Advances in Radiation Oncology (Apr 2024)

Carbon Ion Radiation Therapy for Nonmetastatic Castration-Resistant Prostate Cancer: A Retrospective Analysis

  • Yuhei Miyasaka, MD, PhD,
  • Hidemasa Kawamura, MD, PhD,
  • Hiro Sato, MD, PhD,
  • Nobuteru Kubo, MD, PhD,
  • Hiroyuki Katoh, MD, PhD,
  • Hitoshi Ishikawa, MD, PhD,
  • Hiroshi Matsui, MD, PhD,
  • Yoshiyuki Miyazawa, MD, PhD,
  • Kazuto Ito, MD, PhD,
  • Kazuhiro Suzuki, MD, PhD,
  • Tatsuya Ohno, MD, PhD

Journal volume & issue
Vol. 9, no. 4
p. 101432

Abstract

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Purpose: Treatment outcomes of definitive photon radiation therapy for nonmetastatic castration-resistant prostate cancer (nmCRPC) are reportedly unsatisfactory. Carbon ion radiation therapy (CIRT) has shown favorable tumor control in various malignancies, including radioresistant tumors. Therefore, we retrospectively evaluated the clinical outcomes of CIRT for nmCRPC. Methods and Materials: Patients with nmCRPC (N0M0) treated with CIRT at a total dose of 57.6 Gy (relative biologic effectiveness) in 16 fractions or 51.6 Gy (relative biologic effectiveness) in 12 fractions were included. The castration-resistant status received a diagnosis based on prostate-specific antigen kinetics showing a monotonic increase during primary androgen deprivation therapy or the need to change androgen deprivation therapy. Clinical factors associated with patient prognosis were explored. Twenty-three consecutive patients were identified from our database. The median follow-up period was 63.6 months (range, 14.1-120). Results: Seven patients developed biochemical relapse, 6 had clinical relapse, and 4 died of the disease. The 5-year overall survival, local control rate, biochemical relapse-free survival, and clinical relapse-free survival were 87.5%, 95.7%, 70.3%, and 75.7%, respectively. One patient with diabetes mellitus requiring insulin injections and taking antiplatelet and anticoagulant drugs developed grade 3 hematuria and bladder tamponade after CIRT. None of the patients developed grade 4 or worse toxicity. Conclusions: The present findings indicate the acceptable safety and favorable efficacy of CIRT, encouraging further research on CIRT for nmCRPC.