FOLFIRINOX‑induced reversible dysarthria: A case report and review of previous cases

Introduction

FOLFIRINOX, a combination chemotherapy regimen consisting of fluorouracil, leucovorin, irinotecan and oxaliplatin, is currently a standard treatment for patients with advanced pancreatic cancer who have a good performance status (1). However, FOLFIRINOX can cause severe toxicities, including neutropenia, febrile neutropenia, thrombocytopenia, fatigue and diarrhea, frequently requiring dose reduction or treatment interruption. Irinotecan itself rarely causes dysarthria, which is considered to be a type of acute cholinergic syndrome (2,3). Due to the notable discordance in the incidence of dysarthria between FOLFIRINOX and other irinotecan-containing regimens, we speculate that FOLFIRINOX-induced dysarthria is associated with the sequence of drug administration in this regimen (i.e., intravenous infusion of oxaliplatin, immediately followed by irinotecan). Since oxaliplatin is infused before irinotecan in FOLFIRINOX, oxaliplatin exaggerates the cholinergic effects of irinotecan, making dysarthria increasingly evident.

In the present study we report a case of transient dysarthria, a speech disorder caused by disturbances of the muscles involved in speech, which occurred during the intravenous infusion of irinotecan as part of a FOLFIRINOX regimen in a 64-year-old male patient. We also review other cases previously observed in our hospital. The study was approved by the ethics committee of Nagoya University Hospital (Nagoya, Japan; approval no. 2014-0151).

Case report

A 64-year-old Japanese male was referred to Nagoya University Hospital due to metastatic pancreatic cancer. The patient had a history of diabetes mellitus and was receiving an oral DPP4 inhibitor (Vildagliptin). He had no history of allergy or adverse reactions to specific drugs. He received FOLFIRINOX as first-line chemotherapy, which consisted of oxaliplatin 85 mg/m2 administered intravenously over the course of 2 h, followed by irinotecan 180 mg/m2 over the course of 90 min and l-leucovorin 200 mg/m2 over the course of 2 h, immediately followed by fluorouracil 400 mg/m2 as an intravenous bolus and then 2,400 mg/m2 as a 46-h continuous infusion, usually with anti-emetic premedication with palonosetron and dexamethasone. Prophylactic atropine was not used in the first course. The patient's complete blood count and biochemical test results before the start of chemotherapy were within normal limits. During the first course of FOLFIRINOX, dysarthria developed 90 min after starting the irinotecan infusion and was accompanied by rhinitis, diaphoresis, acute-onset diarrhea and abdominal pain, which are typical signs and symptoms of acute cholinergic syndrome, persisting for ~2 h. These symptoms were alleviated by intramuscular atropine. The patient was conscious and alert, and physical and neurological examinations at the onset of dysarthria revealed no apparent abnormalities. In the second and subsequent courses of chemotherapy, prophylactic treatment with atropine was effective, and the patient did not suffer dysarthria or any other cholinergic symptoms.

Since the approval of FOLFIRINOX for pancreatic cancer in Japan in December 2013, four cases of dysarthria have been encountered among nine patients who received FOLFIRINOX in our hospital (Table I). In all cases, dysarthria occurred during the infusion of irinotecan in the first course of treatment and then resolved rapidly without any sequelae. Certain patients experienced distal extremity paresthesia and pharyngolaryngeal dysesthesia, which are known manifestations of oxaliplatin-induced acute neurotoxicity. All patients remained conscious and alert, and physical and neurological examinations at the onset of dysarthria revealed no other abnormalities. Imaging studies, including computed tomography and magnetic resonance imaging of the brain, were performed on Patient 1, and revealed no abnormalities. Atropine effectively palliated the symptoms at the onset of dysarthria, as well as prophylactically in the subsequent courses.

Table I. Clinical presentation of four patients treated with FOLFIRINOXa.

Table I.

Clinical presentation of four patients treated with FOLFIRINOXa.

			Dysarthria
Patient	Age and gender	Onset from start of irinotecan	Duration	Outcome	Recurrence	Atropine effective	Other symptoms
1	42, female	1 h	10 h	Reversible	Yes, but less intense	Yes	Distal extremity paresthesia
2	58, female	90 min	10 h	Reversible	Yes, but less intense	Yes	None
3	64, male	90 min	2 h (with atropine)	Reversible	No	Yes	Rhinitis, diaphoresis, abdominal pain, diarrhea
4	62, male	Immediate	2 h (with atropine)	Reversible	Yes, but less intense	Yes	Pharyngolaryngeal dysesthesia

a Oxaliplatin 85 mg/m² was administered intravenously over the course of 2 h, followed by irinotecan 180 mg/m² over the course of 90 min and l-leucovorin 200 mg/m² over the course of 2 h, followed immediately by fluorouracil 400 mg/m² as an intravenous bolus and then 2,400 mg/m² as a 46-h continuous infusion, usually with anti-emetic premedication with palonosetron and dexamethasone. Prophylactic atropine was not used in the first course.

Discussion

Two significant clinical lessons have been learned from our experience with these patients. First, FOLFIRINOX frequently causes transient dysarthria. Second, all cases resolved completely, with no need for dose reduction or treatment interruption.

With regard to the first point, since the approval of this regimen in Japan, it has been noted that FOLFIRINOX causes reversible dysarthria more often than previously reported for irinotecan monotherapy and other irinotecan-containing regimens (e.g., FOLFIRI and FOLFOXIRI) (3–12). In our hospital, overt speech disturbance diagnosed as dysarthria developed in 4 of the 9 patients (44.4%) who received FOLFIRINOX. Although dysarthria was not clearly recognized in the original ACCORD11 trial (1), a substantial number of patients developed this symptom in subsequent studies; Gunturu et al (4) reported nine cases of dysarthria among 35 patients (25.7%), and a phase II trial in Japan reported five cases among 36 patients (13.8%) (5). Therefore, the unexpectedly high incidence of dysarthria appears to be a characteristic adverse effect of FOLFIRINOX that extends beyond ethnicity. Conversely, it is known that irinotecan directly causes dysarthria, although only 10 cases have been reported in the literature (2,3,6–13). Although irinotecan exerts its antitumor activity after being metabolized to SN-38 in vivo, dysarthria is apparently caused by the parent compound irinotecan binding to the active site of acetylcholinesterase and eliciting a type of acute cholinergic syndrome (14). The hypoglossal nerve, which plays a major role in speech function through its innervation of tongue muscles, has increased intrinsic sensitivity to cholinergic stimulation owing to the higher density of cholinergic receptors compared with other brainstem nuclei (15,16), which would explain the cause of dysarthria. Other cholinergic symptoms, including rhinitis, diaphoresis and intestinal hyperperistalsis, occasionally occur simultaneously with dysarthria, and atropine effectively palliates the symptoms of dysarthria, supporting the notion that dysarthria is caused by increased acetylcholine activity. Due to the significant discordance in the incidence of dysarthria between FOLFIRINOX and other irinotecan-containing regimens, we speculate that FOLFIRINOX-induced dysarthria is associated with the sequence of drug administration (i.e., intravenous infusion of oxaliplatin, immediately followed by irinotecan). No cases of dysarthria were reported in clinical trials of FOLFOXIRI in advanced colorectal cancer (in which irinotecan was administered prior to oxaliplatin) (17–19). Oxaliplatin frequently causes acute peripheral neurotoxicity, characterized by transient, cold-induced distal and perioral paresthesias and pharyngolaryngeal dysesthesias, attributed to hyperexcitability of peripheral nerves during or immediately following infusion (20). Since oxaliplatin is infused prior to irinotecan in FOLFIRINOX, the hypoglossal nerve stimulation caused by initial treatment with oxaliplatin exaggerates the cholinergic effects of irinotecan, making dysarthria increasingly evident.

The second point was that all reported cases resolved completely, with no need for dose reduction or treatment interruption. As the sudden occurrence of dysarthria is a surprising and uncommon adverse event in traditional cancer chemotherapy, medical oncologists may initially suspect an acute onset of stroke or cerebrovascular disease. However, consistent with our experience, all reported cases were completely reversible, and neither dose reduction nor treatment interruption was necessary.

In conclusion, FOLFIRINOX frequently causes dysarthria, which is transient and resolves spontaneously without any sequelae. Medical oncologists need to correctly identify this characteristic adverse effect of FOLFIRINOX in order to avoid unnecessary dose reduction or treatment interruption.

References