# Perioperative Intravenous Lidocaine and Early Biochemical Outcomes After Robotic-Assisted Radical Prostatectomy: A Clinical Study Within the Framework of Perioperative Metabolic-Inflammatory Modulation

**Authors:** Georgiana Maria Popa, Simona-Alina Abu-Awwad, Ahmed Abu-Awwad, Nicolae Ovidiu Pop, Parascovia Pop, Carmen Ioana Marta, Anca Mihaela Bina, Erika Bimbo Szuhai, Adriana Cacuci, Adrian Gheorghe Osiceanu, Ciprian Dumitru Puscas, Teodor Traian Maghiar, Mihai Octavian Botea

PMC · DOI: 10.3390/metabo16030209 · Metabolites · 2026-03-20

## TL;DR

This study found that using lidocaine during prostate cancer surgery may improve early recovery and reduce inflammation and stress responses.

## Contribution

The study explores lidocaine's effect on postoperative biochemical outcomes and metabolic-inflammation modulation in prostatectomy patients.

## Key findings

- Lidocaine was linked to undetectable PSA levels at 6–12 weeks post-surgery.
- Lidocaine reduced the risk of PSA detectability over time.
- Lidocaine lessened hyperglycemia, lactate elevation, and IL-6 response.

## Abstract

Background: The perioperative period in cancer surgery is characterized by transient metabolic and inflammatory perturbations that may influence early postoperative biochemical dynamics. Surgical stress induces insulin resistance, hyperglycemia, cytokine activation, and metabolic shifts that interact with tumor cell signaling pathways. Intravenous lidocaine has been associated with anti-inflammatory and systemic stabilizing effects beyond analgesia. We investigated whether perioperative lidocaine administration during robotic-assisted radical prostatectomy (RARP) is associated with early postoperative prostate-specific antigen (PSA) dynamics within the context of perioperative metabolic–inflammatory modulation. Methods: In this single-center retrospective cohort study, 180 patients undergoing RARP for localized or locally advanced prostate cancer were stratified according to perioperative intravenous lidocaine exposure. The primary endpoint was undetectable PSA (<0.1 ng/mL) at 6–12 weeks postoperatively. Secondary endpoints included PSA detectability at 3 and 6 months and time to first detectable PSA. Multivariable logistic and Cox regression models were adjusted for established oncologic risk factors. Perioperative glycemic variation, intraoperative lactate dynamics, and postoperative IL-6 levels were analyzed as indicators of stress-induced metabolic activation. Results: Lidocaine exposure was independently associated with higher odds of undetectable PSA at 6–12 weeks (OR 2.10, 95% CI 1.15–3.85) and at subsequent time points. In Cox analysis, lidocaine was associated with a reduced hazard of PSA detectability (HR 0.58, 95% CI 0.37–0.92). Patients receiving lidocaine demonstrated significantly attenuated perioperative hyperglycemia, lower lactate elevation, and reduced IL-6 response. Conclusions: Perioperative intravenous lidocaine administration during RARP was associated with more favorable early PSA dynamics and attenuation of perioperative metabolic–inflammatory activation. Given the retrospective and non-randomized design of the study, these findings should be interpreted as associative and hypothesis-generating, and warrant confirmation in prospective controlled investigations.

## Linked entities

- **Chemicals:** lidocaine (PubChem CID 3676), IL-6 (PubChem CID 165368475)
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** MPO (myeloperoxidase) [NCBI Gene 4353], KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, ELANE (elastase, neutrophil expressed) [NCBI Gene 1991] {aka ELA2, GE, HLE, HNE, NE, PMN-E}, AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** blood loss (MESH:D016063), hypertension (MESH:D006973), hepatic or renal dysfunction (MESH:D008107), hyperglycemia (MESH:D006943), Inflammatory (MESH:D007249), hypersensitivity (MESH:D004342), Surgical (MESH:D007431), hyperalgesic (MESH:D006930), cancer (MESH:D009369), PONV (MESH:D020250), toxicity (MESH:D064420), oncologic (MESH:D000072716), insulin resistance (MESH:D007333), postoperative ileus (MESH:D045823), injury to (MESH:D014947), lymph node (MESH:D000072717), prostate adenocarcinoma (MESH:D000230), hypotension (MESH:D007022), cardiac disease (MESH:D006331), Prostate cancer (MESH:D011471), metastases (MESH:D009362), disease (MESH:D004194)
- **Chemicals:** CO2 (MESH:D002245), sevoflurane (MESH:D000077149), glucose (MESH:D005947), morphine (MESH:D009020), rocuronium (MESH:D000077123), sodium (MESH:D012964), Blood glucose (MESH:D001786), fentanyl (MESH:D005283), propofol (MESH:D015742), lipid (MESH:D008055), Delta (-), Lidocaine (MESH:D008012), catecholamine (MESH:D002395), oxygen (MESH:D010100), Lactate (MESH:D019344)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028550/full.md

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Source: https://tomesphere.com/paper/PMC13028550