Photodynamic therapy for cutaneous hemangiosarcoma in dogs

被引:14
作者
Rocha, Martha S. T. [1 ]
Lucci, Carolina M. [1 ]
dos Santos, Jairo A. M.
Longo, Joao Paulo F. [2 ]
Muehlmann, Luis Alexandre [3 ]
Azevedo, Ricardo B. [2 ]
机构
[1] Univ Brasilia, Dept Physiol Sci, Inst Biol Sci, Brasilia, DF, Brazil
[2] Univ Brasilia, Dept Genet & Morphol, Inst Biol Sci, Brasilia, DF, Brazil
[3] Univ Brasilia, Fac Ceilandia, Brasilia, DF, Brazil
关键词
Animal cancer treatment; Veterinary oncology; PDT; HSA; Nanotechnology; Nanoemulsion; Hemangiosarcoma; Canines; Photodynamic Therapy; DERIVATIVE MONOACID RING; PHOTOSENSITIZERS; CARCINOMA; TUMORS;
D O I
10.1016/j.pdpdt.2019.05.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cutaneous hemangiosarcoma is a malignant neoplasia that frequently occurs in dogs. The most effective treatment requires wide surgical excision of the tumor. To avoid mutilating surgeries, photodynamic therapy (PDT) could serve as an alternative treatment. This study aimed to treat cutaneous hemangiosarcomas in dogs using PDT with aluminium-chloride-phthalocyanine nanoemulsion (AlClPc-nano) as photosensitizer. Eight dogs with histopathological diagnosis of naturally occurring cutaneous hemangiosarcoma were treated. Animals were given intra and peritumoral injections of AICIPc-nano (13.3 mu M). After 15 min, the masses were LED irradiated at a wavelength of 658-662 nm (80 mW potency) for 25 min (120 J/cm(2) fluency). The number of sessions was based on lesion observations, with PDT sessions repeated every 7 days until the mass was no longer macroscopically visible. On that occasion, an excisional biopsy of the area was taken for histopathology analysis. Blood was collected from each animal before each PDT session and excisional biopsy for hematological analysis (blood counts; liver and kidney function). The number of PDT sessions varied from 2 to 4, depending on the size of the initial mass. Seven of the eight cases demonstrated complete remission of neoplasia. Microscopic analysis of the excisional biopsies showed necrosis and hemorrhage only, with no cancer cells, except in one case. During the treatment, inflammation and necrosis were macroscopically observed in the treated areas. The dogs did not show any alteration in blood parameters that could be related to the PDT. In conclusion, PDT with AlClPc-nano is a safe and effective treatment for cutaneous hemangiosarcoma in dogs.
引用
收藏
页码:39 / 43
页数:5
相关论文
共 24 条
  • [1] Photodynamic Efficiency: From Molecular Photochemistry to Cell Death
    Bacellar, Isabel O. L.
    Tsubone, Tayana M.
    Pavani, Christiane
    Baptista, Mauricio S.
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2015, 16 (09) : 20523 - 20559
  • [2] Veterinary photodynamic therapy: A review
    Buchholz, Julia
    Walt, Heinrich
    [J]. PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2013, 10 (04) : 342 - 347
  • [3] Clifford CA, 2000, J VET INTERN MED, V14, P479, DOI 10.1892/0891-6640(2000)014<0479:TOCHAB>2.3.CO
  • [4] 2
  • [5] Photodynamic therapy for cancer
    Dolmans, DEJGJ
    Fukumura, D
    Jain, RK
    [J]. NATURE REVIEWS CANCER, 2003, 3 (05) : 380 - 387
  • [6] DOUGHERTY TJ, 1981, CANCER RES, V41, P401
  • [7] HOSGOOD G, 1991, COMP CONT EDUC PRACT, V13, P1065
  • [8] HISTOPATHOLOGICAL FEATURES OF CUTANEOUS TUMOURS ARISING FROM THE VASCULAR ENDOTHELIAL CELLS IN DOGS
    Jayasree, N.
    Nasreen, A.
    Naik, S. H.
    Murthy, R. V. R.
    Srilatha, Ch
    Sujatha, K.
    [J]. JOURNAL OF EXPERIMENTAL BIOLOGY AND AGRICULTURAL SCIENCES, 2016, 4 : S78 - S82
  • [9] Overcoming the Limits of Hypoxia in Photodynamic Therapy: A Carbonic Anhydrase IX-Targeted Approach
    Jung, Hyo Sung
    Han, Jiyou
    Shi, Hu
    Koo, Seyoung
    Singh, Hardev
    Kim, Hyo-Jin
    Sessler, Jonathan L.
    Lee, Jin Yong
    Kim, Jong-Hoon
    Kim, Jong Seung
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2017, 139 (22) : 7595 - 7602
  • [10] Photodynamic therapy targeted to tumor-induced angiogenic vessels
    Kurohane, K
    Tominaga, A
    Sato, K
    North, JR
    Namba, Y
    Oku, N
    [J]. CANCER LETTERS, 2001, 167 (01) : 49 - 56