Defects in DNA Repair Genes Predict Response to Neoadjuvant Cisplatin-based Chemotherapy in Muscle-invasive Bladder Cancer

被引:409
作者
Plimack, Elizabeth R. [1 ]
Dunbrack, Roland L. [1 ]
Brennan, Timothy A. [2 ]
Andrake, Mark D. [1 ]
Zhou, Yan [1 ]
Serebriiskii, Ilya G. [1 ]
Slifker, Michael [1 ]
Alpaugh, Katherine [1 ]
Dulaimi, Essel [1 ]
Palma, Norma [2 ]
Hoffman-Censits, Jean [3 ]
Bilusic, Marijo [1 ]
Wong, Yu-Ning [1 ]
Kutikov, Alexander [1 ]
Viterbo, Rosalia [1 ]
Greenberg, Richard E. [1 ]
Chen, David Y. T. [1 ]
Lallas, Costas D. [3 ]
Trabulsi, Edouard J. [3 ]
Yelensky, Roman [2 ]
McConkey, David J. [4 ]
Miller, Vincent A. [2 ]
Golemis, Erica A. [1 ]
Ross, Eric A. [1 ]
机构
[1] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[2] Fdn Med Inc, Cambridge, MA USA
[3] Thomas Jefferson Univ Hosp, Philadelphia, PA 19107 USA
[4] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
关键词
Bladder cancer; Urothelial carcinoma; Biomarkers; Cisplatin sensitivity; Cisplatin resistance; ATM; RB1; FANCC; DNA repair; Neoadjuvant chemotherapy; DOUBLE-STRAND BREAKS; ANEMIA-BRCA PATHWAY; UROTHELIAL CARCINOMA; RESISTANCE; DAMAGE; METHOTREXATE; VINBLASTINE; DOXORUBICIN; CYSTECTOMY; MUTATIONS;
D O I
10.1016/j.eururo.2015.07.009
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Cisplatin-based neoadjuvant chemotherapy (NAC) before cystectomy is the standard of care for muscle-invasive bladder cancer (MIBC), with 25-50% of patients expected to achieve a pathologic response. Validated biomarkers predictive of response are currently lacking. Objective: To discover and validate biomarkers predictive of response to NAC for MIBC. Design, setting, and participants: Pretreatment MIBC samples prospectively collected from patients treated in two separate clinical trials of cisplatin-based NAC provided the discovery and validation sets. DNA from pretreatment tumor tissue was sequenced for all coding exons of 287 cancer-related genes and was analyzed for base substitutions, indels, copy number alterations, and selected rearrangements in a Clinical Laboratory Improvements Amendments-certified laboratory. Outcome measurements and statistical analysis: The mean number of variants and variant status for each gene were correlated with response. Variant data from the discovery cohort were used to create a classification tree to discriminate responders from nonresponders. The resulting decision rule was then tested in the independent validation set. Results and limitations: Patients with a pathologic complete response had more alterations than those with residual tumor in both the discovery (p = 0.024) and validation (p = 0.018) sets. In the discovery set, alteration in one or more of the three DNA repair genes ATM, RB1, and FANCC predicted pathologic response (p < 0.001; 87% sensitivity, 100% specificity) and better overall survival (p = 0.007). This test remained predictive for pathologic response in the validation set (p = 0.033), with a trend towards better overall survival (p = 0.055). These results require further validation in additional sample sets. Conclusions: Genomic alterations in the DNA repair-associated genes ATM, RB1, and FANCC predict response and clinical benefit after cisplatin-based chemotherapy for MIBC. The results suggest that defective DNA repair renders tumors sensitive to cisplatin. Patient summary: Chemotherapy given before bladder removal (cystectomy) improves the chance of cure for some but not all patients with muscle-invasive bladder cancer. We found a set of genetic mutations that when present in tumor tissue predict benefit from neoadjuvant chemotherapy, suggesting that testing before chemotherapy may help in selecting patients for whom this approach is recommended. (C) 2015 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:959 / 967
页数:9
相关论文
共 28 条
[1]   RB signaling prevents replication-dependent DNA double-strand breaks following genotoxic insult [J].
Bosco, EE ;
Mayhew, CN ;
Hennigan, RF ;
Sage, J ;
Jacks, T ;
Knudsen, ES .
NUCLEIC ACIDS RESEARCH, 2004, 32 (01) :25-34
[2]   The effects of deregulated DNA damage signalling on cancer chemotherapy response and resistance [J].
Bouwman, Peter ;
Jonkers, Jos .
NATURE REVIEWS CANCER, 2012, 12 (09) :587-598
[3]   Clinicopathological outcomes after radical cystectomy for clinical T2 urothelial carcinoma: further evidence to support the use of neoadjuvant chemotherapy [J].
Canter, Daniel ;
Long, Christopher ;
Kutikov, Alexander ;
Plimack, Elizabeth ;
Saad, Ismail ;
Oblaczynski, Megan ;
Zhu, Fang ;
Viterbo, Rosalia ;
Chen, David Y. T. ;
Uzzo, Robert G. ;
Greenberg, Richard E. ;
Boorjian, Stephen A. .
BJU INTERNATIONAL, 2011, 107 (01) :58-62
[4]   Chemosensitization to cisplatin by inhibitors of the Fanconi anemia/BRCA pathway [J].
Chirnomas, D ;
Taniguchi, T ;
de la Vega, M ;
Vaidya, AP ;
Vasserman, M ;
Hartman, AR ;
Kennedy, R ;
Foster, R ;
Mahoney, J ;
Seiden, MV ;
D'Andrea, AD .
MOLECULAR CANCER THERAPEUTICS, 2006, 5 (04) :952-961
[5]   Identification of Distinct Basal and Luminal Subtypes of Muscle-Invasive Bladder Cancer with Different Sensitivities to Frontline Chemotherapy [J].
Choi, Woonyoung ;
Porten, Sima ;
Kim, Seungchan ;
Willis, Daniel ;
Plimack, Elizabeth R. ;
Hoffman-Censits, Jean ;
Roth, Beat ;
Cheng, Tiewei ;
Mai Tran ;
Lee, I-Ling ;
Melquist, Jonathan ;
Bondaruk, Jolanta ;
Majewski, Tadeusz ;
Zhang, Shizhen ;
Pretzsch, Shanna ;
Baggerly, Keith ;
Siefker-Radtke, Arlene ;
Czerniak, Bogdan ;
Dinney, Colin P. N. ;
McConkey, David J. .
CANCER CELL, 2014, 25 (02) :152-165
[6]   Neoadjuvant Dose-Dense Methotrexate, Vinblastine, Doxorubicin, and Cisplatin With Pegfilgrastim Support in Muscle-Invasive Urothelial Cancer: Pathologic, Radiologic, and Biomarker Correlates [J].
Choueiri, Toni K. ;
Jacobus, Susanna ;
Bellmunt, Joaquim ;
Qu, Angela ;
Appleman, Leonard J. ;
Tretter, Christopher ;
Bubley, Glenn J. ;
Stack, Edward C. ;
Signoretti, Sabina ;
Walsh, Meghara ;
Steele, Graeme ;
Hirsch, Michelle ;
Sweeney, Christopher J. ;
Taplin, Mary-Ellen ;
Kibel, Adam S. ;
Krajewski, Katherine M. ;
Kantoff, Philip W. ;
Ross, Robert W. ;
Rosenberg, Jonathan E. .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (18) :1889-1894
[7]   The DNA Damage Response: Making It Safe to Play with Knives [J].
Ciccia, Alberto ;
Elledge, Stephen J. .
MOLECULAR CELL, 2010, 40 (02) :179-204
[8]   The Fanconi anaemia BRCA pathway [J].
D'Andrea, AD ;
Grompe, M .
NATURE REVIEWS CANCER, 2003, 3 (01) :23-34
[9]   Molecular mechanisms of cisplatin resistance [J].
Galluzzi, L. ;
Senovilla, L. ;
Vitale, I. ;
Michels, J. ;
Martins, I. ;
Kepp, O. ;
Castedo, M. ;
Kroemer, G. .
ONCOGENE, 2012, 31 (15) :1869-1883
[10]   Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing [J].
Gnirke, Andreas ;
Melnikov, Alexandre ;
Maguire, Jared ;
Rogov, Peter ;
LeProust, Emily M. ;
Brockman, William ;
Fennell, Timothy ;
Giannoukos, Georgia ;
Fisher, Sheila ;
Russ, Carsten ;
Gabriel, Stacey ;
Jaffe, David B. ;
Lander, Eric S. ;
Nusbaum, Chad .
NATURE BIOTECHNOLOGY, 2009, 27 (02) :182-189