Preview

Siberian journal of oncology

Advanced search

CLINICAL-IMMUNOLOGICAL ASSESSMENT OF EFFICACY OF NEOADJUVANT PHOTODYNAMIC THERAPY IN SURGICAL MANAGEMENT OF PRIMARY MELANOMA

Abstract

Efficacy of neoadjuvant photodynamic therapy (PDT) with photoditazine and radachlorine was assessed in 42 patients with stage I–III primary melanoma. The control group consisted of 42 patients with melanoma who underwent surgery alone. The 2.5-year overall and recurrence-free survival rates were significantly higher in patients who received neoadjuvant PDT than in the control group patients.  Neoadjuvant PDT performed 2 days before surgery was found to promote the activation of T-and B-cell immunity.   In the experimental study it was shown that the increase in time of laser irradiation of melanoma cell culture accompanied by a significant increase in the proportion of late apoptotic cells.

About the Authors

G. I. Gafton
N.N. Petrov Research Institute of Oncology, St. Petersburg, Pesochny
Russian Federation
Gafton Georgij Ivanovich -  MD, DSc.


V. V. Anisimov
N.N. Petrov Research Institute of Oncology, St. Petersburg, Pesochny
Russian Federation
Anisimov Valentin Vadimovich - MD, DSc., Principal Investigator


M. L. Gelfond
N.N. Petrov Research Institute of Oncology, St. Petersburg, Pesochny
Russian Federation
Gelfond Mark Lvovich -  Senior Researcher


Yu. V. Semiletova
N.N. Petrov Research Institute of Oncology, St. Petersburg, Pesochny
Russian Federation
Semiletova Yulia Vadimovna 


I. A. Baldueva
N.N. Petrov Research Institute of Oncology, St. Petersburg, Pesochny
Russian Federation
Baldueva Irina Aleksandrovna -  MD, DSc.


Т. L. Nekhaeva
N.N. Petrov Research Institute of Oncology, St. Petersburg, Pesochny
Russian Federation
Nekhaeva Tatjana Leonidovna 


A. V. Novik
N.N. Petrov Research Institute of Oncology, St. Petersburg, Pesochny
Russian Federation
Novik Aleksej Viktorovich -  MD., PhD., Senior Researcher


М. Yu. Myasnyankin
N.N. Petrov Research Institute of Oncology, St. Petersburg, Pesochny
Russian Federation
Myasnyankin Michael Jurevich 


References

1. Baldueva I.A. Immunological characteristics of the relationship between the tumor and the body in melanoma // Prakticheskaja onkologija. 2001. № 4 (8). P. 37–41. [in Russian]

2. Vasil’ev N.E. Immunological aspects of photodynamic therapy // Mater. nauch.-prakt. konf. «Primenenie poluprovodnikovyh lazerov v medicine». SPb., 2006. P. 62. [in Russian]

3. Geinitz A.V., Sorokaty A.E., Yagudajev D.M., Trukhmanov R.S. Photodynamic therapy. The history and mechanisms of its action // Lazernaja medicina. 2007. Vol. 11 (3). P. 42–46. [in Russian]

4. Cancer incidence (morbidity and mortality) in Russia in 2009 / Eds. V.I. Chissov, V.V. Starinskij, G.V. Petrova. M., 2011. 260 p. [in Russian]

5. Merabishvilli V.M. Survival of cancer patients. SPb., 2006. 438 p. [in Russian]

6. Mikhaylova I.N., Ivanov P.V., Petenko N.N., Baryshnikov K.A., Morosova L.F., Burova O.S., Cheremushkin E.A., Subramanian S., Chkadua G.Z., Baryshnikov A.Yu., Demidov L.V. Immune reaction of the skin in melanoma patients vaccine therapy // Rossijskij bioterapevticheskij zhurnal. 2010. Vol. 9 (1). P. 63–68. [in Russian]

7. Chernov V.I., Afanasyev S.G., Sinilkin I.G., Tickaja A.A., Avgusti- novich A.V. Radionuclide diagnosis for detection of sentinel lymph nodes // Sibirskij onkologicheskij zhurnal. 2008. № 4. P. 5–10. [in Russian]

8. Almeida R.D., Manadas B.J., Carvalho A.P., Duarte C.B. Intracel- lular signaling mechanisms in photodynamic therapy // Biochim. Biophys. Acta. 2004. Vol. 1704. (2). P. 59–86.

9. Bartholomae W.C., Rininsland F.H., Eisenberg J.C., Boehm B.O., Lehmann P.V., Tary-Lehmann M. T cell immunity induced by live, necrotic and apoptotic tumor cells // J. Immunol. 2004. Vol. 173 (2). P. 1012–1022.

10. Chen B., Roskams T., Xu Y., Agostinis P., de Witte P.A. Photo- dynamic therapy with hypericin induces vascular damage and apoptosis in the RIF-1 mouse tumor model // Int. J. Cancer. 2002. Vol. 98 (2). P. 284–290.

11. Chen W.R., Korbelik M., Bartels K.E., Liu H., Sun J., Nordquist R.E. Enhancement of laser cancer treatment by a chitosan-derived immunoad- juvant // Photochem. Photobiol. 2005. Vol. 81 (1). P. 190–195.

12. Chen W.R., Zhu W.G., Dynlacht J.R., Nordquist R.E. Long-term tumor resistance induced by laser photo-immunotherapy // Int. J. Cancer. 1999. Vol. 81 (5). P. 808–812.

13. Cottrez F., Groux H. Specialization in tolerance: innate CD(4+) CD(25+) versus acquired TR1 and TH3 regulatory T cells // Transplanta- tion. 2004. Vol. 77. Suppl. 1. S. 12–15.

14. Golab J., Wilczynski G., Zagozdzon R., Stokłosa T., Dabrowska A., Rybczyńska J., Wasik M., Machaj E., Ołda T., Kozar K., Kamiński R., Giermasz A., Czajka A., Lasek W., Feleszko W., Jakóbisiak M. Potentia- tion of the anti-tumor effects of Photofrin-based photodynamic therapy by localized treatment with G-CSF // Br. J. Cancer. 2000. Vol. 82 (8). P. 1485–1491.

15. Gollnick S., Evans S., Baumann H., Owczarczak B., Maier P., Vaughan L., Wang W.C., Unger E., Henderson B.W. Role of cytokines in photodynamic therapy-induced local and systemic inflammation // Br. J. Cancer. 2003. Vol. 88 (11). P. 1772–1779.

16. Gollnick S., Vaughan L., Henderson B. Generation of effective antitumor vaccines using photodynamic therapy // Cancer Res. 2002. Vol. 62 (6). P. 1604–1608.

17. Gollnick S.O., Brackett C.M. Enhancement of anti-tumor immunity by photodynamic therapy // Immunol. Res. 2010. Vol. 46 (1–3). P. 216–226. doi: 10.1007/s12026-009-8119-4.

18. Gomer C., Ryter S.W., Ferrario A., Rucker N., Wong S., Fisher A.M. Photodynamic therapy-mediated oxidative stress can induce expression of heat shock proteins // Cancer Res. 1996. Vol. 56 (10). P. 2355–2360.

19. Haylett A.K., Ward T.H., Moore J.V. DNA damage and repair in Gorlin syndrome and normal fibroblasts aer aminolevulinic acid photo- dynamic therapy: a comet assay study // Photochem. Photobiol. 2003. Vol. 78 (4). P. 337–341.

20. Huang Z., Xu H., Meyers A.D., Musani A.I., Wang L., Tagg R., Barqawi A.B., Chen Y.K. Photodynamic therapy for treatment of solid tumors-potential and technical challenges // Technol. Cancer Res. Treat. 2008. Vol. 7 (4). P. 309–320.

21. Kiesslich T., Plaetzer K., Oberdanner C.B., Berlanda J., Ober- mair F.J., Krammer B. Differential effects of glucose deprivation on the cellular sensitivity towards photodynamic treatment-based production of reactive oxygen species and apoptosis-induction // FEBS Lett. 2005. Vol. 579 (1). P. 185–190.

22. Magner W.J., Tomasi T.B. Apoptotic and necrotic cells induced by different agents vary in their expression of MHC and costimulatory genes // Mol. Immunol. 2005. Vol. 42 (9). P. 1033–1042.

23. McNair F.I., Marples B., West C.M., Moore J.V. A comet assay of DNA damage and repair in K562 cells aer photodynamic therapy using haematoporphyrin derivative, methylene blue and meso-tetrahydroxyphenylchlorin // Br. J. Cancer. 1997. Vol. 75 (12). P. 1721–1729.

24. Mitra S., Goren E., Frelinger J., Foster T.H. Activation of heat shock protein 70 promoter with meso-tetrahydroxyphenyl chlorine photodynamic therapy reported by green fluorescent protein in vitro and in vivo // Photochem. Photobiol. 2003. Vol. 78 (6). P. 615–622.

25. Mroz P., Szokalska A., Wu M.X., Hamblin M.R. Photodynamic Therapy of Tumors Can Lead to Development of Systemic AntigenSpecific Immune Response // PLoS ONE. 2010. Vol. 5 (12). P. 151–194. doi: 10.1371/journal.pone.0015194.

26. Oberdanner C.B., Kiesslich T, Krammer B., Plaetzer K. Glucose is required to maintain high ATP-levels for the energy-utilizing steps during PDT-induced apoptosis // Photochem. Photobiol. 2002. Vol. 76 (6). P. 695–703.

27. Oleinick N., Morris R., Belichenko I. The role of apoptosis in response to photodynamic therapy: What, where, why and how // Photochem. Photobiol. Sci. 2002. Vol. 1 (1). P. 1–21.

28. Preise D., Oren R., Glinert I., Kalchenko V., Jung S., Scherz A., Salomon Y. Systemic antitumor protection by vascular-targeted photodynamic therapyinvolves cellular and humoral immunity // Cancer Immunol. Immunother. 2009. Vol. 58 (1). – P. 71–84. doi: 10.1007/s00262-008-0527-0.

29. Preise D., Scherz A., Salomon Y. Antitumor immunity promoted by vascular occluding therapy: lessons from vascular-targeted photodynamic therapy (VTP) // Photochem. Photobiol. Sci. 2011. Vol. 10 (5). P. 681–688. doi: 10.1039/c0pp00315h.

30. Reed M., Miller F., Weiman T., Tseng M.T., Pietsch C.G. The effect of photodynamic therapy on the microcirculation // J. Surg. Res. 1988. Vol. 45 (5). P. 452–459.

31. Scheffer S.R., Nave H., Korangy F., Schlote K., Pabst R., Jaffee E.M., Manns M.P., Greten T.F. Apoptotic, but not necrotic tumor cell vaccines induce a potent immune response in vivo // Int. J. Cancer. 2003. Vol. 103 (2). P. 205–211.

32. Seya T., Akazawa T., Uehori J., Matsumoto M., Azuma I., Toyoshima K. Role of toll-like receptors and their adaptors in adjuvant immunotherapy for cancer // Anticancer Res. 2003. Vol. 23 (6a). P. 4369–4376.

33. Shaif-Muthana M., McIntyre C., Sisley K., Rennie .I, Murray A. Dead or alive: immunogenicity of human melanoma cells when presented by dendritic cells // Cancer Res. 2000. Vol. 60 (22). P. 6441–6447.

34. Sierra-Rivera E., Voorhees G.J., Freedman M.L. Gamma irradiation increases hsp-70 in Chinese hamster ovary cells // Radiat. Res. 1993. Vol. 135 (1). P. 40–45.

35. Van Duijnhoven F.H., Aalbers R.I., Rovers J.P., Terpstra O.T., Kuppen P.J. The immunological consequences of photodynamic treatment of cancer, a literature review // Immunobiology. 2003. Vol. 207 (2). P. 105–113.

36. Woods J.A., Traynor N.J., Brancaleon L., Moseley H. The effect of photofrin on DNA strand breaks and base oxidation in HaCaT keratinocytes: a comet assay study // Photochem. Photobiol. 2004. Vol. 79 (1). P.105–113.

37. Wyld L., Reed M.W., Brown N.J. Differential cell death response to photodynamic therapy is dependent on dose and cell type // Br. J. Can- cer. 2001. Vol. 84 (10). P. 1384–1386.

38. Yenari M., Liu J., Zheng Z., Vexler Z.S., Lee J.E., Giffard R.G. Antiapoptotic and anti-inflammatory mechanisms of heat shock protein protection // Ann. NY Acad. Sci. 2005. Vol. 1053. P. 74–83.

39. Zitvogel L., Casares N., Péquignot M.O., Chaput N., Albert M.L., Kroemer G. Immune response against dying tumor cells // Adv. Immunol. 2004. Vol. 84. P. 131–179.


Review

For citations:


Gafton G.I., Anisimov V.V., Gelfond M.L., Semiletova Yu.V., Baldueva I.A., Nekhaeva Т.L., Novik A.V., Myasnyankin М.Yu. CLINICAL-IMMUNOLOGICAL ASSESSMENT OF EFFICACY OF NEOADJUVANT PHOTODYNAMIC THERAPY IN SURGICAL MANAGEMENT OF PRIMARY MELANOMA. Siberian journal of oncology. 2015;1(2):31-38. (In Russ.)

Views: 775


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 1814-4861 (Print)
ISSN 2312-3168 (Online)