What Is on Your Mind? Impaired Social Cognition in Primary Central Nervous System Lymphoma Patients Despite Ongoing Complete Remission
Abstract
:Simple Summary
Abstract
1. Introduction
2. Materials and Methods
2.1. Participants
2.2. Screening Measures
2.3. Social Cognition Measures
2.3.1. Dispositional Empathy (Interpersonal Reactivity Index)
2.3.2. Behavioral Empathy (Multifaceted Empathy Test)
2.3.3. Social Problem-Solving Fluency Task
“Mark is organizing a concert for charity. His friend loves singing but cannot sing in tune. His friend offers to perform a solo in the concert.”
- 1.
- Control question: Who is organizing the concert?
- 2.
- Social problem-solving questions:
- Why may the situation be awkward for Mark?
- How awkward a situation is it for Mark, out of 100%?
- What could Mark do in this situation? Suggest as many good ideas as you can for dealing with the situation. You have one minute.
- SP example: Explain tactfully that he needs professionals.
- S example: Let his friend sing a solo in the concert.
- P example: Tell his friend that he cannot sing in tune.
- N example: Cancel the concert.
3. Procedure
4. Data Analysis
5. Results
5.1. Social Cognition Measures
5.1.1. Dispositional Empathy
5.1.2. Behavioral Empathy
5.1.3. Social Problem-Solving Fluency Task
5.2. Additional Analyses to Control for Neuropsychological Background Measures and Estimated Overall Intelligence Scores
5.3. Additional Analyses Regarding Different Subgroups of Patients
5.4. Additional Non-Parametric Statistical Analyses
6. Discussion
7. Conclusions
Supplementary Materials
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Batchelor, T.T. Primary central nervous system lymphoma: A curable disease. Hematol. Oncol. 2019, 37, 15–18. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- van der Meulen, M.; Dirven, L.; Habets, E.J.J.; van den Bent, M.J.; Taphoorn, M.J.B.; Bromberg, J.E.C. Cognitive functioning and health-related quality of life in patients with newly diagnosed primary CNS lymphoma: A systematic review. Lancet Oncol. 2018, 19, 407–418. [Google Scholar] [CrossRef]
- Korfel, A.; Schlegel, U. Diagnosis and treatment of primary CNS lymphoma. Nat. Rev. Neurol. 2013, 9, 317–327. [Google Scholar] [CrossRef]
- Seidel, S.; Korfel, A.; Kowalski, T.; Margold, M.; Ismail, F.; Schroers, R.; Baraniskin, A.; Pels, H.; Martus, P.; Schlegel, U. HDMTX-based induction therapy followed by consolidation with conventional systemic chemotherapy and intraventricular therapy (modified Bonn protocol) in primary CNS lymphoma: A monocentric retrospective analysis. Neurol. Res. Pract. 2019, 1, 1–9. [Google Scholar] [CrossRef] [Green Version]
- Seidel, S.; Schlegel, U. Have treatment protocols for primary CNS lymphoma advanced in the past 10 years. Expert Rev. Anticancer Ther. 2019, 19, 909–915. [Google Scholar] [CrossRef]
- Fliessbach, K.; Helmstaedter, C.; Urbach, H.; Althaus, A.; Pels, H.; Linnebank, M.; Juergens, A.; Glasmacher, A.; Schmidt-Wolf, I.G.; Klockgether, T.; et al. Neuropsychological outcome after chemotherapy for primary CNS lymphoma: A prospective study. Neurology 2005, 64, 1184–1188. [Google Scholar] [CrossRef] [PubMed]
- Harder, H.; Holtel, H.; Bromberg, J.E.C.; Poortmans, P.; Haaxma-Reiche, H.; Kluin-Nelemans, H.C.; Menten, J.; van den Bent, M.J. Cognitive status and quality of life after treatment for primary CNS lymphoma. Neurology 2004, 62, 544–547. [Google Scholar] [CrossRef]
- Juergens, A.; Pels, H.; Rogowski, S.; Fliessbach, K.; Glasmacher, A.; Engert, A.; Reiser, M.; Diehl, V.; Vogt-Schaden, M.; Egerer, G.; et al. Long-term survival with favorable cognitive outcome after chemotherapy in primary central nervous system lymphoma. Ann. Neurol. 2010, 67, 182–189. [Google Scholar] [CrossRef]
- Guha-Thakurta, N.; Damek, D.; Pollack, C.; Hochberg, F.H. Intravenous Methotrexate as Initial Treatment for Primary Central Nervous System Lymphoma: Response to Therapy and Quality of Life of Patients. J. Neurooncol. 1999, 43, 259–268. [Google Scholar] [CrossRef]
- Doolittle, N.D.; Korfel, A.; Lubow, M.A.; Schorb, E.; Schlegel, U.; Rogowski, S.; Fu, R.; Dósa, E.; Illerhaus, G.; Kraemer, D.F.; et al. Long-term cognitive function, neuroimaging, and quality of life in primary CNS lymphoma. Neurology 2013, 81, 84–92. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Frith, C.D. The social brain? Philos. Trans. R. Soc. Lond. B Biol. Sci. 2007, 362, 671–678. [Google Scholar] [CrossRef] [PubMed]
- Adolphs, R. The Social Brain: Neural Basis of Social Knowledge. Annu. Rev. Psychol. 2009, 60, 693–716. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ozbay, F.; Johnson, D.C.; Dimoulas, E.; III, M.; Charney, D.; Southwick, S. Social Support and Resilience to Stress: From Neurobiology to Clinical Practice. Psychiatry 2007, 4, 35–40. [Google Scholar]
- Cubis, L.; Ownsworth, T.; Pinkham, M.B.; Foote, M.; Legg, M.; Chambers, S. The importance of staying connected: Mediating and moderating effects of social group memberships on psychological well-being after brain tumor. Psychooncology 2019, 28, 1537–1543. [Google Scholar] [CrossRef] [PubMed]
- Adolphs, R. The neurobiology of social cognition. Curr. Opin. Neurobiol. 2001, 11, 231–239. [Google Scholar] [CrossRef]
- Gaspar, T.; Cabrita, T.R.A.; Gaspar de Matos, M. Psychological and Social Factors That Influence Quality of Life: Gender, Age and Professional Status Differences. Psychol. Res. 2017, 7, 489–498. [Google Scholar] [CrossRef] [Green Version]
- Peretti, S.; Tempesta, D.; Socci, V.; Pino, M.C.; Mazza, M.; Valenti, M.; de Gennaro, L.; Di Dio, C.; Marchetti, A.; Ferrara, M. The role of sleep in aesthetic perception and empathy: A mediation analysis. J. Sleep Res. 2019, 28, 1–14. [Google Scholar] [CrossRef]
- Decety, J.; Lamm, C. Human empathy through the lens of social neuroscience. Sci. World J. 2006, 6, 1146–1163. [Google Scholar] [CrossRef] [Green Version]
- Shamay-Tsoory, S.G.; Aharon-Peretz, J.; Perry, D. Two systems for empathy: A double dissociation between emotional and cognitive empathy in inferior frontal gyrus versus ventromedial prefrontal lesions. Brain 2009, 132, 617–627. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Dvash, J.; Shamay-Tsoory, S.G. Theory of Mind and Empathy as Multidimensional Constructs: Neurological foundations. Top. Lang. Disord. 2014, 34, 282–295. [Google Scholar] [CrossRef] [Green Version]
- Shamay-Tsoory, S.G.; Aharon-Peretz, J. Dissociable prefrontal networks for cognitive and affective theory of mind: A lesion study. Neuropsychologia 2007, 45, 3054–3067. [Google Scholar] [CrossRef] [PubMed]
- Channon, S.; Crawford, S. Mentalising and social problem-solving after brain injury. Neuropsychol. Rehabil. 2010, 20, 739–759. [Google Scholar] [CrossRef]
- Tse, W.S.; Bond, A.J. The impact of depression on social skills. J. Nerv. Ment. Dis. 2004, 192, 260–268. [Google Scholar] [CrossRef]
- Stevens, J.S.; Jovanovic, T. Role of social cognition in post-traumatic stress disorder: A review and meta-analysis. Genes Brain Behav. 2019, 18, 1–10. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Couette, M.; Mouchabac, S.; Bourla, A.; Nuss, P.; Ferreri, F. Social cognition in post-traumatic stress disorder: A systematic review. Br. J. Clin. Psychol. 2020, 59, 117–138. [Google Scholar] [CrossRef] [PubMed]
- Penn, D.L.; Corrigan, P.W.; Bentall, R.P.; Racenstein, J.M.; Newman, L. Social cognition in schizophrenia. Psychol. Bull. 1997, 121, 114–132. [Google Scholar] [CrossRef] [PubMed]
- Javed, A.; Charles, A. The Importance of Social Cognition in Improving Functional Outcomes in Schizophrenia. Front. Psychiatry 2018, 9, 1–14. [Google Scholar] [CrossRef]
- Bishop-Fitzpatrick, L.; Mazefsky, C.A.; Eack, S.M.; Minshew, N.J. Correlates of Social Functioning in Autism Spectrum Disorder: The Role of Social Cognition. Res. Autism Spectr. Disord. 2017, 35, 25–34. [Google Scholar] [CrossRef] [Green Version]
- Barendse, E.M.; Hendriks, M.P.H.; Thoonen, G.; Aldenkamp, A.P.; Kessels, R.P.C. Social behaviour and social cognition in high-functioning adolescents with autism spectrum disorder (ASD): Two sides of the same coin? Cogn. Process. 2018, 19, 545–555. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Cotter, J.; Granger, K.; Backx, R.; Hobbs, M.; Looi, C.Y.; Barnett, J.H. Social cognitive dysfunction as a clinical marker: A systematic review of meta-analyses across 30 clinical conditions. Neurosci. Biobehav. Rev. 2018, 84, 92–99. [Google Scholar] [CrossRef] [PubMed]
- Porcelli, S.; van der Wee, N.; van der Werff, S.; Aghajani, M.; Glennon, J.C.; van Heukelum, S.; Mogavero, F.; Lobo, A.; Olivera, F.J.; Lobo, E.; et al. Social brain, social dysfunction and social withdrawal. Neurosci. Biobehav. Rev. 2019, 97, 10–33. [Google Scholar] [CrossRef]
- Saver, J.L.; Damasio, A.R. Preserved access and processing of social knowledge in a patient with acquired sociopathy due to ventromedial frontal damage. Neuropsychologia 1991, 29, 1241–1249. [Google Scholar] [CrossRef]
- Mattavelli, G.; Pisoni, A.; Casarotti, A.; Comi, A.; Sera, G.; Riva, M.; Bizzi, A.; Rossi, M.; Bello, L.; Papagno, C. Consequences of brain tumour resection on emotion recognition. J. Neuropsychol. 2017, 13, 1–21. [Google Scholar] [CrossRef]
- Nakajima, R.; Yordanova, Y.N.; Duffau, H.; Herbet, G. Neuropsychological evidence for the crucial role of the right arcuate fasciculus in the face-based mentalizing network: A disconnection analysis. Neuropsychologia 2018, 115, 179–187. [Google Scholar] [CrossRef] [PubMed]
- Campanella, F.; Fabbro, F.; Ius, T.; Shallice, T.; Skrap, M. Acute effects of surgery on emotion and personality of brain tumor patients: Surgery impact, histological aspects, and recovery. Neuro Oncol. 2015, 17, 1121–1131. [Google Scholar] [CrossRef] [Green Version]
- Gu, X.; Gao, Z.; Wang, X.; Liu, X.; Knight, R.T.; Hof, P.R.; Fan, J. Anterior insular cortex is necessary for empathetic pain perception. Brain 2012, 135, 2726–2735. [Google Scholar] [CrossRef] [Green Version]
- Sutcliffe, T.; Bjorkquist, O.; Skirnyk, K.; Tate, M. NCOG-09. Comprehensive assessment of long-term social cognition (Theory of Mind) outcomes in glioma patients following standard-of-care treatment. Neuro Oncol. 2017, 19, 139. [Google Scholar] [CrossRef]
- Chen, P.; Wang, G.; Ma, R.; Jing, F.; Zhang, Y.; Wang, Y.; Zhang, P.; Niu, C.; Zhang, X. Multidimensional assessment of empathic abilities in patients with insular glioma. Cogn. Affect. Behav. Neurosci. 2016, 16, 962–975. [Google Scholar] [CrossRef] [Green Version]
- Goebel, S.; Mehdorn, H.M.; Wiesner, C.D. Social cognition in patients with intracranial tumors: Do we forget something in the routine neuropsychological examination? J. Neurooncol. 2018, 140, 687–696. [Google Scholar] [CrossRef] [PubMed]
- Pertz, M.; Okoniewski, A.; Schlegel, U.; Thoma, P. Impairment of sociocognitive functions in patients with brain tumours. Neurosci. Biobehav. Rev. 2020, 108, 370–392. [Google Scholar] [CrossRef] [PubMed]
- Herbet, G.; Lafargue, G.; Moritz-Gasser, S.; Menjot de Champfleur, N.; Costi, E.; Bonnetblanc, F.; Duffau, H. A disconnection account of subjective empathy impairments in diffuse low-grade glioma patients. Neuropsychologia 2015, 70, 165–176. [Google Scholar] [CrossRef]
- Wiemann, G.; Pertz, M.; Kowalski, T.; Seidel, S.; Schlegel, U.; Thoma, P. Complete response to therapy: Why do primary central nervous system lymphoma patients not return to work? J. Neurooncol. 2020, 149, 171–179. [Google Scholar] [CrossRef]
- Lehrl, S. Manual zum MWT-B [Mehrfachwahl-Wortschatz-Intelligenztest]; 5. unveränd. Aufl.; Spitta-Verl.: Balingen, Germany, 2005; ISBN 9783934211049. [Google Scholar]
- Aschenbrenner, S.; Tucha, O.; Lange, K.W. RWT—Regensburger Wortflüssigkeits-Test; Hogrefe: Göttingen, Germany, 2000. [Google Scholar]
- Hautziger, M.; Keller, F.; Kühner, C. BDI-II—Beck-Depressions-Inventar. Klinisch-psychiatrische Ratingskalen für das Kindes-und Jugendalter 2010, 6, 75. [Google Scholar]
- Paulus, C. Der Saarbrücker Persönlichkeitsfragebogen SPF (IRI) zur Messung von Empathie; Universität des Saarlandes: Saarbrücken, Germany, 2007. [Google Scholar]
- Davis, M.H. Measuring individual differences in empathy: Evidence for a multidimensional approach. J. Personal. Soc. Psychol. 1983, 44, 113–126. [Google Scholar] [CrossRef]
- Davis, M.H. A Multidimensional Approach to Individual Differences in Empathy. J. Personal. Soc. Psychol. 1980, 10, 113–126. [Google Scholar]
- Dziobek, I.; Rogers, K.; Fleck, S.; Bahnemann, M.; Heekeren, H.R.; Wolf, O.T.; Convit, A. Dissociation of cognitive and emotional empathy in adults with Asperger syndrome using the Multifaceted Empathy Test (MET). J. Autism Dev. Disord. 2008, 38, 464–473. [Google Scholar] [CrossRef]
- Thoma, P.; Schmidt, T.; Juckel, G.; Norra, C.; Suchan, B. Nice or effective? Social problem solving strategies in patients with major depressive disorder. Psychiatry Res. 2015, 228, 835–842. [Google Scholar] [CrossRef]
- Schmidt, T.; Roser, P.; Juckel, G.; Brüne, M.; Suchan, B.; Thoma, P. Social cognition and social problem solving abilities in individuals with alcohol use disorder. J. Clin. Exp. Neuropsychol. 2016, 38, 974–990. [Google Scholar] [CrossRef]
- Thoma, P.; Sonnenburg, S.; Marcinkowski, N.; Juckel, G.; Edel, M.-A.; Suchan, B. Social problem solving in adult patients with attention deficit hyperactivity disorder. Psychiatry Res. 2020, 285. [Google Scholar] [CrossRef]
- Howell, D.C. Statistical Methods for Psychology, 7th ed.; Wadsworth Cengage Learning: Belmont, CA, USA, 2010; ISBN 9780495597858. [Google Scholar]
- Correa, D.D.; Braun, E.; Kryza-Lacombe, M.; Ho, K.W.; Reiner, A.S.; Panageas, K.S.; Yahalom, J.; Sauter, C.S.; Abrey, L.E.; DeAngelis, L.M.; et al. Longitudinal cognitive assessment in patients with primary CNS lymphoma treated with induction chemotherapy followed by reduced-dose whole-brain radiotherapy or autologous stem cell transplantation. J. Neurooncol. 2019, 144, 553–562. [Google Scholar] [CrossRef]
- Rueckert, L.; Branch, B.; Doan, T. Are Gender Differences in Empathy Due to Differences in Emotional Reactivity? Psychology 2011, 2, 574–578. [Google Scholar] [CrossRef] [Green Version]
- Wideheim, A.-K.; Edvardsson, T.; Påhlson, A.; Ahlström, G. A Family’s Perspective on Living with a Highly Malignant Brain Tumor. Cancer Nurs. 2002, 25, 236–244. [Google Scholar] [CrossRef] [PubMed]
- House, J.S.; Landis, K.R.; Umberson, D. Social relationships and health. Science 1988, 241, 540–545. [Google Scholar] [CrossRef]
- O’Keeffe, F.M.; Murray, B.; Coen, R.F.; Dockree, P.M.; Bellgrove, M.A.; Garavan, H.; Lynch, T.; Robertson, I.H. Loss of insight in frontotemporal dementia, corticobasal degeneration and progressive supranuclear palsy. Brain 2007, 130, 753–764. [Google Scholar] [CrossRef]
- Eslinger, P.J.; Moore, P.; Anderson, C.; Grossman, M. Social cognition, executive functioning, and neuroimaging correlates of empathic deficits in frontotemporal dementia. J. Neuropsychiatry Clin. Neurosci. 2011, 23, 74–82. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Brüne, M.; Brüne-Cohrs, U. Theory of mind-evolution, ontogeny, brain mechanisms and psychopathology. Neurosci. Biobehav. Rev. 2006, 30, 437–455. [Google Scholar] [CrossRef]
- Boele, F.W.; Rooney, A.G.; Grant, R.; Klein, M. Psychiatric symptoms in glioma patients: From diagnosis to management. Neuropsychiatr. Dis. Treat. 2015, 11, 1413–1420. [Google Scholar] [CrossRef] [Green Version]
- Roelofs, R.L.; Wingbermühle, E.; Egger, J.I.M.; Kessels, R.P.C. Social Cognitive Interventions in Neuropsychiatric Patients: A Meta-Analysis. Brain Impair. 2017, 18, 138–173. [Google Scholar] [CrossRef] [Green Version]
- Schulte, F.; Vannatta, K.A.; Barrera, M. Social problem solving and social performance after a group social skills intervention for childhood brain tumor survivors. Psychooncology 2014, 22, 183–189. [Google Scholar] [CrossRef]
PCNSL Patients | |||||
---|---|---|---|---|---|
Total | |||||
Neuropathology | Diffuse large B-cell lymphoma | Other | |||
43 | 0 | 43 | |||
Tissue diagnosis by | Tumor resection | Open biopsy | Stereotactic biopsy | CSF 1 cytology | |
14 | 1 | 26 | 2 | 43 | |
First-line treatment | HDMTX 2-based polychemoimmunotherapy, followed by intensified conventional chemotherapy plus intraventricular treatment for consolidation | HDMTX-based polychemoimmunotherapy, followed by intensified conventional chemotherapy without intraventricular treatment for consolidation | HDMTX-based polychemoimmunotherapy, followed by HDASCT 3 for consolidation | HDMTX-based chemotherapy with temozolomide alone for consolidation | |
32 | 3 | 7 | 1 4 | 43 | |
Tumor relapse | No | Yes | |||
37 | 6 (5 cerebral, 1 ocular only, no systemic relapse) | 43 | |||
Treatment at relapse | Two patients were treated with HDASCT, and three patients were treated with intensified conventional chemotherapy. All five patients received complete remission after salvage treatment. The patient, who suffered from an ocular relapse, received radiation with 36 + 14 Gray fractionized to 5 × 2 Gray to two-thirds of the posterior eye bulb. |
Data | PCNSL Patients | Healthy Controls | Test Statistics |
---|---|---|---|
N | 43 | 43 | |
Median age at testing (years) | 65 (range 37–83) | 66 (range 35–80) | n.s. |
Gender (female:male) | 21:22 | 21:22 | n.s. |
Years of school | 10.56 (2.21) | 11.38 (1.85) | n.s. |
Years of education | 14.92 (3.70) | 15.63 (3.30) | n.s. |
Estimated overall intelligence | 113.63 (13.82) | 121.67 (12.68) | t(82) = 2.780, p = 0.007, d = 0.607 |
Regensburg verbal fluency test (number of words within one minute) | |||
Phonematic verbal fluency | 10.86 (4.05) | 11.70 (4.21) | Main effect of group F(1,84) = 6.077, p = 0.016, η2 = 0.067 main effect of condition F(2,168) = 229.433, p < 0.001, η2 = 0.732 |
Semantic verbal fluency one category | 20.86 (5.79) | 23.56 (5.16) | |
Semantic verbal fluency category switch | 13.37 (3.28) | 15.07 (2.73) | |
Beck Depression Inventory score | 10.30 (9.13) | 5.16 (3.71) | t(55.5) = −3.420, p = 0.001, d = 0.738 |
Data and Measures | Statistical Method |
---|---|
Age | t-test |
Gender | χ2-test |
Years of school | t-test |
Years of education | t-test |
German multiple-choice vocabulary intelligence test | t-test |
Regensburg verbal fluency test | Repeated-measures analysis of variances |
Beck Depression Inventory score | t-test |
Interpersonal Reactivity Index | Repeated-measures analysis of variances |
Multifaceted Empathy Test | Repeated-measures analysis of variances |
Social Problem-Solving Fluency Task, control questions | t-test |
Social Problem-Solving Fluency Task, detection of awkwardness | t-test |
Social Problem-Solving Fluency Task, subjective degree of awkwardness | t-test |
Social Problem-Solving Fluency Task, solution fluency | Repeated-measures analysis of variances |
Social Problem-Solving Fluency Task, selection of optimal alternatives | t-test |
Performance Measure | PCNSL Patients | Healthy Controls | Test Statistics |
---|---|---|---|
N | 43 | 43 | |
Interpersonal Reactivity Index | |||
Empathic concern | 14.51 (2.75) | 14.30 (2.48) | Interaction of subscale and group F(2.7,230.7) = 3.869, p = 0.012, η2 = 0.044 Main effect of subscale F(2.7,230.7) = 56.034, p < 0.001, η2 = 0.400 |
Personal distress | 11.23 (3.34) | 9.79 (2.39) | |
Fantasy | 12.02 (2.88) | 12.30 (2.75) | |
Perspective-taking | 14.12 (2.64) | 15.12 (1.98) | |
Social Problem-Solving Task | |||
Control questions (mean percent correct) | 93.95 (11.78) | 97.09 (5.48) | n.s. |
Detection of awkwardness (mean percent correct) | 64.88 (27.55) | 83.26 (16.29) | t(68.2) = 3.764, p < 0.001, d = 0.812 |
Subjective degree of awkwardness (mean rating percent) | 72.78 (18.49) | 72.63 (11.81) | n.s. |
Selection of optimal (SP 1) alternatives (mean percent correct) | 49.77 (20.64) | 61.40 (19.71) | t(84) = 2.672, p = 0.009, d = 0.576 |
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Share and Cite
Pertz, M.; Kowalski, T.; Thoma, P.; Schlegel, U. What Is on Your Mind? Impaired Social Cognition in Primary Central Nervous System Lymphoma Patients Despite Ongoing Complete Remission. Cancers 2021, 13, 943. https://doi.org/10.3390/cancers13050943
Pertz M, Kowalski T, Thoma P, Schlegel U. What Is on Your Mind? Impaired Social Cognition in Primary Central Nervous System Lymphoma Patients Despite Ongoing Complete Remission. Cancers. 2021; 13(5):943. https://doi.org/10.3390/cancers13050943
Chicago/Turabian StylePertz, Milena, Thomas Kowalski, Patrizia Thoma, and Uwe Schlegel. 2021. "What Is on Your Mind? Impaired Social Cognition in Primary Central Nervous System Lymphoma Patients Despite Ongoing Complete Remission" Cancers 13, no. 5: 943. https://doi.org/10.3390/cancers13050943
APA StylePertz, M., Kowalski, T., Thoma, P., & Schlegel, U. (2021). What Is on Your Mind? Impaired Social Cognition in Primary Central Nervous System Lymphoma Patients Despite Ongoing Complete Remission. Cancers, 13(5), 943. https://doi.org/10.3390/cancers13050943