OBJECTIVES To evaluate the effect of a combination of immunoglobulins (IVIg), cyclophosphamide (CTX), and methylprednisolone (MP) on the clinical course of patients with paraneoplastic neurological syndrome (PNS) and antineuronal antibodies (Abs).
METHODS Seventeen patients with paraneoplastic encephalomyelitis/sensory neuropathy (PEM/SN) with anti-Hu Abs (n=10) or cerebellar degeneration (PCD) with anti-Yo Abs (n=7) received one to nine cycles (mean 3.5) of a combination of IVIg (0.5 g/kg/day from days 1 to 5), CTX (600 mg/m2 at day 1) and MP (1g/day from day 1 to 3). The Rankin scale (RS) was used to evaluate the response. A positive response was considered as either improvement or stabilisation in patients who were still ambulatory (RS⩽3) at the onset of treatment, whereas only improvement, and not stabilisation, was considered a therapeutic benefit in bedridden patients (RS⩾4).
RESULTS Tolerance was good and no patient experienced grade 3/4 toxicity (World Health Organisation). Sixteen patients were evaluable for response. Of the seven patients with RS⩾4, none improved. Of the nine patients with RS⩽3, none improved but three (two SN and one PCD) stabilised for 4, 35, and 16 months.
CONCLUSIONS This study suggests that vigorous immunosuppressive treatment is not useful in severely disabled PNS patients with antineuronal Abs. In a minority of patients (mainly with SN) who are not severely disabled at the onset of treatment, a transient stabilisation is possible and deserves further evaluation.
- paraneoplastic neurological syndromes
- antineuronal Ab
- immunosuppresive treatment
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The presence of high titres of antineuronal antibodies (Abs) directed against antigens present in both neurons and tumour cells suggest that some paraneoplastic neurological syndromes such as paraneoplastic cerebellar degeneration (PCD) with anti-Yo Ab (also known as APCA) or paraneoplastic encephalomyelitis/sensory neuronopathy (PEM/SN) with anti-Hu Ab (also known as ANNA-1) are of autoimmune origin. Unfortunately, with a few exceptions,1-6immunosuppressive treatment such as plasmapheresis, corticosteroids, intravenous immunoglobulin (IVIg), or cyclophosphamide (CTX)7 8 have been disappointing when used alone. However, there is evidence that a combination of IVIg+CTX+methylprednisolone (MP) could be a more efficient approach in various autoimmune diseases, particularly in diseases with an intrathecal synthesis of Ig.9 As intrathecal synthesis of autoantibodies is a frequent finding in PCD with anti-Yo Ab and in PEM/SN with anti-Hu Ab,10 11 the effect of a multimodality immunosuppressive treatment associating CTX, MP, and IV Ig was evaluated in a series of 17 patients.
Patients and methods
Seventeen patients (11 women and six men) aged 50 to 72 years (median=65), with PCD with anti-Yo Ab (n=7) or PEM/SN with anti-Hu Ab (n=10) were treated with IVIg+CTX+MP between 1994 and 1996 (table).
Of 10 patients with anti-Hu Ab, four had CNS involvement (limbic encephalitis, brainstem encephalitis, cerebellar degeneration) and six had a sensory neuronopathy without CNS involvement. Three of these six patients also had signs of dysautonomia.
The seven patients with PCD and anti-Yo Ab had an isolated pancerebellar syndrome.
The median delay between the development of paraneoplastic symptoms and the onset of treatment was 10 months for anti-Hu+ patients (range 3 to 20 months), and 3 months for anti-Yo+ patients (range 0.5 to 5 months). In all cases, the neurological disorder had progressed within the 2 months preceding the therapeutic trial.
NATURE AND TREATMENT OF THE PRIMARY TUMOUR
A tumour was found in all patients as indicated in the table. In the anti-Hu+ patients, the neurological syndrome always preceded the tumour diagnosis (median time 7.5 months; range 3–41). In the anti-Yo+ patients, the neurological syndrome occurred after the tumour diagnosis in three patients (median time 24 months; range 6–43) and before the diagnosis of the tumour in four patients (median time 4 months; range 2–5).
In patients with anti-Hu Ab, the tumour histology was small cell lung cancer (eight patients), neuroendocrine tumour of rectum (one), urothelial carcinoma (one). One patient with small cell lung cancer also had a breast adenocarcinoma. In patients with anti-Yo Ab, the primary tumours were breast (two), ovarian (four), and metastasis of an unknown primary site (one).
Eight patients had treatment of the tumour (chemotherapy and/or radiotherapy) during immunosuppressive therapy. Among the nine others, six had received antineoplastic treatment before immunonsuppressive therapy, and three after.
All seventeen patients received a combination of IVIg, 0.5 g/kg/day for five days (day1 to day 5), intravenous MP, 1 g/day for 3 days (day 1 to day 3), and intravenous CTX, 600 mg/m2 for 1 day (day 4). If the patient was improved or stable after the first cycle, the treatment was repeated three times at 3 week intervals. After the third treatment, if the patient was improved or stable, he received a “maintenance” treatment of IV Ig (0.5 g/kg), intravenous MP (1g), and intravenous CTX (600 mg/m) delivered in 1 day, monthly for 6 months.
Neurological impairment was evaluated by a modified Rankin scale12 (0=asymptomatic patient; 1=non-disabling symptoms which do not interfere with lifestyle; 2=minor disabling symptoms, which lead to some restriction of lifestyle but do not prevent totally independent existence; 3=symptoms significantly interfere with lifestyle or prevent totally independent existence; 4=moderately severe disabling symptoms which clearly prevent independent existence with total support for basic daily activities; 5=severe disabling, totally dependent requiring constant attention day and night; 6=death from neurological symptoms). Patients were considered improved or deteriorated if their Rankin score (RS) changed by at least 1 point. Stabilisation was defined as no change of RS after three courses of therapy.
Survival was determined from onset of treatment to death. The median survival time was defined as the shortest survival time for which the value of the Kaplan-Meier estimator of the survival function was <0.5.13
The detection of anti-Hu and anti-Yo Abs was done by indirect immunoperoxidase on frozen sections of normal human brain cortex or cerebellum, and confirmed by western blot analysis. Serum and CSF anti-Hu and anti-Yo titres were defined as the reciprocal value of the highest dilution that demonstrated neuronal nuclear or Purkinje cell staining. Antibody titrations were done before treatment in serum and in some patients in CSF. When possible, titrations were repeated after treatment.
Patients received one to nine cycles of immunosuppressive therapy (mean 3.5). Tolerance was good and no patient experienced grade 3/4 toxicity (World Health Organisation). Only one patient (9) had a slight reaction characterised by feeling of discomfort with shivering and reversible agitation at the end of the second cycle, which did not recur during the subsequent cycles.
One patient (6) was not evaluable for therapeutic response; he developed symptomatic brain metastasis, and it was not possible to distinguish the respective responsibilities of the paraneoplastic syndrome and of the metastasis in his neurological deterioration.
Of the nine evaluable anti-Hu+ patients, none improved, five (56%) stabilised, and four (44%) deteriorated. Among the six patients who presented with an RS ⩽3 at the beginning of the treatment four ( 3, 4, 5, 8) deteriorated and the two others, including one who also received antitumour treatment, were stabilised (4, 35 months). The three anti-Hu+ patients who had an RS >3 at the beginning of the treatment (7, 9, 10) were stabilised.
All anti-Yo+ patients were evaluable for therapeutic response. Three of them presented with RS⩽3 at the onset. One stabilised during 16 months (13) and two worsened (11, 12). The four patients who had RS>3 at presentation (14, 15, 16, 17) deteriorated.
Post-treatment autoantibody titres in serum samples were available in only five anti-Hu+ patients and two anti-Yo+ patients. In all but one patient, the titres dropped substantially. Mean pretreatment and post-treatment titres were respectively 53 200 (SD 46 639) and 15 400 (SD 15 868) in anti-Hu+patients. In the two anti-Yo+ patients, decreased titres after the treatment were found in one patient (32 000 to 8000) whereas the titre did not change after three courses of treatment in the other patient. Autoantibody titres in CSF could be evaluated twice in only one anti-Hu+ patient (7), in whom it decreased after three courses from 500 to 100. Unfortunately, this patient with a sensory neuropathy had no intrathecal synthesis of the anti-Hu Ab at the onset according to Schuller's formula.14 15
Thus, of the 16 evaluable patients, none improved and only three (18.8%), two patients with SN and one with PCD experienced “useful stabilisation”, defined as stable disease when RS remained⩽3. Median survival for all the patients (after the onset of the treatment) was 5 months (range 2–38+ months). It was 6 (range 3–35+) and 5 (range 2–38+) months for the anti-Hu+ and the anti-Yo+ patients, respectively.
The response of the paraneoplastic neurological syndromes to immunosuppressors or antitumour treatment is greatly influenced by the underlying neuropathology. When the neuronal cell bodies are spared such as in Lambert-Eaton myasthenic syndrome, paraneoplastic vasculitic neuropathy, and some patients with paraneoplastic opsoclonus-myoclonus, recovery has been reported after immunotherapy and anticancer therapy.16-18 Unfortunately, the hallmark of PEM/SN with anti-Hu Ab and of PCD with anti-Yo Ab is a neuronal loss.
In this setting, a therapeutic benefit can be considered as either improvement, which implies that some kind of functional alterations may precede neuronal death, or at least stabilisation in patients who are still ambulatory (RS⩽3). In bedridden patients (RS⩾4) only improvement is relevant and stabilisation cannot be considered a therapeutic benefit because it is useless in terms of quality of life and may occur spontaneously.19
Using these criteria for response, the purpose of this study was to evaluate the effect of a vigorous immunosuppressive treatment combining high doses of steroids, CTX, and IVIg in PNS with anti-Hu or anti-Yo Ab. This regimen was selected because each agent has been occasionally claimed to be useful in PNS4 6 20-22raising the hope that their combination could be additive or synergistic. Furthermore, such combinations have been successful in other autoimmune diseases, including diseases with intrathecal synthesis of IgG, a feature that is also found in many patients with paraneoplastic neurological syndromes and antineuronal Ab.10 11
Despite a good tolerance, our results are clearly disappointing in the patients who were severely disabled at the onset of treatment (RS⩾4) as none of them improved suggesting that immunosuppressors are not useful in this subgroup, whatever the type of paraneoplastic neurological syndromes (PCD or PEM/SN). The most likely hypothesis to explain this finding is that the treatment was started too late at a stage when neuronal loss was already massive and irreversible. Lack of efficacy of immunosupressors in disabled patients has been previously found by our group and others7 8 in 30 patients identified in the literature and in our database. However, Ohet al recently reported on two severely disabled patients with PEM/SN with anti-Hu Ab who improved after immunosuppressors alone (steroids in one and steroids+IVIg+azathioprine in the other)6 but some caution is necessary to interpret this finding because two cases of spontaneous improvement have also been described in the anti-Hu syndrome.23 In fact, improvement after treatment with immunosuppressors in severely disabled patients seems so exceptional (if it does exist) that we think that systematic prescription of very expensive agents (IVIg) or potentially harmful agents that may interfere with chemotherapy of the underlying tumour (CTX) is not indicated in patients with RS⩾4. Nevertheless, a trial of corticosteroids may be worthwhile in this setting according to the literature.
Analysis of the patients who were still ambulatory (RS⩽3) at the onset of treatment is more complex. In these patients, none of them improved but two out of six with an anti-Hu syndrome (both had SN) and one out of three PCD with anti-Yo Ab stabilised for 4, 35, and 16 months, respectively. The “useful” stabilisation experienced by these patients could result from two possibilities. Firstly, the immunosuppressor treatment may have had a real, albeit modest effect that could not be ascribed only to the tumour treatment which was not concomitantly administered in two of these three patients. If this is the case, our data suggest that in the anti-Hu syndrome, immunosuppressors would mainly benefit patients with involvement of the peripheral nervous system. In a previous study we also found that a few patients with SN (two of six with RS⩽3) apparently benefited from IVIg.8 It is of interest to note that five out of the six patients with an anti-Hu syndrome who have been reported to improve after various immunosuppressors (and antitumour treatment in five cases) had an exclusive involvement of the peripheral nervous system with sensory neuropathy as the main finding,1-3 5 6 8leading to the suggestion that the lack of a blood-brain or blood-nerve barrier at the level of the dorsal root ganglia could facilitate the entry and action of immunosuppressors in patients with SN. The second possibility is that our three patients had an indolent form of the disease24 or had a spontaneous stabilisation, an issue that we identified in previous studies.8 Even if we took care to avoid this bias by selecting only patients who were deteriorating neurologically when immunosuppressive therapy was started, we cannot rule out a coincidental association between treatment onset and spontaneous stabilisation of a disease the natural history of which may be heterogeneous. The fact that serum titres of antineuronal Ab dropped substantially in six out of the seven patients in whom we obtained serum samples before and after treatment, including three patients who received immunosuppressors alone, could favour the hypothesis of a real beneficial effect of immunosuppressors. Nevertheless, such findings have been made previously after plasmapheresis or IVIg without a clinical counterpart7 8 25 and we were not able, as others,1 2 5 26 to find a correlation between serum titres of Ab and neurological course. For example, patient 1 who experienced “useful” stabilisation had a 10-fold fall in serum titre after treatment but patient 4 also had a striking drop of serum Ab (16-fold) despite progressive neurological deterioration. We cannot comment on the effect of this therapeutic regimen on intrathecal synthesis of the autoantibodies as the only patient in this series who had repeated CSF examination had pure SN and had no intrathecal synthesis of the anti-Hu Ab, in agreement with our previous findings.11
Only a prospective randomised study could definitely answer to the question of a possible benefit of immunosuppressive therapy. Unfortunately, as previously stated, it is highly unlikely that a double blind randomised trial can ever be designed in these disorders due to their extremely low frequency. At least, analysis of series coming from the same institutions provide more information than simple case reports. Despite its methodological limitations, this trial indicates that combined treatment with IVIg, CTX, and MP in patients with PEM/SN or PCD with antineuronal Ab is well tolerated but does not seem to be useful in debilitated patients (RS⩾4). The question remains open of a transient stabilisation in this regimen in a minority of the patients (mainly with SN) who are still ambulatory at the onset of treatment (RS⩽3). To better delineate the respective roles of immunosuppressors and antitumour treatment in these diseases, we are currently screening our database to see if the addition of immunosuppressive therapy to antitumour treatment modifies the neurological and oncological course compared with antitumour treatment alone, particularly in patients with SN.
This work was supported by the “Association pour la Recherche sur les Tumeurs Cérébrales”. We thank Drs M Uchuya, C Kouhatra, PJ Souquet, B Guillon, and JH Ruel for their help in patient follow up and collecting data, and Dr B Benyahia, MC Nadaud, L Tömpe, B Duprey, and I Lysson for their technical help.