# Efficacy of Neoadjuvant Short-Course Radiation Therapy Followed by Oxaliplatin-Based Chemotherapy for Locally Advanced Rectal Adenocarcinoma: A Single-Center Experience From Saudi Arabia

**Authors:** Tareq Salah, Mohamed Aboziada, Taleb Buhlaiaqh, Nada A Mass, Nedal Bukhari, Bader Alwhaibi, Abdossalam M Makhali, Mervat Mahrous, Sherif Mohamed, Nashwa Abd El-Aziz, Hoda Mokhtar

PMC · DOI: 10.7759/cureus.77604 · Cureus · 2025-01-17

## TL;DR

This study from Saudi Arabia shows that short-course radiation followed by oxaliplatin-based chemotherapy can lead to a 21% complete response rate in locally advanced rectal cancer patients.

## Contribution

The study provides a single-center experience on the efficacy of a specific neoadjuvant treatment regimen for rectal cancer in a Saudi population.

## Key findings

- A 21% pathologic complete response rate was observed in patients treated with short-course radiation followed by oxaliplatin-based chemotherapy.
- Five independent predictors of complete response were identified, including N-stage, CRM status, and surgical approach.
- Nearly half of the patients achieved a near-complete response, suggesting the treatment is effective for a significant portion of cases.

## Abstract

Background

The 5-fluorouracil (5-FU), capecitabine-based long-course or short-course radiotherapy (SCRT) eventually preceded or followed by induction or consolidation chemotherapy (CT) and resection represents the preferred regimen for the treatment of locally advanced rectal cancer (LARC). This study aims to report our experience as a large medical center in Saudi Arabia, with the efficacy of short-course radiation therapy followed by oxaliplatin-based CT in achieving a pathologic complete response (pCR) in patients with LARC.

Materials and methods

This retrospective analysis encompassed 57 patients diagnosed with LARC at a large tertiary center in Riyadh, Saudi Arabia, from June 2020 to December 2022. All participants underwent short-term radiotherapy (25 Grays (Gy) over fractions within one week) followed by CT with 5-FU, leucovorin, and oxaliplatin (FOLFOX) or capecitabine and oxaliplatin (CAPOX), constituting the total neoadjuvant therapy (TNT). Surgical intervention and total mesorectal excision were performed six to eight weeks post-preoperative treatment. The primary endpoint was the pCR rate.

Results

Of the study participants, 34 (60%) were males, with a mean age of 57.6 ± 13.9 years. Two-thirds (n = 37,65%) were classified as T3. The overall response rates were 12 (21%), 12 (21%), 24 (42%), and nine (16%), for complete response (CR), near-complete response (nCR), partial response (PR), and progressive disease (PD), respectively. The multivariable logistic regression model identified five independent predictors for overall CR after adjusting for disease-related factors: N-stage, the circumferential resection margin (CRM), average vascularity (AV), surgical procedure, and postoperative tumor size. Patients with N2 disease had an 18% lower chance of achieving CR (OR = 0.824; 95% CI: 0.634-0.974; p = 0.035). Positive CRM was linked to a 71% reduction in the probability of CR (OR = 0.268; 95% CI: 0.087-0.823; p = 0.021). Each 1 cm increase in AV corresponded to a 28.5% increase in the likelihood of complete response (OR = 1.285; 95% CI: 1.029-1.605; p = 0.027). Patients who underwent AR had 2.8 times greater chances of achieving CR than those who underwent abdominoperineal resection (APR) (OR = 2.801; 95% CI: 1.057-9.324; p = 0.044). Lastly, each 1 cm increase in postoperative tumor size was associated with a 92.5% reduction in the odds of CR (OR = 0.074; 95% CI: 0.017-0.330; p = 0.001).

Conclusions

The current study supports the efficacy of TNT for treating LARC, with a pCR rate of 21% and near-complete response in nearly half of the patients with LARC. Significant predictors of pCR included N-stage, CRM status, AV size, and surgical approach. These insights could refine patient selection for TNT and inform future strategies to optimize treatment outcomes in rectal cancer. Prospective multicenter studies are warranted.

## Linked entities

- **Chemicals:** 5-fluorouracil (PubChem CID 3385), leucovorin (PubChem CID 135403648), oxaliplatin (PubChem CID 9887053), capecitabine (PubChem CID 60953)
- **Diseases:** rectal adenocarcinoma (MONDO:0002169)

## Full-text entities

- **Diseases:** LARC (MESH:D012004), PD (MESH:D018450), N2 disease (MESH:D004194), tumor (MESH:D009369), Rectal Adenocarcinoma (MESH:D000230)
- **Chemicals:** 5-FU, leucovorin, and oxaliplatin (-), Oxaliplatin (MESH:D000077150), FOLFOX (MESH:C410216), capecitabine (MESH:D000069287), 5-FU (MESH:D005472)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC11832227/full.md

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Source: https://tomesphere.com/paper/PMC11832227