TY - JOUR
T1 - A Statistical Approach to Determine the Optimal Duration of Post-Treatment Follow-Up
T2 - Application to Metastatic Nonseminomatous Germ Cell Tumors
AU - Somda, Serge M.A.
AU - Culine, Stéphane
AU - Chevreau, Christine
AU - Fizazi, Karim
AU - Leconte, Eve
AU - Kramar, Andrew
AU - Filleron, Thomas
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - As the number of patients in cancer remission increases every year, an economically attractive option is to reduce duration of follow-up according to prognostic factors. In the present study we propose a statistical method to define an optimal duration of follow-up for patients in remission after treatment for cancer, for detection of recurrences. Background The objective of this study was to present a statistical method to define an optimal duration of follow-up for patients in remission after treatment for cancer, for detection of recurrences. Patients and Methods Surveillance duration was estimated using the 2-step approach proposed by Mould et al. Relapse-free interval was modeled using the parametric cure model proposed by Boag. The optimal length of follow-up was then estimated as the minimal elapsed time after which the probability of a patient to relapse and to be cured with success is below a given threshold value. The method is applied to 2 real data sets of patients treated for metastatic non seminomatous germ-cell tumors: T93BP and T93MP. Results For the T93BP, cure rate was estimated at 91.3% and proportions of patients who relapsed after 3 and 5 years were estimated at 0.5% and 0.2%. With a probability of success of salvage treatment equal to 80% and 50%, numbers of delayed cases after 5 years were 2 and 1. For T93MP, the proportion of patients who presented relapse after 5 and 10 years were estimated at 5.2% and 2.6%. Considering a probability of salvage treatment equal to 20%, the number of delayed cases after 5 and 10 years were 10 and 5. Conclusion Using this methodology, duration of post-therapeutic follow-up might be tailored according to an objective criteria: the number of patients who present relapse after the end of follow-up and who could have been treated with success in case of early detection.
AB - As the number of patients in cancer remission increases every year, an economically attractive option is to reduce duration of follow-up according to prognostic factors. In the present study we propose a statistical method to define an optimal duration of follow-up for patients in remission after treatment for cancer, for detection of recurrences. Background The objective of this study was to present a statistical method to define an optimal duration of follow-up for patients in remission after treatment for cancer, for detection of recurrences. Patients and Methods Surveillance duration was estimated using the 2-step approach proposed by Mould et al. Relapse-free interval was modeled using the parametric cure model proposed by Boag. The optimal length of follow-up was then estimated as the minimal elapsed time after which the probability of a patient to relapse and to be cured with success is below a given threshold value. The method is applied to 2 real data sets of patients treated for metastatic non seminomatous germ-cell tumors: T93BP and T93MP. Results For the T93BP, cure rate was estimated at 91.3% and proportions of patients who relapsed after 3 and 5 years were estimated at 0.5% and 0.2%. With a probability of success of salvage treatment equal to 80% and 50%, numbers of delayed cases after 5 years were 2 and 1. For T93MP, the proportion of patients who presented relapse after 5 and 10 years were estimated at 5.2% and 2.6%. Considering a probability of salvage treatment equal to 20%, the number of delayed cases after 5 and 10 years were 10 and 5. Conclusion Using this methodology, duration of post-therapeutic follow-up might be tailored according to an objective criteria: the number of patients who present relapse after the end of follow-up and who could have been treated with success in case of early detection.
KW - Cure model
KW - Delayed cases
KW - Log-normal
KW - Salvage treatment
KW - Testis
UR - http://www.scopus.com/inward/record.url?scp=84994077983&partnerID=8YFLogxK
U2 - 10.1016/j.clgc.2016.07.023
DO - 10.1016/j.clgc.2016.07.023
M3 - Article
C2 - 27594552
AN - SCOPUS:84994077983
SN - 1558-7673
VL - 15
SP - 230
EP - 236
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
IS - 2
ER -