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01.08.2017 | SHORT REPORT

Addition of an antiangiogenic therapy, bevacizumab, to gemcitabine plus oxaliplatin improves survival in advanced biliary tract cancers

verfasst von: Marie Bréchon, Marie Dior, Johann Dréanic, Bertrand Brieau, Marie-Anne Guillaumot, Catherine Brezault, Olivier Mir, François Goldwasser, Romain Coriat

Erschienen in: Investigational New Drugs | Ausgabe 1/2018

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Summary

Background The prognosis of patients with metastatic carcinoma of the biliary tract (mBTC) is poor and a systemic therapy with gemcitabine and platinum-based is the gold standard. The addition of bevacizumab to the chemotherapy might increase patients’ survival. Our aim was to assess and compare the efficacy of GEMOX (gemcitabine and oxaliplatin regimen) plus bevacizumab to GEMOX alone in mBTC. Methods Patients with mBTC who received the GEMOX-bevacizumab (n = 32; Group A) or GEMOX (n = 25; Group B) regimen as first-line treatment were compared. Treatment was repeated every two weeks until disease progression or unacceptable adverse effects occurred. The primary evaluation criterion was the progression-free survival (PFS). Results A quarter of patients (8/32) from Group A and a fifth of patients (13/25) from Group B had an objective response. The median PFS was 6.48 months and 3.72 months in Group A and B, respectively (p = 0.049). The median OS was 11.31 months and 10.34 months in Group A and B, respectively. Grade 3/4 sepsis was identified in 9.4% and 12% in Group A and B, respectively, (p = 0.64). Conclusion In mBTC, the addition of bevacizumab to GEMOX increased the progression-free survival and was associated with manageable toxicity. These data pave the way for further evaluation of antiangiogenic agents in mBTC.
Literatur
1.
Zurück zum Zitat Bergquist A, von Seth E (2015) Epidemiology of cholangiocarcinoma. Best Pract Res Clin Gastroenterol 29:221–232CrossRefPubMed Bergquist A, von Seth E (2015) Epidemiology of cholangiocarcinoma. Best Pract Res Clin Gastroenterol 29:221–232CrossRefPubMed
2.
3.
Zurück zum Zitat Vauthey JN, Blumgart LH (1994) Recent advances in the management of cholangiocarcinomas. Semin Liver Dis 14:109–114CrossRefPubMed Vauthey JN, Blumgart LH (1994) Recent advances in the management of cholangiocarcinomas. Semin Liver Dis 14:109–114CrossRefPubMed
4.
5.
6.
Zurück zum Zitat Valle J, Wasan H, Palmer DH et al (2010) ABC-02 trial investigators. Cisplatin plus gemcitabine versus gemcitabine for biliary tract cancer. N Engl J Med 362:1273–1281CrossRefPubMed Valle J, Wasan H, Palmer DH et al (2010) ABC-02 trial investigators. Cisplatin plus gemcitabine versus gemcitabine for biliary tract cancer. N Engl J Med 362:1273–1281CrossRefPubMed
7.
Zurück zum Zitat Mir O, Coriat R, Dhooge M et al (2012) Feasibility of gemcitabine and oxaliplatin in patients with advanced biliary tract carcinoma and a performance status of 2. Anti-Cancer Drugs 23:739–744CrossRefPubMed Mir O, Coriat R, Dhooge M et al (2012) Feasibility of gemcitabine and oxaliplatin in patients with advanced biliary tract carcinoma and a performance status of 2. Anti-Cancer Drugs 23:739–744CrossRefPubMed
8.
Zurück zum Zitat Harder J, Riecken B, Kummer O et al (2006) Outpatient chemotherapy with gemcitabine and oxaliplatin in patients with biliary tract cancer. Br J Cancer 95:848–852CrossRefPubMedPubMedCentral Harder J, Riecken B, Kummer O et al (2006) Outpatient chemotherapy with gemcitabine and oxaliplatin in patients with biliary tract cancer. Br J Cancer 95:848–852CrossRefPubMedPubMedCentral
9.
Zurück zum Zitat Riechelmann RP, Townsley CA, Chin SN et al (2007) Expanded phase II trial of gemcitabine and capecitabine for advanced biliary cancer. Cancer 110:1307–1312CrossRefPubMed Riechelmann RP, Townsley CA, Chin SN et al (2007) Expanded phase II trial of gemcitabine and capecitabine for advanced biliary cancer. Cancer 110:1307–1312CrossRefPubMed
10.
Zurück zum Zitat Hida Y, Morita T, Fujita M et al (1999) Vascular endothelial growth factor expression is an independent negative predictor in extrahepatic biliary tract carcinomas. Anticancer Res 19:2257–2260PubMed Hida Y, Morita T, Fujita M et al (1999) Vascular endothelial growth factor expression is an independent negative predictor in extrahepatic biliary tract carcinomas. Anticancer Res 19:2257–2260PubMed
11.
Zurück zum Zitat Ogasawara S, Yano H, Higaki K et al (2001) Expression of angiogenic factors, basic fibroblast growth factor and vascular endothelial growth factor, in human biliary tract carcinoma cell lines. Hepatol Res Off J Jpn Soc Hepatol 20:97–113CrossRef Ogasawara S, Yano H, Higaki K et al (2001) Expression of angiogenic factors, basic fibroblast growth factor and vascular endothelial growth factor, in human biliary tract carcinoma cell lines. Hepatol Res Off J Jpn Soc Hepatol 20:97–113CrossRef
12.
Zurück zum Zitat Hurwitz H, Fehrenbacher L, Novotny W et al (2004) Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. N Engl J Med 350:2335–2342CrossRefPubMed Hurwitz H, Fehrenbacher L, Novotny W et al (2004) Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. N Engl J Med 350:2335–2342CrossRefPubMed
13.
Zurück zum Zitat Giantonio BJ, Catalano PJ, Meropol NJ et al (2007) Eastern cooperative oncology group study E3200. Bevacizumab in combination with oxaliplatin, fluorouracil, and leucovorin (FOLFOX4) for previously treated metastatic colorectal cancer: results from the eastern cooperative oncology group study E3200. J Clin Oncol Off J Am Soc Clin Oncol 25:1539–1544CrossRef Giantonio BJ, Catalano PJ, Meropol NJ et al (2007) Eastern cooperative oncology group study E3200. Bevacizumab in combination with oxaliplatin, fluorouracil, and leucovorin (FOLFOX4) for previously treated metastatic colorectal cancer: results from the eastern cooperative oncology group study E3200. J Clin Oncol Off J Am Soc Clin Oncol 25:1539–1544CrossRef
14.
Zurück zum Zitat Jain RK (2001) Normalizing tumor vasculature with anti-angiogenic therapy: a new paradigm for combination therapy. Nat Med 7:987–989CrossRefPubMed Jain RK (2001) Normalizing tumor vasculature with anti-angiogenic therapy: a new paradigm for combination therapy. Nat Med 7:987–989CrossRefPubMed
15.
Zurück zum Zitat Zhu AX, Meyerhardt JA, Blaszkowsky LS et al (2010) Efficacy and safety of gemcitabine, oxaliplatin, and bevacizumab in advanced biliary-tract cancers and correlation of changes in 18-fluorodeoxyglucose PET with clinical outcome: a phase 2 study. Lancet Oncol 11:48–54CrossRefPubMed Zhu AX, Meyerhardt JA, Blaszkowsky LS et al (2010) Efficacy and safety of gemcitabine, oxaliplatin, and bevacizumab in advanced biliary-tract cancers and correlation of changes in 18-fluorodeoxyglucose PET with clinical outcome: a phase 2 study. Lancet Oncol 11:48–54CrossRefPubMed
16.
Zurück zum Zitat Eisenhauer EA, Therasse P, Bogaerts J et al (2009) New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer Oxf Engl 1990 45:228–247 Eisenhauer EA, Therasse P, Bogaerts J et al (2009) New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer Oxf Engl 1990 45:228–247
17.
Zurück zum Zitat Dhooge M, Coriat R, Mir O et al (2013) Feasibility of gemcitabine plus oxaliplatin in advanced hepatocellular carcinoma patients with child-Pugh B cirrhosis. Oncology 84:32–38CrossRefPubMed Dhooge M, Coriat R, Mir O et al (2013) Feasibility of gemcitabine plus oxaliplatin in advanced hepatocellular carcinoma patients with child-Pugh B cirrhosis. Oncology 84:32–38CrossRefPubMed
18.
Zurück zum Zitat Caussanel JP, Lévi F, Brienza S et al (1990) Phase I trial of 5-day continuous venous infusion of oxaliplatin at circadian rhythm-modulated rate compared with constant rate. J Natl Cancer Inst 82:1046–1050CrossRefPubMed Caussanel JP, Lévi F, Brienza S et al (1990) Phase I trial of 5-day continuous venous infusion of oxaliplatin at circadian rhythm-modulated rate compared with constant rate. J Natl Cancer Inst 82:1046–1050CrossRefPubMed
19.
Zurück zum Zitat Lee H, Wang K, Johnson A et al (2016) Comprehensive genomic profiling of extrahepatic cholangiocarcinoma reveals a long tail of therapeutic targets. J Clin Pathol 69:403–408CrossRefPubMed Lee H, Wang K, Johnson A et al (2016) Comprehensive genomic profiling of extrahepatic cholangiocarcinoma reveals a long tail of therapeutic targets. J Clin Pathol 69:403–408CrossRefPubMed
20.
Zurück zum Zitat Lee J, Park SH, Chang H-M et al (2012) Gemcitabine and oxaliplatin with or without erlotinib in advanced biliary-tract cancer: a multicentre, open-label, randomised, phase 3 study. Lancet Oncol 13:181–188CrossRefPubMed Lee J, Park SH, Chang H-M et al (2012) Gemcitabine and oxaliplatin with or without erlotinib in advanced biliary-tract cancer: a multicentre, open-label, randomised, phase 3 study. Lancet Oncol 13:181–188CrossRefPubMed
21.
22.
Zurück zum Zitat Cacheux W, Boisserie T, Staudacher L et al (2008) Reversible tumor growth acceleration following bevacizumab interruption in metastatic colorectal cancer patients scheduled for surgery. Ann Oncol Off J Eur Soc Med Oncol ESMO 19:1659–1661CrossRef Cacheux W, Boisserie T, Staudacher L et al (2008) Reversible tumor growth acceleration following bevacizumab interruption in metastatic colorectal cancer patients scheduled for surgery. Ann Oncol Off J Eur Soc Med Oncol ESMO 19:1659–1661CrossRef
23.
Zurück zum Zitat Malka D, Cervera P, Foulon S et al (2014) BINGO investigators. Gemcitabine and oxaliplatin with or without cetuximab in advanced biliary-tract cancer (BINGO): a randomised, open-label, non-comparative phase 2 trial. Lancet Oncol 15:819–828CrossRefPubMed Malka D, Cervera P, Foulon S et al (2014) BINGO investigators. Gemcitabine and oxaliplatin with or without cetuximab in advanced biliary-tract cancer (BINGO): a randomised, open-label, non-comparative phase 2 trial. Lancet Oncol 15:819–828CrossRefPubMed
24.
Zurück zum Zitat André T, Tournigand C, Rosmorduc O et al (2004) GERCOR group. Gemcitabine combined with oxaliplatin (GEMOX) in advanced biliary tract adenocarcinoma: a GERCOR study. Ann Oncol Off J Eur Soc Med Oncol ESMO 15:1339–1343CrossRef André T, Tournigand C, Rosmorduc O et al (2004) GERCOR group. Gemcitabine combined with oxaliplatin (GEMOX) in advanced biliary tract adenocarcinoma: a GERCOR study. Ann Oncol Off J Eur Soc Med Oncol ESMO 15:1339–1343CrossRef
Metadaten
Titel
Addition of an antiangiogenic therapy, bevacizumab, to gemcitabine plus oxaliplatin improves survival in advanced biliary tract cancers
verfasst von
Marie Bréchon
Marie Dior
Johann Dréanic
Bertrand Brieau
Marie-Anne Guillaumot
Catherine Brezault
Olivier Mir
François Goldwasser
Romain Coriat
Publikationsdatum
01.08.2017
Verlag
Springer US
Erschienen in
Investigational New Drugs / Ausgabe 1/2018
Print ISSN: 0167-6997
Elektronische ISSN: 1573-0646
DOI
https://doi.org/10.1007/s10637-017-0492-6

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