Background/Aim: Previous evaluation of the safety and clinical efficacy of re-irradiation for pelvic recurrence of rectal cancer after preoperative chemoradiotherapy (PCRT) and rectal surgery is insufficient. We evaluated the safety and efficacy of re-irradiation with carbon-ion radiotherapy (C-ion RT) for pelvic recurrence of rectal cancer after PCRT. Patients and Methods: We reviewed the medical records of patients treated with C-ion RT between August 2011 and December 2021 and analyzed the data of seven consecutive patients. The probabilities of overall survival (OS), local control (LC), and progressionfree survival (PFS) were calculated using the Kaplan-Meier method. Toxicities were classified using the National Cancer Institute's Common Terminology Criteria for Adverse Events (version 4.0). Results: The median follow-up duration after C-ion RT initiation was 30.9 months. Five patients received 73.6 Gy [relative biological effectiveness (RBE)] in 16 fractions, and two patients received 57.6 Gy (RBE) in 12 fractions. All patients completed C-ion RT as scheduled. Two-year estimated OS, LC, and PFS rates after C-ion RT initiation were 100%, 83.3%, and 28.6%, respectively. No patients developed grade ≥3 acute toxicity. Regarding late toxicities, one patient who received Gore-Tex sheets as a spacer before C-ion RT developed grade 3 colon perforation, and then developed a grade 3 urinary tract disorder. One patient developed grade 2 peripheral neuropathy. Conclusion: C-Ion RT showed favorable local efficacy with minimal toxicity. C-Ion RT might be an effective treatment option for pelvic recurrence of rectal cancer after PCRT even when re-irradiation of the pelvis is required.Preoperative chemoradiotherapy (PCRT) for rectal cancer is a feasible treatment option that achieves higher local control (LC) and anorectal preservation rates and omits prophylactic lateral lymph node dissection (1-3). However, up to 10% of patients develop pelvic recurrence after PCRT and rectal surgery (3-5), and chemotherapy alone is insufficient to achieve complete cure. Pelvic exenteration may be indicated, but such surgery is highly invasive and creates difficulties in postoperative management (6, 7). Although X-ray radiotherapy (RT) is one of the treatment options, rectal cancer is known to be a radiation-resistant tumor, and dose constraints of the surrounding gastrointestinal (GI) tract might be exceeded because the pelvic GI tract was already irradiated during PCRT. Therefore, sufficient dose administration with conventional Xray RT is difficult. Recently, clinical outcomes of re-irradiation with stereotactic body radiotherapy (SBRT) for postoperative pelvic recurrence of rectal cancer have been reported, and 2year overall survival (OS) rates are 78.8-84.4% and LC rates are 68.2-69.0%, with a grade ≥3 toxicity rate of 3.3-10.7% (8, 9). These clinical outcomes are unsatisfactory, even with advanced SBRT treatment.Carbon-ion radiotherapy (C-ion RT) has physical and biological advantages compared with X-ray RT, in terms of higher dose ...