Histamine combined with melphalan in isolated limb perfusion for the treatment of locally advanced soft tissue sarcomas: preclinical studies in rats

Histamina combinada ao melfalano na perfusão de membro isolado para o tratamento de sarcomas de partes moles localmente avançado: estudos pré-clínicos em ratos

ORIGINAL ARTICLE

Histamine combined with melphalan in isolated limb perfusion for the treatment of locally advanced soft tissue sarcomas: preclinical studies in rats¹

Histamina combinada ao melfalano na perfusão de membro isolado para o tratamento de sarcomas de partes moles localmente avançado: estudos pré-clínicos em ratos¹

Flavia Brunstein^I; Ivan Dunshee de Abranches Oliveira Santos^II; Lydia Masako Ferreira^III; Sandra T. van Tiel^IV; Alexander M. M. Eggermont^V; Timo L. M. Ten Hagen^VI

^IPlastic Surgery Department – Federal University of Sao Paulo (UNIFESP)-Brazil.

^IIAssociate Professor and Head of the Tumors Division-Plastic Surgery Department - UNIFESP

^IIIHead of the Plastic Surgery Department – UNIFESP

^IVTechnician - Laboratory of Experimental Surgery – Surgical Oncology Department - Erasmus MC, Daniel den Hoed Cancer Center – Rotterdam – the Netherlands

^VHead of the Surgical Oncology Department - Erasmus MC - Daniel den Hoed Cancer Center – Rotterdam – the Netherlands

^VIHead of the Laboratory of Experimental Surgical Oncology – Surgical Oncology Department - Erasmus MC - Daniel den Hoed Cancer Center – Rotterdam – the Netherlands

^{Correspondence}

ABSTRACT

PURPOSE: To evaluate the potential benefit of histamine combined with melphalan in the isolated limb perfusion (ILP) as an alternative to TNF-alfa and melphalan combination, for the treatment of irressectable soft tissue sarcomas of the limbs in Brown Norway (BN) rats.

METHODS: 20 BN rats had small fragments of syngeneic BN-175 fibosarcoma inserted on the right hind limb. In 7-10 days the tumor reached a median diameter of 12-15 mm and they were randomly divided in four groups (sham, melphalan, histamine and escalating doses of histamine combined to melphalan) being submitted to experimental ILP for 30 minutes. Tumors were measured daily with a caliper and the volume was calculated.

RESULTS: Response curves showed a significant effect of the combination of histamine 200 mg/mL with melphalan, with 66% overall response, including 33% complete responses (p< 0.01). There were no systemic collateral effects and locally only mild temporary edema was observed for some animals treated with histamine.

CONCLUSION: Histamine combined with melphalan had a promising effect in the ILP warranting future studies to better explore the mechanism of action as well as its potential use in organ perfusion.

Key words: Sarcomas. Experimental models. Regional treatment. Histamine.

RESUMO

OBJETIVO: Avaliar o potencial benéfico da histamina combinada ao melfalano, na perfusão de membro isolado (PMI), como alternativa à combinação TNF-alfa mais melfalano, no tratamento de sarcomas de partes moles irressecaveis em extremidades, em ratos de linhagem Brown Norway (BN).

MÉTODOS: 20 ratos BN foram submetidos a implantação de fragmentos de fibrosarcoma singênico BN-175 na pata traseira direita. Em cerca de 7-10 dias o tumor atingiu um diâmetro médio de 12-15 mm e foram aleatóriamente divididos em quatro grupos (controle, melfalano, histamina em doses progessivas combinada ao melfalano e histamina) sendo submetidos a PMI experimental por 30 minutos. Os tumores foram então medidos diariamente com o uso de paquímetro e o volume tumoral calculado.

RESULTADOS: As curvas de resposta mostram um efeito significativo da combinação de Histamina na concentração de 200 mg/mL ao melfalano, com 66% de resposta global incluindo 33% de respostas completas (p < 0.01). Não houve efeitos colaterais sistêmicos e localmente apenas edema leve e transitório nos animais tratados com histamine.

CONCLUSÃO: A histamina em combinação com o melfalano apresenta um efeito promissor na PMI garantindo maiores investigações do seu mecanismo de ação e do seu potencial uso na perfusão de órgãos.

Descritores: Sarcomas. Modelos experimentais. Tratamento regional. Histamina

Introduction

Soft tissue sarcomas (STS) are tumors of mesenchymal origin and account for approximately 1% of all adult malignant tumors in the USA¹ and for 5,500 new cases per year in Brazil. Circa 60% of them occur in the extremities and are often large at first diagnosis with an aggressive local growth and propensity for hematogenic spread so that half of the patients will die of disseminated disease. Limb amputation has not shown any benefit in overall survival, thus conservative approaches capable of preserving extremities and maintaining good function are a corner stone of patient approach². Isolated limb perfusion (ILP) was first described as a treatment modality for in transit metastasis of melanoma restricted to the limbs, based on the delivery of high doses of cytostatic drugs (mainly melphalan for the best results and least morbidity) to a tumor-bearing extremity, surgically and temporarily isolated from the systemic circulation by the use of a heart-lung machine^{3, 4, 5}. The rational of the method is that in the ILP setting locoregional concentrations of melphalan, 15 to 20 times higher than after systemic administration, can be achieved without systemic toxicity ^{6, 7}. Complete responses (CR) reached up to 50%⁸ in melanoma patients while in soft tissue sarcomas responses were as poor as 20% Overall Responses (OR), including partial and complete⁹. The combination of TNF-alpha to melphalan brought a new perspective to this modality of treatment with a limb salvage index of 71% and 76% of OR ⁶. In spite of these excellent results, circa 30% of the patients will not respond to standard treatment and might require a limb amputation. Furthermore, TNF-alpha is still not available in many countries both for regulatory and economic reasons restricting the use of this limb salvage procedure to the treatment of in transit metastasis of melanoma. This is still the situation in Brazil, for example, in spite of an experience of more than 10 years with ILP ⁵. Searching for an alternative we evaluated the potential benefit of Histamine (Hi), an inflammatory mediator formed and stored mainly in the granules of mast cells and basophils but also in cells of the epidermis, gastric mucosa, and neurons of the central nervous system as well as in cells in regenerating or rapidly growing tissues. Its classical effect on fine vessels is the formation of edema by an increase in the flow of lymph and its protein content to the extracellular space and also the formation of gaps between endothelial cells, increasing transcapillary vesicular transport¹⁰. Potentially, this could result in an enhanced drug uptake in the tumor and thus lead to improved antitumor responses. We used an established experimental model¹¹, which closely mimics the clinical ILP, in order to evaluate the potential synergy of Hi with melphalan, improving tumor response in soft tissue sarcomas.

Methods

The studies were done at the Laboratory for Experimental Surgical Oncology of the Department of Surgical Oncology of the Erasmus University Medical Center in Rotterdam, the Netherlands. They were in accordance with the Dutch Animal Experimentation Act (1977) and the Guidelines on the protection of experimental animals of the European Community council (1986). Furthermore, the specific protocols for this study were approved by the Erasmus University Rotterdam Animal Committee – the Netherlands. Male inbred Brown Norway (BN) rats were obtained from Harlan-CPB (Austerlitz, the Netherlands), weighing 250-300 g and were fed a standard laboratory diet ad libitum (Hope Farms Woerden, the Netherlands). Frozen small fragments (3 mm) of the syngeneic BN-175 sarcoma maintained in liquid nitrogen under -80⁰C were quickly defrost and inserted subcutaneously in the dorsum of BN rats for expansion. Upon a diameter of around 3 cm the animal was killed under anesthesia by cervical dislocation and the tumor excised and then divided in small fragments of viable tumor tissue of circa 3 mm diameter. Next, these small fragments were inserted subcutaneously in the right hind leg of the animals in groups no bigger than 15 animals. For this, a little incision on the skin above the ankle was made, with the dissection of the tissue and its closure with clip¹². Tumor growth was evaluated by daily measures of the main diameters with a caliper and the calculation of the volume using the formula 0.4 (A² x B) (where B represents the largest tumor diameter and A is the diameter perpendicular to it). When tumor diameter exceeded 25 mm or at the end of the experiment rats were killed by cervical dislocation, under anesthesia. In seven to ten days, the diameter reached values between 12-15 mm and the tumors were amenable to the procedure¹² (Figure 1a). Under anesthesia, using 0.5 ìg/kg intraperitoneal ketamine and 0.5 ìg/kg intramuscular hypnomidate, the rats were fixed in dorsal position to the operating table with adhesive tape. The inguinal vessels (Figure 1b) were reached through an incision parallel to the inguinal ligament with the use of a surgical microscope. Before manipulating the vessels, 50 IU of heparin were administered in bolus by the penile vein. Next, the femoral artery and vein were canulated with silicon tubes measuring 0.012 inches internal diameter and 0.025 of external diameter and 0.025 and 0.047 inches, respectively (Dow Corning, Michigan, USA). The tubes were connected via a roller pump to an oxygenated reservoir containing 5 mL perfusate. A groin tourniquet occluded collateral vessels, warranting a proper isolation of the limb, controlled by the maintenance of a stable volume (Figures 1c and d).

The limb was maintained at a temperature of 38ºC by the use of a water mattress around the limb covered by an aluminum foil. A thermometer controlled the temperature during the whole procedure that lasted 30 minutes. At the end of the ILP a washout was done with 2 mL of oxygenated haemaccel. Next the cannulas were taken out and the vessels ligated. Skin was closed with continuous suture and the animal was put under a heating light till complete recovery, in order to avoid hypothermia. According to the group the animal was randomized to, the 5 mL perfusate would consist of: 1) haemaccel alone (Boehring Pharma, Amsterdam, the Netherlands); 2) haemaccel plus 40 mg melphalan (AlkeranÒ Wellcome, Beckenham, United Kingdom); 3) haemaccel, 40 mg melphalan and escalating doses of Hi (kindly provided by Maxim Pharmaceuticals Inc., San Diego, CA), ranging from 100 to 2000 mg or 4) haemaccel plus 1000 mg Hi. Tumor dimensions were measured every day for volume evaluation. Response was classified as: progressive disease (PD) increase of more than 25%; no change (NC) volume kept in the range of –25% to +25% of the initial one; partial remission (PR) decrease between –25% and –90%, or complete response (CR) final tumor volume less than 10% of initial, as compared to volume on day nine. Limb function was clinically observed as the ability to walk and stand on the perfused limb after ILP. On a scale from grade 0 to 2, grade 0 is a severely impaired function where the rat drags its hind limb; 1, a slightly impaired function (can not use it in a normal way, but stand on it); finally 2 is an intact function (normal walking and standing pattern). Tumor growth curves were plotted as means and standard deviation (SD) of the data from all animals. Statistical evaluation was done by repeated measures ANOVA analyses of the three most representative days: 4, 8 and 10 using SAS Software Release 8.2 for Windows 2000 (SAS Institute Inc., Cary, NC, USA) using PROC MIXED. Main effects of treatment and day (three levels: day 4, 8 and 10) were included in the models as was the interaction between treatment and day. For days where response was statistically significant, interaction terms were further investigated by testing for differences following treatment on that day.

Results

Tumors grew exponentially in the BN rats after control ILP, as expected. The use of Hi plus melphalan led to tumor regression in 66% of the treated animals, including 33% with no palpable tumors (CR), approximately 10 days after treatment (p<0.01) (Fig 2 and 3). This effect was only observed when Hi dose reached 1,000 mg (concentration of 200 mg/mL) and would not improve even after doubling the concentration to 400 mg/mL. It is also of note that Hi alone had an effect very similar to melphalan alone, when the curves are evaluated together (Fig 3). Yet, looking closer at the pattern of response the first resulted in a reduced or stable tumor growth rate with 50% SD while the second led to 17% PR. Perfusion with Hi, either alone or combined with melphalan, did not cause systemic side effects. As for regional toxicity only some transient edema after Hi ILP, both with and without melphalan, was observed leading to temporary grade 1 toxicity in two rats for each group.

Discussion

First of all is important to stress that the experimental model of ILP requires a learning curve before obtaining trustable results. One of the main issues playing a role on quality is the time taken between anesthesia and the isolation and canulation of the femoral vessels. This might determine a significant leakage and, in this case just opposite to what is seen in the clinical setting there is not much to do besides reducing flow speed. Once more than 4 mL is lost the limb will present such a significant edema in the post-operative period that further evaluation of the treatment administered is prevented. Also the morbidity in these situations would result in such a suffering of the subject that, according to ethical recommendations, it would be better to sacrifice the animal. We showed for the first time the promising activity of Histamine plus melphalan in ILP, for the treatment of soft tissue sarcomas. Among the advantages of Hi as compared to TNF-alpha we could include its pharmacokinetics with a short half-life in the serum of only 0.35 minutes against 20 minutes for TNF-a¹³. Hi is metabolized through two major pathways in man: the more important involves ring methylation and is catalyzed by the enzyme histamine-N-methyltransferase, which is widely distributed. Most of the product, N-methylhistamine is converted by monoamine oxidase (MAO) to N-methyl imidazole acetic acid.

Alternatively Hi undergoes oxidative deamination catalyzed mainly by the nonspecific enzyme diamine oxidase (DAO). The products are imidazole acetic acid and its riboside. The metabolites with little or no activity are excreted in the urine¹⁰. Although these data come from studies with lower dosages or endogenous Hi they describe a widely distributed and fast metabolizing system, which would suggest a potentially safer drug in case of some leakage during the ILP. Furthermore, our finding opens new possibilities of application in potentially less well-isolated settings as for example the isolated liver perfusion. Still, more studies on the pharmacokinetics for the higher doses and evaluation in the clinical setting are mandatory for the clinical translation of Hi.

Another advantage, mainly for exploring its use in organ perfusion, would be its lack of toxicity towards the liver as compared to TNF-a, which exhibits a small window for dosage increase.

Conclusion

Hi plus melphalan in the ILP seems a promising alternative and worth being evaluated in the clinical setting. Further studies are required to better detail its mechanism of action.

Acknowledgements

We thank Maxim Pharmaceuticals Inc., San Diego, CA for kindly providing Histamine Dihydrochloride injection for the studies

We thank Gerard JJM Borsboom from the Department of Public Health, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands for expert assistance with statistical evaluation.

Received: March 3, 2005

Revised: April 12, 2005

Aproved: May 17, 2005

Conflict of interest: none

Financial source: grant from CAPES/MEC – Brazil

How to cite this article: Brunstein F, Santos IDAO, Ferreira LM, van Tiel ST, Eggermont AMM, Hagen TLMT. Histamine combined with melphalan in isolated limb perfusion for the treatment of locally advanced soft tissue sarcomas: preclinical studies in rats. Acta Cir Bras [serial online] 2005 Jul-Aug;20(4). Available from: http://www.scielo.br/acb

* Color figures available from http://www.scielo.br/acb

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1

. Laboratory of Experimental Surgical Oncology Daniel den Hoed Cancer Center Erasmus MC - Rotterdam the Netherlands.

Publication Dates

• Publication in this collection
  20 July 2005
• Date of issue
  Aug 2005

History

• Accepted
  17 May 2005
• Reviewed
  12 Apr 2005
• Received
  03 Mar 2005