TY - JOUR
T1 - Testicular Cancer Survivorship
T2 - Research Strategies and Recommendations
AU - Travis, Lois B.
AU - Beard, Clair
AU - Allan, James M.
AU - Dahl, Alv A.
AU - Feldman, Darren R.
AU - Oldenburg, Jan
AU - Daugaard, Gedske
AU - Kelly, Jennifer L.
AU - Dolan, M. Eileen
AU - Hannigan, Robyn
AU - Constine, Louis S.
AU - Oeffinger, Kevin C.
AU - Okunieff, Paul
AU - Armstrong, Greg
AU - Wiljer, David
AU - Miller, Robert C.
AU - Gietema, Jourik A.
AU - van Leeuwen, Flora E.
AU - Williams, Jacqueline P.
AU - Nichols, Craig R.
AU - Einhorn, Lawrence H.
AU - Fossa, Sophie D.
PY - 2010/8/4
Y1 - 2010/8/4
N2 - Testicular cancer represents the most curable solid tumor, with a 10-year survival rate of more than 95%. Given the young average age at diagnosis, it is estimated that effective treatment approaches, in particular, platinum-based chemotherapy, have resulted in an average gain of several decades of life. This success, however, is offset by the emergence of considerable long-term morbidity, including second malignant neoplasms, cardiovascular disease, neurotoxicity, nephrotoxicity, pulmonary toxicity, hypogonadism, decreased fertility, and psychosocial problems. Data on underlying genetic or molecular factors that might identify those patients at highest risk for late sequelae are sparse. Genome-wide association studies and other translational molecular approaches now provide opportunities to identify testicular cancer survivors at greatest risk for therapy-related complications to develop evidence-based long-term follow-up guidelines and interventional strategies. We review research priorities identified during an international workshop devoted to testicular cancer survivors. Recommendations include 1) institution of lifelong follow-up of testicular cancer survivors within a large cohort setting to ascertain risks of emerging toxicities and the evolution of known late sequelae, 2) development of comprehensive risk prediction models that include treatment factors and genetic modifiers of late sequelae, 3) elucidation of the effect(s) of decades-long exposure to low serum levels of platinum, 4) assessment of the overall burden of medical and psychosocial morbidity, and 5) the eventual formulation of evidence-based long-term follow-up guidelines and interventions. Just as testicular cancer once served as the paradigm of a curable malignancy, comprehensive follow-up studies of testicular cancer survivors can pioneer new methodologies in survivorship research for all adult-onset cancer. J Natl Cancer Inst 2010; 102: 1114-1130
AB - Testicular cancer represents the most curable solid tumor, with a 10-year survival rate of more than 95%. Given the young average age at diagnosis, it is estimated that effective treatment approaches, in particular, platinum-based chemotherapy, have resulted in an average gain of several decades of life. This success, however, is offset by the emergence of considerable long-term morbidity, including second malignant neoplasms, cardiovascular disease, neurotoxicity, nephrotoxicity, pulmonary toxicity, hypogonadism, decreased fertility, and psychosocial problems. Data on underlying genetic or molecular factors that might identify those patients at highest risk for late sequelae are sparse. Genome-wide association studies and other translational molecular approaches now provide opportunities to identify testicular cancer survivors at greatest risk for therapy-related complications to develop evidence-based long-term follow-up guidelines and interventional strategies. We review research priorities identified during an international workshop devoted to testicular cancer survivors. Recommendations include 1) institution of lifelong follow-up of testicular cancer survivors within a large cohort setting to ascertain risks of emerging toxicities and the evolution of known late sequelae, 2) development of comprehensive risk prediction models that include treatment factors and genetic modifiers of late sequelae, 3) elucidation of the effect(s) of decades-long exposure to low serum levels of platinum, 4) assessment of the overall burden of medical and psychosocial morbidity, and 5) the eventual formulation of evidence-based long-term follow-up guidelines and interventions. Just as testicular cancer once served as the paradigm of a curable malignancy, comprehensive follow-up studies of testicular cancer survivors can pioneer new methodologies in survivorship research for all adult-onset cancer. J Natl Cancer Inst 2010; 102: 1114-1130
KW - LONG-TERM SURVIVORS
KW - GERM-CELL-CANCER
KW - QUALITY-OF-LIFE
KW - SINGLE NUCLEOTIDE POLYMORPHISMS
KW - CISPLATIN-INDUCED CYTOTOXICITY
KW - GENOME-WIDE ASSOCIATION
KW - CORONARY-ARTERY-DISEASE
KW - ETOPOSIDE-INDUCED CYTOTOXICITY
KW - PATIENTS RECEIVING CISPLATIN
KW - RANDOMIZED CONTROLLED-TRIAL
U2 - 10.1093/jnci/djq216
DO - 10.1093/jnci/djq216
M3 - Editorial
SN - 0027-8874
VL - 102
SP - 1114
EP - 1130
JO - JOURNAL OF THE NATIONAL CANCER INSTITUTE
JF - JOURNAL OF THE NATIONAL CANCER INSTITUTE
IS - 15
ER -