This article has Open Peer Review reports available.
Detecting acute neurotoxicity during platinum chemotherapy by neurophysiological assessment of motor nerve hyperexcitability
© Hill et al; licensee BioMed Central Ltd. 2010
Received: 28 March 2010
Accepted: 23 August 2010
Published: 23 August 2010
Platinum-based drugs, such as cisplatin and oxaliplatin, are well-known for inducing chronic sensory neuropathies but their acute and motor neurotoxicities are less well characterised. Use was made of nerve conduction studies and needle electromyography (EMG) to assess motor nerve excitability in cancer patients during their first treatment cycle with platinum-based chemotherapy in this study.
Twenty-nine adult cancer patients had a neurophysiological assessment either before oxaliplatin plus capecitabine, on days 2 to 4 or 14 to 20 after oxaliplatin plus capecitabine, or on days 2 to 4 after carboplatin plus paclitaxel or cisplatin, undertaken by a neurophysiologist who was blinded to patient and treatment details. Patients completed a symptom questionnaire at the end of the treatment cycle.
Abnormal spontaneous high frequency motor fibre action potentials were detected in 100% of patients (n = 6) and 72% of muscles (n = 22) on days 2 to 4 post-oxaliplatin, and in 25% of patients (n = 8) and 13% of muscles (n = 32) on days 14 to 20 post-oxaliplatin, but in none of the patients (n = 14) or muscles (n = 56) tested prior to oxaliplatin or on days 2 to 4 after carboplatin plus paclitaxel or cisplatin. Repetitive compound motor action potentials were less sensitive and less specific than spontaneous high frequency motor fibre action potentials for detection of acute oxaliplatin-induced motor nerve hyperexcitability but were present in 71% of patients (n = 7) and 32% of muscles (n = 32) on days 2 to 4 after oxaliplatin treatment. Acute neurotoxicity symptoms, most commonly cold-induced paraesthesiae and jaw or throat tightness, were reported by all patients treated with oxaliplatin (n = 22) and none of those treated with carboplatin plus paclitaxel or cisplatin (n = 6).
Abnormal spontaneous high frequency motor fibre activity is a sensitive and specific endpoint of acute oxaliplatin-induced motor nerve hyperexcitability, detectable on EMG on days 2 to 4 post-treatment. Objective EMG assessment of motor nerve excitability could compliment patient-reported symptomatic endpoints of acute oxaliplatin-induced neurotoxicity in future studies.
Cancer chemotherapy based on cisplatin, carboplatin and oxaliplatin, usually combined with radiation, capecitabine, paclitaxel or other agents, is the mainstay of treatment for many cancer patients, including those with lung, colorectum, stomach, head and neck, cervix, oesophagus, bladder, ovary and testis cancer . However, platinum-induced chronic neuro-sensory toxicities are treatment-limiting, in particular glove and stocking distal paraesthesiae and dysesthesiae with loss of tendon reflexes and peripheral sensation, and ototoxicity with tinnitus and hearing loss [2–4]. Neuro-sensory toxicities typically develop after repeated dosing, progress cumulatively with continued treatment and persist long beyond the completion of treatment. In addition, oxaliplatin has been reported to cause a distinct acute and reversible neurotoxicity syndrome with motor symptoms , which has not been reported with other platinum-based drugs to date. While the chronic neuro-sensory toxicities of platinum-based drugs are well known, their acute and motor neurotoxicity are less well characterised.
In a previous study of cancer patients treated with oxaliplatin [5, 6], striking neurophysiological abnormalities were demonstrated suggesting a state of acute peripheral nerve hyperexcitability due to altered axonal ion channel activity. These neurophysiological abnormalities included repetitive compound motor action potentials (CMAPs) during nerve conduction studies after a single electrical stimulus following the main CMAP, and high frequency motor fibre action potentials on needle electromyography (EMG) that occurred spontaneously and upon needle insertion or voluntary muscle contraction. Since these original reports, few or no subsequent studies by other groups have independently confirmed the occurrence of repetitive CMAPs and/or abnormal motor fibre action potentials in patients treated with oxaliplatin or other chemotherapy drugs.
In the current study, use was made of nerve conduction studies and EMG to assess motor nerve excitability in cancer patients during their first treatment cycle of platinum-based chemotherapy. We sought to define clinical procedures for the objective assessment of acute oxaliplatin-induced motor nerve hyperexcitability by optimising the time-points and endpoints for its neurophysiological detection. In addition, we aimed to independently confirm whether repetitive CMAPs and/or abnormal motor fibre action potentials were detectable after oxaliplatin treatment, and to obtain preliminary evidence of their occurrence after treatment with other platinum drugs. Neurophysiological studies are inherently subjective as they require qualitative interpretation. To reduce observer bias in the current study, a control group of patients was included who were tested prior to receiving platinum-based chemotherapy and the neurophysiologist was blinded to patient group and treatment details.
Eligible subjects were adult cancer patients who were to receive standard chemotherapy with oxaliplatin (130 mg/m2), cisplatin (100 mg/m2) or carboplatin (AUC 6 mg*min/ml) alone or in combination with other agents repeated three weekly, and who had given written informed consent. Subjects who had previously received platinum-based chemotherapy and those with previous or existing peripheral neuropathy or medical contraindications to clinical neurophysiological procedures were ineligible. The study was approved by the Auckland Ethics Committee × (Approval no AKX 04/06/165).
Study Procedures and Groups
Study procedures included neurophysiological assessment and symptom evaluation both carried out during the first treatment cycle of platinum-based chemotherapy. The neurophysiological assessment was carried out once only to avoid subject drop-out, which was associated with repeated assessments in previous studies . Study patients were allocated to one of four groups according to their treatment and the timing of their neurophysiological assessment, as follows: group 1, assessment prior to oxaliplatin; group 2, assessment on days 2 to 4 after oxaliplatin; group 3, assessment on days 14 to 20 after oxaliplatin, and; group 4, assessment on days 2 to 4 after carboplatin plus paclitaxel or cisplatin.
The neurophysiological assessment included a standard neurological examination, nerve conduction studies and EMG, carried out by a neurology specialist (PB) who was blinded to the patient and treatment details. To maintain blinding, the neurologist did not take a neurological history and ensured that patients did not volunteer any neurological symptoms.
The neurophysiological assessment was similar to that previously reported [5, 6]. Standard nerve conduction techniques, electrode positions and stimulation sites were used. Limb temperature was monitored and maintained above 32°C. Neurophysiological testing was carried out in the limbs opposite to the arm used for the chemotherapy infusion. Sensory studies comprised sural, radial, median and ulnar sensory nerve action potentials (SNAPs). Motor studies were performed in median, ulnar, peroneal and tibial nerves. The presence of repetitive compound muscle action potentials (CMAPs) was assessed in the four motor nerves tested using an F-wave programme, with a slower sweep speed than conventional CMAP recordings. EMG was performed in first dorsal interosseous (FDIO), extensor digitorum communis (EDC), tibialis anterior and gastrocnemius muscles. Most patients had all 4 sensory and motor nerve studies performed, and all 4 muscles sampled by EMG, though a few did not have the complete set of these tests.
A simple scoring system for increased motor unit activity was created:
0 No abnormal motor unit activity
1 Increased insertional activity
2 Spontaneous high frequency motor unit activity with muscle clinically at rest, with bursts lasting for duration of less than 2 seconds
3 Spontaneous high frequency motor unit activity with muscle clinically at rest, with bursts lasting for duration of 2 to 5 seconds
4 Spontaneous high frequency motor unit activity with muscle clinically at rest, with bursts lasting for duration of more than 5 seconds
Patients completed a short symptom questionnaire, immediately before their neurophysiological assessment and at the end of the first treatment cycle, documenting the presence, absence, severity, onset time and duration of jaw or throat tightness, perioral paraesthesiae, muscle cramps, cold-induced paraesthesiae, glove and stocking numbness and tingling, infusional arm discomfort, loss of sensation of breathing, visual disturbance and any other neurotoxicity symptoms. The neurologist (PB) remained blinded to the result of this questionnaire. Symptom data from one oxaliplatin patient was unavailable because of sudden cardiac death.
A group size of 6 to 8 subjects was considered adequate to provide sufficient data for each time point and treatment group to give a reasonable estimate of the proportion of patients with motor nerve hyperexcitability. Data were analysed using descriptive statistics and reported as the number and proportion of patients, muscles and nerves affected by motor nerve hyperexcitability for each group. The standard error of each proportion was calculated as follows; standard error = √p(1-p)/n), where p is proportion and n is sample size. No formal evaluation of the statistical significance of differences between groups was planned or carried out. Test sensitivity was calculated from the number of patients, muscles or nerves displaying motor nerve hyperexcitability expressed as a percentage of the total number of patients, muscles or nerves tested on days 2 to 4 after oxaliplatin. Test specificity was calculated as the number of patients, muscles or nerves not displaying motor nerve hyperexcitability expressed as a percentage of the total number of patients, muscles or nerves tested before oxaliplatin or on days 2 to 4 after carboplatin plus paclitaxel or cisplatin.
Patients and Treatment
Number of Patients
28 to 79 years
Colorectal Dukes C
Head and Neck
Non-Small Cell Lung Cancer
One or more1
One or more regimens2
Oxaliplatin (130 mg/m2) with Capecitabine (1000 to 2000 mg BID po days 1 to 14)
Cisplatin (100 mg/m2)
Carboplatin (AUC 6 mg*min/ml) with Paclitaxel (200 mg/m2)
Spontaneous high frequency motor unit activity
Comparison of neurophysiological endpoints of acute oxaliplatin-induced motor nerve hyperexcitability
Number of Abnormal Tests/Total Number of Tests (%)
Spontaneous High Frequency Motor Unit Action Potentials
Repetitive Compound Motor Action Potentials
Muscles or Nerves
Muscles or Nerves
Muscles or Nerves
Muscles or Nerves
Muscles or Nerves
Muscles or Nerves
Abnormal, spontaneous high frequency motor unit activity was detected in all patients tested on days 2 to 4 after oxaliplatin (6 of 6; 100%) but in fewer patients tested on days 14 to 20 after oxaliplatin (2 of 8; 25%) and no patients tested prior to oxaliplatin (0 of 8; 0%), or on days 2 to 4 after carboplatin plus paclitaxel or cisplatin (0 of 6; 0%). Abnormal, spontaneous high frequency motor unit activity was detected in most muscles tested on days 2 to 4 after oxaliplatin (16/22; 72%) but in fewer muscles tested on days 14 to 20 after oxaliplatin (4 of 32; 12%) and in none of the muscles tested prior to oxaliplatin (0 of 32; 0%), or on days 2 to 4 after carboplatin plus paclitaxel or cisplatin (0 of 24; 0%).
The sensitivity of spontaneous high frequency motor unit activity for detecting acute motor nerve hyperexcitability on days 2 to 4 after oxaliplatin was 100% and 72% for patients and muscles respectively, and its specificity was 100% for both patients and muscles (Table 2).
No abnormalities in sensory nerve conduction studies were seen.
Repetitive CMAPs (Fig 2C) were present in most patients tested on days 2 to 4 after oxaliplatin (5 of 7; 71%) but in fewer patients tested before oxaliplatin (1 of 8; 13%), on days 14 to 20 after oxaliplatin (2 of 8; 25%) or on days 2 to 4 after carboplatin plus paclitaxel or cisplatin (1 of 6; 17%). Repetitive CMAPs were present in about one third of the nerves tested on days 2 to 4 after oxaliplatin (9 of 28; 32%) but in fewer nerves tested before oxaliplatin (1 of 32; 3.2%), on days 14 to 20 after oxaliplatin (3 of 31; 10%) or on days 2 to 4 after carboplatin plus paclitaxel or cisplatin (2 of 24; 8%).
The sensitivity of repetitive CMAPs for detecting acute motor nerve hyperexcitability on days 2 to 4 after oxaliplatin was 71% and 32% for patients and nerves, respectively. The specificity of repetitive CMAPs for detecting acute motor nerve hyperexcitability on days 2 to 4 after oxaliplatin was 86% and 95% for patients and nerves, respectively (Table 2).
Cold-induced paraesthesiae were reported by all patients treated with oxaliplatin (22 of 22; 100%) with its onset ranging from 0 to 48 hours post-treatment (median 0 hours) and duration ranging from 3 to 21 days (median 8 days). Jaw or throat tightness was reported by 15 of 22 patients (68%) treated with oxaliplatin with its onset ranging from 0 to 26 hours post-oxaliplatin (median 2 hours) and duration ranging from < 1 to 21 days (median 6 days). Pain in the upper limb used for the oxaliplatin infusion was reported by 12 of 22 patients (55%) treated with oxaliplatin but only in those receiving the drug via peripheral vein canula and in no patients given oxaliplatin via central venous line. Infusion arm discomfort came on 0 to 2 hours after oxaliplatin infusion (median 0 hours) and lasted from less than 1 day to 19 days (median 7.5 days). Other symptoms reported by oxaliplatin-treated patients included glove and stocking paraesthesiae unrelated to cold exposure (8 patients), muscle cramps (4 patients), transient change in vision (2 patients) and shortness of breath (1 patient).
None of the patients treated with carboplatin plus paclitaxel or cisplatin reported cold-induced paraesthesiae, jaw or throat tightness, infusion arm discomfort, glove and stocking paraesthesiae unrelated to cold exposure, muscle cramps, transient change in vision or shortness of breath.
In this study, we showed that abnormal, spontaneous high frequency motor unit action potentials were a sensitive and specific endpoint of acute oxaliplatin-induced motor nerve hyperexcitability. These abnormal, spontaneous high frequency motor unit action potentials, which resembled discharges seen in neuromyotonia, were detectable on EMG testing on days 2 to 4 post-treatment with the muscle clinically at rest independently of EMG needle insertion. They were detected in 100% of patients and 72% of muscles on days 2 to 4 after treatment with oxaliplatin plus capecitabine but in none of the patients or muscles tested before oxaliplatin treatment or after treatment with carboplatin plus paclitaxel or cisplatin. Abnormal, spontaneous high frequency motor unit activity was more frequent on days 2 to 4 than on days 14 to 20 post-treatment, and was more sensitive and more specific than repetitive CMAPs for detecting acute oxaliplatin-induced motor nerve hyperexcitability. Repetitive CMAPs were abnormal action potentials occurring after a single electrical stimulus following the main CMAP. These findings confirm a previous report [5, 6] of spontaneous high frequency motor unit action potentials and repetitive CMAPs after oxaliplatin treatment and refined clinical procedures for the neurophysiological assessment of chemotherapy-induced motor nerve hyperexcitability.
The neurophysiological features of acute oxaliplatin-induced motor nerve hyperexcitability found in this study, and those described previously [5, 6] are similar to those seen in acquired neuromyotonia. Neuromyotonia is often associated with autoantibodies against potassium channels , and it has been postulated that disruption of K+ channels is a key element in the production of neuromyotonia. However, in a mouse diaphragm model, K+ channel blockade did not replicate the neurophysiological features of oxaliplatin. Instead, the increase in spontaneous activity induced by oxaliplatin in this model was prevented by the voltage-gated Na+ channel blocker tetrodotoxin. The authors concluded that the most likely mechanism of oxaliplatin neurotoxicity is a direct effect on voltage-gated Na+ channels rather than an effect on K+ channels or nerve terminal Ca2+ regulation. Others have also found evidence of Na+ channel dysfunction with oxaliplatin use [9, 10] although this has not been a consistent finding .
Repetitive CMAPs may be generated at the synapse or in the motor nerve axon . Synaptic CMAPs may occur when there is excessive acetyl choline (ACh) in the synapse, and they can also occur with normal amounts of ACh in the synapse in the slow channel syndrome . There is no reason to suppose that repetitive CMAPs in the setting of oxaliplatin use are due to excessive ACh in the synapse. Instead, the repetitive CMAPs that were observed following a single electrical stimulus were almost certainly generated in the motor nerve axons themselves. Repetitive CMAPs similar to those recorded here have been described in neuromyotonia, and the authors concluded from their studies that the focus of abnormal excitation must have been in the distal part of the nerve. Presumably disruption of function of sodium channels is also the reason for the appearance of the repetitive CMAPs with oxaliplatin use, as well as causing the spontaneous high frequency motor unit activity seen on EMG.
Neurophysiological studies are more subjective than may be appreciated, and for this reason considerable lengths were taken to eliminate bias from the current study by including relevant control groups and ensuring the neurophysiologist was blinded to the treatment group and patient details. In particular, determining whether there is abnormal insertional EMG activity is very subjective, and this is likely to have contributed to false positive tests recorded in control patients. However, the more robust finding of abnormal spontaneous high frequency motor unit activity was not detected in any of the control patients who were tested before receiving oxaliplatin or after other chemotherapeutic agents. Similarly, it was difficult at times to determine whether there were one or more abnormal repetitive CMAPs following a single stimulus, and whether this had occurred because some patients were not adequately relaxed for testing. However, the impression was that repetitive CMAPs were much more prominent after oxaliplatin than in any other circumstance, but it was not possible to devise any method for quantifying this abnormality to improve its specificity.
Motor nerve hyperexcitability with subsequent abnormal muscle contraction could be a basis for some of the acute neurotoxicity symptoms reported by patients after oxaliplatin treatment. Approximately 70% of patients treated with oxaliplatin in the current study complained of jaw or throat tightness, and 4 of 22 patients reported muscle cramps. However, motor symptoms occurred less frequently than abnormal, spontaneous high frequency motor unit activity as determined by EMG assessment of subclinical motor nerve hyperexcitability. Cold-induced paraesthesiae were reported universally by oxaliplatin-treated patients in the current study, with or without other sensory symptoms, which may be due to sensory nerve hyperexcitability that was undetectable by conventional neurophysiological testing.
Park et al  found evidence of sensory nerve hyperexcitability and functional channelopathy of axonal sodium channels when they undertook axonal excitability studies in 58 patients who were treated with oxaliplatin. Significant changes were evident in both sensory and motor axons in recovery cycle parameters immediately following oxaliplatin infusions. The extent of oxaliplatin-induced abnormality in motor axons was proportional to the degree of change in sensory axons. Abnormalities became progressively worse in sensory axons, while motor axonal excitability remained unchanged with repeated doses of oxaliplatin. Sensory excitability abnormalities that developed during early treatment cycles were able to predict the development of chronic sensory neuropathy on an individual patient basis in 80% of patients, in their study. The neurophysiological studies undertaken by Park et al  were notably different from those performed in the current study. Their studies required specialised equipment, but our studies comprised conventional clinical neurophysiological studies, and included detailed EMG studies. As such, the studies are complementary. The testing in the current study, which was less sophisticated than that undertaken by Park et al , did not identify sensory abnormalities acutely, but found clear evidence of motor nerve excitability acutely that resolved over subsequent weeks.
Finally, our study suggests that the mechanism of acute oxaliplatin-induced motor nerve hyperexcitability differs from the mechanisms involved in the chronic neuro-sensory toxicities of oxaliplatin and related chemotherapeutic agents. We showed evidence of acute motor nerve hyperexcitability on nerve conduction studies and EMG after oxaliplatin treatment, but not following treatment with carboplatin plus paclitaxel or cisplatin. In contrast, cisplatin, carboplatin plus paclitaxel and oxaliplatin are well known for inducing chronic neuro-sensory toxicity in a high percentage of treated patients that typically present with chronic neuro-sensory symptoms and loss of sensation with motor function spared [2, 3, 14]. Differences between the acute and chronic neurotoxicity profiles of different chemotherapy drugs, and in their relative specificity for inducing toxicity to peripheral sensory versus motor nerves, suggests that these are distinct and mechanistically unrelated neurotoxicities. The mechanisms of acute and chronic neurotoxicities of platinum drugs are unknown. However, acute motor nerve hyperexcitability induced by oxaliplatin may be due to chelation of calcium or other endogenous divalent cations by its oxalate leaving group , but not by the leaving groups of other platinum drugs. In contrast, the chronic neuro-sensory toxicities of cisplatin, carboplatin and oxaliplatin maybe due to neuronal accumulation of platinum , which is a common element of all chemotherapeutic agents of the class.
Abnormal, spontaneous high frequency motor fibre activity is a sensitive and specific endpoint of acute oxaliplatin-induced motor nerve hyperexcitability, detectable on EMG on days 2 to 4 post-treatment. Objective EMG assessment of motor nerve excitability could compliment patient-reported symptomatic endpoints of acute oxaliplatin-induced neurotoxicity in future studies, and is suitable for use in multicentre clinical trials as EMG is widely available as a routine diagnostic clinical procedure.
The authors are grateful to the patients and their families for their participation in the study, and the Cancer Society of New Zealand for research grant support.
- Kelland L: The resurgence of platinum-based cancer chemotherapy. Nat Rev Cancer. 2007, 7: 573-584. 10.1038/nrc2167.View ArticlePubMedGoogle Scholar
- Mollman JE: Cisplatin neurotoxicity. N Engl J Med. 1990, 322: 126-127. 10.1056/NEJM199001113220210.View ArticlePubMedGoogle Scholar
- Grothey A: Oxaliplatin-safety profile: neurotoxicity. Semin Oncol. 2003, 30: 5-13. 10.1016/S0093-7754(03)00399-3.View ArticlePubMedGoogle Scholar
- McKeage MJ: Comparative adverse effect profiles of platinum drugs. Drug Saf. 1995, 13: 228-244. 10.2165/00002018-199513040-00003.View ArticlePubMedGoogle Scholar
- Wilson RH, Lehky T, Thomas RR, Quinn MG, Floeter MK, Grem JL: Acute oxaliplatin-induced peripheral nerve hyperexcitability. J Clin Oncol. 2002, 20: 1767-1774. 10.1200/JCO.2002.07.056.View ArticlePubMedGoogle Scholar
- Lehky TJ, Leonard GD, Wilson RH, Grem JL, Floeter MK: Oxaliplatin-induced neurotoxicity: acute hyperexcitability and chronic neuropathy. Muscle Nerve. 2004, 29: 387-392. 10.1002/mus.10559.View ArticlePubMedGoogle Scholar
- Shillito P, Molenaar PC, Vincent A, Leys K, Zheng W, Vandenberg RJ, Plomp JJ, Vankempen GTH, Chauplannaz G, Wintzen AR, et al: Acquired neuromyotonia - evidence for autoantibodies directed against K+ channels of peripheral-nerves. Annals of Neurology. 1995, 38: 714-722. 10.1002/ana.410380505.View ArticlePubMedGoogle Scholar
- Webster RG, Brain KL, Wilson RH, Grem JL, Vincent A: Oxaliplatin induces hyperexcitability at motor and autonomic neuromuscular junctions through effects on voltage-gated sodium channels. Br J Pharmacol. 2005, 146: 1027-1039. 10.1038/sj.bjp.0706407.View ArticlePubMedPubMed CentralGoogle Scholar
- Park SB, Lin CSY, Krishnan AV, Goldstein D, Friedlander ML, Kiernan MC: Oxaliplatin-induced neurotoxicity: changes in axonal excitability precede development of neuropathy. Brain. 2009, 132: 2712-2723. 10.1093/brain/awp219.View ArticlePubMedGoogle Scholar
- Adelsberger H, Quasthoff S, Grosskreutz J, Lepier A, Eckel F, Lersch C: The chemotherapeutic oxaliplatin alters voltage-gated Na(+) channel kinetics on rat sensory neurons. Eur J Pharmacol. 2000, 406: 25-32. 10.1016/S0014-2999(00)00667-1.View ArticlePubMedGoogle Scholar
- Broomand A, Jerremalm E, Yachnin J, Ehrsson H, Elinder F: Oxaliplatin neurotoxicity--no general ion channel surface-charge effect. J Negat Results Biomed. 2009, 8: 2-10.1186/1477-5751-8-2.View ArticlePubMedPubMed CentralGoogle Scholar
- VanDijk JG, Lammers GJ, Wintzen AR, Molenaar PC: Repetitive CMAPs: Mechanisms of neural and synaptic genesis. Muscle & Nerve. 1996, 19: 1127-1133.View ArticleGoogle Scholar
- Engel AG, Lambert EH, Mulder DM, Torres CF, Sahashi K, Bertorini TE, Whitaker JN: A newly recognized congenital myasthenic syndrome attributed to a prolonged open time of the acetylcholine-induced ion channel. Annals of Neurology. 1982, 11: 553-569. 10.1002/ana.410110603.View ArticlePubMedGoogle Scholar
- Postma TJ, Vermorken JB, Liefting AJ, Pinedo HM, Heimans JJ: Paclitaxel-induced neuropathy. Ann Oncol. 1995, 6: 489-494.PubMedGoogle Scholar
- Gamelin L, Capitain O, Morel A, Dumont A, Traore S, Anne LB, Gilles S, Boisdron-Celle M, Gamelin E: Predictive factors of oxaliplatin neurotoxicity: The involvement of the oxalate outcome pathway. Clinical Cancer Research. 2007, 13: 6359-6368. 10.1158/1078-0432.CCR-07-0660.View ArticlePubMedGoogle Scholar
- Screnci D, McKeage MJ, Galettis P, Hambley TW, Palmer BD, Baguley BC: Relationships between hydrophobicity, reactivity, accumulation and peripheral nerve toxicity of a series of platinum drugs. Br J Cancer. 2000, 82: 966-972. 10.1054/bjoc.1999.1026.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/10/451/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.