Evidence map›Paper›PMID 33208548›Full record

Observational studyNeurology2021

Paraneoplastic Myeloneuropathies: Clinical, Oncologic, and Serologic Accompaniments.

Shailee Shah, Rocio Vazquez Do Campo, Neeraj Kumar, Andrew McKeon, Eoin P Flanagan, Christopher Klein, Sean J Pittock, Divyanshu Dubey

Abstract readObservational Study
In one paragraph

Observational study in Neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

  1. Review
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  6. Article
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  9. Article
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  11. Article
  12. Paraneoplastic Neurologic Disorders.Current neurology and neuroscience reports · 2023
    Review
  13. Article
  14. A review of the neurological complications of breast cancer.Journal of family medicine and primary care · 2022
    Review
  15. Article
  16. Paraneoplastic neurological syndrome: growing spectrum and relevance.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Review
  17. Review
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  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Shailee ShahFrom the Departments of Neurology (S.S., R.V.D.C., N.K., A.M., E.P.F., C.K., S.J.P., D.D.) and Laboratory Medicine and Pathology (A.M., E.P.F., C.K., S.J.P., D.D.), Mayo Clinic College of Medicine, Rochester, MN.ORCID 0000-0002-3451-0303
Rocio Vazquez Do CampoFrom the Departments of Neurology (S.S., R.V.D.C., N.K., A.M., E.P.F., C.K., S.J.P., D.D.) and Laboratory Medicine and Pathology (A.M., E.P.F., C.K., S.J.P., D.D.), Mayo Clinic College of Medicine, Rochester, MN.ORCID 0000-0001-8980-8185
Neeraj KumarFrom the Departments of Neurology (S.S., R.V.D.C., N.K., A.M., E.P.F., C.K., S.J.P., D.D.) and Laboratory Medicine and Pathology (A.M., E.P.F., C.K., S.J.P., D.D.), Mayo Clinic College of Medicine, Rochester, MN.
Andrew McKeonFrom the Departments of Neurology (S.S., R.V.D.C., N.K., A.M., E.P.F., C.K., S.J.P., D.D.) and Laboratory Medicine and Pathology (A.M., E.P.F., C.K., S.J.P., D.D.), Mayo Clinic College of Medicine, Rochester, MN.
Eoin P FlanaganFrom the Departments of Neurology (S.S., R.V.D.C., N.K., A.M., E.P.F., C.K., S.J.P., D.D.) and Laboratory Medicine and Pathology (A.M., E.P.F., C.K., S.J.P., D.D.), Mayo Clinic College of Medicine, Rochester, MN.
Christopher KleinFrom the Departments of Neurology (S.S., R.V.D.C., N.K., A.M., E.P.F., C.K., S.J.P., D.D.) and Laboratory Medicine and Pathology (A.M., E.P.F., C.K., S.J.P., D.D.), Mayo Clinic College of Medicine, Rochester, MN.
Sean J PittockFrom the Departments of Neurology (S.S., R.V.D.C., N.K., A.M., E.P.F., C.K., S.J.P., D.D.) and Laboratory Medicine and Pathology (A.M., E.P.F., C.K., S.J.P., D.D.), Mayo Clinic College of Medicine, Rochester, MN.
Divyanshu DubeyFrom the Departments of Neurology (S.S., R.V.D.C., N.K., A.M., E.P.F., C.K., S.J.P., D.D.) and Laboratory Medicine and Pathology (A.M., E.P.F., C.K., S.J.P., D.D.), Mayo Clinic College of Medicine, Rochester, MN. dubey.divyanshu@mayo.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo test the hypothesis that myeloneuropathy is a presenting phenotype of paraneoplastic neurologic syndromes we retrospectively reviewed clinical, radiologic, and serologic features of 32 patients with concomitant paraneoplastic spinal cord and peripheral nervous system involvement.

methodsObservational study investigating patients with myeloneuropathy and underlying cancer or onconeural antibody seropositivity.

resultsAmong 32 patients with paraneoplastic myeloneuropathy, 20 (63%) were women with median age 61 years (range 27-84 years). Twenty-six patients (81%) had classified onconeural antibodies (amphiphysin, n = 8; antineuronal nuclear antibody [ANNA] type 1 [anti-Hu], n = 5; collapsin response mediator protein 5 [CRMP5] [anti-CV2], n = 6; Purkinje cell cytoplasmic antibody type 1 [PCA1] [anti-Yo], n = 1; Purkinje cell cytoplasmic antibody type 2 [PCA2], n = 2; kelch-like protein 11 [KLHL11], n = 1; and combinations thereof: ANNA1/CRMP5, n = 1; ANNA1/amphiphysin, n = 1; ANNA3/CRMP5, n = 1). Cancer was confirmed in 25 cases (onconeural antibodies, n = 19; unclassified antibodies, n = 3; no antibodies, n = 3). Paraneoplastic myeloneuropathies had asymmetric paresthesias (84%), neuropathic pain (78%), subacute onset (72%), sensory ataxia (69%), bladder dysfunction (69%), and unintentional weight loss >15 pounds (63%). Neurologic examination demonstrated concomitant distal or asymmetric hyporeflexia and hyperreflexia (81%), impaired vibration and proprioception (69%), Babinski response (68%), and asymmetric weakness (66%). MRI showed longitudinally extensive (45%), tract-specific spinal cord T2 hyperintensities (39%) and lumbar nerve root enhancement (38%). Ten of 28 (36%) were unable to ambulate independently at last follow-up (median 24 months, range 5-133 months). Combined oncologic and immunologic therapy had more favorable modified Rankin Scale scores at post-treatment follow-up compared to those receiving either oncologic or immunologic therapy alone (2 [range 1-4] vs 4 [range 2-6],

conclusionsParaneoplastic etiologies should be considered in the evaluation of subacute myeloneuropathies. Recognition of key characteristics of paraneoplastic myeloneuropathy may facilitate early tumor diagnosis and initiation of immunosuppressive treatment.

Indexed as

AdultAgedAged, 80 and overAutoantibodiesFemaleHEK293 CellsHumansMaleMiddle AgedParaneoplastic PolyneuropathyParaneoplastic Syndromes, Nervous SystemRetrospective StudiesAutoantibodies

Identifiers

PMID33208548
PMCPMC7905784

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.