Prognostic impact of pan-immune-inflammation value and prognostic nutritional index in metastatic colorectal cancer patients treated with regorafenib
Abstract
Objectives: Metastatic colorectal cancer (mCRC) remains a major cause of cancer-related mortality, with limited therapeutic options available after the failure of standard treatments. Regorafenib, an oral multichines inhibitor, has shown a survival advantage in treatment refractory mCRC. This research aims to evaluate the real-world effectiveness of regorafenib and to investigate the prognostic significance of inflammatory and nutritional indicators, specifically the Pan-Immune-Inflammation Value (PIV) and Prognostic Nutritional Index (PNI).
Methods: We conducted a retrospective analysis of 166 mCRC patients who received regorafenib 2014 to 2024. Demographic, clinical, and pathological data, treatment responses, and laboratory indicators were gathered. Survival outcomes were evaluated by Kaplan–Meier analysis, whereas prognostic variables were analyzed using Cox regression.
Results: The average age was 58 years, and 59% of patients were male. The overall disease control rate with regorafenib was 33%, and the objective response rate was 11%. The median progression-free survival (PFS) was 3.8 months, and the median overall survival (OS) was 9.1 months. A high PIV (≥309.1) was associated with significantly shorter overall survival (7.1 vs. 11.8 months, P=0.001), whereas a high PNI (≥47.9) was correlated with longer overall survival (10.7 vs. 6.7 months, P=0.02). Multivariate analysis confirmed PIV and PNI as independent prognostic indicators.
Conclusions: Regorafenib provides a modest survival advantage and disease stabilization in previously treated mCRC patients. PIV and PNI are independent prognostic biomarkers that may assist in patient stratification and therapy optimization. Further studies are warranted to refine predictive markers and dosing strategies.
Keywords
Ethical Statement
References
- 1. Siegel RL, Giaquinto AN, Jemal A. Cancer statistics, 2024. CA Cancer J Clin. 2024;74(1):12-49. doi: 10.3322/caac.21820.
- 2. Cervantes A, Adam R, Roselló S, et al; ESMO Guidelines Committee. Metastatic colorectal cancer: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up. Ann Oncol. 2023;34(1):10-32. doi: 10.1016/j.annonc.2022.10.003.
- 3. Siegel RL, Miller KD, Goding Sauer A, et al. Colorectal cancer statistics, 2020. CA Cancer J Clin. 2020;70(3):145-164. doi: 10.3322/caac.21601.
- 4. Cancer Stat Facts: Colon and Rectum Cancer. National Cancer Institute Surveillance Epidemiology and End Results Program website. 2018. https://seer.cancer.gov/statfacts/html/colorect.html.
- 5. Hurwitz H, Fehrenbacher L, Novotny W, et al. Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. N Engl J Med. 2004;350(23):2335-2342. doi: 10.1056/NEJMoa032691.
- 6. Saltz LB, Clarke S, Díaz-Rubio E, et al. Bevacizumab in combination with oxaliplatin-based chemotherapy as first-line therapy in metastatic colorectal cancer: a randomized phase III study. J Clin Oncol. 2008;26(12):2013-2019. doi: 10.1200/JCO.2007.14.9930.
- 7. Douillard JY, Oliner KS, Siena S, et al. Panitumumab-FOLFOX4 treatment and RAS mutations in colorectal cancer. N Engl J Med. 2013;369(11):1023-1034. doi: 10.1056/NEJMoa1305275.
- 8. Van Cutsem E, Köhne CH, Láng I, et al. Cetuximab plus irinotecan, fluorouracil, and leucovorin as first-line treatment for metastatic colorectal cancer: updated analysis of overall survival according to tumor KRAS and BRAF mutation status. J Clin Oncol. 2011;29(15):2011-2019. doi: 10.1200/JCO.2010.33.5091.
Details
Primary Language
English
Subjects
Clinical Oncology , Cancer Therapy (Excl. Chemotherapy and Radiation Therapy)
Journal Section
Research Article
Authors
Sedat Yıldırım
*
0000-0002-2423-6902
Türkiye
Özkan Alan
0000-0001-2345-6789
Türkiye
Akif Doğan
0000-0003-4275-2414
Türkiye
Seval Ay Ersoy
0000-0002-7555-2657
Türkiye
Hatice Odabaş
0000-0002-5757-4705
Türkiye
Early Pub Date
October 3, 2025
Publication Date
November 4, 2025
Submission Date
August 25, 2025
Acceptance Date
September 27, 2025
Published in Issue
Year 2025 Volume: 11 Number: 6