TY - JOUR
T1 - Multi-institutional assessment of adverse health outcomes among north American testicular cancer survivors after modern cisplatin-based chemotherapy
AU - Platinum Study Group
AU - Fung, Chunkit
AU - Sesso, Howard D.
AU - Williams, Annalynn M.
AU - Kerns, Sarah L.
AU - Monahan, Patrick
AU - Zaid, Mohammad Abu
AU - Feldman, Darren R.
AU - Hamilton, Robert J.
AU - Vaughn, David J.
AU - Beard, Clair J.
AU - Kollmannsberger, Christian K.
AU - Cook, Ryan
AU - Althouse, Sandra
AU - Ardeshir-Rouhani-Fard, Shirin
AU - Lipshultz, Steve E.
AU - Einhorn, Lawrence H.
AU - Fossa, Sophie D.
AU - Travis, Lois B.
AU - Curreri, Stephanie
AU - Brames, Mary Jacqueline
AU - Norton, Kelli
AU - Jacobsen, Erin
AU - Silber, Deborah
AU - Anson-Cartwright, Lynn
AU - Cox, Nancy J.
AU - Dolan, M. Eileen
AU - Jacobs, Linda
AU - Panzer, Sarah Lena
AU - Pucci, Donna
AU - Baker, Debbie
AU - Casaceli, Cindy
AU - Johnson, Eileen
AU - Sahasrabudhe, Deepak
AU - Frisina, Robert D.
AU - Bosl, George
AU - Gospodarowicz, Mary
AU - Robison, Leslie L.
N1 - Publisher Copyright:
© 2017 by American Society of Clinical Oncology.
PY - 2017/4/10
Y1 - 2017/4/10
N2 - Purpose To provide new information on adverse health outcomes (AHOs) in testicular cancer survivors (TCSs) after four cycles of etoposide and cisplatin (EPX4) or three or four cycles of bleomycin, etoposide, cisplatin (BEPX3/BEPX4). Methods Nine hundred fifty-two TCSs > 1 year postchemotherapy underwent physical examination and completed a questionnaire. Multinomial logistic regression estimated AHOs odds ratios (ORs) in relation to age, cumulative cisplatin and/or bleomycin dose, time since chemotherapy, sociodemographic factors, and health behaviors. Results Median age at evaluation was 37 years; median time since chemotherapy was 4.3 years. Chemotherapy consisted largely of BEPX3 (38.2%), EPX4 (30.9%), and BEPX4 (17.9%). None, one to two, three to four, or five or more AHOs were reported by 20.4%, 42.0%, 25.1%, and 12.5% of TCSs, respectively. Median number after EPX4 or BEPX3 was two (range, zero to nine and zero to 11, respectively; P > .05) and two (range, zero to 10) after BEPX4. When comparing individual AHOs for EPX4 versus BEPX3, Raynaud phenomenon (11.6% v 21.4%; P < .01), peripheral neuropathy (29.2% v 21.4%; P = .02), and obesity (25.5% v 33.0%; P = .04) differed. Larger cumulative bleomycin doses (OR, 1.44 per 90,000 IU) were significantly associated with five or more AHOs. Increasing age was a significant risk factor for one to two, three to four, or five or more AHOs versus zero AHOs (OR, 1.22, 1.50, and 1.87 per 5 years, respectively; P < .01); vigorous physical activity was protective (OR, 0.62, 0.51, and 0.41, respectively; P < .05). Significant risk factors for three to four and five or more AHOs included current (OR, 3.05 and 3.73) or former (OR, 1.61 and 1.76) smoking (P < .05). Self-reported health was excellent/very good in 59.9% of TCSs but decreased as AHOs increased (P < .001). Conclusion Numbers of AHOs after EPX4 or BEPX3 appear similar, with median follow-up of 4.3 years. A healthy lifestyle was associated with reduced number of AHOs.
AB - Purpose To provide new information on adverse health outcomes (AHOs) in testicular cancer survivors (TCSs) after four cycles of etoposide and cisplatin (EPX4) or three or four cycles of bleomycin, etoposide, cisplatin (BEPX3/BEPX4). Methods Nine hundred fifty-two TCSs > 1 year postchemotherapy underwent physical examination and completed a questionnaire. Multinomial logistic regression estimated AHOs odds ratios (ORs) in relation to age, cumulative cisplatin and/or bleomycin dose, time since chemotherapy, sociodemographic factors, and health behaviors. Results Median age at evaluation was 37 years; median time since chemotherapy was 4.3 years. Chemotherapy consisted largely of BEPX3 (38.2%), EPX4 (30.9%), and BEPX4 (17.9%). None, one to two, three to four, or five or more AHOs were reported by 20.4%, 42.0%, 25.1%, and 12.5% of TCSs, respectively. Median number after EPX4 or BEPX3 was two (range, zero to nine and zero to 11, respectively; P > .05) and two (range, zero to 10) after BEPX4. When comparing individual AHOs for EPX4 versus BEPX3, Raynaud phenomenon (11.6% v 21.4%; P < .01), peripheral neuropathy (29.2% v 21.4%; P = .02), and obesity (25.5% v 33.0%; P = .04) differed. Larger cumulative bleomycin doses (OR, 1.44 per 90,000 IU) were significantly associated with five or more AHOs. Increasing age was a significant risk factor for one to two, three to four, or five or more AHOs versus zero AHOs (OR, 1.22, 1.50, and 1.87 per 5 years, respectively; P < .01); vigorous physical activity was protective (OR, 0.62, 0.51, and 0.41, respectively; P < .05). Significant risk factors for three to four and five or more AHOs included current (OR, 3.05 and 3.73) or former (OR, 1.61 and 1.76) smoking (P < .05). Self-reported health was excellent/very good in 59.9% of TCSs but decreased as AHOs increased (P < .001). Conclusion Numbers of AHOs after EPX4 or BEPX3 appear similar, with median follow-up of 4.3 years. A healthy lifestyle was associated with reduced number of AHOs.
UR - https://www.scopus.com/pages/publications/85017304402
U2 - 10.1200/JCO.2016.70.3108
DO - 10.1200/JCO.2016.70.3108
M3 - Article
C2 - 28240972
AN - SCOPUS:85017304402
SN - 0732-183X
VL - 35
SP - 1211
EP - 1222
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 11
ER -