TY - JOUR
T1 - Oxaliplatin-Induced Peripheral Neuropathy and Identification of Unique Severity Groups in Colorectal Cancer
AU - Griffith, Kathleen A.
AU - Zhu, Shijun
AU - Johantgen, Meg
AU - Kessler, Michael D.
AU - Renn, Cynthia
AU - Beutler, Andreas S.
AU - Kanwar, Rahul
AU - Ambulos, Nicholas
AU - Cavaletti, Guido
AU - Bruna, Jordi
AU - Briani, Chiara
AU - Argyriou, Andreas A.
AU - Kalofonos, Haralabos P.
AU - Yerges-Armstrong, Laura M.
AU - Dorsey, Susan G.
N1 - Funding Information:
This work was supported by the National Institutes of Health (P30NR014129 to SGD), National Institutes of Health (K01HL116770 to LMYA), and FondazioneCariplo (2013-0842 to G. C.). K. A.G. holds a TNSc copyright. When licensed, she is paid royalties. There was no license for its use in this study. TNSc is copyrighted by Johns Hopkins University. The authors declare no conflicts of interest.
Publisher Copyright:
© 2017 American Academy of Hospice and Palliative Medicine
PY - 2017/11
Y1 - 2017/11
N2 - Context: Oxaliplatin-induced peripheral neuropathy (OIPN) is a dose-limiting toxicity of oxaliplatin and affects most colorectal cancer patients. OIPN is commonly evaluated by patient symptom report, using scales to reflect impairment. They do not discriminate between unique grouping of symptoms and signs, which impedes prompt identification of OIPN. Objective: The objective of this study was to identify clusters of symptoms and signs that differentiated underlying clinical severity and segregated patients within our population into OIPN subgroups. Methods: Chemotherapy-naive colorectal cancer patients (N = 148) receiving oxaliplatin were administered the Total Neuropathy Score clinical (TNSc©), which includes symptom report (sensory, motor, autonomic) and sensory examination (pin sense, vibration, reflexes). The TNSc was administered before chemotherapy initiation (T0) and after cumulative doses of oxaliplatin 510–520 mg/m2 (T1) and 1020–1040 mg/m2 of oxaliplatin (T2). Using mean T2 TNSc scores, latent class analysis grouped patients into OIPN severity cohorts. Results: Latent class analysis categorized patients into four distinct OIPN groups: low symptoms and low signs (n = 54); low symptoms and intermediate signs (n = 44); low symptoms and high signs (n = 21); and high symptoms and high signs (n = 29). No differences were noted among OIPN groups on age, sex, chemotherapy regimen, or cumulative oxaliplatin dose. Conclusion: We identified OIPN patient groups with distinct symptoms/signs, demonstrating variability of OIPN presentation regardless of cumulative oxaliplatin dose. Over half of the sample had positive findings on OIPN examination despite little or no symptoms. Sensory examination of all patients receiving oxaliplatin is indicated for timely identification of OIPN, which will allow earlier symptom management.
AB - Context: Oxaliplatin-induced peripheral neuropathy (OIPN) is a dose-limiting toxicity of oxaliplatin and affects most colorectal cancer patients. OIPN is commonly evaluated by patient symptom report, using scales to reflect impairment. They do not discriminate between unique grouping of symptoms and signs, which impedes prompt identification of OIPN. Objective: The objective of this study was to identify clusters of symptoms and signs that differentiated underlying clinical severity and segregated patients within our population into OIPN subgroups. Methods: Chemotherapy-naive colorectal cancer patients (N = 148) receiving oxaliplatin were administered the Total Neuropathy Score clinical (TNSc©), which includes symptom report (sensory, motor, autonomic) and sensory examination (pin sense, vibration, reflexes). The TNSc was administered before chemotherapy initiation (T0) and after cumulative doses of oxaliplatin 510–520 mg/m2 (T1) and 1020–1040 mg/m2 of oxaliplatin (T2). Using mean T2 TNSc scores, latent class analysis grouped patients into OIPN severity cohorts. Results: Latent class analysis categorized patients into four distinct OIPN groups: low symptoms and low signs (n = 54); low symptoms and intermediate signs (n = 44); low symptoms and high signs (n = 21); and high symptoms and high signs (n = 29). No differences were noted among OIPN groups on age, sex, chemotherapy regimen, or cumulative oxaliplatin dose. Conclusion: We identified OIPN patient groups with distinct symptoms/signs, demonstrating variability of OIPN presentation regardless of cumulative oxaliplatin dose. Over half of the sample had positive findings on OIPN examination despite little or no symptoms. Sensory examination of all patients receiving oxaliplatin is indicated for timely identification of OIPN, which will allow earlier symptom management.
KW - Chemotherapy-induced peripheral neuropathy
KW - chronic pain
KW - latent class analysis
KW - measurement
KW - oxaliplatin
KW - pain
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U2 - 10.1016/j.jpainsymman.2017.07.033
DO - 10.1016/j.jpainsymman.2017.07.033
M3 - Article
C2 - 28743660
AN - SCOPUS:85030751992
SN - 0885-3924
VL - 54
SP - 701-706.e1
JO - Journal of pain and symptom management
JF - Journal of pain and symptom management
IS - 5
ER -