Ультразвуковая аблация опухоли: иммунные эффекты и перспективы интеграции в современные программы лечения генерализованного рака

Автор: Мачак Г.Н.

Журнал: Злокачественные опухоли @malignanttumors

Рубрика: Оригинальные исследования

Статья в выпуске: 2 т.8, 2018 года.

Бесплатный доступ

Несмотря на революционные открытия последних лет в области молекулярной онкологии и иммунологии, выживаемость при генерализованных формах злокачественных новообразований не превышает 20-30 %, поэтому поиск новых терапевтических подходов остается актуальной задачей. Дальнейший прогресс, в частности, связывают с повышением иммуногенности опухолей, индукцией воспалительного фенотипа и блокадой механизмов иммуносупрессии. Решению этих задач может способствовать ультразвуковая аблация (УЗА), которая занимает особое место среди аналогичных методик, поскольку вызывает быстрый иммунный ответ, обладает неинвазивностью и низкой локальной токсичностью, позволяет манипулировать параметрами физического воздействия, допускает многократное применение, относительно недорога и не требует длительной госпитализации. Помимо циторедукции и снижения системных иммунносупрессивных сигналов, УЗА создает в организме депо лизированных клеток и считается способом вакцинирования in situ. Постаблативная иммуногенная клеточная смерть стимулирует начальные фазы иммунного цикла и способствует генерации популяций CD4+ и CD8+ цитотоксических Т-лимфоцитов...

Еще

Злокачественные новообразования, метастазы, ультразвуковая аблация, иммунотерапия, абскопальный эффект

Короткий адрес: https://sciup.org/140243785

IDR: 140243785   |   DOI: 10.18027/2224-5057-2018-8-2-31-42

Список литературы Ультразвуковая аблация опухоли: иммунные эффекты и перспективы интеграции в современные программы лечения генерализованного рака

  • Joshi S. S., Maron S. B., Catenacci D. V. Pembrolizumab for treatment of advanced gastric and gastroesophageal junction adenocarcinoma. Future Oncol. 2018. Vol. 14 (5). P. 417-430. doi: 10.2217/fon-2017-0436.
  • Peters S., Kerr K. M., Stahel R. PD-1 blockade in advanced NSCLC: A focus on pembrolizumab. Cancer Treat. Rev. 2018. Vol. 62. P. 39-49. doi: 10.1016/j. ctrv.2017.10.002.
  • Schachter J., Ribas A., Long G. V., Arance A., Grob J. J., Mortier L. et al. Pembrolizumab versus ipilimumab for advanced melanoma: final overall survival results of a multicentre, randomised, open-label phase 3 study (KEYNOTE-006). Lancet. 2017. Vol. 390 (10105). P. 1853-1862. doi: 10.1016/S0140-6736(17)31601-X.
  • Chen D. S., Mellman I. Elements of cancer immunity and the cancer-immune set point. Nature. 2017. Vol. 541 (7637). P. 321-330. doi: 10.1038/nature21349.
  • Alatrash G., Daver N., Mittendorf E. A. Targeting Immune Checkpoints in Hematologic Malignancies. Pharmacol. Rev. 2016. Vol. 68 (4). P. 1014-1025.
  • Atkins M. B., Larkin J. Immunotherapy Combined or Sequenced With Targeted Therapy in the Treatment of Solid Tumors: Current Perspectives. J. Natl. Cancer Inst. 2016. Vol. 108 (6). djv414. 10.1093/jnci/djv414
  • DOI: :10.1093/jnci/djv414
  • Motzer R. J., Tannir N. M., McDermott D. F., Aren Frontera O., Melichar B., Choueiri T. K. et al. Nivolumab plus Ipilimumab versus Sunitinib in Advanced Renal-Cell Carcinoma. N. Engl. J. Med. 2018. Vol. 378 (14). P. 1277-1290. 10.1056/NEJMoa1712126
  • DOI: :10.1056/NEJMoa1712126
  • Powles T., Eder J. P., Fine G. D., Braiteh F. S., Loriot Y., Cruz C. et al. MPDL3280A (anti -PD-L1) treatment leads to clinical activity in metastatic bladder cancer. Nature. 2014. Vol. 515. P. 558-562.
  • Topalian S. L., Hodi F. S., Brahmer J. R., Gettinger S. N., Smith D. C., McDermott D. F. et al. Safety, activity, and immune correlates of anti -PD-1 antibody in cancer. N. Engl. J. Med. 2012. Vol. 366. P. 2443-2454.
  • Topalian S. L., Sznol M., McDermott D. F., Kluger H. M., Carvajal R. D., Sharfman W. H. et al. Survival, durable tumor remission, and long-term safety in patients with advanced melanoma receiving nivolumab. J. Clin. Oncol. 2014. Vol. 32. P. 1020-1030.
  • Sharma P., Allison J. P. The future of immune checkpoint therapy. Science. 2015. Vol. 348 (6230). P. 56-61. 10.1126/science. aaa8172
  • DOI: :10.1126/science.aaa8172
  • Ventola C. L. Cancer Immunotherapy, Part 3: Challenges and Future Trends. P&T. 2017. Vol. 42 (8). P. 514-521.
  • Koyama S., Akbay E. A., Li Y. Y. et al. Adaptive resistance to therapeutic PD-1 blockade is associated with upregulation of alternative immune checkpoints. Nat. Commun. 2016. Vol. 7. P. 10501.
  • Mothersill C., Rusin A., Fernandez-Palomo C., Seymour C. History of bystander effects research 1905-present; what is in a name? Int. J. Radiat. Biol. 2017. Vol. 29. P. 1-12. 10.1080/09553002.2017.1398436
  • DOI: :10.1080/09553002.2017.1398436
  • Siva S., MacManus M. P., Martin R. F., Martin O. A. Abscopal effects of radiation therapy: a clinical review for the radiobiologist. Cancer Lett. 2015. Vol. 356 (1). P. 82-90. 10.1016/j. canlet. 2013.09.018. Epub 2013 Oct 12
  • DOI: :10.1016/j.canlet.2013.09.018.Epub2013Oct12
  • Grass G. D., Krishna N., Kim S. The immune mechanisms of abscopal effect in radiation therapy. Curr. Probl. Cancer. 2016. Vol. 40 (1). P. 10-24. 10.1016/j. currproblcancer. 2015.10.003. Epub 2015 Nov 21
  • DOI: :10.1016/j.currproblcancer.2015.10.003.Epub2015Nov21
  • Levy A., Chargari C., Marabelle A., Perfettini J. L., Magne N., Deutsch E. Can immunostimulatory agents enhance the abscopal effect ofradiotherapy? Eur. J. Cancer. 2016. Vol. 62. P. 36-45. 10.1016/j. ejca. 2016.03.067. Epub 2016 May 18
  • DOI: :10.1016/j.ejca.2016.03.067.Epub2016May18
  • Postow M. A., Callahan M. K., Barker C. A., Yamada Y., Yuan J., Kitano S. et al. Immunologic correlates of the abscopal effect in a patient with melanoma. N. Engl. J. Med. 2012. Vol. 366 (10). P. 925-931. doi
  • DOI: :10.1056/NEJMoa1112824
  • Shi L., Chen L., Wu C., Zhu Y., Xu B., Zheng X. et al. PD-1 blockade boosts radiofrequency ablation-elicited adaptive immuneresponses against tumor. Clin. Cancer Res. 2016. Vol. 22. P. 1173-1184.
  • Silvestrini M. T., Ingham E. S., Mahakian L. M., Kheirolomoom A., Liu Y., Fite B. Z. et al. Priming is key to effective incorporation of image-guided thermal ablation into immunotherapy protocols. JCI Insight. 2017. Vol. 2 (6). e90521. 10.1172/jci.insight. 90521
  • DOI: :10.1172/jci.insight.90521
  • Pampena M. B., Barrio M. M., Julia E. P., Blanco P. A., von Euw E. M., Mordoh J. et al. Early Events of the Reaction Elicited by CSF-470 Melanoma Vaccine Plus Adjuvants: An In Vitro Analysis of Immune Recruitment and Cytokine Release. Front Immunol. 2017. Vol. 8. P. 1342. 10.3389/fimmu.2017.01342
  • DOI: :10.3389/fimmu.2017.01342
  • Silva A., Mount A., Krstevska K., Pejoski D., Hardy M. P., Owczarek C. et al. The combination of ISCOMATRIX adjuvant and TLR agonists induces regression of established solid tumors in vivo. J. Immunol. 2015. Vol. 194 (5). P. 2199-2207. 10.4049/jimmunol.1402228
  • DOI: :10.4049/jimmunol.1402228
  • Kushner B. H., Cheung I. Y., Modak S., Kramer K., Ragupathi G., Cheung N. K. Phase I trial of a bivalent gangliosides vaccine in combination with -glucan for high-risk neuroblastoma in second or later remission. Clin. Cancer Res. 2014. Vol. 20 (5). P. 1375-1382. 10.1158/1078-0432.CCR-13-1012
  • DOI: :10.1158/1078-0432.CCR-13-1012
  • Adams S. Toll-like receptor agonists in cancer therapy. Immunotherapy. 2009. Vol. 1 (6). P. 949-964. 10.2217/imt.09.70
  • DOI: :10.2217/imt.09.70
  • Liu C., Xie Y., Sun B., Geng F., Zhang F., Guo Q. et al. MUC1-and Survivin-based DNA Vaccine Combining Immunoadjuvants CpG and interleukin-2 in a Bicistronic Expression Plasmid Generates Specific Immune Responses and Antitumour Effects in a Murine Colorectal Carcinoma Model. Scand. J. Immunol. 2018. Vol. 87 (2). P. 63-72. 10.1111/sji.12633
  • DOI: :10.1111/sji.12633
  • Shukla N. M., Arimoto K. I., Yao S., Fan J. B., Zhang Y., Sato-Kaneko F. et al. Identification of Compounds That Prolong Type I Interferon Signaling as Potential Vaccine Adjuvants. SLAS Discov. 2018. May 11. 2472555218774308. 10.1177/2472555218774308
  • DOI: :10.1177/2472555218774308
  • Rammensee H. G., Singh-Jasuja H. HLA ligandome tumor antigen discovery for personalized vaccine approach. Expert Rev. Vaccines. 2013. Vol. 12. P. 1211-1217. 10.1586/14760584.2013.836911
  • DOI: :10.1586/14760584.2013.836911
  • Kooreman N. G., Kim Y., de Almeida P. E., Termglinchan V., Diecke S., Shao N. Y. et al. Autologous iPSC-Based Vaccines Elicit Antitumor Responses In Vivo. Cell Stem. Cell. 2018. Vol. 22 (4). P. 501-513. e7 10.1016/j. stem. 2018.01.016. Epub 2018 Feb 15
  • DOI: :10.1016/j.stem.2018.01.016.Epub2018Feb15
  • Bull J. M. C. A review of immune therapy in cancer and a question: can thermal therapy increase tumor response? Int. J. Hyperthermia. 2017. Vol. 3. P. 1-13. 10.1080/02656736.2017.1387938
  • DOI: :10.1080/02656736.2017.1387938
  • Mauri G., Nicosia L., Xu Z., Di Pietro S., Monfardini L., Bonomo G. et al. Focused ultrasound: tumour ablation and its potential to enhance immunological therapy to cancer. Br. J. Radiol. 2018. Vol. 91 (1083). 20170641. 10.1259/bjr.20170641
  • DOI: :10.1259/bjr.20170641
  • Wu F. High Intensity Focused Ultrasound (HIFU) Ablation. In: Keisari Y. (eds). Tumor Ablation. The Tumor Microenvironment. Springer Science+Business Media Dordrecht, 2013. Vol. 5. P. 61-76
  • DOI: 10.1007/978-94-007-4694-7_2
  • Tranberg K. G. Percutaneous ablation of liver tumours. Best Pract. Res. Clin. Gastroenterol. 2004. Vol. 18. P. 125-145.
  • Ohno T., Kawano K., Sasaki A. et al. Expansion of an ablated site and induction of apoptosis after microwave coagulation therapy in rat liver. J. Hepatobiliary Pancreat. Surg. 2001. Vol. 8. P. 360-366.
  • Canney M. S., Khokhlova V. A., Bessonova O. V., Bailey M. R., Crum L. A. Shock-induced heating and millisecond boiling in gels and tissue due to high intensity focused ultrasound. Ultrasound Med. Biol. 2010. Vol. 36. P. 250-267. 10.1016/j.ultrasmedbio. 2009.09.010
  • DOI: :10.1016/j.ultrasmedbio.2009.09.010
  • Maxwell A. D., Wang T. Y., Cain C. A., Fowlkes J. B., Sapozhnikov O. A., Bailey M. R., Xu Z. Cavitation clouds created by shock scattering from bubbles during histotripsy. J. Acoust. Soc. Am. 2011. Vol. 130. P. 1888-1898. doi
  • DOI: :10.1121/1.3625239
  • Waitz R., Solomon S. B., Petre E. N., Trumble A. E., Fasso M., Norton L. et al. Potent induction of tumor immunity by combining tumor cryoablation with anti-CTLA-4 therapy. Cancer Res. 2012. Vol. 72 (2). P. 430-439.
  • Davidovich P., Kearney C. J., Martin S. J. Inflammatory outcomes of apoptosis, necrosis and necroptosis. Biol. Chem. 2014. Vol. 395 (10). P. 1163-1171.
  • Julier Z., Park A. J., Briquez P. S., Martino M. M. Promoting tissue regeneration by modulating the immune system. Acta Biomater. 2017. Vol. 53. P. 13-28. doi
  • DOI: :10.1016/j.actbio.2017.01.056
  • Wu F., Zhou L., Chen W. R. Host antitumour immune responses to HIFU ablation. Int. J. Hyperthermia. 2007. Vol. 23. P. 165-171
  • Ghanamah M., Berber E., Siperstein A. Pattern of carcinoembryonic antigen drop after laparoscopic radiofrequency ablation of liver metastasis from colorectal carcinoma. Cancer. 2006. Vol. 107. P. 149-153.
  • den Brok M. H. M. G. M., Sutmuller R. P. M, Nierkens S., Bennink E. J., Frielink C., Toonen L. W. J. Efficient loading of dendritic cells following cryo and radiofrequency ablation in combination with immune modulation induces anti-tumour immunity. Br. J. Cancer. 2006. Vol. 95. P. 896-905.
  • Ito F., Ku A. W., Bucsek M. J., Muhitch J. B., Vardam-Kaur T., Kim M. et al. Immune adjuvant activity of pre-resectional radiofrequency ablation protects against local and systemic recurrence in aggressive murine colorectal cancer. PLoS One. 2015. Vol. 10. e0143370. doi
  • DOI: :10.1371/journal.pone.0143370
  • Xing Y., Lu X., Pua EC., Zhong P. The effect of high intensity focused ultrasound treatment on metastases in a murine melanoma model. Biochem. Biophys. Res. Commun. 2008. Vol. 375 (4). P. 645-650. 10.1016/j.bbrc. 2008.08.072
  • DOI: :10.1016/j.bbrc.2008.08.072
  • Chu K. F., Dupuy D. E. Thermal ablation of tumours: biological mechanisms and advances in therapy. Nat. Rev. Cancer. 2014. Vol. 14 (3). P. 199-208.
  • Kramer G., Steiner G. E., Grobl M., Hrachowitz K., Reithmayr F., Paucz L. et al. Response to sublethal heat treatment of prostatic tumor cells and of prostatic tumor infiltrating T-cells. Prostate. 2004. Vol. 58 (2). P. 109-120.
  • Hu Z., Yang X. Y., Liu Y., Morse M. A., Lyerly H. K., Clay T. M., Zhong P. Release of endogenous danger signals from HIFU-treated tumor cells and their stimulatory effects on APCs. Biochem. Biophys. Res. Commun. 2005. Vol. 335. P. 124-131 10.1016/j. bbrc. 2005.07.071
  • DOI: :10.1016/j.bbrc.2005.07.071
  • Wu F., Wang Z. B., Cao Y. D., Zhou Q., Zhang Y., Xu Z. L., Zhu X. Q. Expression of tumor antigens and heat-shock protein 70 in breast cancer cells after high-intensity focused ultrasound ablation. Ann. Surg. Oncol. 2007. Vol. 14. P. 1237-1242. doi
  • DOI: :10.1245/s10434-006-9275-6
  • Haen S. P., Gouttefangeas C., Schmidt D., Boss A., Clasen S., von Herbay A. et al. Elevated serum levels of heat shock protein 70 can be detected after radiofrequency ablation. Cell Stress Chaperones. 2011. Vol. 16 (5). P. 495-504. 10.1007/s12192-011-0261-y
  • DOI: :10.1007/s12192-011-0261
  • Evrard S., Menetrier-Caux C., Biota C., Neaud V., Mathoulin-Pelissier S., Blay J.Y., Rosenbaum J. Cytokines pattern after surgical radiofrequency ablation of liver colorectal metastases. Gastroenterol. Clin. Biol. 2007. Vol. 31. P. 141-145.
  • Hori K., Mihich E., Ehrke M.J. Role of tumor necrosis factor and interleukin 1 in gammainterferon-promoted activation of mouse tumoricidal macrophages. Cancer Res. 1989. Vol. 49. P. 2606-2614.
  • Kirn A., Bingen A., Steffan A.M., Wild M.T., Keller F., Cinqualbre J. Endocytic capacities of Kupffer cells isolated from the human adult liver. Hepatology.1982. Vol. 2. P. 216-222.
  • Napoletano C., Taurino F., Biffoni M., De Majo A., Coscarella G., Bellati F. et al. A RFA strongly modulates the immune system and anti-tumor immune responses in metastatic liver patients. Int. J. Oncol. 2008. Vol. 32. P. 481-490.
  • Hu Z., Yang X.Y., Liu Y., Sankin G.N., Pua E.C., Morse M.A. et al. Investigation of HIFU-induced anti-tumor immunity in a murine tumor model. J. Transl. Med. 2007. Vol. 5. P. 34
  • DOI: 10.1186/1479-5876-5-34
  • Xing Y., Lu X., Pua E.C., Zhong P. The effect of high intensity focused ultrasound treatment on metastases in a murine melanoma model. Biochem. Biophys. Res. Commun. 2008. Vol. 375(4). P. 645-650
  • DOI: 10.1016/j.bbrc.2008.08.072
  • Dromi S.A., Walsh M.P., Herby S., Traughber B., Xie J., Sharma K.V. et al. Radiofrequency ablation induces antigenpresenting cell infiltration and amplification of weak tumor-induced immunity. Radiology. 2009. Vol. 251(1). P. 58-66
  • DOI: 10.1148/radiol.2511072175
  • Huang X., Yuan F., Liang M., Lo H.W., Shinohara M.L., Robertson C., Zhong P. M-HIFU inhibits tumor growth, suppresses STAT3 activity and enhances tumor specific immunity in a transplant tumor model of prostate cancer. PLoS ONE. 2012. Vol. 7. e41632
  • DOI: 10.1371/journal.pone.0041632
  • Xu Z.L., Zhu X.Q., Lu P., Zhou Q., Zhang J., Wu F. Activation of tumor-infiltrating antigen presenting cells by high intensity focused ultrasound ablation of human breast cancer. Ultrasound Med. Biol. 2009. Vol. 35. P. 50-57
  • DOI: 10.1016/j.ultrasmedbio.2008.08.005
  • Zerbini A., Pilli M., Fagnoni F., Pelosi G., Pizzi M.G., Schivazappa S. et al. Increased immunostimulatory activity conferred to antigenpresenting cells by exposure to antigen extract from hepatocellular carcinoma afterradiofrequency thermal ablation. J. Immunother. 2008. Vol. 31(3). P. 271-282
  • DOI: 10.1097/CJI.0b013e318160ff1c
  • Zhang Y., Deng J., Feng J., Wu F. Enhancement of antitumor vaccine in ablated hepatocellular carcinoma by high-intensity focused ultrasound: a preliminary report. World J. Gastroenterol. 2010. Vol. 16. P. 3584-3591.
  • Deng J., ZhangY., Feng J., Wu F. Dendritic cells loaded with ultrasound-ablated tumour induce in vivo specific antitumour immune responses. Ultrasound Med. Biol. 2010. Vol. 36. P. 441-448.
  • Rosberger D.F., Coleman D.J., Silverman R., Woods S., Rondeau M., Cunningham-Rundles S. Immunomodulation in choroidal melanoma: Reversal of inverted CD4/CD8 ratios following treatment with ultrasonic hyperthermia. Biotechnol. Ther. 1994. Vol. 5. P. 59-68.
  • Wu F., Wang Z.B., Lu P., Xu Z.L., Chen W.Z., Zhu H., Jin C.B. Activated anti-tumor immunity in cancer patients after high intensity focused ultrasound ablation. Ultrasound Med. Biol. 2004. Vol. 30. P. 1217-1222
  • DOI: 10.1016/j.ultrasmedbio.2004.08.003
  • Wang X., Sun J. High-intensity focused ultrasound in patients with late-stage pancreatic carcinoma. Chin. Med. J. (Engl.). 2002. Vol. 115. P. 1332-1335.
  • Yang W., Wang W., Liu B., Zhu B., Li J., Xu D. et al. Immunomodulation characteristics by thermal ablation therapy in cancer patients. Asia Pac. J. Clin. Oncol. 2018. Jan 8
  • DOI: 10.1111/ajco.12836
  • Wissniowski T.T., Hansler J., Neureiter D., Frieser M., Schaber S., Esslinger B. et al. Activation of tumor-specific T lymphocytes by radio-frequency ablation of the VX2 hepatoma in rabbits. Cancer Res. 2003. Vol. 63(19). P. 6496-500.
  • van den Bijgaart R.J., Eikelenboom D.C., Hoogenboom M., Futterer J.J., den Brok M.H., Adema G.J. Thermal and mechanical high-intensity focused ultrasound: perspectives on tumor ablation, immune effects and combination strategies. Cancer Immunol. Immunother. 2017. Vol. 66(2). P. 247-258
  • DOI: 10.1007/s00262-016-1891-9
  • Zhou Q., Zhu X.Q., Zhang J., Xu J.L., Lu P., Wu F. Changes in circulating immunosuppressive cytokine levels of cancer patients after high intensity focused ultrasound treatment. Ultrasound Med. Biol. 2008. Vol. 34. P. 81-87
  • DOI: 10.1016/j.ultrasmedbio.2007.07.013
  • Xia J.Z., Xie F.L., Ran L.F., Xie X.P., Fan Y.M., Wu F. High-intensity focused ultrasound tumor ablation activates autologous tumor-specific cytotoxic T lymphocytes. Ultrasound Med. Biol. 2012. Vol. 38(8). P. 1363-1371. 10.1016/j. ultrasmedbio.2012.03.009
  • DOI: :10.1016/j.ultrasmedbio.2012.03.009
  • Yang R., Reilly C.R., Rescorla F.J., Sanghvi N.T., Fry F.J., Franklin T.D. Jr, Grosfeld J.L. Effects of high-intensity focused ultrasound in the treatment of experimental neuroblastoma. J. Pediatr. Surg. 1992. Vol. 27. P. 246-250.
  • Ran L.F., Xie X.P., Xia J.Z., Xie F.L., Fan Y.M., Wu F. Specific antitumour immunity of HIFU-activated cytotoxic T lymphocytes after adoptive transfusion in tumour-bearing mice. Int. J. Hyperthermia. 2016. Vol. 32(2). P. 204-210
  • DOI: 10.3109/02656736.2015.1112438
  • den Brok M.H., Sutmuller R.P., van der Voort R., Bennink E.J., Figdor C.G., Ruers T.J., Adema G.J. In situ tumor ablation creates an antigen source for the generation of antitumor immunity. Cancer Res. 2004. Vol. 64(11). P. 4024-4029.
  • Lu P., Zhu X.Q., Xu Z.L., Zhou Q., Zhang J., Wu F. Increased infiltration of activated tumor-infiltrating lymphocytes after high intensity focused ultrasound ablation of human breast cancer. Surgery. 2009. Vol. 145. P. 286-293
  • DOI: 10.1016/j.surg.2008.10.010
  • Dong B.W., Zhang J., Liang P., Yu X.L., Su L., Yu D.J. et al. Sequential pathological and immunologic analysis of percutaneousmicrowave coagulation therapy of hepatocellular carcinoma. Int. J. Hyperthermia. 2003. Vol. 19(2). P. 119-133.
  • Zerbini A., Pilli M., Penna A., Pelosi G., Schianchi C., Molinari A. et al. Radiofrequency thermal ablation of hepatocellular carcinoma liver nodules can activate and enhance tumor-specific T-cell responses. Cancer Res. 2006. Vol. 66(2). P. 1139-1146.
  • Hansler J., Wissniowski T.T., Schuppan D., Witte A., Bernatik T., Hahn E.G., Strobel D. Activation and dramatically increased cytolytic activity of tumor specific T lymphocytes after radio-frequency ablation in patients with hepatocellular carcinoma and colorectal liver metastases. World J. Gastroenterol. 2006. Vol. 12(23). P. 3716-3721.
  • Zerbini A., Pilli M., Laccabue D., Pelosi G., Molinari A., Negri E. et al. Radiofrequency thermal ablation for hepatocellular carcinoma stimulates autologous NK-cell response. Gastroenterology. 2010. Vol. 138(5). P. 1931-1942
  • DOI: 10.1053/j.gastro.2009.12.051
  • Widenmeyer M., Shebzukhov Y., Haen S.P., Schmidt D., Clasen S., Boss A. et al. Analysis of tumor antigen-specific T cells and antibodies in cancer patients treated with radiofrequency ablation. Int. J. Cancer. 2011. Vol. 128(11). P. 2653-2662
  • DOI: 10.1002/ijc.25601
  • Hiroishi K., Eguchi J., Baba T., Shimazaki T., Ishii S., Hiraide A. et al. Strong CD8(+) T-cell responses against tumor-associated antigens prolong the recurrence-free interval after tumor treatment in patients withhepatocellular carcinoma. J. Gastroenterol. 2010. Vol. 45(4). P. 451-458
  • DOI: 10.1007/s00535-009-0155-2
  • Herbst R.S., Soria J.C., Kowanetz M., Fine G.D., Hamid O., Gordon M.S. et al. Predictive correlates of response to the anti-PD-L1 antibody MPDL3280A in cancer patients. Nature. 2014. Vol. 515. P. 563-567.
  • Taube J.M., Klein A., Brahmer J.R., Xu H., Pan X., Kim J.H. et al. Association of PD-1, PD-1 ligands, and other features of the tumor immune microenvironment with response to anti-PD-1 therapy. Clin. Cancer Res. 2014. Vol. 20. P. 5064-5074.
  • Tumeh P.C., Harview C.L., Yearley J.H., Shintaku I.P., Taylor E.J., Robert L. et al. PD-1 blockade induces responses by inhibiting adaptive immune resistance. Nature. 2014. Vol. 515. P. 568-571.
  • Diab A., McArthur H.L., Solomon S.B., Sacchini V., Comstock C., Maybody M. et al. A pilot study of preoperative (Pre-op), singledose ipilimumab (Ipi) and/or cryoablation (Cryo) in women (pts) with early-stage/resectable breast cancer (ESBC). ASCO Meeting Abstracts. 2014. Vol. 32. P. 1098.
  • Page D.B., Yuan J., Redmond D., Wen Y.H., Durack J.C., Emerson R. et al. Deep Sequencing of T-cell Receptor DNA as a Biomarker of Clonally Expanded TILs in Breast Cancer after Immunotherapy. Cancer Immunol. Res. 2016. Vol. 4(10). P. 835-844.
  • Hodi F.S., Chesney J., Pavlick A.C., Robert C., Grossmann K.F., McDermott D.F. et al. Combined nivolumab and ipilimumab versus ipilimumab alone in patients with advanced melanoma: 2-year overall survival outcomes in a multicentre, randomised, controlled, phase 2 trial. Lancet Oncol. 2016. Vol. 17(11). P. 1558-1568
  • DOI: 10.1016/S1470-2045(16)30366-7
  • Sznol M., Ferrucci P.F., Hogg D., Atkins M.B., Wolter P., Guidoboni M. et al. Pooled Analysis Safety Profile of Nivolumab and Ipilimumab Combination Therapy in Patients With Advanced Melanoma. J. Clin. Oncol. 2017. Vol. 35(34). P. 3815-3822
  • DOI: 10.1200/JCO.2016.72.1167
  • Sibaud V., David I., Lamant L., Resseguier S., Radut R., Attal J. et al. Acute skin reaction suggestive of pembrolizumab-induced radiosensitization. Melanoma Res. 2015. Vol. 25(6). P. 555-558
  • DOI: 10.1097/CMR.0000000000000191
  • Chang X. Radiofrequency ablation of primary tumors combined with anti-programmed death-1 (PD-1) antibody results in an enhanced antitumor effect against advanced renal cell carcinoma. J. Urology. 2016. Vol. 195. No.4S, Suppl. Abstract MP03-07.
  • Chen Z., Shen S., Peng B., Tao J. Intratumoural GM-CSF microspheres and CTLA-4 blockade enhance the antitumour immunity induced by thermal ablation in a subcutaneous murine hepatoma model. Int. J. Hyperthermia. 2009. Vol. 25(5). P. 374-382
  • DOI: 10.1080/02656730902976807
  • Chen D.S., Mellman I. Oncology meets immunology: the cancer-immunity cycle. Immunity. 2013. Vol. 39. P. 1-10.
  • Kim J.M., Chen D.S. Immune escape to PD-L1/PD-1 blockade: seven steps to success (or failure). Annals of Oncology. Vol. 27. P. 1492-1504. 2016
  • DOI: 10.1093/annonc/mdw217
  • Ferguson T.A., Choi J., Green D.R. Armed response: how dying cells influence T-cell functions. Immunol. 2011. Vol. 241. P. 77-88.
  • Golden E.B., Apetoh L. Radiotherapy and immunogenic cell death. Semin. Radiat. Oncol. Vol. 25(1). P. 11-17. 10.1016/j. semradonc.2014.07.005
  • DOI: :10.1016/j.semradonc.2014.07.005
  • Tesniere A., Apetoh L., Ghiringhelli F., Joza N., Panaretakis T., Kepp O. et al. Immunogenic cancer cell death: a key-lock paradigm. Curr. Opin. Immunol. 2008. Vol. 20. P. 504-511
  • DOI: 10.1016/j.coi.2008.05.007
  • Chalovich J.M., Eisenberg E. NIH Public Access. Biophys. Chem. 2012. Vol. 257. P. 2432-2437.
  • Curley C.T., Sheybani N.D., Bullock T.N., Price R.J. Focused Ultrasound Immunotherapy for Central Nervous System Pathologies: Challenges and Opportunities. Theranostics. 2017. Vol. 7(15). P. 3608-3623
  • DOI: 10.7150/thno.21225
  • Blank C.U., Haanen J.B., Ribas A., Schumacher TN. CANCER IMMUNOLOGY. The "cancer immunogram". Science. 2016. Vol. 352(6286). P. 658-60
  • DOI: 10.1126/science.aaf2834
Еще
Статья научная