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Poster Display session

90P - Intensity-modulated radiation therapy can reduce acute toxicities in long-course neoadjuvant radiation therapy combined with S-1 for locally advanced rectal cancer

Date

07 Dec 2024

Session

Poster Display session

Presenters

Saori Tatsuno

Citation

Annals of Oncology (2024) 35 (suppl_4): S1432-S1449. 10.1016/annonc/annonc1687

Authors

S. Tatsuno1, H. Doi1, M. Inada1, J. Fukuda1, N. Ishida1, T. Uehara1, K. Nakamatsu1, M. Hosono1, J. Kawamura2, Y. Matsuo1

Author affiliations

  • 1 Radiation Oncology, Kindai University - Faculty of Medicine, 589-8511 - Osaka/JP
  • 2 Surgery, Kindai University - Faculty of Medicine, 589-8511 - Osaka/JP

Resources

This content is available to ESMO members and event participants.

Abstract 90P

Background

Intensity-modulated radiation therapy (IMRT) may reduce radiation-induced toxicity in neoadjuvant radiation therapy (NA-RT) for locally advanced rectal cancer (LARC). The purpose of this study was to compare outcomes and toxicity between three-dimensional conformal radiation therapy (3D-CRT) and IMRT in patients undergoing long-course NA-RT for LARC.

Methods

We retrospectively analyzed a total of 47 consecutive patients who received NA-RT for LARC between January 2011 and September 2022. Seven and 40 patients were diagnosed as clinical stages II and III, respectively. The prescribed dose per fraction was 1.8 Gy for total doses 45 or 50.4 Gy. Seventeen and 30 patients received 3DCRT and IMRT, respectively. NA-RT was delivered with concurrent chemotherapy of oral administration of S-1.

Results

Planned NA-RT was completed without any treatment interruption in 43 patients, except for four patients; two patients experienced treatment interruption and two patients discontinued due to grade ≥3 toxicities. The median follow-up term was 31.4 (range, 7.1-136.6) months. The 2-year local control (LC) rate, progression-free survival (PFS) rate, and overall survival (OS) rate were 90.9% (95% confidence interval [CI], 77.6–96.5), 82.3 (95% CI, 67.6–90.8) and 93.0% (95% CI, 79.7–97.7), respectively. No significant differences were observed between patients receiving 3DCRT and IMRT in LC, PFS, and OS (P = 0.488, 0.259, and 0.636, respectively). Patients receiving IMRT showed significantly fewer non-hematological grade ≥2 acute toxicities than those receiving 3DCRT (P = 0.018), although there were no significant differences in non-hematological grade ≥3 acute toxicities between patients receiving IMRT and 3DCRT (P = 1.000). In addition, patients who received IMRT tended to have less intestinal toxicity of grade ≥2 than those who received 3DCRT (P = 0.057).

Conclusions

Long-course NA-RT combined with oral administration of S-1 showed good clinical outcomes. IMRT significantly reduced the grade ≥2 acute toxicities without compromising oncologic outcome compared to 3DCRT. Therefore, IMRT was considered as a current standard treatment in terms of total neoadjuvant therapy era.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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