• Makoto Nagashima, Mitsuru Ooshiro, Ayako Moriyama, Yui Sugishita, Kengo Kadoya, Ayami Sato, Tomoaki Kitahara, Ryuichi Takagi, Tasuku Urita, Yutaka Yoshida, Hiroshi Tanaka, Takashi Oshiro, Shinichi Okazumi, and Ryoji Katoh.
• Department of Surgery, Toho University Sakura Medical Center, 564-1 Shimoshizu, Sakura, 285-8741, Japan, nagashima@sakura.med.toho-u.ac.jp.
• Support Care Cancer. 2014 Jun 1; 22 (6): 1579-84.

BackgroundThe oxaliplatin-based regimen FOLFOX is widely used to treat patients with advanced colorectal cancer (CRC). However, dose-limiting toxicity after continuous oxaliplatin administration can lead to peripheral neuropathy. Several agents, including opioids, that have been employed to treat oxaliplatin-induced peripheral neuropathy (OIPN) have been examined in clinical settings regarding their protective and therapeutic effects. However, the pharmacotherapy of these agents has not yet been established. Therefore, we investigated the efficacy and tolerability of oxycodone for OIPN and subsequently with FOLFOX therapy in CRC patients.MethodsThis was a single-center retrospective study of 64 CRC patients who underwent FOLFOX therapy at the Toho University Sakura Medical Center (Sakura, Japan). Controlled-release (CR) oxycodone was concomitantly administered to 29 patients (OXY group), whereas the additional 35 patients (non-OXY group) were not given oxycodone during the FOLFOX treatment course. The incidence and severity of OIPN and the number of FOLFOX cycles were measured and compared between the two groups. Neurological toxicities were assessed according to the Common Terminology Criteria for Advanced Events, version 3.0.ResultsAll study patients had OIPN. Most patients experienced grade 1 or 2 sensory neuropathy. Grade 3 sensory neuropathy was observed in two patients in the non-OXY group. All patients in the OXY group completed the scheduled FOLFOX therapy, whereas FOLFOX therapy was discontinued in ten patients in the non-OXY group due to severe peripheral neuropathy. The median numbers of FOLFOX cycles in the OXY and non-OXY groups were 13 (range, 6-46) and 7 (range, 2-18), respectively (P < 0.05). The median cumulative oxaliplatin doses were 1072.3 mg/m(2) (range, 408.7-3385.3 mg/m(2)) in the OXY group and 483.0 mg/m(2) (range 76.2-1414.1 mg/m(2)) in the non-OXY group (P < 0.05).ConclusionsOur findings indicate that CR oxycodone might attenuate the severity of OIPN and extend the use of FOLFOX therapy.

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