Abstract

Background and PurposeA phase 2 study LAPACT indicated nab-paclitaxel plus gemcitabine (AG) improved outcomes of patients with locally advanced pancreatic cancer (LAPC). Conventional radiotherapy failed to show benefit, indicating high dose to volume with high risk of recurrence is needed. The high dose can be delivered through hypofractionated tomotherapy with simultaneous integrated boost (SIB). However, there is a lack of such prospective trials and more data are needed to validate the role of AG plus hypofractionated tomotherapy with SIB in patients with LAPC.Materials and MethodsPatients with LAPC receiving AG plus tomotherapy at the Nanjing Drum Tower Hospital between 2018 and 2021 were retrospectively analyzed. The treatment was scheduled as follows: nab-paclitaxel 125 mg/m2 plus gemcitabine 1,000 mg/m2 on days 1 and 8 every three weeks for at least two cycles, followed by hypofractionated tomotherapy with SIB (high dose field: 50 Gy/10 fractions, the remainder: 30 Gy/10 fractions). Then patients were given AG until intolerance or disease progression.ResultsOverall, 22 patients completing the chemoradiotherapy were included. The median follow-up was 15.2 months. After the chemoradiotherapy, 5 patients achieved a partial response (PR), 15 had a stable disease (SD), and another 2 patients were with progressive disease (PD). The median progression-free survival (PFS) and overall survival (OS) were 12.8 months (95% confidence interval [CI] 4.3–21.3 months) and 16.3 months (95% CI 10.9–21.6 months), respectively. The optimal carbohydrate antigen (CA) 19-9 response and chemotherapy cycles ≥6 were correlated with favorable PFS and OS. The most common recurrent pattern was peritoneal dissemination (22.7%) and the locoregional recurrence rate was relatively low (4.5%). Treatments were well-tolerated. The most common grade ≥3 adverse event was thrombocytopenia (13.6%).ConclusionThis study demonstrated the feasibility of AG followed by hypofractionated tomotherapy with SIB in patients with LAPC. The hypofractionated tomotherapy with SIB was safe and showed high local control rate. Further study with a larger population to validate our data is underway.

Highlights

  • Pancreatic cancer is the seventh leading cause of cancer death worldwide, with an estimation of 466,003 deaths and 495,733 new cases worldwide in 2020 according to the GLOBOCAN 2020 [1]

  • The eligibility criteria included: pathologically confirmed pancreatic adenocarcinoma; unresectable locally advanced pancreatic cancer (LAPC) evaluated by radiologists and surgeons; receiving treatment of AG followed by hypofractionated tomotherapy with simultaneous integrated boost (SIB) between May 2018 and March 2021

  • We found that optimal CA19-9 response and more chemotherapy cycles (HR = 0.267, 95% confidence interval (CI) 0.091–0.786, P = 0.016) were significantly correlated with prolonged progression-free survival (PFS) (Table 3)

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Summary

Introduction

Pancreatic cancer is the seventh leading cause of cancer death worldwide, with an estimation of 466,003 deaths and 495,733 new cases worldwide in 2020 according to the GLOBOCAN 2020 [1]. Non-metastatic pancreatic cancer can be classified into 3 groups: resectable, borderline resectable and locally advanced pancreatic cancer (LAPC) [3]. The deaths of patients with LAPC are mainly caused by metastatic spread and uncontrolled local growth [7]. FOLFIRINOX (folinic acid, 5-fluorouracil, irinotecan, and oxaliplatin) and AG (nab-paclitaxel plus gemcitabine), which were initially applied for patients with metastatic disease, have been evaluated for patients with LAPC. A phase 2 study LAPACT indicated nab-paclitaxel plus gemcitabine (AG) improved outcomes of patients with locally advanced pancreatic cancer (LAPC).

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