Skip to main content
Top
Published in: Cancer Immunology, Immunotherapy 8/2015

01-08-2015 | Original Article

Cytokine production in patients with papillary thyroid cancer and associated autoimmune Hashimoto thyroiditis

Authors: Snezana Zivancevic-Simonovic, Olgica Mihaljevic, Ivana Majstorovic, Suzana Popovic, Slavica Markovic, Olivera Milosevic-Djordjevic, Zorica Jovanovic, Ljiljana Mijatovic-Teodorovic, Dusan Mihajlovic, Miodrag Colic

Published in: Cancer Immunology, Immunotherapy | Issue 8/2015

Login to get access

Abstract

Hashimoto thyroiditis (HT) is the most frequent thyroid autoimmune disease, while papillary thyroid cancer (PTC) is one of the most common endocrine malignancies. A few patients with HT also develop PTC. The aim of this study was to analyze cytokine profiles in patients with PTC accompanied with autoimmune HT in comparison with those in patients with PTC alone or HT alone and healthy subjects. Cytokine levels were determined in supernatants obtained from phytohemagglutinin (PHA)-stimulated whole blood cultures in vitro. The concentrations of selected cytokines: Th1—interferon gamma (IFN-γ); Th2—interleukin 4 (IL-4), interleukin 5 (IL-5), interleukin 6 (IL-6), interleukin 10 (IL-10) and interleukin 13 (IL-13); Th9—interleukin 9 (IL-9); and Th17—interleukin 17 (IL-17A) were measured using multiplex cytokine detection systems for human Th1/Th2/Th9/Th17/Th22. We found that PTC patients with HT produced significantly higher concentrations of IL-4, IL-6, IL-9, IL-13 and IFN-γ than PTC patients without HT. In conclusion, autoimmune HT affects the cytokine profile of patients with PTC by stimulating secretion of Th1/Th2/Th9 types of cytokines. Th1/Th2 cytokine ratios in PTC patients with associated autoimmune HT indicate a marked shift toward Th2 immunity.
Literature
2.
go back to reference Mazziotti G, Sorvillo F, Naclerio C et al (2003) Type-1 response in peripheral CD4+ and CD8+ T cells from patients with Hashimoto’s thyroiditis. Eur J Endocrinol 148:383–388PubMedCrossRef Mazziotti G, Sorvillo F, Naclerio C et al (2003) Type-1 response in peripheral CD4+ and CD8+ T cells from patients with Hashimoto’s thyroiditis. Eur J Endocrinol 148:383–388PubMedCrossRef
3.
go back to reference Figueroa-Vega N, Alfonso-Pérez M, Benedicto I et al (2010) Increased circulating proinflammatory cytokines and Th17 lymphocytes in Hashimoto’s thyroiditis. J Clin Endocrinol Metab 2010(95):953–962CrossRef Figueroa-Vega N, Alfonso-Pérez M, Benedicto I et al (2010) Increased circulating proinflammatory cytokines and Th17 lymphocytes in Hashimoto’s thyroiditis. J Clin Endocrinol Metab 2010(95):953–962CrossRef
4.
go back to reference Skapenko A, Niedobitek GU, Kalden JR et al (2004) Generation and regulation of human Th1-biased immune responses in vivo: a critical role for IL-4 and IL-10. J Immunol 172:6427–6434PubMedCrossRef Skapenko A, Niedobitek GU, Kalden JR et al (2004) Generation and regulation of human Th1-biased immune responses in vivo: a critical role for IL-4 and IL-10. J Immunol 172:6427–6434PubMedCrossRef
5.
go back to reference Marazuela M, García-López MA, Figueroa-Vega N et al (2006) Regulatory T cells in human autoimmune thyroid disease. J Clin Endocrinol Metab 91:3639–3646PubMedCrossRef Marazuela M, García-López MA, Figueroa-Vega N et al (2006) Regulatory T cells in human autoimmune thyroid disease. J Clin Endocrinol Metab 91:3639–3646PubMedCrossRef
6.
go back to reference Davies L, Welch HG (2006) Increasing incidence of thyroid cancer in the United States, 1973–2002. JAMA 295:2164–2167PubMedCrossRef Davies L, Welch HG (2006) Increasing incidence of thyroid cancer in the United States, 1973–2002. JAMA 295:2164–2167PubMedCrossRef
7.
go back to reference Riesco-Eizaguirre G, Santisteban P (2007) New insights in thyroid follicular cell biology and its impact in thyroid cancer therapy. Endocr Relat Cancer 14:957–977PubMedCrossRef Riesco-Eizaguirre G, Santisteban P (2007) New insights in thyroid follicular cell biology and its impact in thyroid cancer therapy. Endocr Relat Cancer 14:957–977PubMedCrossRef
8.
go back to reference Ozgen AG, Karadeniz M, Erdogan M et al (2009) The (-174) G/C polymorphism in the interleukin-6 gene is associated with risk of papillary thyroid carcinoma in Turkish patients. J Endocrinol Invest 32:491–494PubMedCrossRef Ozgen AG, Karadeniz M, Erdogan M et al (2009) The (-174) G/C polymorphism in the interleukin-6 gene is associated with risk of papillary thyroid carcinoma in Turkish patients. J Endocrinol Invest 32:491–494PubMedCrossRef
9.
go back to reference Cunha LL, Aj Tincani, Assumpcao LV et al (2011) Interleukin-10 but not interleukin-18 may be associated with the immune response against well-differentiated thyroid cancer. Clinics (Sao Paulo) 66:1203–1208CrossRef Cunha LL, Aj Tincani, Assumpcao LV et al (2011) Interleukin-10 but not interleukin-18 may be associated with the immune response against well-differentiated thyroid cancer. Clinics (Sao Paulo) 66:1203–1208CrossRef
10.
go back to reference Simonovic SZ, Mihaljevic O, Majstorovic I et al (2015) Cytokine production in peripheral blood cells of patients with differentiated thyroid cancer: elevated Th2/Th9 production before and reduced Th2 cytokine production after radioactive iodine therapy. Cancer Immunol Immunother 64:75–82PubMedCrossRef Simonovic SZ, Mihaljevic O, Majstorovic I et al (2015) Cytokine production in peripheral blood cells of patients with differentiated thyroid cancer: elevated Th2/Th9 production before and reduced Th2 cytokine production after radioactive iodine therapy. Cancer Immunol Immunother 64:75–82PubMedCrossRef
11.
go back to reference Stassi G, Todaro M, Zerilli M et al (2003) Thyroid cancer resistance to chemotherapeutic drugs via autocrine production of interleukin-4 and interleukin-10. Cancer Res 63:6784–6790PubMed Stassi G, Todaro M, Zerilli M et al (2003) Thyroid cancer resistance to chemotherapeutic drugs via autocrine production of interleukin-4 and interleukin-10. Cancer Res 63:6784–6790PubMed
12.
go back to reference Jankovic B, Le KT, Hershman JM (2013) Hashimoto’s thyroiditis and papillary thyroid carcinoma: is there a correlation? J Clin Endocrinol Metab 98:474–482PubMedCrossRef Jankovic B, Le KT, Hershman JM (2013) Hashimoto’s thyroiditis and papillary thyroid carcinoma: is there a correlation? J Clin Endocrinol Metab 98:474–482PubMedCrossRef
13.
go back to reference Weber F (2014) Lymphocytes and thyroid cancer: more to it than meets the eye? Endocr Relat Cancer 21:C1–C5PubMedCrossRef Weber F (2014) Lymphocytes and thyroid cancer: more to it than meets the eye? Endocr Relat Cancer 21:C1–C5PubMedCrossRef
14.
go back to reference Cunha LL, Marcello MA, Ward LS (2014) The role of the inflammatory microenvironment in thyroid carcinogenesis. Endocr Relat Cancer 21:R85–R103PubMedCrossRef Cunha LL, Marcello MA, Ward LS (2014) The role of the inflammatory microenvironment in thyroid carcinogenesis. Endocr Relat Cancer 21:R85–R103PubMedCrossRef
15.
go back to reference Kashima K, Yokoyama S, Noguchi S et al (1998) Chronic thyroiditis as a favorable prognostic factor in papillary thyroid carcinoma. Thyroid 8:197–202PubMedCrossRef Kashima K, Yokoyama S, Noguchi S et al (1998) Chronic thyroiditis as a favorable prognostic factor in papillary thyroid carcinoma. Thyroid 8:197–202PubMedCrossRef
16.
go back to reference Singh B, Shaha AR, Trivedi H et al (1999) Coexistent Hashimoto’s thyroiditis with papillary thyroid carcinoma: impact of presentation, management and outcome. Surgery 126:1070–1077PubMedCrossRef Singh B, Shaha AR, Trivedi H et al (1999) Coexistent Hashimoto’s thyroiditis with papillary thyroid carcinoma: impact of presentation, management and outcome. Surgery 126:1070–1077PubMedCrossRef
17.
go back to reference Kim EY, Kim WG, Kim WB et al (2009) Coexistence of chronic lymphocytic thyroiditis is associated with lower recurrence rates in patients with papillary thyroid carcinoma. Clin Endocrinol (Oxf) 71:581–586CrossRef Kim EY, Kim WG, Kim WB et al (2009) Coexistence of chronic lymphocytic thyroiditis is associated with lower recurrence rates in patients with papillary thyroid carcinoma. Clin Endocrinol (Oxf) 71:581–586CrossRef
18.
go back to reference Lee JH, Kim Y, Choi JW et al (2013) The association between papillary thyroid carcinoma and histologically proven Hashimoto’s thyroiditis: a meta-analysis. Eur J Endocrinol 168:343–349PubMedCrossRef Lee JH, Kim Y, Choi JW et al (2013) The association between papillary thyroid carcinoma and histologically proven Hashimoto’s thyroiditis: a meta-analysis. Eur J Endocrinol 168:343–349PubMedCrossRef
19.
go back to reference Kebebew E, Treseler P, Ituarte P, Clark O (2001) Coexisting chronic lymphocytic thyroiditis and papillary thyroid cancer revisited. World J Surg 25:632–637PubMedCrossRef Kebebew E, Treseler P, Ituarte P, Clark O (2001) Coexisting chronic lymphocytic thyroiditis and papillary thyroid cancer revisited. World J Surg 25:632–637PubMedCrossRef
20.
go back to reference Cunha LL, Ward LS (2012) Concurrent lymphocytic thyroiditis is associated to less aggressive papillary thyroid carcinomas. Eur Arch Otorhinolaryngol 269:699–700PubMedCrossRef Cunha LL, Ward LS (2012) Concurrent lymphocytic thyroiditis is associated to less aggressive papillary thyroid carcinomas. Eur Arch Otorhinolaryngol 269:699–700PubMedCrossRef
21.
go back to reference Schuetz M, Duan H, Wahl K et al (2006) T Lymphocyte cytokine production patterns in Hashimoto patients with elevated calcitonin levels and their relationship to tumor initiation. Anticancer Res 26:4591–4596PubMed Schuetz M, Duan H, Wahl K et al (2006) T Lymphocyte cytokine production patterns in Hashimoto patients with elevated calcitonin levels and their relationship to tumor initiation. Anticancer Res 26:4591–4596PubMed
22.
go back to reference Nikiforov YE (2012) Thyroid tumors: classification, staging, and general considerations. In: Nikiforov YE, Biddinger PW, Thompson LDR (eds) Diagnostic pathology and molecular genetics of the thyroid, 2nd edn. Wolters Kluwer/Lippincott Williams & Wilkins, Philadelphia, pp 108–119 Nikiforov YE (2012) Thyroid tumors: classification, staging, and general considerations. In: Nikiforov YE, Biddinger PW, Thompson LDR (eds) Diagnostic pathology and molecular genetics of the thyroid, 2nd edn. Wolters Kluwer/Lippincott Williams & Wilkins, Philadelphia, pp 108–119
23.
go back to reference Budhu A, Wang XW (2006) The role of cytokines in hepatocellular carcinoma. J Leukoc Biol 80:1197–1213PubMedCrossRef Budhu A, Wang XW (2006) The role of cytokines in hepatocellular carcinoma. J Leukoc Biol 80:1197–1213PubMedCrossRef
24.
go back to reference Bodelon C, Polley MY, Kemp TJ et al (2013) Circulating levels of immune and inflammatory markers and long versus short survival in early-stage lung cancer. Ann Oncol 24:2073–2079PubMedCentralPubMedCrossRef Bodelon C, Polley MY, Kemp TJ et al (2013) Circulating levels of immune and inflammatory markers and long versus short survival in early-stage lung cancer. Ann Oncol 24:2073–2079PubMedCentralPubMedCrossRef
25.
go back to reference Ellyard JI, Simson L, Parish CR (2007) Th2-mediated anti-tumour immunity: friend or foe? Tissue Antigens 70:1–11PubMedCrossRef Ellyard JI, Simson L, Parish CR (2007) Th2-mediated anti-tumour immunity: friend or foe? Tissue Antigens 70:1–11PubMedCrossRef
26.
go back to reference Mattes J, Hulett M, Xie W et al (2003) Immunotherapy of cytotoxic T cell-resistant tumors by T helper 2 cells: an eotaxin and STAT6-dependent process. J Exp Med 197:387–393PubMedCentralPubMedCrossRef Mattes J, Hulett M, Xie W et al (2003) Immunotherapy of cytotoxic T cell-resistant tumors by T helper 2 cells: an eotaxin and STAT6-dependent process. J Exp Med 197:387–393PubMedCentralPubMedCrossRef
28.
go back to reference Schroder K, Hertzog PJ, Ravasi T et al (2004) Interferon-Υ: an overview of signals, mechanisms and functions. J Leukoc Biol 75:163–189PubMedCrossRef Schroder K, Hertzog PJ, Ravasi T et al (2004) Interferon-Υ: an overview of signals, mechanisms and functions. J Leukoc Biol 75:163–189PubMedCrossRef
29.
go back to reference Del Prete GF, Tiri A, Mariotti S et al (1987) Enhanced production of gamma-interferon by thyroid-derived T cell clones from patients with Hashimoto’s thyroiditis. Clin Exp Immunol 69:323–331PubMedCentralPubMed Del Prete GF, Tiri A, Mariotti S et al (1987) Enhanced production of gamma-interferon by thyroid-derived T cell clones from patients with Hashimoto’s thyroiditis. Clin Exp Immunol 69:323–331PubMedCentralPubMed
31.
go back to reference Miller CH, Maher SG, Young HA (2009) Clinical use of interferon-gamma. Ann N Y Acad Sci 1182:69–79PubMedCrossRef Miller CH, Maher SG, Young HA (2009) Clinical use of interferon-gamma. Ann N Y Acad Sci 1182:69–79PubMedCrossRef
32.
go back to reference Hossain MS, Bhimani C, Zhengjia C et al (2011) Profiling counter-regulatory and cytotoxic immune pathways with cellular biomarkers in thyroid cancer patients. [abstract]. In: Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research; 2011 Apr 2–6; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 71(8 Suppl):Abstract nr 5525. doi:10.1158/1538-7445.AM2011-5525 Hossain MS, Bhimani C, Zhengjia C et al (2011) Profiling counter-regulatory and cytotoxic immune pathways with cellular biomarkers in thyroid cancer patients. [abstract]. In: Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research; 2011 Apr 2–6; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 71(8 Suppl):Abstract nr 5525. doi:10.​1158/​1538-7445.​AM2011-5525
33.
go back to reference Kang S, Tanaka T, Kishimoto T (2015) Therapeutic uses of anti-interleukin-6 receptor antibody. Int Immunol 27:21–29PubMedCrossRef Kang S, Tanaka T, Kishimoto T (2015) Therapeutic uses of anti-interleukin-6 receptor antibody. Int Immunol 27:21–29PubMedCrossRef
34.
35.
go back to reference Baki M, Akman FE, Vural P et al (2012) The combination of interleukin-10 -1082 and tumor necrosis factor α -308 or interleukin-6 -174 genes polymorphisms suggests an association with susceptibility to Hashimoto’s thyroiditis. Int Immunopharmacol 12:543–546PubMedCrossRef Baki M, Akman FE, Vural P et al (2012) The combination of interleukin-10 -1082 and tumor necrosis factor α -308 or interleukin-6 -174 genes polymorphisms suggests an association with susceptibility to Hashimoto’s thyroiditis. Int Immunopharmacol 12:543–546PubMedCrossRef
36.
go back to reference Weetman AP, Bright-Thomas R, Freeman M (1990) Regulation of interleukin-6 release by human thyrocytes. J Endocrinol 127:357–361PubMedCrossRef Weetman AP, Bright-Thomas R, Freeman M (1990) Regulation of interleukin-6 release by human thyrocytes. J Endocrinol 127:357–361PubMedCrossRef
37.
go back to reference Ajjan RA, Watson PF, Weetman AP (1996) Cytokines and thyroid function. Adv Neuroimmunol 6:359–386PubMedCrossRef Ajjan RA, Watson PF, Weetman AP (1996) Cytokines and thyroid function. Adv Neuroimmunol 6:359–386PubMedCrossRef
38.
go back to reference Ruggeri RM, Sciacchitano S, Vitale A et al (2009) Serum hepatocyte growth factor (HGF) is increased in Hashimoto’s thyroiditis whether or not it is associated with nodular goiter as compared with healthy non-goitrous individuals. J Endocrinol Invest 32:465–469PubMedCrossRef Ruggeri RM, Sciacchitano S, Vitale A et al (2009) Serum hepatocyte growth factor (HGF) is increased in Hashimoto’s thyroiditis whether or not it is associated with nodular goiter as compared with healthy non-goitrous individuals. J Endocrinol Invest 32:465–469PubMedCrossRef
39.
go back to reference Sieminska L, Wojciechowska C, Kos-Kudla B et al (2010) Serum concentrations of leptin, adiponectin, and interleukin-6 in postmenopausal women with Hashimoto’s thyroiditis. Endokrynol Pol 61:112–116PubMed Sieminska L, Wojciechowska C, Kos-Kudla B et al (2010) Serum concentrations of leptin, adiponectin, and interleukin-6 in postmenopausal women with Hashimoto’s thyroiditis. Endokrynol Pol 61:112–116PubMed
40.
41.
go back to reference Kura Y, De Velasco MA, Kobayashi Y, et al (2013) Interleukin-6 (IL-6) as a therapeutic target in prostate cancer. [abstract]. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6–10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 73(8 Suppl):Abstract nr 1226. doi:10.1158/1538-7445.AM2013-1226 Kura Y, De Velasco MA, Kobayashi Y, et al (2013) Interleukin-6 (IL-6) as a therapeutic target in prostate cancer. [abstract]. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6–10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 73(8 Suppl):Abstract nr 1226. doi:10.​1158/​1538-7445.​AM2013-1226
42.
go back to reference Zhang Y, Yan W, Collins MA et al (2013) Interleukin-6 is required for pancreatic cancer progression by promoting MAPK signaling activation and oxidative stress resistance. Cancer Res 73:6359–6374PubMedCrossRef Zhang Y, Yan W, Collins MA et al (2013) Interleukin-6 is required for pancreatic cancer progression by promoting MAPK signaling activation and oxidative stress resistance. Cancer Res 73:6359–6374PubMedCrossRef
43.
go back to reference Ujiie H, Tomida M, Akiyama H et al (2012) Serum hepatocyte growth factor and interleukin-6 are effective prognostic markers for non-small cell lung cancer. Anticancer Res 32:3251–3258PubMed Ujiie H, Tomida M, Akiyama H et al (2012) Serum hepatocyte growth factor and interleukin-6 are effective prognostic markers for non-small cell lung cancer. Anticancer Res 32:3251–3258PubMed
44.
go back to reference Huang BY, Hseuh C, Chao TC et al (2011) Well-differentiated thyroid carcinoma with concomitant Hashimoto’s thyroiditis present with less aggressive clinical stage and low recurrence. Endocr Pathol 22:144–149PubMedCrossRef Huang BY, Hseuh C, Chao TC et al (2011) Well-differentiated thyroid carcinoma with concomitant Hashimoto’s thyroiditis present with less aggressive clinical stage and low recurrence. Endocr Pathol 22:144–149PubMedCrossRef
45.
go back to reference Ng TH, Britton GJ, Hill EV et al (2013) Regulation of adaptive immunity; the role of interleukin-10. Front Immunol 4:129–140PubMedCentralPubMed Ng TH, Britton GJ, Hill EV et al (2013) Regulation of adaptive immunity; the role of interleukin-10. Front Immunol 4:129–140PubMedCentralPubMed
46.
47.
go back to reference de Waal-Malefyt R, Yssel H, de Vries JE (1993) Direct effects of IL-10 on subsets of human CD4+ T cell clones and resting T cells. Specific inhibition of IL-2 production and proliferation. J Immunol 150:4754–4765PubMed de Waal-Malefyt R, Yssel H, de Vries JE (1993) Direct effects of IL-10 on subsets of human CD4+ T cell clones and resting T cells. Specific inhibition of IL-2 production and proliferation. J Immunol 150:4754–4765PubMed
48.
go back to reference Cyktor JC, Turner J (2011) Interleukin-10 and immunity against prokaryotic and eukaryotic intracellular pathogens. Infect Immunol 79:2964–2973CrossRef Cyktor JC, Turner J (2011) Interleukin-10 and immunity against prokaryotic and eukaryotic intracellular pathogens. Infect Immunol 79:2964–2973CrossRef
49.
go back to reference Franks AL, Slansky JE (2012) Multiple associations between a broad spectrum of autoimmune diseases, chronic inflammatory diseases and cancer. Anticancer Res 32:1119–1136PubMedCentralPubMed Franks AL, Slansky JE (2012) Multiple associations between a broad spectrum of autoimmune diseases, chronic inflammatory diseases and cancer. Anticancer Res 32:1119–1136PubMedCentralPubMed
50.
go back to reference Luheshi N, Davies GC, Poon E et al (2013) Th1 and Th2 cytokines determine how CD40 activation changes human macrophage function in vitro. [abstract]. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6–10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 73(8 Suppl):Abstract nr 1542. doi:10.1158/1538-7445.AM2013-1542 Luheshi N, Davies GC, Poon E et al (2013) Th1 and Th2 cytokines determine how CD40 activation changes human macrophage function in vitro. [abstract]. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6–10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 73(8 Suppl):Abstract nr 1542. doi:10.​1158/​1538-7445.​AM2013-1542
51.
go back to reference Becker JC, Andersen MH, Schrama D et al (2013) Immune-suppressive properties of the tumor microenvironment. Cancer Immunol Immunother 62:1137–1148PubMedCrossRef Becker JC, Andersen MH, Schrama D et al (2013) Immune-suppressive properties of the tumor microenvironment. Cancer Immunol Immunother 62:1137–1148PubMedCrossRef
52.
go back to reference Atsumi T, Singh R, Sabharwal L et al (2014) Inflammation amplifier, a new paradigm in cancer biology. Cancer Res 74:8–14PubMedCrossRef Atsumi T, Singh R, Sabharwal L et al (2014) Inflammation amplifier, a new paradigm in cancer biology. Cancer Res 74:8–14PubMedCrossRef
53.
go back to reference Murray JI, West NR, Murphy LC et al (2014) Intratumoral inflammation and endocrine resistance in breast cancer. Endocr Relat Cancer 22:R51–R67PubMedCrossRef Murray JI, West NR, Murphy LC et al (2014) Intratumoral inflammation and endocrine resistance in breast cancer. Endocr Relat Cancer 22:R51–R67PubMedCrossRef
Metadata
Title
Cytokine production in patients with papillary thyroid cancer and associated autoimmune Hashimoto thyroiditis
Authors
Snezana Zivancevic-Simonovic
Olgica Mihaljevic
Ivana Majstorovic
Suzana Popovic
Slavica Markovic
Olivera Milosevic-Djordjevic
Zorica Jovanovic
Ljiljana Mijatovic-Teodorovic
Dusan Mihajlovic
Miodrag Colic
Publication date
01-08-2015
Publisher
Springer Berlin Heidelberg
Published in
Cancer Immunology, Immunotherapy / Issue 8/2015
Print ISSN: 0340-7004
Electronic ISSN: 1432-0851
DOI
https://doi.org/10.1007/s00262-015-1705-5

Other articles of this Issue 8/2015

Cancer Immunology, Immunotherapy 8/2015 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine