Journal of Clinical Oncology, Vol 23, No 6 (February 20), 2005: pp. 1200-1208
© 2005 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2005.08.003
Randomized Trial of 30 Versus 20 Gy in the Adjuvant Treatment of Stage I Testicular Seminoma: A Report on Medical Research Council Trial TE18, European Organisation for the Research and Treatment of Cancer Trial 30942 (ISRCTN18525328)
William G. Jones,
Sophie D. Fossa,
Graham M. Mead,
J. Trevor Roberts,
Michael Sokal,
Alan Horwich,
Sally P. Stenning
From the Cookridge Hospital, Leeds; Southampton General Hospital, Southampton; Northern Centre for Cancer Treatment, Newcastle upon Tyne; Nottingham City Hospital, Nottingham; Royal Marsden Hospital, Sutton; MRC Clinical Trials Unit, London, United Kingdom; and Norwegian Radium Hospital, Oslo, Norway, on behalf of the Medical Research Council Testicular Tumour Working Party (now NCRI Testis Cancer Clinical Studies Group) and the European Organisation for Research and Treatment of Cancer Genitourinary Cancer Group
Address reprint requests to Sally P. Stenning, MSc, TE18 Trial, MRC Clinical Trials Unit, Cancer Division, 222 Euston Rd, London, NW1 2DA United Kingdom; e-mail: TE18{at}ctu.mrc.ac.uk
PURPOSE: To assess the possibility of reducing radiotherapy doses without compromising efficacy in the management of patients with stage I seminoma.
PATIENTS AND METHODS: Patients were randomly assigned 20 Gy/10 fractions over 2 weeks or 30 Gy/15 fractions during 3 weeks after orchidectomy. They completed a symptom diary card during treatment and quality-of-life forms pre- and post-treatment. The trial was powered to exclude absolute differences in 2-year relapse rates of 3% to 4% ( = .05 [one sided]; 90% power).
RESULTS: From 1995 to 1998, 625 patients were randomly assigned to treatment. Four weeks after starting radiotherapy, significantly more patients receiving 30 Gy reported moderate or severe lethargy (20% v 5%) and an inability to carry out their normal work (46% v 28%). However, by 12 weeks, levels in both groups were similar. With a median follow-up of 61 months, 10 and 11 relapses, respectively, have been reported in the 30- and 20-Gy groups (hazard ratio, 1.11; 90% CI, 0.54 to 2.28). The absolute difference in 2-year relapse rates is 0.7%; the lower 90% confidence limit is 2.9%. Only one patient has died from seminoma (allocated to the 20-Gy treatment group).
CONCLUSION: Treatment with 20 Gy in 10 fractions is unlikely to produce relapse rates more than 3% higher than for standard 30 Gy radiation therapy, and data on an additional 469 patients randomly assigned in a subsequent trial support and strengthen these results. Reductions in morbidity enable patients to return to work more rapidly. Prolonged follow-up is required before any inference can be made about any impact of allocated treatment on new primary cancer diagnoses.
Support for central trial coordination was provided through core funding from the Medical Research Council, London, United Kingdom.
Presented in part at 5th International Germ Cell Tumour Conference, Leeds, United Kingdom, September 13-15, 2001; European Cancer Conference (ECCO) 11, Lisbon, Portugal, October 21-25, 2001, and the 38th Annual Meeting of the American Society of Clinical Oncology, May 18-21, 2002, Orlando, FL.
Authors' disclosures of potential conflicts of interest are found at the end of this article.

CiteULike Complore Connotea Del.icio.us Digg Facebook Reddit Technorati Twitter What's this?
This article has been cited by other articles:

|
 |

|
 |
 
H.-J. Schmoll, K. Jordan, R. Huddart, M. P. Laguna, A. Horwich, K. Fizazi, V. Kataja, and On behalf of the ESMO Guidelines Working Group
Testicular seminoma: ESMO Clinical Recommendations for diagnosis, treatment and follow-up
Ann. Onc.,
May 1, 2009;
20(suppl_4):
iv83 - iv88.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
X. Garcia-del-Muro, P. Maroto, J. Guma, J. Sastre, M. Lopez Brea, J. A. Arranz, N. Lainez, D. S. de Prado, J. Aparicio, J. M. Piulats, et al.
Chemotherapy As an Alternative to Radiotherapy in the Treatment of Stage IIA and IIB Testicular Seminoma: A Spanish Germ Cell Cancer Group Study
J. Clin. Oncol.,
November 20, 2008;
26(33):
5416 - 5421.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T. Powles, D. Robinson, J. Shamash, H. Moller, N. Tranter, and T. Oliver
The long-term risks of adjuvant carboplatin treatment for stage I seminoma of the testis
Ann. Onc.,
March 1, 2008;
19(3):
443 - 447.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Schairer, M. Hisada, B. E. Chen, L. M. Brown, R. Howard, S. D. Fossa, M. Gail, and L. B. Travis
Comparative Mortality for 621 Second Cancers in 29356 Testicular Cancer Survivors and 12420 Matched First Cancers
J Natl Cancer Inst,
August 15, 2007;
99(16):
1248 - 1256.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. D. Fossa, E. Gilbert, G. M. Dores, J. Chen, K. A. McGlynn, S. Schonfeld, H. Storm, P. Hall, E. Holowaty, A. Andersen, et al.
Noncancer Causes of Death in Survivors of Testicular Cancer
J Natl Cancer Inst,
April 4, 2007;
99(7):
533 - 544.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. de Wit and K. Fizazi
Controversies in the Management of Clinical Stage I Testis Cancer
J. Clin. Oncol.,
December 10, 2006;
24(35):
5482 - 5492.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T. Oliver, G. Mead, M. Mason, S. Stenning, K. Dieckmann, H. Steiner, M. De Santis, J. Aparicio, I. Skoneczna, and C. Kratzik
The Sword of Damocles and the Treatment of Stage I Seminoma
J. Clin. Oncol.,
June 1, 2006;
24(16):
2599 - 2600.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. J. Loehrer Sr and G. J. Bosl
Carboplatin for Stage I Seminoma and the Sword of Damocles
J. Clin. Oncol.,
December 1, 2005;
23(34):
8566 - 8569.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Aparicio, J. R. Germa, X. G. del Muro, P. Maroto, J. A. Arranz, A. Saenz, A. Barnadas, J. Dorca, J. Guma, D. Olmos, et al.
Risk-Adapted Management for Patients With Clinical Stage I Seminoma: The Second Spanish Germ Cell Cancer Cooperative Group Study
J. Clin. Oncol.,
December 1, 2005;
23(34):
8717 - 8723.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Saxman
Doctor ... Will I Still Be Able To Have Children?
J Natl Cancer Inst,
November 2, 2005;
97(21):
1557 - 1559.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Brydoy, S. D. Fossa, O. Klepp, R. M. Bremnes, E. A. Wist, T. Wentzel-Larsen, and O. Dahl
Paternity Following Treatment for Testicular Cancer
J Natl Cancer Inst,
November 2, 2005;
97(21):
1580 - 1588.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
L. B. Travis, S. D. Fossa, S. J. Schonfeld, M. L. McMaster, C. F. Lynch, H. Storm, P. Hall, E. Holowaty, A. Andersen, E. Pukkala, et al.
Second Cancers Among 40 576 Testicular Cancer Patients: Focus on Long-term Survivors
J Natl Cancer Inst,
September 21, 2005;
97(18):
1354 - 1365.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Chan
Randomized Trial of 30 Versus 20 Gy in the Adjuvant Treatment of Stage I Testicular Seminoma: A Report on Medical Research Council Trial TE18, European Organisation for Research and Treatment of Cancer Trial 30942 (ISRCTN18525328)
J. Clin. Oncol.,
September 20, 2005;
23(27):
6806 - 6806.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S.P. Stenning, W.G. Jones, and S.D. Fossa
In Reply:
J. Clin. Oncol.,
September 20, 2005;
23(27):
6806 - 6807.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. J. Dignam
Early Viewing of Noninferiority Trials in Progress
J. Clin. Oncol.,
August 20, 2005;
23(24):
5461 - 5463.
[Full Text]
[PDF]
|
 |
|
|