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Volumn 22, Issue 13, 2016, Pages 3227-3237

Phase I safety, pharmacokinetic, and pharmacodynamic study of the poly(ADP-ribose) polymerase (PARP) inhibitor veliparib (ABT-888) in combination with irinotecan in patients with advanced solid tumors

(25)  LoRusso, Patricia M a,f   Li, Jing a   Burger, Angelika a   Heilbrun, Lance K a   Sausville, Edward A b   Boerner, Scott A a,e   Smith, Daryn a   Pilat, Mary Jo a   Zhang, Jie a   Tolaney, Sara M c   Cleary, James M c   Chen, Alice P d   Rubinstein, Lawrence d   Boerner, Julie L a   Bowditch, Adam a   Cai, Dongpo c   Bell, Tracy c   Wolanski, Andrew c   Marrero, Allison M e   Zhang, Yiping e   more..


Author keywords

[No Author keywords available]

Indexed keywords

DNA; HISTONE H2AX; IRINOTECAN; NIBRIN; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE 1; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE 2; VELIPARIB; ANTINEOPLASTIC AGENT; BENZIMIDAZOLE DERIVATIVE; CAMPTOTHECIN; CELL CYCLE PROTEIN; H2AFX PROTEIN, HUMAN; HISTONE; NBN PROTEIN, HUMAN; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE INHIBITOR; NUCLEAR PROTEIN; PARP1 PROTEIN, HUMAN; PARP2 PROTEIN, HUMAN;

EID: 84977103990     PISSN: 10780432     EISSN: 15573265     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-15-0652     Document Type: Article
Times cited : (86)

References (46)
  • 1
    • 67650471685 scopus 로고    scopus 로고
    • Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers
    • Fong PC, Boss DS, Yap TA, Tutt A, Wu P, Mergui-Roelvink M, et al. Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers. N Engl J Med 2009;361:123-34.
    • (2009) N Engl J Med , vol.361 , pp. 123-134
    • Fong, P.C.1    Boss, D.S.2    Yap, T.A.3    Tutt, A.4    Wu, P.5    Mergui-Roelvink, M.6
  • 3
    • 77951445939 scopus 로고    scopus 로고
    • Poly(adp-ribose) polymerase inhibitors: A novel drug class with a promising future
    • Gartner EM, Burger AM, Lorusso PM. Poly(adp-ribose) polymerase inhibitors: A novel drug class with a promising future. Cancer J 2010;16:83-90.
    • (2010) Cancer J , vol.16 , pp. 83-90
    • Gartner, E.M.1    Burger, A.M.2    Lorusso, P.M.3
  • 5
    • 80052238687 scopus 로고    scopus 로고
    • Phase I study of PARP inhibitor ABT-888 in combination with topotecan in adults with refractory solid tumors and lymphomas
    • Kummar S, Chen A, Ji J, Zhang Y, Reid JM, Ames M, et al. Phase I study of PARP inhibitor ABT-888 in combination with topotecan in adults with refractory solid tumors and lymphomas. Cancer Res 2011;71:5626-34.
    • (2011) Cancer Res , vol.71 , pp. 5626-5634
    • Kummar, S.1    Chen, A.2    Ji, J.3    Zhang, Y.4    Reid, J.M.5    Ames, M.6
  • 6
    • 84863236347 scopus 로고    scopus 로고
    • A phase I study of veliparib in combination with metronomic cyclophosphamide in adults with refractory solid tumors and lymphomas
    • Kummar S, Ji J, Morgan R, Lenz HJ, Puhalla SL, Belani CP, et al. A phase I study of veliparib in combination with metronomic cyclophosphamide in adults with refractory solid tumors and lymphomas. Clin Cancer Res 2012;18:1726-34.
    • (2012) Clin Cancer Res , vol.18 , pp. 1726-1734
    • Kummar, S.1    Ji, J.2    Morgan, R.3    Lenz, H.J.4    Puhalla, S.L.5    Belani, C.P.6
  • 7
    • 80355139266 scopus 로고    scopus 로고
    • Phase I trial of veliparib (ABT-888), a poly(ADP-ribose) polymerase (PARP) inhibitor, in combination with doxorubicin and cyclophosphosphamide in breast cancer and other solid tumors
    • Tan A, Toppmeyer D, Stein M, Moss R, Gounder M, Lindquist D, et al. Phase I trial of veliparib (ABT-888), a poly(ADP-ribose) polymerase (PARP) inhibitor, in combination with doxorubicin and cyclophosphosphamide in breast cancer and other solid tumors. J Clin Oncol 29:2011 (suppl; abstr 3041).
    • (2011) J Clin Oncol , vol.29
    • Tan, A.1    Toppmeyer, D.2    Stein, M.3    Moss, R.4    Gounder, M.5    Lindquist, D.6
  • 8
    • 84872217951 scopus 로고    scopus 로고
    • A phase I dose-escalation study of ABT-888 (veliparib) in combination with carboplatin in HER2-negative metastatic breast cancer (MBC)
    • Viswanathan S, Wesolowski R, Layman R, ALejandra G, Miller B, Chalmers J, et al. A phase I dose-escalation study of ABT-888 (veliparib) in combination with carboplatin in HER2-negative metastatic breast cancer (MBC). J Clin Oncol 29:2011 (suppl; abstr TPS106).
    • (2011) J Clin Oncol , vol.29
    • Viswanathan, S.1    Wesolowski, R.2    Layman, R.3    Alejandra, G.4    Miller, B.5    Chalmers, J.6
  • 9
    • 84919775982 scopus 로고    scopus 로고
    • Phase II trial of single agent PARP inhibitor ABT-888 (veliparib) followed by post-progression therapy of veliparib with carboplatin in patients with BRCA-associated metastatic breast cancer: California Cancer Consortium trial PHII-96
    • Somlo G, Frankel PH, Luu TH, Ma C, Arun B, Garcia AB, et al. Phase II trial of single agent PARP inhibitor ABT-888 (veliparib) followed by post-progression therapy of veliparib with carboplatin in patients with BRCA-associated metastatic breast cancer: California Cancer Consortium trial PHII-96. J Clin Oncol 32:5s, 2014 (suppl; abstr 1021).
    • (2014) J Clin Oncol , vol.32 , pp. 5s
    • Somlo, G.1    Frankel, P.H.2    Luu, T.H.3    Ma, C.4    Arun, B.5    Garcia, A.B.6
  • 10
    • 84905183020 scopus 로고    scopus 로고
    • Phase I trial of olaparib in combination with cisplatin for the treatment of patients with advanced breast, ovarian and other solid tumors
    • Balmaña J, Tung NM, Isakoff SJ, Grana B, Ryan PD, Saura C, et al. Phase I trial of olaparib in combination with cisplatin for the treatment of patients with advanced breast, ovarian and other solid tumors. Ann Oncol 2014;25:1656-63.
    • (2014) Ann Oncol , vol.25 , pp. 1656-1663
    • Balmaña, J.1    Tung, N.M.2    Isakoff, S.J.3    Grana, B.4    Ryan, P.D.5    Saura, C.6
  • 11
    • 84977179838 scopus 로고    scopus 로고
    • A phase I study of veliparib (ABT-888) in combination with low-dose fractionated whole abdominal radiation therapy (LDFWAR) in patients with advanced solid malignancies and peritoneal carcinomatosis
    • Reiss K, Herman J, ZAhurak M, Brade A, Dawson L, Scardina A, et al. A phase I study of veliparib (ABT-888) in combination with low-dose fractionated whole abdominal radiation therapy (LDFWAR) in patients with advanced solid malignancies and peritoneal carcinomatosis. J Clin Oncol 32:5s, 2014 (suppl; abstr 4139).
    • (2014) J Clin Oncol , vol.32 , pp. 5s
    • Reiss, K.1    Herman, J.2    Zahurak, M.3    Brade, A.4    Dawson, L.5    Scardina, A.6
  • 12
    • 84923698550 scopus 로고    scopus 로고
    • The safety and tolerability of veliparib plus capecitabine and radiation in subjects with locally advanced rectal cancer: Results of a phase 1b study
    • Czito B, Mulcahy M, WR S, Vaghefi H, Jameson G, Deluca A, et al. The safety and tolerability of veliparib plus capecitabine and radiation in subjects with locally advanced rectal cancer: Results of a phase 1b study. J Clin Oncol 32:5s, 2014 (suppl; abstr 3634).
    • (2014) J Clin Oncol , vol.32 , pp. 5s
    • Czito, B.1    Mulcahy, M.2    WR, S.3    Vaghefi, H.4    Jameson, G.5    Deluca, A.6
  • 14
    • 60549117554 scopus 로고    scopus 로고
    • Discovery of the Poly(ADP-ribose) polymerase (PARP) inhibitor 2-[(R)-2-methylpyrrolidin-2-yl]-1H-benzimidazole-4-carboxamide (ABT-888) for the treatment of cancer
    • Penning TD, Zhu GD, Gandhi VB, Gong J, Liu X, Shi Y, et al. Discovery of the Poly(ADP-ribose) polymerase (PARP) inhibitor 2-[(R)-2-methylpyrrolidin-2-yl]-1H-benzimidazole-4-carboxamide (ABT-888) for the treatment of cancer. J Med Chem 2009;52:514-23.
    • (2009) J Med Chem , vol.52 , pp. 514-523
    • Penning, T.D.1    Zhu, G.D.2    Gandhi, V.B.3    Gong, J.4    Liu, X.5    Shi, Y.6
  • 15
    • 34249006299 scopus 로고    scopus 로고
    • ABT-888, an orally active poly(ADP-ribose) polymerase inhibitor that potentiates DNA-damaging agents in preclinical tumor models
    • Donawho CK, Luo Y, Luo Y, Penning TD, Bauch JL, Bouska JJ, et al. ABT-888, an orally active poly(ADP-ribose) polymerase inhibitor that potentiates DNA-damaging agents in preclinical tumor models. Clin Cancer Res 2007;13:2728-37.
    • (2007) Clin Cancer Res , vol.13 , pp. 2728-2737
    • Donawho, C.K.1    Luo, Y.2    Luo, Y.3    Penning, T.D.4    Bauch, J.L.5    Bouska, J.J.6
  • 16
    • 84894121635 scopus 로고    scopus 로고
    • Stereospecific PARP trapping by BMN 673 and comparison with olaparib and rucaparib
    • Murai J, Huang SY, Renaud A, Zhang Y, Ji J, Takeda S, et al. Stereospecific PARP trapping by BMN 673 and comparison with olaparib and rucaparib. Mol Cancer Ther 2014;13:433-43.
    • (2014) Mol Cancer Ther , vol.13 , pp. 433-443
    • Murai, J.1    Huang, S.Y.2    Renaud, A.3    Zhang, Y.4    Ji, J.5    Takeda, S.6
  • 17
    • 66849106010 scopus 로고    scopus 로고
    • Phase 0 clinical trial of the poly (ADP-ribose) polymerase inhibitor ABT-888 in patients with advanced malignancies
    • Kummar S, Kinders R, Gutierrez ME, Rubinstein L, Parchment RE, Phillips LR, et al. Phase 0 clinical trial of the poly (ADP-ribose) polymerase inhibitor ABT-888 in patients with advanced malignancies. J Clin Oncol 2009;27:2705-11.
    • (2009) J Clin Oncol , vol.27 , pp. 2705-2711
    • Kummar, S.1    Kinders, R.2    Gutierrez, M.E.3    Rubinstein, L.4    Parchment, R.E.5    Phillips, L.R.6
  • 18
    • 84927918390 scopus 로고    scopus 로고
    • Final results of a phase 1 study of the single-agent veliparib in patients with either BRCA1/2-mutated cancer, platinum-refractory ovarian, or basal-like breast cancer
    • Puhalla S, Beumer JH, Pahuja S, Appleman LJ, Tawbi HA, Stoller RG, et al. Final results of a phase 1 study of the single-agent veliparib in patients with either BRCA1/2-mutated cancer, platinum-refractory ovarian, or basal-like breast cancer. J Clin Oncol 32:5s, 2014 (suppl; abstr 2570).
    • (2014) J Clin Oncol , vol.32 , pp. 5s
    • Puhalla, S.1    Beumer, J.H.2    Pahuja, S.3    Appleman, L.J.4    Tawbi, H.A.5    Stoller, R.G.6
  • 19
    • 10744226451 scopus 로고    scopus 로고
    • Anticancer chemosensitization and radiosensitization by the novel poly(ADP-ribose) polymerase-1 inhibitor AG14361
    • Calabrese CR, Almassy R, Barton S, Batey MA, Calvert AH, Canan-Koch S, et al. Anticancer chemosensitization and radiosensitization by the novel poly(ADP-ribose) polymerase-1 inhibitor AG14361. J Natl Cancer Inst 2004;96:56-67.
    • (2004) J Natl Cancer Inst , vol.96 , pp. 56-67
    • Calabrese, C.R.1    Almassy, R.2    Barton, S.3    Batey, M.A.4    Calvert, A.H.5    Canan-Koch, S.6
  • 20
    • 28544441999 scopus 로고    scopus 로고
    • The novel poly(ADP-Ribose) polymerase inhibitor, AG14361, sensitizes cells to topoisomerase I poisons by increasing the persistence of DNA strand breaks
    • Smith LM, Willmore E, Austin CA, Curtin NJ. The novel poly(ADP-Ribose) polymerase inhibitor, AG14361, sensitizes cells to topoisomerase I poisons by increasing the persistence of DNA strand breaks. Clin Cancer Res 2005;11:8449-57.
    • (2005) Clin Cancer Res , vol.11 , pp. 8449-8457
    • Smith, L.M.1    Willmore, E.2    Austin, C.A.3    Curtin, N.J.4
  • 21
    • 34548072788 scopus 로고    scopus 로고
    • The selective poly(ADP-ribose) polymerase-1(2) inhibitor, CEP-8983, increases the sensitivity of chemoresistant tumor cells to temozolomide and irinotecan but does not potentiate myelotoxicity
    • Miknyoczki S, Chang H, Grobelny J, Pritchard S, Worrell C, McGann N, et al. The selective poly(ADP-ribose) polymerase-1(2) inhibitor, CEP-8983, increases the sensitivity of chemoresistant tumor cells to temozolomide and irinotecan but does not potentiate myelotoxicity. Mol Cancer Ther 2007;6:2290-302.
    • (2007) Mol Cancer Ther , vol.6 , pp. 2290-2302
    • Miknyoczki, S.1    Chang, H.2    Grobelny, J.3    Pritchard, S.4    Worrell, C.5    McGann, N.6
  • 22
    • 0242588748 scopus 로고    scopus 로고
    • Chemopotentiation of temozolomide, irinotecan, and cisplatin activity by CEP-6800, a poly(ADP-ribose) polymerase inhibitor
    • Miknyoczki SJ, Jones-Bolin S, Pritchard S, Hunter K, Zhao H, Wan W, et al. Chemopotentiation of temozolomide, irinotecan, and cisplatin activity by CEP-6800, a poly(ADP-ribose) polymerase inhibitor. Mol Cancer Ther 2003;2:371-82.
    • (2003) Mol Cancer Ther , vol.2 , pp. 371-382
    • Miknyoczki, S.J.1    Jones-Bolin, S.2    Pritchard, S.3    Hunter, K.4    Zhao, H.5    Wan, W.6
  • 23
    • 84879555636 scopus 로고    scopus 로고
    • The PARP inhibitor ABT-888 synergizes irinotecan treatment of colon cancer cell lines
    • Davidson D, Wang Y, Aloyz R, Panasci L. The PARP inhibitor ABT-888 synergizes irinotecan treatment of colon cancer cell lines. Invest New Drugs 2013;31:461-8.
    • (2013) Invest New Drugs , vol.31 , pp. 461-468
    • Davidson, D.1    Wang, Y.2    Aloyz, R.3    Panasci, L.4
  • 24
    • 33845672155 scopus 로고    scopus 로고
    • Inhibition of poly(ADP-ribose) polymerase prevents irinotecan-induced intestinal damage and enhances irinotecan/temozolomide efficacy against colon carcinoma
    • Tentori L, Leonetti C, Scarsella M, Muzi A, Mazzon E, Vergati M, et al. Inhibition of poly(ADP-ribose) polymerase prevents irinotecan-induced intestinal damage and enhances irinotecan/temozolomide efficacy against colon carcinoma. FASEB J 2006;20:1709-11.
    • (2006) FASEB J , vol.20 , pp. 1709-1711
    • Tentori, L.1    Leonetti, C.2    Scarsella, M.3    Muzi, A.4    Mazzon, E.5    Vergati, M.6
  • 25
    • 84909995009 scopus 로고    scopus 로고
    • Preferential potentiation of topoisomerase I poison cytotoxicity by PARP inhibition in S phase
    • Znojek P, Willmore E, Curtin NJ. Preferential potentiation of topoisomerase I poison cytotoxicity by PARP inhibition in S phase. Br J Cancer 2014;111:1319-26.
    • (2014) Br J Cancer , vol.111 , pp. 1319-1326
    • Znojek, P.1    Willmore, E.2    Curtin, N.J.3
  • 26
    • 84901218339 scopus 로고    scopus 로고
    • Rationale for poly(ADP-ribose) polymerase (PARP) inhibitors in combination therapy with camptothecins or temozolomide based on PARP trapping versus catalytic inhibition
    • Murai J, Zhang Y, Morris J, Ji J, Takeda S, Doroshow JH, et al. Rationale for poly(ADP-ribose) polymerase (PARP) inhibitors in combination therapy with camptothecins or temozolomide based on PARP trapping versus catalytic inhibition. J Pharmacol Exp Ther 2014;349:408-16.
    • (2014) J Pharmacol Exp Ther , vol.349 , pp. 408-416
    • Murai, J.1    Zhang, Y.2    Morris, J.3    Ji, J.4    Takeda, S.5    Doroshow, J.H.6
  • 27
    • 84856738573 scopus 로고    scopus 로고
    • Enhanced killing of cancer cells by poly(ADP-ribose) polymerase inhibitors and topoisomerase I inhibitors reflects poisoning of both enzymes
    • Patel AG, Flatten KS, Schneider PA, Dai NT, McDonald JS, Poirier GG, et al. Enhanced killing of cancer cells by poly(ADP-ribose) polymerase inhibitors and topoisomerase I inhibitors reflects poisoning of both enzymes. J Biol Chem 2012;287:4198-210.
    • (2012) J Biol Chem , vol.287 , pp. 4198-4210
    • Patel, A.G.1    Flatten, K.S.2    Schneider, P.A.3    Dai, N.T.4    McDonald, J.S.5    Poirier, G.G.6
  • 29
    • 2342459714 scopus 로고    scopus 로고
    • Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan
    • Innocenti F, Undevia SD, Iyer L, Chen PX, Das S, Kocherginsky M, et al. Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan. J Clin Oncol 2004;22:1382-8.
    • (2004) J Clin Oncol , vol.22 , pp. 1382-1388
    • Innocenti, F.1    Undevia, S.D.2    Iyer, L.3    Chen, P.X.4    Das, S.5    Kocherginsky, M.6
  • 30
    • 0036025450 scopus 로고    scopus 로고
    • UGT1A1∗28 polymorphism as a determinant of irinotecan disposition and toxicity
    • Iyer L, Das S, Janisch L, Wen M, Ramirez J, Karrison T, et al. UGT1A1∗28 polymorphism as a determinant of irinotecan disposition and toxicity. Pharmacogenomics J 2002;2:43-7.
    • (2002) Pharmacogenomics J , vol.2 , pp. 43-47
    • Iyer, L.1    Das, S.2    Janisch, L.3    Wen, M.4    Ramirez, J.5    Karrison, T.6
  • 31
    • 84977181009 scopus 로고    scopus 로고
    • Pharmacia and Upjohn Company. New York, NY: Pfizer Inc. Revised December
    • Pharmacia and Upjohn Company. Camptosar (irinotecan hydrochloride injection) drug package insert. New York, NY: Pfizer Inc. Revised December 2014. Available from: http://labeling.pfizer.com/ShowLabeling.aspx?id=533.
    • (2014) Camptosar (Irinotecan Hydrochloride Injection) Drug Package Insert
  • 32
    • 74049132367 scopus 로고    scopus 로고
    • Simultaneous determination of ABT-888, a poly (ADP-ribose) polymerase inhibitor, and its metabolite in human plasma by liquid chromatography/tandem mass spectrometry
    • Wiegand R, Wu J, Sha X, LoRusso P, Li J. Simultaneous determination of ABT-888, a poly (ADP-ribose) polymerase inhibitor, and its metabolite in human plasma by liquid chromatography/tandem mass spectrometry. J Chromatography B 2010;878:333-9.
    • (2010) J Chromatography B , vol.878 , pp. 333-339
    • Wiegand, R.1    Wu, J.2    Sha, X.3    LoRusso, P.4    Li, J.5
  • 33
    • 0242362622 scopus 로고    scopus 로고
    • Sensitive HPLC-fluorescence method for irinotecan and four major metabolites in human plasma and saliva: Application to pharmacokinetic studies
    • Poujol S, Pinguet F, Malosse F, Astre C, Ychou M, Culine S, et al. Sensitive HPLC-fluorescence method for irinotecan and four major metabolites in human plasma and saliva: application to pharmacokinetic studies. Clin Chem 2003;49:1900-8.
    • (2003) Clin Chem , vol.49 , pp. 1900-1908
    • Poujol, S.1    Pinguet, F.2    Malosse, F.3    Astre, C.4    Ychou, M.5    Culine, S.6
  • 34
    • 58149263490 scopus 로고    scopus 로고
    • Preclinical modeling of a phase 0 clinical trial: Qualification of a pharmacodynamic assay of poly (ADP-ribose) polymerase in tumor biopsies of mouse xenografts
    • Kinders RJ, Hollingshead M, Khin S, Rubinstein L, Tomaszewski JE, Doroshow JH, et al. Preclinical modeling of a phase 0 clinical trial: qualification of a pharmacodynamic assay of poly (ADP-ribose) polymerase in tumor biopsies of mouse xenografts. Clin Cancer Res 2008;14:6877-85.
    • (2008) Clin Cancer Res , vol.14 , pp. 6877-6885
    • Kinders, R.J.1    Hollingshead, M.2    Khin, S.3    Rubinstein, L.4    Tomaszewski, J.E.5    Doroshow, J.H.6
  • 35
    • 78349238215 scopus 로고    scopus 로고
    • Development of a validated immunofluorescence assay for gammaH2AX as a pharmacodynamic marker of topoisomerase I inhibitor activity
    • Kinders RJ, Hollingshead M, Lawrence S, Ji J, Tabb B, Bonner WM, et al. Development of a validated immunofluorescence assay for gammaH2AX as a pharmacodynamic marker of topoisomerase I inhibitor activity. Clin Cancer Res 2010;16:5447-57.
    • (2010) Clin Cancer Res , vol.16 , pp. 5447-5457
    • Kinders, R.J.1    Hollingshead, M.2    Lawrence, S.3    Ji, J.4    Tabb, B.5    Bonner, W.M.6
  • 36
    • 0033987392 scopus 로고    scopus 로고
    • Pharmacokinetic, metabolic, and pharmacodynamic profiles in a dose-escalating study of irinotecan and cisplatin
    • de Jonge MJ, Verweij J, de Bruijn P, Brouwer E, Mathijssen RH, van Alphen RJ, et al. Pharmacokinetic, metabolic, and pharmacodynamic profiles in a dose-escalating study of irinotecan and cisplatin. J Clin Oncol 2000;18:195-203.
    • (2000) J Clin Oncol , vol.18 , pp. 195-203
    • De Jonge, M.J.1    Verweij, J.2    De Bruijn, P.3    Brouwer, E.4    Mathijssen, R.H.5    Van Alphen, R.J.6
  • 38
    • 84872547120 scopus 로고    scopus 로고
    • Drugging topoisomerases: Lessons and challenges
    • Pommier Y. Drugging topoisomerases: Lessons and challenges. ACS Chem Biol 2013;8:82-95.
    • (2013) ACS Chem Biol , vol.8 , pp. 82-95
    • Pommier, Y.1
  • 39
    • 84859761985 scopus 로고    scopus 로고
    • Tyrosyl-DNA phosphodiesterase 1 (TDP1) repairs DNA damage induced by topoisomerases I and II and base alkylation in vertebrate cells
    • Murai J, Huang SY, Das BB, Dexheimer TS, Takeda S, Pommier Y. Tyrosyl-DNA phosphodiesterase 1 (TDP1) repairs DNA damage induced by topoisomerases I and II and base alkylation in vertebrate cells. J Biol Chem 2012;287:12848-57.
    • (2012) J Biol Chem , vol.287 , pp. 12848-12857
    • Murai, J.1    Huang, S.Y.2    Das, B.B.3    Dexheimer, T.S.4    Takeda, S.5    Pommier, Y.6
  • 42
    • 79956053314 scopus 로고    scopus 로고
    • Poly(ADP-ribose) polymerase and XPF-ERCC1 participate in distinct pathways for the repair of topoisomerase I-induced DNA damage in mammalian cells
    • Zhang YW, Regairaz M, Seiler JA, Agama KK, Doroshow JH, Pommier Y. Poly(ADP-ribose) polymerase and XPF-ERCC1 participate in distinct pathways for the repair of topoisomerase I-induced DNA damage in mammalian cells. Nucleic Acids Res 2011;39:3607-20.
    • (2011) Nucleic Acids Res , vol.39 , pp. 3607-3620
    • Zhang, Y.W.1    Regairaz, M.2    Seiler, J.A.3    Agama, K.K.4    Doroshow, J.H.5    Pommier, Y.6
  • 44
    • 84919920835 scopus 로고    scopus 로고
    • Targeting DNA repair with combination veliparib (ABT-888) and temozolomide in patients with metastatic castration-resistant prostate cancer
    • Hussain M, Carducci MA, Slovin S, Cetnar J, Qian J, McKeegan EM, et al. Targeting DNA repair with combination veliparib (ABT-888) and temozolomide in patients with metastatic castration-resistant prostate cancer. Invest New Drugs 2014;32:904-12.
    • (2014) Invest New Drugs , vol.32 , pp. 904-912
    • Hussain, M.1    Carducci, M.A.2    Slovin, S.3    Cetnar, J.4    Qian, J.5    McKeegan, E.M.6
  • 45
    • 85017471079 scopus 로고    scopus 로고
    • A phase I study of niraparib in combination with temozolomide (TMZ) in patients with advanced cancer
    • Kurzrock R, Galanis E, Johnson DR, Kansra V, Wilcoxen K, Mcclure T, et al. A phase I study of niraparib in combination with temozolomide (TMZ) in patients with advanced cancer. J Clin Oncol 32:5s, 2014 (suppl; abstr 2092).
    • (2014) J Clin Oncol , vol.32 , pp. 5s
    • Kurzrock, R.1    Galanis, E.2    Johnson, D.R.3    Kansra, V.4    Wilcoxen, K.5    Mcclure, T.6
  • 46
    • 79952281417 scopus 로고    scopus 로고
    • A phase I study of the safety and tolerability of olaparib (AZD2281, KU0059436) and dacarbazine in patients with advanced solid tumours
    • Khan OA, Gore M, Lorigan P, Stone J, Greystoke A, Burke W, et al. A phase I study of the safety and tolerability of olaparib (AZD2281, KU0059436) and dacarbazine in patients with advanced solid tumours. Br J Cancer 2011;104:750-5.
    • (2011) Br J Cancer , vol.104 , pp. 750-755
    • Khan, O.A.1    Gore, M.2    Lorigan, P.3    Stone, J.4    Greystoke, A.5    Burke, W.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.