancreaticoduodenectomy for pancreatic adenocarcinoma? A propensity score analysis. Ann Surg Oncol. 2009;16:2116–22.

    Article  PubMed  Google Scholar 

  10. Keane FK, Wo JY, Ferrone CR, et al. Intraoperative radiotherapy in the era of intensive neoadjuvant chemotherapy and chemoradiotherapy for pancreatic adenocarcinoma. Am J Clin Oncol. 2018;41:607–12.

    Article  PubMed  Google Scholar 

  11. Sekigami Y, Michelakos T, Fernandez-Del Castillo C, et al. Intraoperative radiation mitigates the effect of microscopically positive tumor margins on survival among pancreatic adenocarcinoma patients treated with neoadjuvant FOLFIRINOX and chemoradiation. Ann Surg Oncol. 2021;28:4592–601.

    Article  PubMed  Google Scholar 

  12. Sindelar WF, Kinsella TJ. Studies of intraoperative radiotherapy in carcinoma of the pancreas. Ann Oncol. 1999;10(Suppl 4):226–30.

    Article  PubMed  Google Scholar 

  13. Adham M, Singhirunnusorn J. Surgical technique and results of total mesopancreas excision (TMpE) in pancreatic tumors. Eur J Surg Oncol. 2012;38:340–5.

    Article  CAS  PubMed  Google Scholar 

  14. Hackert T, Strobel O, Michalski CW, et al. The TRIANGLE operation - radical surgery after neoadjuvant treatment for advanced pancreatic cancer: a single arm observational study. HPB (Oxford). 2017;19:1001–7.

    Article  Google Scholar 

  15. Hill CS, Fu W, Hu C, et al. Location, location, location: what should be targeted beyond gross disease for localized pancreatic ductal adenocarcinoma? Proposal of a standardized clinical tumor volume for pancreatic ductal adenocarcinoma of the head: the “triangle volume.” Pract Radiat Oncol. 2022;12:215–25.

    Article  PubMed  Google Scholar 

  16. Blair AB, Rosati LM, Rezaee N, et al. Postoperative complications after resection of borderline resectable and locally advanced pancreatic cancer: the impact of neoadjuvant chemotherapy with conventional radiation or stereotactic body radiation therapy. Surgery. 2018;163:1090–6.

    Article  PubMed  Google Scholar 

  17. Oar A, Lee M, Le H, et al. Australasian gastrointestinal trials group (AGITG) and trans-tasman radiation oncology group (TROG) guidelines for pancreatic stereotactic body radiation therapy (SBRT). Pract Radiat Oncol. 2020;10:e136–46.

    Article  PubMed  Google Scholar 

  18. Onishi H, Shirato H, Nagata Y, et al. Hypofractionated stereotactic radiotherapy (HypoFXSRT) for stage I non-small cell lung cancer: updated results of 257 patients in a Japanese multi-institutional study. J Thorac Oncol. 2007;2:S94-100.

    Article  PubMed  Google Scholar 

  19. Reyngold M, O’Reilly EM, Varghese AM, et al. Association of ablative radiation therapy with survival among patients with inoperable pancreatic cancer. JAMA Oncol. 2021;7:735–8.

    Article  PubMed  Google Scholar 

  20. Ohri N, Tomé WA, Méndez Romero A, et al. Local control after stereotactic body radiation therapy for liver tumors. Int J Radiat Oncol Biol Phys. 2021;110:188–95.

    Article  PubMed  Google Scholar 

  21. Whitehead AL, Julious SA, Cooper CL, et al. Estimating the sample size for a pilot randomised trial to minimise the overall trial sample size for the external pilot and main trial for a continuous outcome variable. Stat Methods Med Res. 2016;25:1057–73.

    Article  PubMed  Google Scholar 

  22. Bell ML, Whitehead AL, Julious SA. Guidance for using pilot studies to inform the design of intervention trials with continuous outcomes. Clin Epidemiol. 2018;10:153–7.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Dindo D, Demartines N, Clavien P-A. Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg. 2004;240:205–13.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Barbour AP, Samra JS, Haghighi KS, et al. The AGITG GAP study: a phase II study of perioperative gemcitabine and nab-paclitaxel for resectable pancreas cancer. Ann Surg Oncol. 2020;27:2506–15.

    Article  PubMed  Google Scholar 

  25. Jones RP, Psarelli E-E, Jackson R, et al. Patterns of recurrence after resection of pancreatic ductal adenocarcinoma: a secondary analysis of the espac-4 randomized adjuvant chemotherapy trial. JAMA Surg. 2019;154:1038–48.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Cardillo N, Seible DM, Fero KE, et al. Clinical impact of local progression in pancreatic cancer. J Natl Compr Canc Netw. 2018;16:711–7.

    Article  PubMed  Google Scholar 

  27. Palta M, Godfrey D, Goodman KA, et al. Radiation therapy for pancreatic cancer: executive summary of an ASTRO clinical practice guideline. Pract Radiat Oncol. 2019;9:322–32.

    Article  PubMed  Google Scholar 

  28. Brunner TB, Haustermans K, Huguet F, et al. ESTRO ACROP guidelines for target volume definition in pancreatic cancer. Radiother Oncol. 2021;154:60–9.

    Article  PubMed  Google Scholar 

  29. Kharofa J, Mierzwa M, Olowokure O, et al. Pattern of marginal local failure in a phase II trial of neoadjuvant chemotherapy and stereotactic body radiation therapy for resectable and borderline resectable pancreas cancer. Am J Clin Oncol. 2019;42:247–52.

    Article  CAS  PubMed  Google Scholar 

  30. Miller JA, Toesca DAS, Baclay JRM, et al. Pancreatic stereotactic body radiation therapy with or without hypofractionated elective nodal irradiation. Int J Radiat Oncol Biol Phys. 2021;S0360–3016(21):02600–6.

    Google Scholar 

Download references


Mr. El-Hebri for his generous donation to fund this study


This study was funded by a generous donation from Mr. El-Hebri.

Author information

Authors and Affiliations



AVR and AKN were responsible for writing the manuscript. All authors read and reviewed the manuscript, and gave approval for submission. .

Corresponding author

Correspondence to Abhinav V. Reddy.

Ethics declarations

Ethics approval and consent to participate

The protocol has been reviewed and approved by the institutional review board of our hospital (IRB00294801). This study has been registered at (NCT05141513).

Consent for publication

Not applicable.

Competing interests


Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Reddy, A.V., Hill, C.S., Zheng, L. et al. A safety study of intraoperative radiation therapy following stereotactic body radiation therapy and multi-agent chemotherapy in the treatment of localized pancreatic adenocarcinoma: study protocol of a phase I trial. Radiat Oncol 17, 173 (2022).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: