Multiple psychosocial factors appear to affect cancer progression in various populations; however, research investigating the relationship between psychosocial factors and outcomes following hematopoietic stem cell transplantation (HCT) is scarce. Subject to adverse immunological and psychological conditions, HCT patients may be especially vulnerable to psychosomatic health sequelae; therefore, we studied whether optimism and anxiety influence the pertinent clinical outcome of days to neutrophil engraftment (DTE).
54 adults undergoing either autologous or allogeneic HCT completed self-report questionnaires measuring optimism and anxiety. We assessed the association between these psychosocial variables and DTE.
Greater optimism and less anxiety were associated with the favorable outcome of fewer DTE in autologous HCT recipients, though this relationship was no longer significant when reducing the sample size to only subjects who filled out their baseline survey by the time of engraftment.
Our findings are suggestive that optimism and anxiety may be associated with time to neutrophil recovery in autologous, but not allogeneic, adult HCT recipients. Further investigation in larger, more homogeneous subjects with consistent baseline sampling is warranted.
Citation: Knight JM, Moynihan JA, Lyness JM, Xia Y, Tu X, Messing S, et al. (2014) Peri-Transplant Psychosocial Factors and Neutrophil Recovery following Hematopoietic Stem Cell Transplantation. PLoS ONE 9(6): e99778. doi:10.1371/journal.pone.0099778
Editor: Graca Almeida-Porada, Wake Forest Institute for Regenerative Medicine, United States of America
Received: January 19, 2014; Accepted: May 19, 2014; Published: June 10, 2014
Copyright: © 2014 Knight et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the National Institutes of Health (5R24 AG031089-02, T32 073452, R21 AT000895). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Psychosocial factors affect cancer progression in multiple populations –. However, research investigating these relationships following hematopoietic stem cell transplantation (HCT) is scarce, with few studies investigating the differential effect of emotions on outcomes and immune recovery –. The number of transplants continues to increase, with 8,000 allogeneic and 11,000 autologous HCTs performed in the United States in 2011 . Their use, safety, efficacy, and availability for hematologic malignancies and disorders have greatly expanded, making it important to identify positive and negative prognostic factors and immunologic mechanisms in this population.
HCTs are associated with unique immunological and psychological conditions. Patients receiving transplants are more immunosuppressed than other cancer patients secondary to ablation of their native marrow. Furthermore, the clinical course of HCT may be more distressing than other cancer treatments, with potentially prolonged periods of physical and emotional isolation depending on the type of transplant, institutional practice, and potential complications . There is generally a significant decline in quality of life in the immediate post-transplant period .
Positive psychosocial variables such as optimism predict not only emotional, but also physical well-being after HCT, including survival , . The psychoneuroimmune mechanisms mediating these associations are unknown. Negative pre-transplant emotions, including depression and anxiety, have been associated with worse post-transplant outcomes and survival , , , ; however, other studies have not confirmed this association , .
Neutropenia is a major contributor to morbidity following transplant ; the longer the period of neutropenia, the greater the potential for infectious complications . Conversely, survival is improved with earlier neutrophil engraftment . Days to neutrophil engraftment (DTE) may, therefore, contribute to differences in mortality among HCT patients with differing pre-transplant psychological profiles. Recently, anxiety and depression were observed to be associated with slower immune recovery as measured by white blood cell (WBC) count following autologous transplant . This relationship has never been examined in allogeneic recipients.
We investigated the association of optimism and anxiety with time to neutrophil recovery in a population of adult HCT recipients undergoing either autologous or allogeneic transplant. We hypothesized that greater optimism and less anxiety around the time of transplant would be associated with less time to neutrophil recovery.
Patients entered the study between Day −20 and Day +3, with Day 0 being the day of stem cell transplant. The goal was to enroll participants as close to Day −8 as possible, but preferably at least prior to transplant. Most commonly, enrollment occurred at the last pre-transplant outpatient visit prior to transplant. Reasons for variation in enrollment time included lack of access to the patient at their pre-transplant visit due to patient, provider, or study staff conflicts or overlap. If a patient was unable to be approached at a pre-transplant visit, they were approached as soon as possible following hospital admission for transplant. On occasion this resulted in enrolling participants after their transplant if admission occurred on a Friday and the conditioning period was short, as occurs with multiple myeloma (conditioning with high dose melphalan on Day −1). One hundred and twenty-two patients were approached by a member of the research team for study participation; 64 (52%) agreed to participate and 54 provided complete psychosocial data. Any patient admitted to the Bone Marrow Transplant Program at the University of Rochester Medical Center for transplantation of any type, age ≥18 years of age or older and able to give informed consent and complete the study questionnaires was eligible to participate. There were no medical condition exclusions. Factors noted to affect neutrophil recovery rates including age, race, gender, conditioning regimen (myeloablative/non-myeloablative), stem cell source (bone marrow or peripheral blood), and number of CD34+ cells infused/kg of recipient body weight were controlled for. Allogeneic and autologous transplants were evaluated separately. All participants received homogeneous granulocyte colony stimulating factor (GCSF); therefore, it was not necessary to include GCSF as a covariate. Due to the small number of minorities, race was dichotomized as Caucasian or non-Caucasian.
Upon obtaining written informed consent (as close to Day −8 as possible), a member of the research team provided participants with the self-administered surveys and was available as long as necessary to answer any questions and ensure participants understood how to complete them. Participants were asked to complete the surveys independently to avoid any possible influence from the research staff. They were also asked to complete them as soon as possible to be picked up the following day by a research team member. There was variation in the time of survey completion, ranging from Day −20 to Day +32. Fifty-seven percent of subjects completed the surveys prior to transplant, 82% by Day +3, and 85% by Day +14.These variations were due to either or both a) variation in time of study enrollment or b) a delay in participants filling out the survey on their own and returning it. Reasons for delays in enrollment are noted as above. The psychological parameters assessed were:
The Life Orientation Test (LOT) assesses individual differences in generalized optimism versus pessimism. The 10-item revised version (LOT-R)  focuses explicitly on expectations for the future (scored 0–24).
The 20-item State-Trait Anxiety Inventory, Trait Version (STAI-T)  was assessed in this study (scored 20–80). Only the trait component of the STAI was evaluated as we were most interested in the effects of anxiety as a stable personality trait. This measure was also chosen due to the more consistent relationship between trait anxiety and changes in immune function – rather than the more ambiguous relationship between state anxiety and immune function –.
These psychosocial measures were utilized as part of a music therapy intervention study in which 32 participants were randomized to the music therapy intervention and 32 randomized to an expressive reading arm; both groups received the same time and attention support. Other psychosocial measures evaluated as part of the initial study included coping style, social support, locus of control, and religiousness. We chose to evaluate optimism and anxiety due to their availability and evidence in the literature to support their relationship with transplant outcomes.
DTE was measured as the day post-transplant that the absolute neutrophil count (ANC) was >500/mm3 for ≥3 consecutive days, a clinically meaningful endpoint at which time the risk for serious bacterial or fungal infections starts to decrease .
Data are expressed as means ± SD for continuous variables and as the number (percentage) for categorical variables. DTE also included the range for each transplant type. Comparisons of patient characteristics for the transplant types were 2-sided and included the use of t-tests, chi-square, or Fisher's exact test, as appropriate to the data. P values of <.05 were considered to be statistically significant. Multiple regression analyses were conducted using a general linear model program. The analyses were carried out separately for autologous and allogeneic transplants. The outcome DTE was analyzed by optimism and anxiety separately while controlling both demographic and clinical covariates of age, race, gender, conditioning regimen, stem cell source, and number of CD34+ cells. T-tests assessed the differences for autologous and allogeneic transplants in optimism and anxiety overall as well as for those who filled out their survey by Day +3 and those who did not. Analyses were additionally run for only those participants who filled out their survey by Day +3, effectively reducing any bias that knowledge of engraftment status might have on perceived anxiety or optimism. All analyses were carried out using SAS/STAT software, Version 9.3 of the SAS System (Copyright © July, 2011, SAS Institute Inc) on a Windows 7 platform.
Patients' pre-transplant diagnoses included lymphomas (N = 27; 42.19%), leukemias (N = 21; 32.81%), solid tumors (N = 2; 3.13%), multiple myeloma (N = 10; 15.63%), and other hematologic disorders (4; 6.25%). Table 1 presents the baseline descriptive characteristics for the 64 patients (33 men, 31 women) participating in the study. Reported optimism levels had a mean and SD of 16.44 (5.38) and range of 4–24 while reported anxiety levels were 38.44 (9.22) with a range of 24–59. There was no significant difference in levels of anxiety or optimism between autologous and allogeneic recipients (p = 0.89 and p = 0.71, respectively). These traits were very highly negatively correlated (Pearson r = −0.70, p<0.0001). While the initial study was a randomized controlled trial evaluating the efficacy of music therapy, both treatment arms were an active intervention (music therapy vs. expressive reading), and there were no differences in psychosocial or other outcomes between groups.
Greater optimism and less anxiety were significantly associated with fewer DTE among autologous HCT recipients; however, these psychosocial factors were not significantly associated with DTE when evaluating the more restricted sample of participants who filled out their surveys by Day +3 (Table 2). There was no significant association between optimism or anxiety and DTE among allogeneic recipients collectively (β = −0.0059, p = 0.97; β = −0.1446, p = 0.11, respectively) or for only those who filled out their surveys by Day +3 (β = −0.0994, p = 0.68; β = −0.1866, p = 0.27, respectively). There were no significant differences for either autologous or allogeneic transplant recipients in scores on the anxiety or optimism measures when compared by time of survey completion (Table 3).
We partially confirmed our hypothesis: greater optimism and less anxiety in the peri-transplant period were significantly associated with fewer DTE in autologous HCT recipients, although this relationship was no longer significant with the reduced sample size evaluating only subjects who completed their survey by Day +3. The effect remained similar, however, as indicated by the standardized estimates. Fewer DTE would be expected to result in a shorter period of extreme infectious susceptibility and increased survival.
These results suggest one possible mechanistic explanation to the growing body of literature on the effects of psychosocial factors on HCT outcomes , , , ; however, due to the nature of this study and our limited sample size, this is purely associational data that should prompt further exploration in larger, more homogeneous samples. Longer DTE may be an early event in the dysregulated immunological cascade predisposing psychosocially-impaired transplant recipients to higher levels of morbidity and mortality. The exact mechanism linking psychological factors and neutropenia remains to be elucidated and is likely not straightforward. Acute stress and inflammatory cytokines can actually induce early mobilization of neutrophils , , though this effect may be enhanced or impaired pending exposure to different sex hormones . Also in support of the adverse effects of psychological stress, catecholamines decrease function and phagocytic capabilities of neutrophils , ; therefore, it may be necessary to measure function and not simply absolute neutrophil numbers in future studies. Finally, differences in effect on neutrophils between acute and chronic psychosocial states will need to be evaluated when elucidating this mechanism.
We did not observe significant findings with allogeneic transplant patients; we suggest that the additional significant physiological burdens involved in their treatment might diminish the impact of psychosocial factors on DTE for this group. Another possibility is that the psychosocial effect may be somehow imprinted on the transplanted cells themselves, preventing the observation of this effect when the donor psychosocial status is unknown, as occurs in this study with allogeneic transplantation. Finally, allogeneic recipients take immunosuppressive agents to mitigate graft versus host disease; these may also mask the relationship between psychosocial factors and immune outcomes.
Our results are consistent with prior work demonstrating an impact of anxiety on immune recovery post-transplant . We extended this previous work by investigating the relationship among allogeneic recipients and also examining optimism as an additional psychosocial factor of importance. Our assessment of immune recovery was slightly different; MgGregor et al  evaluated WBC counts over days 5–22, while we looked at the more specific WBC subset of interest during immediate immune recovery – neutrophils – and evaluated an endpoint used in clinical practice - DTE. In the only previous study evaluating optimism and transplant outcome, pre-transplant optimism predicted better survival in the first two months post-HCT, but not at six months . Our results provide one explanation for the dissipation of this effect on survival over time, as neutrophil engraftment is a more proximal event.
There are some significant limitations to our study. We investigated a very heterogeneous group (i.e., diagnoses, baseline levels of illness and supportive care); future analyses should either be powered to control for these differences or examine a more homogeneous group. Our most significant limitation is the variability in timing of when the baseline surveys were completed, which when restricted to those who filled out their surveys by the time of engraftment resulted in psychosocial factors and DTE not being significantly associated. This could mean that in fact knowledge of engraftment influenced optimism and anxiety; however, there are three reasons why this knowledge may not have significantly influenced anxiety or optimism in our study. First, we evaluated trait and not state anxiety, with studies demonstrating substantial stability of both the short- (20–100 days) and long-term (years) STAI-T measure . The LOT-R also tends to evaluate dispositional or “trait” optimism . Traits are less subject to influence by a discrete event. Second, none of the anxiety or optimism scores between or among autologous and allogeneic recipients were significantly different as a function of time of survey completion, albeit we did have a small sample within which to detect a difference. Third, there are a multitude of other physical and medical factors and complications that could also have arisen during that time period to reasonably affect psychosocial status. Alternatively, it is possible that with a restricted sample size we simply lost power to detect significance; this may be the case given that our results were similar in direction and size while no longer significant. Our findings therefore should be considered preliminary and should be replicated in a larger sample with more consistent timing of the baseline survey before more definitive conclusions may be drawn.
In conclusion, our findings suggest that optimism and anxiety may be associated with time to neutrophil recovery in autologous stem cell transplant patients, though this relationship was no longer significant with the reduced sample size evaluating subjects completing their psychosocial surveys by Day +3, with more favorable peri-transplant psychosocial factors associated with shorter time to neutrophil recovery. Further research is needed with larger and more homogeneous cohorts of HCT patients with consistent baseline sampling to investigate the impact of psychosocial factors on DTE and other immunologic transplant sequelae with the goal of improving outcomes in this physically and psychologically stressed population.
This work was previously presented in part at the Academy of Psychosomatic Medicine 57th Annual Meeting, Marco Island, FL, November 13, 2010 and at the American Psychosomatic Society 69th Annual Meeting, San Antonio, TX, March 13, 2011.
Conceived and designed the experiments: BCH LH ROO DG JLL OJZS. Performed the experiments: BCH ROO DG JLL OJZS. Analyzed the data: JMK JAM JML YX XT SM. Contributed reagents/materials/analysis tools: JLL. Wrote the paper: JMK JAM JML YX XT SM OJZS.
- 1. Reiche EM, Nunes SO, Morimoto HK (2004) Stress, depression, the immune system, and cancer. Lancet Oncol 5: 617–625. doi: 10.1016/s1470-2045(04)01597-9
- 2. Antoni MH, Lutgendorf SK, Cole SW, Dhabhar FS, Sephton SE, et al. (2006) The influence of bio-behavioural factors on tumour biology: Pathways and mechanisms. Nat Rev Cancer 6: 240–248. doi: 10.1038/nrc1820
- 3. Thaker PH, Sood AK (2008) Neuroendocrine influences on cancer biology. Semin Cancer Biol 18: 164–170. doi: 10.1016/j.semcancer.2007.12.005
- 4. Hoodin F, Uberti JP, Lynch TJ, Steele P, Ratanatharathorn V (2006) Do negative or positive emotions differentially impact mortality after adult stem cell transplant? Bone Marrow Transplant 38: 255–264. doi: 10.1038/sj.bmt.1705419
- 5. Gregurek R, Labar B, Mrsić M, Batinić D, Ladika I, et al. (1996) Anxiety as a possible predictor of acute GVHD. Bone Marrow Transplant 18: 585.
- 6. Lee SJ, Loberiza FR, Rizzo JD, Soiffer RJ, Antin JH, et al. (2003) Optimistic expectations and survival after hematopoietic stem cell transplantation. Biol Blood Marrow Transplant 9: 389–396. doi: 10.1016/s1083-8791(03)00103-4
- 7. McGregor BA, Syrjala KL, Dolan ED, Langer SL, Redman M (2012) The effect of pre-transplant distress on immune reconstitution among adult autologous hematopoietic cell transplantation patients. Brain Behav Immun 30: S142–S148. doi: 10.1016/j.bbi.2012.07.020
- 8. Costanzo ES, Juckett MB, Coe CL (2012) Biobehavioral influences on recovery following hematopoietic stem cell transplantation. Brain Behav Immun 30: S68–S74. doi: 10.1016/j.bbi.2012.07.005
- 9. Knight JM, Lyness JM, Sahler OJZ, Liesveld JL, Moynihan JA (2013) Psychosocial factors and hematopoietic stem cell transplantation: Potential biobehavioral pathways. Psychoneuroendocrinology 38: 2383–2393. doi: 10.1016/j.psyneuen.2013.06.016
- 10. Pasquini MC WZ (2012) Current use and outcome of hematopoietic stem cell transplantation. CIBMTR Summary Slides. Available at: http://www.cibmtr.org.
- 11. Norkin M, Hsu JW, Wingard JR (2012) Quality of life, social challenges, and psychosocial support for long-term survivors after allogeneic hematopoietic stem-cell transplantation. Semin Hematol 49: 104–109. doi: 10.1053/j.seminhematol.2011.10.004
- 12. Hochhausen N, Altmaier EM, McQuellon R, Davies SM, Papadopolous E, et al. (2007) Social support, optimism, and self-efficacy predict physical and emotional well-being after bone marrow transplantation. J Psychosoc Oncol 25: 87–101. doi: 10.1300/j077v25n01_05
- 13. Andrykowski MA, Brady MJ, Henslee-Downey PJ (1994) Psychosocial factors predictive of survival after allogeneic bone marrow transplantation for leukemia. Psychosom Med 56: 432–439. doi: 10.1097/00006842-199409000-00008
- 14. Jenkins PL, Lester H, Alexander J, Whittaker J (1994) A prospective study of psychosocial morbidity in adult bone marrow transplant recipients. Psychosomatics 35: 361–367. doi: 10.1016/s0033-3182(94)71757-6
- 15. Chang G, Orav EJ, Tong M, Antin JH (2004) Predictors of 1-year survival assessed at the time of bone marrow transplantation. Psychosomatics: Journal of Consultation Liaison Psychiatry 45: 378–385. doi: 10.1176/appi.psy.45.5.378
- 16. Mouthon MA, Van der Meeren A, Gaugler MH, Visser TP, Squiban C, et al. (1999) Thrombopoietin promotes hematopoietic recovery and survival after high-dose whole body irradiation. International Journal of Radiation Oncology* Biology* Physics 43: 867–875. doi: 10.1016/s0360-3016(98)00477-5
- 17. Saito T, Kanda Y, Nakai K, Kim SW, Arima F, et al. (2003) Immune reconstitution following reduced-intensity transplantation with cladribine, busulfan, and antithymocyte globulin: Serial comparison with conventional myeloablative transplantation. Bone Marrow Transplant 32: 601–608. doi: 10.1038/sj.bmt.1704205
- 18. Bensinger WI, Storb R (2001) Allogeneic peripheral blood stem cell transplantation. Rev Clin Exp Hematol 5: 67–86. doi: 10.1046/j.1468-0734.2001.00033.x
- 19. Scheier MF, Carver CS, Bridges MW (1994) Distinguishing optimism from neuroticism (and trait anxiety, self-mastery, and self-esteem): A reevaluation of the life orientation test. J Pers Soc Psychol 67: 1063–1078. doi: 10.1037//0022-3522.214.171.1243
- 20. Spielberger CD (1989) State-trait anxiety inventory: A comprehensive bibliography. Palo Alto, CA: Consulting Psychologists Press.
- 21. Afsar FS, Isleten F, Sonmez N (2010) Children with atopic dermatitis do not have more anxiety or different cortisol levels compared with normal children. J Cutan Med Surg 14: 13–18.
- 22. Hashizume H, Horibe T, Ohshima A, Ito T, Yagi H, et al. (2005) Anxiety accelerates T-helper 2-tilted immune responses in patients with atopic dermatitis. Br J Dermatol 152: 1161–1164. doi: 10.1111/j.1365-2133.2005.06449.x
- 23. Katsuura S, Kamezaki Y, Yamagishi N, Kuwano Y, Nishida K, et al. (2011) Circulating vascular endothelial growth factor is independently and negatively associated with trait anxiety and depressive mood in healthy japanese university students. Int J Psychophysiol 81: 38–43. doi: 10.1016/j.ijpsycho.2011.04.004
- 24. Salome N, Tasiemski A, Dutriez I, Wigger A, Landgraf R, et al. (2008) Immune challenge induces differential corticosterone and interleukin-6 responsiveness in rats bred for extremes in anxiety-related behavior. Neuroscience 151: 1112–1118. doi: 10.1016/j.neuroscience.2007.12.010
- 25. Elsenbruch S, Lucas A, Holtmann G, Haag S, Gerken G, et al. (2006) Public speaking stress-induced neuroendocrine responses and circulating immune cell redistribution in irritable bowel syndrome. Am J Gastroenterol 101: 2300–2307. doi: 10.1111/j.1572-0241.2006.00837.x
- 26. Lekander M, Furst CJ, Rotstein S, Blomgren H, Fredrikson M (1995) Anticipatory immune changes in women treated with chemotherapy for ovarian cancer. Int J Behav Med 2: 1–12. doi: 10.1207/s15327558ijbm0201_1
- 27. Matzner P, Hazut O, Naim R, Shaashua L, Sorski L, et al. (2013) Resilience of the immune system in healthy young students to 30-hour sleep deprivation with psychological stress. Neuroimmunomodulation 20: 194–204. doi: 10.1159/000348698
- 28. Trigg ME (2002) Post-transplant immune recovery and the implication for infection risk. Int J Hematol 76: 199–205. doi: 10.1007/bf03165245
- 29. Hoodin F, Weber S (2003) A systematic review of psychosocial factors affecting survival after bone marrow transplantation. Psychosomatics 44: 181–195. doi: 10.1176/appi.psy.44.3.181
- 30. Dhabhar FS, Malarkey WB, Neri E, McEwen BS (2012) Stress-induced redistribution of immune cells—from barracks to boulevards to battlefields: A tale of three hormones—curt richter award winner. Psychoneuroendocrinology 37: 1345–1368. doi: 10.1016/j.psyneuen.2012.05.008
- 31. Cecilio CA, Costa EH, Ucelli P, Chaves CA, Toffoli MC, et al. (1997) The neutrophil migration induced by tumour necrosis factor alpha in mice is unaffected by glucocorticoids. Mediators Inflamm 6: 46–52. doi: 10.1080/09629359791929
- 32. Barker LA, Dazin PF, Levine JD, Green PG (2005) Sympathoadrenal-dependent sexually dimorphic effect of nonhabituating stress on in vivo neutrophil recruitment in the rat. Br J Pharmacol 145: 872–879. doi: 10.1038/sj.bjp.0706257
- 33. Kaufmann I, Eisner C, Richter P, Huge V, Beyer A, et al. (2007) Psychoneuroendocrine stress response may impair neutrophil function in complex regional pain syndrome. Clin Immunol 125: 103–111. doi: 10.1016/j.clim.2007.07.004
- 34. Trabold B, Gruber M, Frohlich D (2007) Functional and phenotypic changes in polymorphonuclear neutrophils induced by catecholamines. Scand Cardiovasc J 41: 59–64. doi: 10.1080/14017430601085948
- 35. Watson D, Walker LM (1996) The long-term stability and predictive validity of trait measures of affect. J Pers Soc Psychol 70: 567–577. doi: 10.1037/0022-35126.96.36.1997
- 36. Burke KL, Joyner AB, Czech DR, Wilson MJ (2000) An investigation of concurrent validity between two optimism/pessimism questionnaires: The life orientation test-revised and the optimism/pessimism scale. Current Psychology 19: 129–136. doi: 10.1007/s12144-000-1009-5