Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmune disorder of neuromuscular transmission with presynaptic involvement (1). The syndrome exhibits characteristic proximal limb weakness, autonomic disturbance and depressed tendon reflexes. LEMS is a rare disease with an estimated annual incidence of 0.48–0.75 cases per million individuals in the Netherlands, and a prevalence of 3.42 cases per million individuals (2). Diagnosis of LEMS is based on clinical symptoms and electrophysiological studies, including the repetitive nerve stimulation test (2). LEMS is associated with cancer in the form of paraneoplastic syndrome in 50–60% of cases, the majority of which are small cell lung cancer (SCLC) (3). Treatment is based on anti-cancer therapy for those patients with associated cancers, given in combined with symptomatic and immunosuppressive therapy (4). LEMS patients with SCLC are more likely to reveal a better prognosis than patients with SCLC alone, probably due to early identification of SCLC (5). The potassium-channel blocker, 3,4-diaminopyridine (3,4-DAP), prolongs the duration of nerve action potentials and increases the release of acetylcholine at the presynaptic membrane of the neuromuscular junction, effectively treating the symptoms of LEMS (6–8). The present study describes the case of a patient with LEMS and SCLC, who showed a marked clinical improvement following treatment with 3,4-DAP, compared with anticancer therapy alone, which only caused temporary improvement. The patient provided written informed consent.

A 62-year-old male presented to the Hallym University Hospital (Chuncheon, Republic of Korea) in December 2013 with progressive quadriparesis, which had been apparent for >2 weeks and was more prominent in the legs compared with the arms. A diagnosis of myasthenia gravis (MG) was suspected initially due to progressive quadriparesis, as described above. In addition, thymoma was also suspected due to its high proportion of comorbidity with MG. The patient underwent a chest computed tomography (CT) scan to evaluate a thymoma. A subcarinal mass was subsequently detected. A bronchoscopic biopsy revealed a malignant small round cell tumor that was suggestive of small cell carcinoma, and the patient was diagnosed with SCLC. The patient visited the Research Institute and Hospital of the National Cancer Center (Goyang, Republic of Korea) for additional evaluation in January 2014. The patient experienced progressive weakness and fatigue, which appeared to be worse in the evening. The patient also complained of a dry mouth and mild dysarthria, with intermittent aspiration of water. The family history was normal, and the patient had a history of smoking one packet of cigarettes per day, for 38 years. A neurological examination revealed overall proximal weakness [Medical Research Council (MRC) grade IV+] and hypoactive tendon reflexes with normal sensory function (9). Since a diagnosis of LEMS was suspected, a repetitive nerve stimulation test was performed on the right abductor digiti minimi, trapezius and orbicularis oculi muscles using the method previously described by Oh (10). The results were compatible with LEMS (Fig. 1). Abnormal decremental responses with low-rate stimulation and incremental responses with high-rate stimulation were observed. An anti-acetylcholine receptor antibody assay yielded a negative result.

Four cycles of chemotherapy (etoposide and carboplatin) and concurrent thoracic irradiation (6,380 cGy/29 Fx) were performed, which resulted in a modest response of the SCLC (partial remission status). The MRC grading system divides muscle strength into 3 levels in grade IV. GIV+ means definite but slight weakness, GIV means able to move the joint against a combination of gravity and some resistance, and GIV- means capable of minimal resistance. Subsequent to the treatment for cancer, a mild improvement in the muscle weakness (MRC grade IV+) was recognized. However, the muscle weakness of the patient worsened again (MRC grade III to IV-) 1 month after the concurrent chemoradiation therapy (CCRT). The patient was initially treated with pyridostigmine alone (60 mg, 3 times per day), as 3,4-DAP is an orphan drug not easily available in South Korea, but the symptoms remained unimproved for 2 weeks. Therefore, the patient was prescribed 3,4-DAP (10 mg, 3 times per day) from the Korean Orphan Drug Center (Seoul, South Korea) and pyridostigmine (60 mg, 3 times per day). The symptoms markedly improved following the administration of 3,4-DAP. A neurological examination performed 1 year later demonstrated no muscle weakness (MRC grade V) and no significant adverse effects were indicated.

Previous studies in South Korea have reported a favorable response of LEMS to anticancer therapy that is used to treat SCLC alone (11–13). Specific anticancer therapies often improve LEMS, possibly by inhibiting the tumor-derived antigenic stimuli, including surface voltage-gated calcium channels (VGCCs), which provoke the production of anti-VGCC antibodies (14). By contrast, the patient in the present study experienced temporarily improved muscle weakness that then worsened, even with anticancer therapy. However, the patient showed a marked clinical improvement following the administration of 3,4-DAP. A number of previous studies in United States and Japan have demonstrated that patients with LEMS, who were treated with 3,4-DAP therapy exhibited significant improvements in muscle strength (8,15,16). In accordance with the previous studies, the patient was diagnosed with muscle weakness caused by LEMS with SCLC, which was improved using 3,4-DAP therapy combined with CCRT. To the best of our knowledge, the present study is the first to report this finding in South Korea.

Aminopyridines potentiate chemical transmission at the central and peripheral synapses by targeting the VGCC and facilitating the release of acetylcholine at the motor nerve terminals. The chemical 3,4-DAP, at doses sufficient to improve neuromuscular transmission, produces few central nervous system adverse effects as its penetration into the brain is limited (6). However, epileptic seizures and arrhythmias have been previously described in patients that use high doses (6,7).

The present study illustrates that 3,4-DAP is a useful treatment choice in patients with LEMS, particularly in patients that do not improve fully following anticancer therapy.