A Novel Haemostatic Agent for Robotic Partial Nephrectomy

Kidney Cancer, Renal Cell Carcinoma

Robotic Partial Nephrectomy, PuraBond

Kidney cancer is one of only a few cancers with an increasing incidence over the past two decades. Renal cell carcinoma (RCC) accounts for over 85% of all kidney tumours, which makes up 2-3% of all adult malignancies. Approximately, 70% of RCCs are incidentally discovered on axial imaging of the abdomen with \>50% of RCCs being low-stage (T1-T2 N0M0). Despite advancements in drug discovery for advanced RCC, mortality rates have not changed over the past two decades, however for patients with the low-stage disease, surgical extirpation offers excellent 5-year survival rates of 95%. Nephron-sparing surgery (NSS) provides effective curative therapy for patients with localized renal cell carcinoma with the benefit of kidney preservation and excellent cancer-specific survival. However, the most frequent complications during NSS, after tumour resection are bleeding, urinary fistula formation, and ischemic renal damage. More precisely, the urological complication was defined as significant haemorrhage \>500 mL necessitating intervention or transfusion, urine leakage (drainage of greater than 50 mL daily for more than one week with fluid biochemistry compatible with urine) and acute renal failure (resulting in any dialysis, ureteral obstruction or kidney loss). In the field of partial nephrectomy procedures, it is therefore crucial achieving adequate haemostasis intraoperatively during post tumour excision while the artery is clamped and after being unclamped.

Kidney cancer is one of only a few cancers with an increasing incidence over the past two decades. Renal cell carcinoma (RCC) accounts for over 85% of all kidney tumours, which makes up 2-3% of all adult malignancies. Approximately, 70% of RCCs are incidentally discovered on axial imaging of the abdomen with \>50% of RCCs being low-stage (T1-T2 N0M0). Despite advancements in drug discovery for advanced RCC, mortality rates have not changed over the past two decades, however for patients with the low-stage disease, surgical extirpation offers excellent 5-year survival rates of 95%. Nephron-sparing surgery (NSS) provides effective curative therapy for patients with localized renal cell carcinoma with the benefit of kidney preservation and excellent cancer-specific survival. However, the most frequent complications during NSS, after tumour resection are bleeding, urinary fistula formation, and ischemic renal damage. More precisely, the urological complication was defined as significant haemorrhage \>500 mL necessitating intervention or transfusion, urine leakage (drainage of greater than 50 mL daily for more than one week with fluid biochemistry compatible with urine) and acute renal failure (resulting in any dialysis, ureteral obstruction or kidney loss). In the field of partial nephrectomy procedures, it is therefore crucial achieving adequate haemostasis intraoperatively during post tumour excision while the artery is clamped and after being unclamped. Haemostatic agent can be used after Robotic-assisted laparoscopic partial nephrectomy (RLPN) or after the sutureless technique with bipolar cauterization of the surgical bed for the haemostatic control in the treatment of small cortical masses. It can be always used for tumours ≤1.5 cm and can be a valid option also for tumours between 1.6 and 2.5 cm, aside from their spatial extension. As such, there is a need for the exploration of the use of novel haemostatic agents, such as self-assembling peptide (SAP)-based haemostat, to manage bleeding during partial nephrectomy. The SAPs are oligopeptides (8 - 16 amino acids) composed of alternating hydrophilic and hydrophobic amino acids. These peptide chains can rapidly form nanofibers and create 3D microenvironments at a physiological pH and osmolarity. As peptides are nontoxic, biocompatible, and biodegradable, the SAPs can be used without an apparent immunological response, are also easy handling and are easy to inject due to their water solubility. Due to all these properties, SAPs are suitable for clinical use. One of the most widely studied SAPs is RADA16. It contains the amino acids alanine, lysine, and glutamate in repeated sequences of 4 X \[Arg-Ala-Asp-Ala\] (RADA16). RADA16 has proven utility as an effective topical haemostatic agent in a variety of surgical and pathological scenarios. PuraStat and PuraBond (same product manufactured by 3-D Matrix Europe SAS, Caluire-et-Cuire, France) are CE-marked medical devices delivered by pre-filled syringes as viscous aqueous solutions of synthetic 2.5% RADA16. When RADA16 comes in to contact with blood or other physiological fluids, it forms a hydrogel. The hydrogel formation acts as a mechanical barrier and blocks the flow of the blood from the wound and thereby, demonstrates excellent topical haemostatic control. Initial preclinical studies investigating this peptide have shown other benefits in addition to its haemostatic properties, including improved wound healing. Since 2014, PuraStat/PuraBond haemostatic efficacy has been significant successfully assessed in clinical studies, including in GI endoscopy, ENT, cardiovascular and general surgery (liver surgery) to support its use in humans demonstrated \>90% of achieved haemostasis within 2min. There is a recent Australian case series published in Oct 2023 evaluating 29 patients undergoing nerve sparing robot-assisted radical prostatectomy, concluding it is a safe haemostatic agent. However, there are no current studies published regarding self-assembling peptide haemostatic agents in partial nephrectomy. This study aims to generate clinical evidence investigating the feasibility and safety of PuraBond in achieving haemostasis in partial nephrectomy.

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United Kingdom