PURPOSE:
A
prospective phase II multicenter study was performed in two steps in
paclitaxel-treated ovarian cancer patients in France. A French version
of the four-item Functional Assessment of Cancer Therapy/Gynecologic
Oncology Group-Neurotoxicity (FACT/GOG-Ntx) questionnaire was validated.
This was then used to evaluate neurotoxicity in relation to
erythropoietin treatment.
METHODS:
Patients received
standard second-line paclitaxel-based chemotherapy and erythropoietin
for anemia. Neurotoxicity and hemoglobin levels were evaluated every
cycle with the FACT/GOG-Ntx and NCI-CTCAE. The translated questionnaire
was tested in 20 patients to confirm the translation accuracy. The final
questionnaire was validated in 98 patients with internal consistency
(Cronbach's coefficient) and item correlation (Pearson's r coefficient)
tests. Neurotoxicity severity was analyzed according to erythropoietin
intake (first three cycles versus no or late intake) and correlated with
anemia.
RESULTS:
Patients received a median of six
paclitaxel cycles (range 1-9). Neurotoxicity was validated in 484
questionnaires. Internal consistency was excellent with Cronbach's
coefficients of ≥0.89 at inclusion, after 3 cycles and at study end.
Inter-question correlation was high with Pearson's coefficients of
0.65-0.85. FACT/GOG-Ntx and NCI-CTCAE severity scoring was similar.
Globally, the incidence of severe neurotoxicity (FACT/GOG-Ntx and
NCI-CTCAE) was found significantly higher in patients with severe
anemia. Of 98 evaluable patients, 31 received erythropoietin during the
first three cycles. Mean hemoglobin level was significantly lower in
this group from baseline to cycle 4; however, these anemic patients with
early EPO intake did not develop an increase rate of severe
neurotoxicity.
CONCLUSIONS:
The French FACT/GOG-Ntx
questionnaire is a reliable and valid tool for assessing
chemotherapy-induced neuropathy. This study raises the possibility that
erythropoietin might play a neuroprotective role when administered with
paclitaxel.
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