Incidence of Severe Nephrotoxicity With Cisplatin Based on Renal Function Eligibility Criteria Indirect Comparison Meta-analysis

被引:14
作者
Dahal, Arati [1 ]
Bellows, Brandon K. [2 ]
Sonpavde, Guru [4 ]
Tantravahi, Srinivas K. [3 ]
Choueiri, Toni K. [5 ,6 ]
Galsky, Matthew D. [7 ]
Agarwal, Neeraj [3 ]
机构
[1] Univ Washington, Sch Publ Hlth, Dept Hlth Serv, Seattle, WA 98195 USA
[2] Univ Utah, Pharmacotherapy Outcomes Res Ctr, 2000 Circle Hope,Ste 2123, Salt Lake City, UT 84112 USA
[3] Univ Utah, Huntsman Canc Inst, 2000 Circle Hope,Ste 2123, Salt Lake City, UT 84112 USA
[4] UAB Comprehens Canc Ctr, Birmingham, AL USA
[5] Brigham & Womens Hosp, Dana Farber Canc Inst, 75 Francis St, Boston, MA 02115 USA
[6] Harvard Med Sch, Boston, MA USA
[7] Mt Sinai Med Ctr, Mt Sinai Sch Med, Tisch Canc Inst, New York, NY 10029 USA
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 2016年 / 39卷 / 05期
关键词
meta-analysis; cisplatin; cancer; nephrotoxicity; indirect comparison; CELL LUNG-CANCER; RANDOMIZED PHASE-II; GEMCITABINE PLUS CISPLATIN; ONCOLOGY-GROUP; 1ST-LINE TREATMENT; CONTINUOUS-INFUSION; CLINICAL-TRIALS; BREAST-CANCER; MITOMYCIN-C; CHEMOTHERAPY;
D O I
10.1097/COC.0000000000000081
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The objective of this meta-analysis was to indirectly compare incidence of nephrotoxicity in trials using cisplatin (CIS) for treatment of solid tumors when renal function was assessed using serum creatinine (SCr) or creatinine clearance (CrCl) for eligibility criteria. Methods: Randomized trials comparing CIS-containing with non-CIS-containing chemotherapy regimens were identified in PubMed. Included studies were performed from 1990 to 2010, used SCr or CrCl as an eligibility criterion, and reported incidence of grade >= 3 nephrotoxicity for both treatment arms using World Health Organization (WHO) or National Cancer Institute (NCI) toxicity criteria. The relative risk (RR) of grade >= 3 nephrotoxicity associated with CIS versus non-CIS regimens was examined. Subgroup analyses, adjusted indirect comparison, and metaregression were used to compare SCr and CrCl. Results: The literature search identified 2359 studies, 42 studies met all the inclusion criteria (N=9521 patients). SCr was used as an eligibility criterion in 20 studies (N=4704), CrCI was used in 9 studies (N=1650), and either was used in 13 studies (N=3167). The overall RR for developing nephrotoxicity with CIS versus non-CIS treatment was 1.75 (P=0.005). Subgroup analyses showed an increased risk when SCr was used (RR= 2.60, P=0.005) but not when CrCl was used (RR= 1.50, P=0.19). Both the adjusted indirect comparison and metaregression showed a nonsignificantly reduced risk of nephrotoxicity when CrCl was used. Conclusions: CIS-based therapy was associated with a significant increase in severe nephrotoxicity. The risk of severe nephrotoxicity appears to be lower when CrCl was used to determine whether people should be treated with CIS.
引用
收藏
页码:497 / 506
页数:10
相关论文
共 66 条
[1]   Phase III trial in metastatic gastroesophageal adenocarcinoma with fluorouracil, leucovorin plus either oxaliplatin or cisplatin:: A study of the arbeitsgemeinschaft internistische onkologie [J].
Al-Batran, Salah-Eddin ;
Hartmann, Joerg Thomas ;
Probst, Stephan ;
Schmalenberg, Harald ;
Hollerbach, Stephan ;
Hofheinz, Ralf ;
Rethwisch, Volker ;
Seipelt, Gernot ;
Homann, Nils ;
Wilhelm, Gerhard ;
Schuch, Gunter ;
Stoehlmacher, Jan ;
Derigs, Hans Guenter ;
Hegewisch-Becker, Susanna ;
Grossmann, Johannes ;
Pauligk, Claudia ;
Atmaca, Akin ;
Bokemeyer, Carsten ;
Knuth, Alexander ;
Jaeger, Elke .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (09) :1435-1442
[2]   Statistics Notes - Interaction revisited: the difference between two estimates [J].
Altman, DG ;
Bland, JM .
BMJ-BRITISH MEDICAL JOURNAL, 2003, 326 (7382) :219-219
[3]   Temozolomide and cisplatin versus temozolomide in patients with advanced melanoma: a randomized phase II study of the Hellenic Cooperative Oncology Group [J].
Bafaloukos, D ;
Tsoutsos, D ;
Kalofonos, H ;
Chalkidou, S ;
Panagiotou, P ;
Linardou, E ;
Briassoulis, E ;
Efstathiou, E ;
Polyzos, A ;
Fountzilas, G ;
Christodoulou, C ;
Kouroussis, C ;
Iconomou, T ;
Gogas, H .
ANNALS OF ONCOLOGY, 2005, 16 (06) :950-957
[4]   Cisplatin-vindesine-mitomycin (MVP) vs cisplatin-ifosfamide-vinorelbine (PIN) vs carboplatin-vinorelbine (CaN) in patients with advanced non-small-cell lung cancer (NSCLC): a FONICAP randomized phase II study [J].
Baldini, E ;
Tibaldi, C ;
Ardizzoni, A ;
Salvati, F ;
Antilli, A ;
Portalone, L ;
Barbera, S ;
Romano, F ;
De Marinis, F ;
Migliorino, MR ;
Noseda, MA ;
Borghini, U ;
Crippa, M ;
Ferrara, G ;
Raimondi, M ;
Fioretti, M ;
Bandera, M ;
Pennucci, MC ;
Galeasso, G ;
Cacciani, GC ;
Lepidini, G ;
Sunseri, G ;
Lanfranco, C ;
Rinaldi, M ;
Lionetto, R ;
Conte, PF ;
Rosso, R .
BRITISH JOURNAL OF CANCER, 1998, 77 (12) :2367-2370
[5]   Time to progression in metastatic breast cancer patients treated with epirubicin is not improved by the addition of either cisplatin or lonidamine: Final results of a phase III study with a factorial design [J].
Berruti, A ;
Bitossi, R ;
Gorzegno, G ;
Bottini, A ;
Alquati, P ;
De Matteis, A ;
Nuzzo, F ;
Giardina, G ;
Danese, S ;
De Lena, M ;
Lorusso, V ;
Farris, A ;
Sarobba, MG ;
DeFabiani, E ;
Bonazzi, G ;
Castiglione, F ;
Bumma, C ;
Moro, G ;
Bruzzi, P ;
Dogliotti, L .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (20) :4150-4159
[6]   Docetaxel/gemcitabine or cisplatin/gemcitabine followed by docetaxel in the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC):: results of a multicentre randomized phase II trial [J].
Binder, D. ;
Schweisfurth, H. ;
Grah, C. ;
Schaeper, C. ;
Temmesfeld-Wollbrueck, B. ;
Siebert, G. ;
Suttorp, N. ;
Beinert, T. .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2007, 60 (01) :143-150
[7]   A phase III trial of docetaxel/carboplatin versus mitomycin C/ifosfamide/cisplatin (MIC) or mitomycin C/vinblastine/cisplatin (MVP) in patients with advanced non-small-cell lung cancer: a randomised multicentre trial of the British Thoracic Oncology Group (BTOG1) [J].
Booton, R. ;
Lorigan, P. ;
Anderson, H. ;
Baka, S. ;
Ashcroft, L. ;
Nicolson, M. ;
O'Brien, M. ;
Dunlop, D. ;
O'Byrne, K. ;
Laurence, V. ;
Snee, M. ;
Dark, G. ;
Thatcher, N. .
ANNALS OF ONCOLOGY, 2006, 17 (07) :1111-1119
[8]   Efficacy of platinum-based regimens in non-small cell lung cancer. A negative report from the Cuneo lung cancer study group [J].
Buccheri, G ;
Ferrigno, D .
LUNG CANCER, 1997, 18 (01) :57-70
[9]   The results of direct and indirect treatment comparisons in meta-analysis of randomized controlled trials [J].
Bucher, HC ;
Guyatt, GH ;
Griffith, LE ;
Walter, SD .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1997, 50 (06) :683-691
[10]   Phase III multicenter randomized trial of the dartmouth regimen versus dacarbazine in patients with metastatic melanoma [J].
Chapman, PB ;
Einhorn, LH ;
Meyers, ML ;
Saxman, S ;
Destro, AN ;
Panageas, KS ;
Begg, CB ;
Agarwala, SS ;
Schuchter, LM ;
Ernstoff, MS ;
Houghton, AN ;
Kirkwood, JM .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (09) :2745-2751