Literature DB >> 21282539

Randomized trial of carboplatin versus radiotherapy for stage I seminoma: mature results on relapse and contralateral testis cancer rates in MRC TE19/EORTC 30982 study (ISRCTN27163214).

R Timothy D Oliver1, Graham M Mead, Gordon J S Rustin, Johnathan K Joffe, Nina Aass, Robert Coleman, Rhian Gabe, Philip Pollock, Sally P Stenning.   

Abstract

PURPOSE: Initial results of a randomized trial comparing carboplatin with radiotherapy (RT) as adjuvant treatment for stage I seminoma found carboplatin had a noninferior relapse-free rate (RFR) and had reduced contralateral germ cell tumors (GCTs) in the short-term. Updated results with a median follow-up of 6.5 years are now reported. PATIENTS AND METHODS: Random assignment was between RT and one infusion of carboplatin dosed at 7 × (glomerular filtration rate + 25) on the basis of EDTA (n = 357) and 90% of this dose if determined on the basis of creatinine clearance (n = 202). The trial was powered to exclude a doubling in RFRs assuming a 96-97% 2-year RFR after radiotherapy (hazard ratio [HR], approximately 2.0).
RESULTS: Overall, 1,447 patients were randomly assigned in a 3-to-5 ratio (carboplatin, n = 573; RT, n = 904). RFRs at 5 years were 94.7% for carboplatin and 96.0% for RT (RT-C 90% CI, 0.7% to 3.5%; HR, 1.25; 90% CI, 0.83 to 1.89). One death as a result of seminoma (in RT arm) occurred. Patients receiving at least 99% of the 7 × AUC dose had a 5-year RFR of 96.1% (95% CI, 93.4% to 97.7%) compared with 92.6% (95% CI, 88.0% to 95.5%) in those who received lower doses (HR, 0.51; 95% CI, 0.24 to 1.07; P = .08). There was a clear reduction in the rate of contralateral GCTs (carboplatin, n = 2; RT, n = 15; HR, 0.22; 95% CI, 0.05 to 0.95; P = .03), and elevated pretreatment follicle-stimulating hormone (FSH) levels (> 12 IU/L) was a strong predictor (HR, 8.57; 95% CI, 1.82 to 40.38).
CONCLUSION: These updated results confirm the noninferiority of single dose carboplatin (at 7 × AUC dose) versus RT in terms of RFR and establish a statistically significant reduction in the medium term of risk of second GCT produced by this treatment.

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Year:  2011        PMID: 21282539     DOI: 10.1200/JCO.2009.26.4655

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  50 in total

1.  Testicular cancer: Optimal management of stage I seminoma in 2015.

Authors:  Guy C Toner
Journal:  Nat Rev Urol       Date:  2015-04-21       Impact factor: 14.432

Review 2.  Estimation of Kidney Function in Oncology: Implications for Anticancer Drug Selection and Dosing.

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3.  Controversies in the management of stage I seminoma: adjuvant carboplatin revisited.

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4.  [Risk of second malignancies after platinum-based chemotherapy of testicular cancer].

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Review 5.  [Diagnosis, treatment and follow-up of testicular cancer].

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6.  Controversies in the Management of Clinical Stage I Seminoma: Carboplatin a Decade in-Time to Start Backing Out.

Authors:  Rune A W van de Wetering; Stefan Sleijfer; Darren R Feldman; Samuel A Funt; George J Bosl; Ronald de Wit
Journal:  J Clin Oncol       Date:  2018-02-01       Impact factor: 44.544

7.  Surveillance policy for Japanese patients with stage I testicular germ cell cancer in the multi-detector computed tomography era.

Authors:  Takeshi Yuasa; Naoko Inoshita; Hajime Tanaka; Shinji Urakami; Shinya Yamamoto; Yasuhisa Fujii; Hitoshi Masuda; Iwao Fukui; Yuichi Ishikawa; Junji Yonese
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8.  Improving Carboplatin Dosing Based on Estimated GFR.

Authors:  Jan H Beumer; Lesley A Inker; Andrew S Levey
Journal:  Am J Kidney Dis       Date:  2017-12-06       Impact factor: 8.860

Review 9.  Testicular cancer: germ cell tumours.

Authors:  Peter Chung; Padraig Warde
Journal:  BMJ Clin Evid       Date:  2016-01-07

10.  A comparison of measured and estimated glomerular filtration rate for carboplatin dose calculation in stage I testicular seminoma.

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