5-Fluorouracil plus L-leucovorin and oxaliplatin treatment for esophageal squamous cell carcinoma: A multicenter retrospective study

Author:

Shiraishi Kazuhiro1,Okada Mao1,Yamamoto Shun1,Matsubara Yuki2,Masuishi Toshiki2,Shimozaki Keitaro3,Yamamoto Yoshiyuki4,Hirose Suguru4,Sugiyama Keiji5,Furuta Mitsuhiro6,Machida Nozomu6,Takahashi Naoki7,Yoshii Takako7,Kito Yosuke8,Tsuzuki Takao9,Boku Shogen10,Tsuchihashi Kenji11,Akinori Sugaya12,Takayama Toshizo13,Komori Azusa14,Mitani Seiichiro15,Matsumoto Toshihiko16,Hirata Kenro17,Nishimura Takashi18

Affiliation:

1. National Cancer Center Hospital

2. Aichi Cancer Center Hospital

3. Japanese Foundation for Cancer Research

4. University of Tsukuba

5. National Hospital Organization Nagoya Medical Center

6. Kanagawa Cancer

7. Saitama Cancer Center

8. Ishikawa Prefectural Central Hospital

9. Japanese Red Cross Society Himeji Hospital

10. Kansai Medical University Hospital

11. Kyushu University

12. Ibaraki Prefectural Central Hospital

13. Daido Hospital

14. Oita University Faculty of Medicine

15. Kindai University

16. Kobe City Medical Center General Hospital

17. Keio University School of Medicine

18. Jikei University School of Medicine

Abstract

Abstract

Background Cisplatin-based chemotherapy is the standard treatment for advanced esophageal squamous cell carcinoma (ESCC). However, the 5-fluorouracil plus L-leucovorin and oxaliplatin (FOLFOX) regimen is available in Japan as an alternative to cisplatin-based chemotherapy, but its efficacy and safety remain unclear. Hence, we aimed to retrospectively evaluate patients with advanced ESCC who received FOLFOX therapy. Methods Patients with advanced ESCC who received FOLFOX therapy at 18 institutions between April 2019 and October 2020 were included. Fifty-two patients were received first-line FOLFOX treatment, while 39 patients received later-line FOLFOX treatment. Results The median progression-free survival, median overall survival, and objective response rate were 3.8 months (95% confidence interval [CI]: 3.0–5.0), 13.9 months (95% CI: 10.3–17.9 months), and 35% in the first-line group and 2.4 months (95% CI: 2.1–3.8 months), 7.2 months (95% CI: 5.3–9.8 months), and 4% in the later-line group, respectively. The most frequent grade 3 or 4 adverse events were neutropenia (23%) and anemia (12%) in the first-line group and neutropenia (18%), anorexia (13%), anemia (10%), and nausea (10%) in the later-line group. Conclusion First-line FOLFOX treatment is suitable for patients with advanced ESCC. However, FOLFOX has shown limited efficacy as a later-line treatment.

Publisher

Research Square Platform LLC

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