Poly(ADP)-Ribose Polymerase Inhibition: Frequent Durable Responses in BRCA Carrier Ovarian Cancer Correlating With Platinum-Free Interval

被引:777
作者
Fong, Peter C.
Yap, Timothy A.
Boss, David S.
Carden, Craig P.
Mergui-Roelvink, Marja
Gourley, Charlie
De Greve, Jacques
Lubinski, Jan
Shanley, Susan
Messiou, Christina
A'Hern, Roger
Tutt, Andrew
Ashworth, Alan
Stone, John
Carmichael, James
Schellens, Jan H. M.
de Bono, Johann S.
Kaye, Stan B.
机构
[1] Royal Marsden Natl Hlth Serv Fdn Trust, Drug Dev Unit, Sutton SM2 5PT, Surrey, England
[2] Inst Canc Res, Sutton, Surrey, England
[3] Univ Edinburgh Canc Res, Inst Genet & Mol Med, Edinburgh, Midlothian, Scotland
[4] Kings Coll London, Breakthrough Breast Canc Res Unit, London WC2R 2LS, England
[5] Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
[6] AstraZeneca, Macclesfield, Cheshire, England
[7] Netherlands Canc Inst, Amsterdam, Netherlands
[8] Univ Utrecht, Dept Pharmaceut Sci, Utrecht, Netherlands
[9] Univ Ziekenhuis, Brussel Oncol Ctr, Brussels, Belgium
[10] Int Hereditary Canc Ctr, Szczecin, Poland
关键词
POLY(ADP-RIBOSE) POLYMERASE; MUTANT-CELLS; RESISTANCE; MUTATIONS; BREAST; TUMORS; PTEN; HYPERMETHYLATION; GUIDELINES; DEFICIENT;
D O I
10.1200/JCO.2009.26.9589
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Selective tumor cell cytotoxicity can be achieved through a synthetic lethal strategy using poly(ADP)-ribose polymerase (PARP) inhibitor therapy in BRCA1/2 mutation carriers in whom tumor cells have defective homologous recombination (HR) DNA repair. Platinum-based chemotherapy responses correlate with HR DNA repair capacity. Olaparib is a potent, oral PARP inhibitor that is well tolerated, with antitumor activity in BRCA1/2 mutation carriers. Patients and Methods Patients with BRCA1/2-mutated ovarian cancer were treated with olaparib within a dose-escalation and single-stage expansion of a phase I trial. Antitumor activity was subsequently correlated with platinum sensitivity. Results Fifty patients were treated: 48 had germline BRCA1/2 mutations; one had a BRCA2 germline sequence change of unknown significance, and another had a strong family history of BRCA1/2-associated cancers who declined mutation testing. Of the 50 patients, 13 had platinum-sensitive disease, 24 had platinum-resistant disease, and 13 had platinum-refractory disease (according to platinum-free interval). Twenty (40%; 95% CI, 26% to 55%) achieved Response Evaluation Criteria in Solid Tumors (RECIST) complete or partial responses and/or tumor marker (CA125) responses, and three (6.0%) maintained RECIST disease stabilization for more than 4 months, giving an overall clinical benefit rate of 46% (95% CI, 32% to 61%). Median response duration was 28 weeks. There was a significant association between the clinical benefit rate and platinum-free interval across the platinum-sensitive, resistant, and refractory subgroups (69%, 45%, and 23%, respectively). Post hoc analyses indicated associations between platinum sensitivity and extent of olaparib response (radiologic change, P = .001; CA125 change, P = .002). Conclusion Olaparib has antitumor activity in BRCA1/2 mutation ovarian cancer, which is associated with platinum sensitivity.
引用
收藏
页码:2512 / 2519
页数:8
相关论文
共 29 条
[1]   Ovarian cancer: Strategies for overcoming resistance to chemotherapy [J].
Agarwal, R ;
Kaye, SB .
NATURE REVIEWS CANCER, 2003, 3 (07) :502-516
[2]  
[Anonymous], 2006, Cancer Therapy Evaluation Program, Common Terminology Criteria for Adverse Events, Version 3.0
[3]   A synthetic lethal therapeutic approach: Poly(ADP) ribose polymerase inhibitors for the treatment of cancers deficient in DNA double-strand break repair [J].
Ashworth, Alan .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (22) :3785-3790
[4]  
Audeh MW, 2009, J CLIN ONCOL, V27
[5]  
Baldwin RL, 2000, CANCER RES, V60, P5329
[6]   Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase [J].
Bryant, HE ;
Schultz, N ;
Thomas, HD ;
Parker, KM ;
Flower, D ;
Lopez, E ;
Kyle, S ;
Meuth, M ;
Curtin, NJ ;
Helleday, T .
NATURE, 2005, 434 (7035) :913-917
[7]   Resistance to therapy caused by intragenic deletion in BRCA2 [J].
Edwards, Stacey L. ;
Brough, Rachel ;
Lord, Christopher J. ;
Natrajan, Rachael ;
Vatcheva, Radost ;
Levine, Douglas A. ;
Boyd, Jeff ;
Reis-Filho, Jorge S. ;
Ashworth, Alan .
NATURE, 2008, 451 (7182) :1111-U8
[8]   Promoter hypermethylation and BRCA1 inactivation in sporadic breast and ovarian tumors [J].
Esteller, M ;
Silva, JM ;
Dominguez, G ;
Bonilla, F ;
Matias-Guiu, X ;
Lerma, E ;
Bussaglia, E ;
Prat, J ;
Harkes, IC ;
Repasky, EA ;
Gabrielson, E ;
Schutte, M ;
Baylin, SB ;
Herman, JG .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (07) :564-569
[9]   Probability of BRCA1/2 mutation varies with ovarian histology:: results from screening 442 ovarian cancer families [J].
Evans, D. G. R. ;
Young, K. ;
Bulman, M. ;
Shenton, A. ;
Wallace, A. ;
Lalloo, F. .
CLINICAL GENETICS, 2008, 73 (04) :338-345
[10]   Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy [J].
Farmer, H ;
McCabe, N ;
Lord, CJ ;
Tutt, ANJ ;
Johnson, DA ;
Richardson, TB ;
Santarosa, M ;
Dillon, KJ ;
Hickson, I ;
Knights, C ;
Martin, NMB ;
Jackson, SP ;
Smith, GCM ;
Ashworth, A .
NATURE, 2005, 434 (7035) :917-921