Premium
Palmar‐plantar erythrodysesthesia syndrome following treatment with high‐dose methotrexate or high‐dose cytarabine
Author(s) -
Karol Seth E.,
Yang Wenjian,
Smith Colton,
Cheng Cheng,
Stewart Clinton F.,
Baker Sharyn D.,
Sandlund John T.,
Rubnitz Jeffrey E.,
Bishop Michael W.,
Pappo Alberto S.,
Jeha Sima,
Pui ChingHon,
Relling Mary V.
Publication year - 2017
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/cncr.30762
Subject(s) - medicine , methotrexate , cytarabine , surgery , chemotherapy
BACKGROUND Palmar‐plantar erythrodysesthesia syndrome (PPES) is an uncommon side effect of high‐dose cytarabine or methotrexate. Prior case reports of PPES have been limited, and the predisposing factors for the development of PPES remain unknown. METHODS A review of databases identified 22 patients (1.3%) who developed 39 episodes of PPES among 1720 patients after treatment with high‐dose cytarabine or methotrexate. RESULTS Symptoms lasted a mean of 6.4 days. Hands and feet were both involved in 68% of the initial episodes. Parenteral opioids were required for pain control by 27% of the patients. In comparison with the 1698 children treated with similar therapy, the children who developed PPES were older (mean age at diagnosis, 14.3 vs 7.7 years; P = 7.5 × 10 –7 ). The frequency of PPES was less common in patients receiving methotrexate alone (7 of 946 or 0.7%) versus cytarabine (7 of 205 or 3.4%; P = .005) but was not different for those receiving both high‐dose methotrexate and cytarabine (8 of 569 or 1.4%; P = .32). Prolonged infusions of methotrexate were associated with less frequent PPES in comparison with rapid infusions ( P = 1.5 × 10 –5 ), as was the co‐administration of dexamethasone with cytarabine ( P = 2.5 × 10 –6 ). Self‐described race and sex were not associated with PPES. In a multivariate analysis, older age and high‐dose cytarabine administration without dexamethasone remained associated with PPES ( P = 1.1 × 10 –4 and P = .038, respectively). A genome‐wide association study did not identify any associations with PPES meeting the genome‐wide significance threshold, but top variants were enriched for skin expression quantitative trait loci, including rs11764092 in AUTS2 ( P = 6.45 × 10 –5 ). CONCLUSIONS These data provide new insight into the incidence of PPES as well as its risk factors. Cancer 2017;123:3602‐8. © 2017 American Cancer Society .