- Open Access
Patterns of tumor response in canine and feline cancer patients treated with electrochemotherapy: preclinical data for the standardization of this treatment in pets and humans
© Spugnini et al; licensee BioMed Central Ltd. 2007
Received: 24 August 2007
Accepted: 02 October 2007
Published: 02 October 2007
Electrochemotherapy (ECT) is a novel anticancer therapy that is currently being evaluated in human and pet cancer patients. ECT associates the administration of an anti-tumor agent to the delivery of trains of appropriate waveforms. The increased uptake of chemotherapy leads to apoptotic death of the neoplasm thus resulting in prolonged local control and extended survival. In this paper we describe the histological features of a broad array of spontaneous tumors of companion animals receiving pulse-mediated chemotherapy. Multivariate statistical analysis of the percentage of necrosis and apoptosis in the tumors before and after ECT treatment, shows that only a high percentage of necrosis and apoptosis after the ECT treatment were significantly correlated with longer survivals of the patients (p < 0.0001 and p = 0.004, respectively). Further studies on this topic are warranted in companion animals with spontaneous tumors to identify new molecular targets for electrochemotherapy and to the develop new therapeutical protocols to be translated to humans.
Local management of solid neoplasms in humans generally involves multimodality approaches whose cornerstones are surgery combined with radiation therapy [1, 2]. The usual radiation protocols are based on preoperative, intra-operative, or post-operative external beam treatment or adjuvant brachytherapy . The aim of these strategies is to optimize local control while minimizing side effects, especially in the case of limb neoplasms. For these reasons low dose external beam fractionation is usually preferred, however in case of large cancers that involve deep underlying structures, preoperative radiation therapy might be chosen . Unfortunately the rate of local wound complication associated with aggressive surgical management and radiation therapy is still elevated . Electrochemotherapy (ECT) is a new approach to solid tumors that associates the administration of a chemotherapy agent to the application of square or biphasic electric pulses (EP) so to increase the uptake of drug by the cancer cells [6, 7]. This approach can lead to tumor destruction through apoptotic death at least when using bleomycin as anticancer agent , resulting in tumor control or palliation with minimal side effects. Over the past years our group focused on the development of novel ECT protocols in pets affected by advanced cancer as a model for down-staged human patients. After preliminary studies involving also the development of custom-tailored electrodes [9, 10] we studied the impact of ECT on several cohorts of canine and feline patients affected by spontaneously occurring tumors [11–13].
The high rate of local control in our preliminary investigation  that accounted for an overall 80% response (40% long lasting), prompted us to mount several phase II studies.
Many tumor histotypes show a marked responsiveness to pulse-mediated chemotherapy, leading to tumor shrinkage and clinical remission. In particular, ECT seems promising at controlling oral mucosal melanomas either as a single modality therapy or in conjunction with surgical cytoreduction . Moreover, ECT can be employed not only to directly attack neoplasms but can also be used in an adjuvant fashion to treat residual disease, thus sterilizing the surgical field in case of incomplete excision as per radiation therapy [11–13]. Of interest, tumors reported to be resistant to this clinical strategy  became highly responsive when it has been coupled with surgery as evidenced by a recent publication .
Despite the consistent number of preclinical and clinical publications on this topic, there are few data on the histopathological modifications induced by this therapy . Mir and coll. described massive necrosis induced by ECT in cats harboring post-vaccinal sarcomas, characterized by diffuse infiltration of the tumor perimeter by macrophages, lymphocytes and eosinophils .
The lack of extensive investigation in this field prompted us to run a thorough revision of our histological samples to gather a broader picture of patterns of tumor response and eventually to identify possible prognostic factors.
Tumor types treated with ECT in 127 companion animals with spontaneously occurring neoplasms
Number of patients
Soft tissue sarcoma
19 + 39
Soft tissue sarcoma
Mast cell tumor
Squamous cell carcinoma
Biopsies (surgical and punch samplings) were collected before the beginning of ECT, after one session (one week after the treatment) and at the completion of the protocol (two weeks after the end of the protocol). More than 370 specimens were analyzed. Histopathology specimens embedded in paraffin have been cut into 6 μm sections and stained following standard protocols, using Hematoxylin/Eosin, Hematoxylin/Van Gieson, and toluidine blue staining (to identify poorly differentiated mast cell tumors) . The TUNEL reaction was performed using the peroxidase-based Apoptag kit (Oncor, Gaithersburg, MD), as previously described . In order to confirm the diagnoses, histological examination of the biopsies were independently performed by two pathologists (FB and AB) that were not informed of the clinical outcome of the veterinary patients that were staged, treated and followed up by another investigator (EPS).
Histopathological patterns were tested for significance regarding response to first treatment, response to second session of ECT and the recurrence within the first six months of follow-up. Patients died of unrelated disease were censored in the analysis. Variables tested were: percentage of necrosis, apoptotic index. All analyses were performed following an intention to treat analysis method. The time to progression was calculated as the period from the date of starting treatment to the first observation of disease progression or to death from any cause. Survival plot were performed by Kaplan-Meier product-limit method . The differences in terms of survival according to the degree of apoptosis and necrosis (both pre- and post-treatment) were evaluated by the log-rank test . Finally, the Cox proportional hazards model was applied to the multivariate survival analysis . SPSS software (version 11.05, SPSS, Chicago) was used for statistical analysis. A P value of less than 0.05 was considered to indicate statistical significance.
Main histopathological features of the ECT-treated cancers
Phase of treatment*
Early phase (First session of ECT)
acute inflammatory response followed by necrosis and apoptosis
End of treatment (second session of ECT)
no inflammatory response, necrosis, scar tissue and apoptosis of the residual tumor cells
Correlation with survival in multivariate analysis of the histopathological parameters selected
Relative risk (95% C.I.)
Necrosis post > 55
0.066 (0.024 – 0.179)
Necrosis post ≤ 55
Apoptosis pre > 3
0.534 (0.267 – 1.072)
Apoptosis pre ≤ 3
Apoptosis post > 9
0.352 (0.173 – 0.715)
Apoptosis post ≤ 9
ECT has several advantages on other anti-tumor techniques: ease of administration, low cost, minimal toxicity (usually limited to mild focal inflammation at the treated site), and high response rate. Our morphological study shows on a broad selection of tumors of companion animals a progressive and highly selective destruction that frequently allowed conservative surgeries in the case of extensive tumors. The histopathological analysis of the treated tumor revealed that cancer cells did not undergo the typical response to bleomycin consisting with enlargement and polynucleation , but evidenced marked necrosis circumscribed to the tumour tissue, and an associated acute inflammatory response mediated by lymphocytes and plasma cells. In the second phase of the treatment, neoplastic apoptotic cells are detected in most of the tumour mass, with no signs of acute inflammation. This apoptotic pattern could be a consequence not only of the ECT but also a phenomenon mediated by cellular immunity, depending on the presence of a mixed T and B lymphocyte population (data not shown). When we statistically analysed the levels of necrosis and apoptosis in the tumours before and after ECT treatment, we found that either high necrosis and high apoptosis in the treated tumours were correlated with an higher survival. As it was logical to think, the percentage of necrosis in the untreated tumours did not display any significant correlation, while an high apoptotic rate in the untreated tumours was, indeed, significantly correlated with survival. These data are in agreement with several observation that in several human and animal different tumour histotypes, the apoptotic rate is an important prognostic factor . Nevertheless, when we performed a multivariate analysis with the same histopathological parameters, we found that only an high level of necrosis and apoptosis after the ECT treatment, significantly correlated with a longer survival. This result reinforces the idea that it is the destruction of the tumours by the ECT treatment that is responsible for the survival of the patients.
On the other hand, this pattern of tumor lysis seems to play a key role in the prevention of local recurrence and distant dissemination for melanomas treated with this technique. In fact, we recently described a vitiligo-like lesion in canine malignant melanomas of the oral cavity where the absence of any pigment at the treatment site in the long term survivors might imply the aiming of the immune system to melanin and other deep melanoma antigens . Another pattern of response, at the moment observed only in three cases of feline high grade sarcomas, suggests that ECT seems to promote a selection of tumor cells, leading to a local recurrence in the form of a less aggressive histotype: a neurofibroma-like lesion rather than an high grade sarcoma.
To the best of our knowledge, this is the most extensive description of histopathological patterns of response to electrochemotherapy in tumors of companion animals, showing previously undescribed mechanisms of response. The morphological analysis further confirm the efficacy and selectivity of this novel anticancer treatment as evidenced by the lack of sufferance elicited in the normal tissues surrounding the neoplasms. Studies are currently ongoing at our laboratory to further define the nature of the immune response elicited by the ECT treatment, in order to refine and ameliorate the efficacy of our protocols.
Spontaneous tumors of pets share striking clinical, histopathological and molecular similarities with their human counterparts, thus providing an invaluable bench to clinic bridging .
The results of our studies are being currently translated to humans . Indeed, the data presented in this article, combined with the preclinical results obtained in companion animals will be instrumental to identify new molecular targets and to plan more efficacious and less invasive ECT protocols to be transferred to humans.
This work has been supported by "Grant 2005" of the Italian Ministry of Health to E.P.S., and by grants from International Society for the Study of Comparative Oncology, Inc. (ISSCO, President HE Kaiser) Silver Spring, MD, USA and FUTURA-Onlus to A. Baldi.
- O'Sullivan B, Davis AM, Turcotte R, Bell R, Catton C, Chabot P, Wunder J, Kandel R, Goddard K, Sadura A, Pater J, Zee B: Preoperative versus postoperative radiotherapy in soft-tissue sarcoma of the limbs: a randomized trial. Lancet. 2002, 359: 2235-2241. 10.1016/S0140-6736(02)09292-9.View ArticlePubMedGoogle Scholar
- Owens JM, Roberts DB, Myers JN: The role of postoperative adjuvant radiation therapy in the treatment of mucosal melanomas of the head and neck region. Arch Otolaryngol Head Neck Surg. 2003, 129: 864-868. 10.1001/archotol.129.8.864.View ArticlePubMedGoogle Scholar
- Suit HD, Mankin HJ, Wood WC, Proppe KH: Preoperative, intraoperative, and postoperative radiation in the treatment of primary soft tissue sarcoma. Cancer. 1985, 55: 2659-2667. 10.1002/1097-0142(19850601)55:11<2659::AID-CNCR2820551122>3.0.CO;2-Q.View ArticlePubMedGoogle Scholar
- Sadoski C, Suit HD, Rosenberg A, Rosenberg A, Mankin H, Efird J: Preoperative radiation, surgical margins, and local control of extremity sarcomas of soft tissues. J Surg Oncol. 1993, 52: 223-230. 10.1002/jso.2930520405.View ArticlePubMedGoogle Scholar
- Bujko K, Suit HD, Springfield DS, Convery K: Wound healing after preoperative radiation for sarcoma of soft tissues. Surg Gynecol Obstet. 1993, 176 (2): 124-134.PubMedGoogle Scholar
- Belehradek M, Domenge C, Luboinski B: Electrochemotherapy, a new antitumor treatment. First clinical phase I-II trial. Cancer. 1993, 72: 3694-3700. 10.1002/1097-0142(19931215)72:12<3694::AID-CNCR2820721222>3.0.CO;2-2.View ArticlePubMedGoogle Scholar
- Daskalov I, Mudrov N, Peycheva E: Exploring new instrumentation parameters for electrochemotherapy. Attacking tumors with bursts of biphasic pulses instead of single pulses. IEEE Eng Med Biol Mag. 1999, 18 (1): 62-66. 10.1109/51.740982.View ArticlePubMedGoogle Scholar
- Tounekti O, Pron G, Belehradek J, Mir LM: Bleomycin, an apoptosis-mimetic drug that induces two types of cell death depending on the number of molecules internalized. Cancer Res. 1990, 53: 5462-5469.Google Scholar
- Spugnini EP, Porrello A: Potentiation of chemotherapy in companion animals with spontaneous large neoplasms by application of biphasic electric pulses. J Exp Clin Cancer Res. 2003, 22: 571-580.PubMedGoogle Scholar
- Spugnini EP, Citro G, Porrello A: Rational design of new electrodes for electrochemotherapy. J Exp Clin Cancer Res. 2005, 24: 245-254.PubMedGoogle Scholar
- Spugnini EP, Dragonetti E, Vincenzi B, Onori N, Citro G, Baldi A: Pulse mediated chemotherapy enhances local control and survival in a spontaneous canine model of primary mucosal melanoma. Melanoma Res. 2006, 16: 23-27. 10.1097/01.cmr.0000195702.73192.a0.View ArticlePubMedGoogle Scholar
- Spugnini EP, Baldi A, Vincenzi B, Bongiorni F, Bellelli C, Citro G, Porrello A: Intraoperative versus postoperative electrochemotherapy in high grade soft tissue sarcomas: a preliminary study in a spontaneous feline model. Cancer Chemother Pharmacol. 2007, 59: 375-381. 10.1007/s00280-006-0281-y.View ArticlePubMedGoogle Scholar
- Spugnini EP, Vincenzi B, Baldi F, Citro G, Baldi A: Adjuvant electrochemotherapy for the treatment of incompletely resected canine mast cell tumors. Anticancer Res. 2006, 26: 4585-4589.PubMedGoogle Scholar
- Mir LM, Devauchelle P, Quintin-Colonna F, Delisle F, Doliger S, Fradelizi D, Belehradek J, Orlowski S: First clinical trial of cat soft-tissue sarcomas treatment by electrochemotherapy. Br J Cancer. 1997, 76: 1617-1622.PubMed CentralView ArticlePubMedGoogle Scholar
- Salomskaite-Davalgiene S, Venslauskas MS, Pauziene N: Histological analysis of electrochemotherapy influence in Lewis lung carcinoma. Medicina (Kaunas). 2002, 38: 540-544.Google Scholar
- Strefezzi RDeF, Xavier JG, Catão-Dias JL: Morphometry of canine cutaneous mast cell tumors. Vet Pathol. 2003, 40: 268-275. 10.1354/vp.40-3-268.View ArticleGoogle Scholar
- Baldi A, Abbate A, Bussani R, Patti G, Melfi R, Angelini A, Dobrina A, Rossiello R, Silvestri F, Baldi F, Di Sciascio G: Apoptosis and post-infarction left venricular remodeling. J Mol Cell Cardiol. 2002, 34: 165-174. 10.1006/jmcc.2001.1498.View ArticlePubMedGoogle Scholar
- Kaplan E, Meier P: Nonparametric estimation from incomplete observations. J Am Stat Assoc. 1958, 53: 457-481. 10.2307/2281868.View ArticleGoogle Scholar
- Peto R, Pike MC, Armitage P: Design and analysis of randomised clinical trials requiring prolonged observation of each patient. Br J Cancer. 1977, 35: 1-39.PubMed CentralView ArticlePubMedGoogle Scholar
- Cox DR: Regression models and life tables. J R Stat Soc. 1972, 34: 187-220.Google Scholar
- Groeger AM, Esposito V, De Luca A, Cassandro R, Tonini G, Ambrogi V, Baldi F, Goldfarb R, Mineo TC, Baldi A, Wolner E: Prognostic value of immunohistochemical expression of p53, BAX, BCL-2 and BCL-Xl in resected non small cell lung cancer. Histopathology. 2004, 44: 54-63. 10.1111/j.1365-2559.2004.01750.x.View ArticlePubMedGoogle Scholar
- Porrello A, Cardelli P, Spugnini EP: Pet models in cancer research: general principles. J Exp Clin Cancer Res. 2004, 23: 181-193.PubMedGoogle Scholar
- Peycheva E, Daskalov I, Tsoneva I: Electrochemotherapy of Mycosis fungoides by interferon-alpha. Bioelectrochemistry. 2007, 70: 283-286. 10.1016/j.bioelechem.2006.10.006.View ArticlePubMedGoogle Scholar
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