Skip to main content
Top
Published in: Current Oncology Reports 4/2010

01-07-2010

Bladder Cancer: Can We Move Beyond Chemotherapy?

Author: Arlene Siefker-Radtke

Published in: Current Oncology Reports | Issue 4/2010

Login to get access

Abstract

Since the advent of cisplatin-based chemotherapy, cytotoxic combination chemotherapy remains the mainstay of treatment for locally advanced and metastatic urothelial malignancies. The current paradigm of combining novel agents with cytotoxic chemotherapy without any understanding of the underlying biology of urothelial cancer has limited the impact of developing novel agents for this disease. Current research investigating the biology of bladder cancer, including the role of p53, EMT, EGFR-related pathways, and anti-angiogenic pathways, may potentially impact the future development of novel agents targeting urothelial malignancies. Additionally, the use of novel gene therapy to mediate enhanced interferon expression in the bladder using adenoviral vectors, and enhancing tumor recognition strategies using the immune system with vaccines and anti-CTLA4 antibodies, are of interest. It is hoped that through these efforts we may soon move beyond the traditional cytotoxic chemotherapy paradigm, developing combinations that are more active and less toxic for all patients with urothelial cancer.
Literature
1.
go back to reference Sternberg CN, Yagoda A, Scher HI, et al.: Preliminary results of M-VAC (methotrexate, vinblastine, doxorubicin and cisplatin) for transitional cell carcinoma of the urothelium. J Urol 1985, 133:403–407.PubMed Sternberg CN, Yagoda A, Scher HI, et al.: Preliminary results of M-VAC (methotrexate, vinblastine, doxorubicin and cisplatin) for transitional cell carcinoma of the urothelium. J Urol 1985, 133:403–407.PubMed
2.
go back to reference von der Maase H, Hansen SW, Roberts JT, et al.: Gemcitabine and cisplatin versus methotrexate, vinblastine, doxorubicin, and cisplatin in advanced or metastatic bladder cancer: results of a large, randomized, multinational, multicenter, phase III study. J Clin Oncol 2000, 18:3068–3077.PubMed von der Maase H, Hansen SW, Roberts JT, et al.: Gemcitabine and cisplatin versus methotrexate, vinblastine, doxorubicin, and cisplatin in advanced or metastatic bladder cancer: results of a large, randomized, multinational, multicenter, phase III study. J Clin Oncol 2000, 18:3068–3077.PubMed
3.
go back to reference Grossman HB, Natale RB, Tangen CM, et al.: Neoadjuvant chemotherapy plus cystectomy compared with cystectomy alone for locally advanced bladder cancer [erratum appears in N Engl J Med 2003, 349:1880]. N Engl J Med 2003, 349:859–866.CrossRefPubMed Grossman HB, Natale RB, Tangen CM, et al.: Neoadjuvant chemotherapy plus cystectomy compared with cystectomy alone for locally advanced bladder cancer [erratum appears in N Engl J Med 2003, 349:1880]. N Engl J Med 2003, 349:859–866.CrossRefPubMed
4.
go back to reference Logothetis CJ, Dexeus FH, Finn L, et al.: A prospective randomized trial comparing MVAC and CISCA chemotherapy for patients with metastatic urothelial tumors. J Clin Oncol 1990, 8:1050–1055.PubMed Logothetis CJ, Dexeus FH, Finn L, et al.: A prospective randomized trial comparing MVAC and CISCA chemotherapy for patients with metastatic urothelial tumors. J Clin Oncol 1990, 8:1050–1055.PubMed
5.
go back to reference Logothetis CJ, Finn LD, Smith T, et al.: Escalated MVAC with or without recombinant human granulocyte-macrophage colony-stimulating factor for the initial treatment of advanced malignant urothelial tumors: results of a randomized trial. J Clin Oncol 1995, 13:2272–2277.PubMed Logothetis CJ, Finn LD, Smith T, et al.: Escalated MVAC with or without recombinant human granulocyte-macrophage colony-stimulating factor for the initial treatment of advanced malignant urothelial tumors: results of a randomized trial. J Clin Oncol 1995, 13:2272–2277.PubMed
6.
go back to reference Seidman AD, Scher HI, Gabrilove JL, et al.: Dose-intensification of MVAC with recombinant granulocyte colony-stimulating factor as initial therapy in advanced urothelial cancer. J Clin Oncol 1993, 11:408–414.PubMed Seidman AD, Scher HI, Gabrilove JL, et al.: Dose-intensification of MVAC with recombinant granulocyte colony-stimulating factor as initial therapy in advanced urothelial cancer. J Clin Oncol 1993, 11:408–414.PubMed
7.
go back to reference Loehrer PJ Sr, Elson P, Dreicer R, et al.: Escalated dosages of methotrexate, vinblastine, doxorubicin, and cisplatin plus recombinant human granulocyte colony-stimulating factor in advanced urothelial carcinoma: an Eastern Cooperative Oncology Group trial. J Clin Oncol 1994, 12:483–488.PubMed Loehrer PJ Sr, Elson P, Dreicer R, et al.: Escalated dosages of methotrexate, vinblastine, doxorubicin, and cisplatin plus recombinant human granulocyte colony-stimulating factor in advanced urothelial carcinoma: an Eastern Cooperative Oncology Group trial. J Clin Oncol 1994, 12:483–488.PubMed
8.
go back to reference Bamias A, Aravantinos G, Deliveliotis C, et al.: Docetaxel and cisplatin with granulocyte colony-stimulating factor (G-CSF) versus MVAC with G-CSF in advanced urothelial carcinoma: a multicenter, randomized, phase III study from the Hellenic Cooperative Oncology Group. J Clin Oncol 2004, 22:220–228.CrossRefPubMed Bamias A, Aravantinos G, Deliveliotis C, et al.: Docetaxel and cisplatin with granulocyte colony-stimulating factor (G-CSF) versus MVAC with G-CSF in advanced urothelial carcinoma: a multicenter, randomized, phase III study from the Hellenic Cooperative Oncology Group. J Clin Oncol 2004, 22:220–228.CrossRefPubMed
9.
go back to reference Siefker-Radtke AO, Millikan RE, Tu SM, et al.: Phase III trial of fluorouracil, interferon alpha-2b, and cisplatin versus methotrexate, vinblastine, doxorubicin, and cisplatin in metastatic or unresectable urothelial cancer. J Clin Oncol 2002, 20:1361–1367.CrossRefPubMed Siefker-Radtke AO, Millikan RE, Tu SM, et al.: Phase III trial of fluorouracil, interferon alpha-2b, and cisplatin versus methotrexate, vinblastine, doxorubicin, and cisplatin in metastatic or unresectable urothelial cancer. J Clin Oncol 2002, 20:1361–1367.CrossRefPubMed
10.
go back to reference Sternberg CN, de Mulder PH, Schornagel JH, et al.: Randomized phase III trial of high-dose-intensity methotrexate, vinblastine, doxorubicin, and cisplatin (MVAC) chemotherapy and recombinant human granulocyte colony-stimulating factor versus classic MVAC in advanced urothelial tract tumors: European Organization for Research and Treatment of Cancer Protocol no. 30924. J Clin Oncol 2001, 19:2638–2646.PubMed Sternberg CN, de Mulder PH, Schornagel JH, et al.: Randomized phase III trial of high-dose-intensity methotrexate, vinblastine, doxorubicin, and cisplatin (MVAC) chemotherapy and recombinant human granulocyte colony-stimulating factor versus classic MVAC in advanced urothelial tract tumors: European Organization for Research and Treatment of Cancer Protocol no. 30924. J Clin Oncol 2001, 19:2638–2646.PubMed
11.
go back to reference Siefker-Radtke A, Millikan, RE, Kamat, AM, et al.: A phase II trial of sequential neoadjuvant chemotherapy with ifosfamide, doxorubicin, and gemcitabine (IAG), followed by cisplatin, gemcitabine, and ifosfamide (CGI) in locally advanced urothelial cancer: Final results from the M. D. Anderson Cancer Center. J Clin Oncol 2008, 26:269s. Siefker-Radtke A, Millikan, RE, Kamat, AM, et al.: A phase II trial of sequential neoadjuvant chemotherapy with ifosfamide, doxorubicin, and gemcitabine (IAG), followed by cisplatin, gemcitabine, and ifosfamide (CGI) in locally advanced urothelial cancer: Final results from the M. D. Anderson Cancer Center. J Clin Oncol 2008, 26:269s.
12.
go back to reference Bajorin DF, McCaffrey JA, Dodd PM, et al.: Ifosfamide, paclitaxel, and cisplatin for patients with advanced transitional cell carcinoma of the urothelial tract: final report of a phase II trial evaluating two dosing schedules. Cancer 2000, 88:1671–1678.CrossRefPubMed Bajorin DF, McCaffrey JA, Dodd PM, et al.: Ifosfamide, paclitaxel, and cisplatin for patients with advanced transitional cell carcinoma of the urothelial tract: final report of a phase II trial evaluating two dosing schedules. Cancer 2000, 88:1671–1678.CrossRefPubMed
13.
go back to reference •• Siefker-Radtke A, Kamat A, Williams D, et al.: A phase II randomized four-regimen selection trial incorporating response for sequential chemotherapy in metastatic, unresectable urothelial cancer: Final results from the M. D. Anderson Cancer Center. J Clin Oncol 2009, 27:251s. This clinical trial used a novel statistical design in sequential therapy that incorporates response to continue treatment that is working, with early re-randomization in the setting of suboptimal response. •• Siefker-Radtke A, Kamat A, Williams D, et al.: A phase II randomized four-regimen selection trial incorporating response for sequential chemotherapy in metastatic, unresectable urothelial cancer: Final results from the M. D. Anderson Cancer Center. J Clin Oncol 2009, 27:251s. This clinical trial used a novel statistical design in sequential therapy that incorporates response to continue treatment that is working, with early re-randomization in the setting of suboptimal response.
14.
go back to reference • Milowsky MI, Nanus DM, Maluf FC, et al.: Final results of sequential doxorubicin plus gemcitabine and ifosfamide, paclitaxel, and cisplatin chemotherapy in patients with metastatic or locally advanced transitional cell carcinoma of the urothelium. J Clin Oncol 2009, 27:4062–4067. This is a sequential clinical trial design using a fixed schedule of chemotherapy. • Milowsky MI, Nanus DM, Maluf FC, et al.: Final results of sequential doxorubicin plus gemcitabine and ifosfamide, paclitaxel, and cisplatin chemotherapy in patients with metastatic or locally advanced transitional cell carcinoma of the urothelium. J Clin Oncol 2009, 27:4062–4067. This is a sequential clinical trial design using a fixed schedule of chemotherapy.
15.
go back to reference Thall PF, Millikan RE, Sung HG: Evaluating multiple treatment courses in clinical trials. Stat Med 2000, 19:1011–1028.CrossRefPubMed Thall PF, Millikan RE, Sung HG: Evaluating multiple treatment courses in clinical trials. Stat Med 2000, 19:1011–1028.CrossRefPubMed
16.
go back to reference • Siefker-Radtke AO, Kamat AM, Grossman HB, et al.: Phase II clinical trial of neoadjuvant alternating doublet chemotherapy with ifosfamide/doxorubicin and etoposide/cisplatin in small-cell urothelial cancer. J Clin Oncol 2009, 27:2592–2597. This is the first clinical trial in small cell urothelial cancer. Though it is a small clinical trial, it suggests a potential impact for neoadjuvant chemotherapy in small cell of the bladder. • Siefker-Radtke AO, Kamat AM, Grossman HB, et al.: Phase II clinical trial of neoadjuvant alternating doublet chemotherapy with ifosfamide/doxorubicin and etoposide/cisplatin in small-cell urothelial cancer. J Clin Oncol 2009, 27:2592–2597. This is the first clinical trial in small cell urothelial cancer. Though it is a small clinical trial, it suggests a potential impact for neoadjuvant chemotherapy in small cell of the bladder.
17.
go back to reference Siefker-Radtke AO, Gee J, Shen Y, et al.: Multimodality management of urachal carcinoma: the M. D. Anderson Cancer Center experience. J Urol 2003, 169:1295–1298.CrossRefPubMed Siefker-Radtke AO, Gee J, Shen Y, et al.: Multimodality management of urachal carcinoma: the M. D. Anderson Cancer Center experience. J Urol 2003, 169:1295–1298.CrossRefPubMed
18.
go back to reference Shariat SF, Lotan Y, Karakiewicz PI, et al.: p53 predictive value for pT1-2 N0 disease at radical cystectomy. J Urol 2009, 182:907–913.CrossRefPubMed Shariat SF, Lotan Y, Karakiewicz PI, et al.: p53 predictive value for pT1-2 N0 disease at radical cystectomy. J Urol 2009, 182:907–913.CrossRefPubMed
19.
go back to reference Millikan R, Dinney C, Swanson D, et al.: Integrated therapy for locally advanced bladder cancer: final report of a randomized trial of cystectomy plus adjuvant M-VAC versus cystectomy with both preoperative and postoperative M-VAC. J Clin Oncol 2001, 19:4005–4013.PubMed Millikan R, Dinney C, Swanson D, et al.: Integrated therapy for locally advanced bladder cancer: final report of a randomized trial of cystectomy plus adjuvant M-VAC versus cystectomy with both preoperative and postoperative M-VAC. J Clin Oncol 2001, 19:4005–4013.PubMed
20.
go back to reference Mhawech-Fauceglia P, Fischer G, Beck A, et al.: Raf1, Aurora-A/STK15 and E-cadherin biomarkers expression in patients with pTa/pT1 urothelial bladder carcinoma; a retrospective TMA study of 246 patients with long-term follow-up. Eur J Surg Oncol 2006, 32:439–444.CrossRefPubMed Mhawech-Fauceglia P, Fischer G, Beck A, et al.: Raf1, Aurora-A/STK15 and E-cadherin biomarkers expression in patients with pTa/pT1 urothelial bladder carcinoma; a retrospective TMA study of 246 patients with long-term follow-up. Eur J Surg Oncol 2006, 32:439–444.CrossRefPubMed
21.
go back to reference Slaton JW, Millikan R, Inoue K, et al.: Correlation of metastasis related gene expression and relapse-free survival in patients with locally advanced bladder cancer treated with cystectomy and chemotherapy. J Urol 2004, 171:570–574.CrossRefPubMed Slaton JW, Millikan R, Inoue K, et al.: Correlation of metastasis related gene expression and relapse-free survival in patients with locally advanced bladder cancer treated with cystectomy and chemotherapy. J Urol 2004, 171:570–574.CrossRefPubMed
22.
go back to reference Sen S, Zhou H, Zhang RD, et al.: Amplification/overexpression of a mitotic kinase gene in human bladder cancer. J Natl Cancer Inst 2002, 94:1320–1329.PubMed Sen S, Zhou H, Zhang RD, et al.: Amplification/overexpression of a mitotic kinase gene in human bladder cancer. J Natl Cancer Inst 2002, 94:1320–1329.PubMed
23.
go back to reference Park HS, Park WS, Bondaruk J, et al.: Quantitation of Aurora kinase A gene copy number in urine sediments and bladder cancer detection. J Natl Cancer Inst 2008, 100:1401–1411.CrossRefPubMed Park HS, Park WS, Bondaruk J, et al.: Quantitation of Aurora kinase A gene copy number in urine sediments and bladder cancer detection. J Natl Cancer Inst 2008, 100:1401–1411.CrossRefPubMed
24.
go back to reference Nguyen PL, Swanson PE, Jaszcz W, et al.: Expression of epidermal growth factor receptor in invasive transitional cell carcinoma of the urinary bladder. A multivariate survival analysis. Am J Clin Pathol 1994, 101:166–176.PubMed Nguyen PL, Swanson PE, Jaszcz W, et al.: Expression of epidermal growth factor receptor in invasive transitional cell carcinoma of the urinary bladder. A multivariate survival analysis. Am J Clin Pathol 1994, 101:166–176.PubMed
25.
go back to reference Blehm KN, Spiess PE, Bondaruk JE, et al.: Mutations within the kinase domain and truncations of the epidermal growth factor receptor are rare events in bladder cancer: implications for therapy. Clin Cancer Res 2006, 12:4671–4677.CrossRefPubMed Blehm KN, Spiess PE, Bondaruk JE, et al.: Mutations within the kinase domain and truncations of the epidermal growth factor receptor are rare events in bladder cancer: implications for therapy. Clin Cancer Res 2006, 12:4671–4677.CrossRefPubMed
26.
go back to reference Black PC, Brown GA, Inamoto T, et al.: Sensitivity to epidermal growth factor receptor inhibitor requires E-cadherin expression in urothelial carcinoma cells. Clin Cancer Res 2008, 14:1478–1486.CrossRefPubMed Black PC, Brown GA, Inamoto T, et al.: Sensitivity to epidermal growth factor receptor inhibitor requires E-cadherin expression in urothelial carcinoma cells. Clin Cancer Res 2008, 14:1478–1486.CrossRefPubMed
27.
go back to reference •• Adam L, Zhong M, Choi W, et al.: miR-200 expression regulates epithelial-to-mesenchymal transition in bladder cancer cells and reverses resistance to epidermal growth factor receptor therapy. Clin Cancer Res 2009, 15:5060–5072. This recent publication suggests a role for miR-200 as a regulatory mechanism for EMT in urothelial cancer. •• Adam L, Zhong M, Choi W, et al.: miR-200 expression regulates epithelial-to-mesenchymal transition in bladder cancer cells and reverses resistance to epidermal growth factor receptor therapy. Clin Cancer Res 2009, 15:5060–5072. This recent publication suggests a role for miR-200 as a regulatory mechanism for EMT in urothelial cancer.
28.
go back to reference Jimenez RE, Hussain M, Bianco FJ Jr, et al.: Her-2/neu overexpression in muscle-invasive urothelial carcinoma of the bladder: prognostic significance and comparative analysis in primary and metastatic tumors. Clin Cancer Res 2001, 7:2440–2447.PubMed Jimenez RE, Hussain M, Bianco FJ Jr, et al.: Her-2/neu overexpression in muscle-invasive urothelial carcinoma of the bladder: prognostic significance and comparative analysis in primary and metastatic tumors. Clin Cancer Res 2001, 7:2440–2447.PubMed
29.
go back to reference Lonn U, Lonn S, Friberg S, et al.: Prognostic value of amplification of c-erb-B2 in bladder carcinoma. Clin Cancer Res 1995, 1:1189–1194.PubMed Lonn U, Lonn S, Friberg S, et al.: Prognostic value of amplification of c-erb-B2 in bladder carcinoma. Clin Cancer Res 1995, 1:1189–1194.PubMed
30.
go back to reference Lee SE, Chow NH, Chi YC, et al.: Expression of c-erbB-2 protein in normal and neoplastic urothelium: lack of adverse prognostic effect in human urinary bladder cancer. Anticancer Res 1994, 14:1317–1324.PubMed Lee SE, Chow NH, Chi YC, et al.: Expression of c-erbB-2 protein in normal and neoplastic urothelium: lack of adverse prognostic effect in human urinary bladder cancer. Anticancer Res 1994, 14:1317–1324.PubMed
31.
go back to reference Hussain M, Petrylak D, Dunn R, et al.: Trastuzumab (T), Paclitaxel (P), Carboplatin (C), and Gemcitabine (G) in advanced HER2-positive urothelial carcinoma: Results of a multi-center phase II NCI trial. J Clin Oncol 2005, 23:379s.CrossRef Hussain M, Petrylak D, Dunn R, et al.: Trastuzumab (T), Paclitaxel (P), Carboplatin (C), and Gemcitabine (G) in advanced HER2-positive urothelial carcinoma: Results of a multi-center phase II NCI trial. J Clin Oncol 2005, 23:379s.CrossRef
32.
go back to reference Goddard JC, Sutton CD, Furness PN, et al.: Microvessel density at presentation predicts subsequent muscle invasion in superficial bladder cancer. Clin Cancer Res 2003, 9:2583–2586.PubMed Goddard JC, Sutton CD, Furness PN, et al.: Microvessel density at presentation predicts subsequent muscle invasion in superficial bladder cancer. Clin Cancer Res 2003, 9:2583–2586.PubMed
33.
go back to reference Bochner BH, Cote RJ, Weidner N, et al.: Angiogenesis in bladder cancer: relationship between microvessel density and tumor prognosis. J Natl Cancer Inst 1995, 87:1603–1612.CrossRefPubMed Bochner BH, Cote RJ, Weidner N, et al.: Angiogenesis in bladder cancer: relationship between microvessel density and tumor prognosis. J Natl Cancer Inst 1995, 87:1603–1612.CrossRefPubMed
34.
go back to reference Crew JP, O'Brien T, Bradburn M, et al.: Vascular endothelial growth factor is a predictor of relapse and stage progression in superficial bladder cancer. Cancer Res 1997, 57:5281–5285.PubMed Crew JP, O'Brien T, Bradburn M, et al.: Vascular endothelial growth factor is a predictor of relapse and stage progression in superficial bladder cancer. Cancer Res 1997, 57:5281–5285.PubMed
35.
go back to reference Yang CC, Chu KC, Yeh WM: The expression of vascular endothelial growth factor in transitional cell carcinoma of urinary bladder is correlated with cancer progression. Urol Oncol 2004, 22:1–6.PubMed Yang CC, Chu KC, Yeh WM: The expression of vascular endothelial growth factor in transitional cell carcinoma of urinary bladder is correlated with cancer progression. Urol Oncol 2004, 22:1–6.PubMed
36.
go back to reference Bernardini S, Fauconnet S, Chabannes E, et al.: Serum levels of vascular endothelial growth factor as a prognostic factor in bladder cancer. J Urol 2001, 166:1275–1279.CrossRefPubMed Bernardini S, Fauconnet S, Chabannes E, et al.: Serum levels of vascular endothelial growth factor as a prognostic factor in bladder cancer. J Urol 2001, 166:1275–1279.CrossRefPubMed
37.
go back to reference Benedict WF, Tao Z, Kim CS, et al.: Intravesical Ad-IFNalpha causes marked regression of human bladder cancer growing orthotopically in nude mice and overcomes resistance to IFN-alpha protein. Mol Ther 2004, 10:525–532.CrossRefPubMed Benedict WF, Tao Z, Kim CS, et al.: Intravesical Ad-IFNalpha causes marked regression of human bladder cancer growing orthotopically in nude mice and overcomes resistance to IFN-alpha protein. Mol Ther 2004, 10:525–532.CrossRefPubMed
38.
go back to reference Nagabhushan TL, Maneval DC, Benedict WF, et al.: Enhancement of intravesical delivery with Syn3 potentiates interferon-alpha2b gene therapy for superficial bladder cancer. Cytokine Growth Factor Rev 2007, 18:389–394.CrossRefPubMed Nagabhushan TL, Maneval DC, Benedict WF, et al.: Enhancement of intravesical delivery with Syn3 potentiates interferon-alpha2b gene therapy for superficial bladder cancer. Cytokine Growth Factor Rev 2007, 18:389–394.CrossRefPubMed
39.
go back to reference •• Sharma P, Shen Y, Wen S, et al.: CD8 tumor-infiltrating lymphocytes are predictive of survival in muscle-invasive urothelial carcinoma. Proc Natl Acad Sc U S A 2007, 104:3967–3972. This recent tissue-based study suggests the potential impact of tumor recognition by the immune system. •• Sharma P, Shen Y, Wen S, et al.: CD8 tumor-infiltrating lymphocytes are predictive of survival in muscle-invasive urothelial carcinoma. Proc Natl Acad Sc U S A 2007, 104:3967–3972. This recent tissue-based study suggests the potential impact of tumor recognition by the immune system.
40.
go back to reference Sharma P, Gnjatic S, Jungbluth AA, et al.: Frequency of NY-ESO-1 and LAGE-1 expression in bladder cancer and evidence of a new NY-ESO-1 T-cell epitope in a patient with bladder cancer. Cancer Immun 2003, 3:19.PubMed Sharma P, Gnjatic S, Jungbluth AA, et al.: Frequency of NY-ESO-1 and LAGE-1 expression in bladder cancer and evidence of a new NY-ESO-1 T-cell epitope in a patient with bladder cancer. Cancer Immun 2003, 3:19.PubMed
41.
go back to reference •• Sharma P, Bajorin DF, Jungbluth AA, et al.: Immune responses detected in urothelial carcinoma patients after vaccination with NY-ESO-1 protein plus BCG and GM-CSF. J Immunother 2008, 31:849–857. This clinical trial uses vaccine to induce immune responses in urothelial cancer patients. •• Sharma P, Bajorin DF, Jungbluth AA, et al.: Immune responses detected in urothelial carcinoma patients after vaccination with NY-ESO-1 protein plus BCG and GM-CSF. J Immunother 2008, 31:849–857. This clinical trial uses vaccine to induce immune responses in urothelial cancer patients.
Metadata
Title
Bladder Cancer: Can We Move Beyond Chemotherapy?
Author
Arlene Siefker-Radtke
Publication date
01-07-2010
Publisher
Current Science Inc.
Published in
Current Oncology Reports / Issue 4/2010
Print ISSN: 1523-3790
Electronic ISSN: 1534-6269
DOI
https://doi.org/10.1007/s11912-010-0104-5

Other articles of this Issue 4/2010

Current Oncology Reports 4/2010 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