Loneliness and mental health during the COVID-19 pandemic in older breast cancer survivors and noncancer controls.

BACKGROUND: The coronavirus disease 2019 (COVID-19) pandemic has had wide-ranging health effects and increased isolation. Older with cancer patients might be especially vulnerable to loneliness and poor mental health during the pandemic.
METHODS: The authors included active participants enrolled in the longitudinal Thinking and Living With Cancer study of nonmetastatic breast cancer survivors aged 60 to 89 years (n = 262) and matched controls (n = 165) from 5 US regions. Participants completed questionnaires at parent study enrollment and then annually, including a web-based or telephone COVID-19 survey, between May 27 and September 11, 2020. Mixed-effects models were used to examine changes in loneliness (a single item on the Center for Epidemiologic Studies-Depression [CES-D] scale) from before to during the pandemic in survivors versus controls and to test survivor-control differences in the associations between changes in loneliness and changes in mental health, including depression (CES-D, excluding the loneliness item), anxiety (the State-Trait Anxiety Inventory), and perceived stress (the Perceived Stress Scale). Models were adjusted for age, race, county COVID-19 death rates, and time between assessments.
RESULTS: Loneliness increased from before to during the pandemic (0.211; P = .001), with no survivor-control differences. Increased loneliness was associated with worsening depression (3.958; P < .001) and anxiety (3.242; P < .001) symptoms and higher stress (1.172; P < .001) during the pandemic, also with no survivor-control differences.
CONCLUSIONS: Cancer survivors reported changes in loneliness and mental health similar to those reported by women without cancer. However, both groups reported increased loneliness from before to during the pandemic that was related to worsening mental health, suggesting that screening for loneliness during medical care interactions will be important for identifying all older women at risk for adverse mental health effects of the pandemic.

Introduction

The coronavirus disease 2019 (COVID‐19) pandemic has been a period of unprecedented psychosocial stress for many individuals, including decreased social contact and lower availability of support and services, with the potential for profound impacts on mental health., , , , Research suggests that the prevalence of depression and anxiety symptoms in the general population increased during the pandemic compared with estimates from the previous year., , , , , , , Loneliness, or feelings of social disconnection resulting from a discrepancy between an individual's actual and desired social relationships, also increased during this time., , , Loneliness has been identified as an independent risk factor for morbidity and mortality that is comparable in its effects on mortality to smoking 15 cigarettes per day in cancer and noncancer populations., , , Research suggests that older adults experience higher levels of loneliness and are more vulnerable to its negative health consequences, including depression, hypertension, and cognitive declines, than younger adults.

Older adults and individuals with preexisting medical conditions such as cancer were particularly advised to physically isolate from others during the pandemic because of high risk for severe complications of COVID‐19. Social isolation thus may contribute to increased feelings of loneliness among older cancer survivors. Prepandemic vulnerabilities for loneliness, depression, and anxiety may also be magnified during the pandemic in older breast cancer survivors compared with those without cancer because of concerns about COVID‐19 infection, potential disruptions to medical care, and additional stressors that they might face. Reports from other countries suggest that patients with cancer and survivors have experienced increases in loneliness, and worsening mental health, including depression, anxiety, and stress, during the pandemic compared with their family members and the general population. However, there remains little evidence about the impact of the pandemic on loneliness and its association with mental health among older cancer survivors in the United States.

We examined changes in loneliness and mental health during the COVID‐19 pandemic in a sample of older breast cancer survivors and matched noncancer controls enrolled in the longitudinal Thinking and Living With Cancer (TLC) study. We hypothesized that cancer survivors would experience larger increases in loneliness than controls and that increases in loneliness would be associated with worsening depression and anxiety symptoms and higher stress during the pandemic in survivors compared with controls.

Materials and Methods

Participants were enrolled in the ongoing, multisite longitudinal TLC study investigating the effects of cancer treatment on cognitive function in women aged ≥60 years with newly diagnosed nonmetastatic (AJCC stage 0‐III) breast cancer and frequency‐matched noncancer controls. The institutional review boards of all participating study sites (Georgetown University, Memorial Sloan Kettering Cancer Center, Moffitt Cancer Center, City of Hope Comprehensive Cancer Center, Hackensack University Medical Center, and Indiana University School of Medicine) approved the protocol (ClinicalTrials.gov identifier NCT03451383).

Eligibility for the TLC study included no history of stroke, head injury, major psychiatric or neurodegenerative disorder, prior chemotherapy or hormonal therapy, or treatment for another cancer within the past 5 years. Women taking psychoactive medications were eligible if the dose was stable for at least 2 months before study enrollment. Details about the study have been published elsewhere., Briefly, breast cancer survivors were enrolled in the study after surgery but before initiation of radiation or systemic therapy. As part of the TLC parent study, all survivors and frequency‐matched noncancer controls completed questionnaires at study enrollment and then annually for up to 60 months.

Of the 1282 women enrolled in the TLC parent study as of March 1, 2020, 533 active participants (ie, those who had not yet completed the study, dropped out, or died) were contacted to complete an additional web‐based or telephone survey during the COVID‐19 pandemic. Compared with nonactive participants, active participants had completed more years of education (mean ± SD: 15.6 ± 2.2 vs 15.2 ± 2.3; P = .006), and a larger proportion was White (83.9% vs 78.1%; P = .011) and was married or living as married (61.0% vs 53.8%; P = .011).

Participants completed the COVID‐19 survey online (80.7%) or by telephone (19.3%) between May 27 and September 11, 2020, to assess the impact of the pandemic on psychosocial functioning. Of the 533 active participants, 279 cancer survivors and 166 noncancer controls responded to the survey. We excluded 13 survivors who were missing cancer treatment information at study enrollment, 3 survivors and 1 control who reported contracting COVID‐19, and 1 survivor who was missing treatment information at enrollment and also reported contracting COVID‐19, for a final sample of 262 survivors (81.6% of active survivors) and 165 controls (85.1% of active controls) (Fig. 1). Compared with responders, nonresponders had higher depression symptoms at study enrollment (mean ± SD: 7.3 ± 6.8 vs 5.3 ± 6.5; P = .011), and a larger proportion was non‐White (27.3% vs 13.8%; P = .002). The proportion of responders differed across study sites for controls (P = .004) but not for survivors (P = .074); therefore, analyses were adjusted for study site using county‐specific COVID‐19 death rates (see description in Measures, below).

Figure 1

This Consolidated Standards for Reporting Trials (CONSORT) diagram for the Thinking and Living with Cancer Study illustrates the sample of (A) older breast cancer survivors and (B) matched controls without cancer. Participants were excluded if they were not active (ie, had completed the study, dropped out, or died) at the time of the coronavirus disease 2019 (COVID‐19) survey, were missing cancer treatment information at study enrollment, or reported a COVID‐19 diagnosis. The percentages of participants who completed and declined the COVID‐19 survey were calculated based on the number of participants who were active and eligible to complete the survey.

Measures

Loneliness was evaluated using the single item “I felt lonely during the past week” from the Center for Epidemiologic Studies–Depression (CES‐D) Scale,, , , which participants completed at all TLC parent study assessments and during the COVID‐19 survey. Response options ranged from 0 (rarely or none of the time) to 3 (most of the time). The COVID‐19 survey also included the 3‐item loneliness scale adapted from the University of California‐Los Angeles loneliness scale. Previous research with older adults indicated that the CES‐D loneliness item correlated highly with the 3‐item scale, and the 2 measures were highly correlated in this sample (r = 0.61; P < .001). The CES‐D loneliness item was also more highly correlated with items on the 3‐item loneliness scale (r = −0.47 to 0.59; average, r = 0.51) than it was with the other items on the CES‐D scale (r = 0.09‐0.53; average, r = 0.32). All study analyses focused on the CES‐D loneliness item because it was available at TLC study assessments before and during the pandemic.

Participants completed the CES‐D scale to assess depressive symptoms at each parent study assessment, and this scale was also included on the COVID‐19 survey, with higher scores indicating greater depression. We removed the loneliness item from the CES‐D for analyses of depression, and internal consistency for the CES‐D remained high both with (Cronbach α = .88) and without (Cronbach α = 0.88) the loneliness item. Participants also completed the State‐Trait Anxiety Inventory (STAI)‐State subscale to assess anxiety symptoms at each parent study assessment and on the COVID‐19 survey, with higher scores indicating greater anxiety. As part of the COVID‐19 survey, participants also completed the Perceived Stress Scale,, which assessed the degree to which women appraised their life as stressful (eg, feeling unable to control important things in life) in the past month.

Several demographic characteristics were considered as covariates, including age, race (non‐White vs White), county rates of COVID‐19 deaths, and time (in months) from participants' last pre–COVID‐19 study assessment to the COVID‐19 survey., County COVID‐19 death rates were calculated as the cumulative number of COVID‐19 deaths per 1000 individuals from the start of data reporting in each US county to the date of survey completion for each participant, divided by the 2019 population estimate for that county. Data for cumulative deaths in each county were obtained from The New York Times based on reports from state and local health agencies., For the analysis that examined longitudinal changes in loneliness, we included living circumstances (living alone vs with others) and the Medical Outcomes Study Social Support Survey emotional (eg, someone to confide in) and tangible (eg, someone to help with daily chores) social support subscales at the time of the COVID‐19 survey as additional covariates.

Statistical Analysis

Descriptive analyses compared survivors and controls at study enrollment, at their last pre–COVID‐19 assessment, and at the COVID‐19 survey. To examine whether there were differences between survivors and controls in longitudinal changes in loneliness from study enrollment to the last pre–COVID‐19 assessment and from the last pre–COVID‐19 assessment to the COVID‐19 survey, we used a piecewise, linear mixed‐effects model with fixed timepoints at study enrollment, the last pre–COVID‐19 study assessment, and the COVID‐19 survey. Because of variation among participants in the number of follow‐up assessments they had completed at the time of the COVID‐19 survey, we aligned outcomes with the last pre–COVID‐19 assessment. The model included interaction terms for timepoint (study enrollment and the COVID‐19 survey vs the last pre–COVID‐19 assessment) and group (survivors vs controls), adjusting for age, race (non‐White vs White), county COVID‐19 death rate, months from the last pre–COVID‐19 assessment to the COVID‐19 survey, living circumstances, and emotional and tangible support.

To test the hypothesis that increases in loneliness would have a greater impact on depression, anxiety, and perceived stress during the pandemic in survivors versus controls, we conducted separate linear mixed‐effects models for each outcome with timepoints at the last pre–COVID‐19 study assessment and at the COVID‐19 survey. For these models, we calculated a loneliness difference score (CES‐D loneliness score at the COVID‐19 survey minus the CES‐D loneliness score at the last pre–COVID‐19 assessment). The models included a 3‐way interaction term for timepoint, loneliness difference score, and group to test for differences between survivors and controls. The models adjusted for age, race, county COVID‐19 death rate, and months from the last pre–COVID‐19 assessment to the COVID‐19 survey. If a 3‐way interaction term was not statistically significant, it was removed from the model and group was added as a covariate. Follow‐up analyses probed significant 2‐way interactions between timepoint and the loneliness difference score on depression and anxiety symptoms to provide point estimates for simple slopes representing change in depression and anxiety symptoms at different levels of the loneliness difference score: a 1‐point increase in loneliness (difference score of +1), no change in loneliness (difference score of 0), and a 1‐point decrease in loneliness (difference score of −1).

All tests of statistical significance were 2‐sided using a P < .05 threshold. Analyses were performed using SAS version 9.4 (SAS Institute Inc).

Results

The mean age of survivors and controls was approximately 68 years, and most self‐identified as White, reported being married, and were not currently employed (Table 1). Descriptive statistics for the psychosocial variables appear in Table 2. Consistent with prior reports in noncancer populations, both survivors and controls reported increases in depression and anxiety symptoms during the pandemic.

TABLE 1

Demographic and Clinical Characteristics Among Older Breast Cancer Survivors and Frequency‐Matched Noncancer Controls

Demographic and Clinical Variables	No. (%)		P a
	Survivors, n = 262	Controls, n = 165
Age: Mean ± SD, y	67.9 ± 5.3	68.0 ± 6.0	.834
Race			.274
Non‐White	40 (15.3)	19 (11.5)
White	222 (84.7)	146 (88.5)
Marital status			.184
Married or living as married	156 (64.2)	91 (57.6)
Other	87 (35.8)	67 (42.4)
Education: Mean ± SD, y	15.6 ± 2.2	15.8 ± 2.1	.361
Employment status			.630
Currently employed	85 (35.0)	59 (37.3)
Not currently employed	158 (65.0)	99 (62.7)
Year of study enrollment			<.001
2014	4 (1.5)	2 (1.2)
2015	31 (11.8)	1 (0.6)
2016	23 (8.8)	9 (5.5)
2017	44 (16.8)	57 (34.5)
2018	90 (34.4)	47 (28.5)
2019	50 (19.1)	48 (29.1)
2020	20 (7.6)	1 (0.6)
AJCC Cancer stage			—
0	55 (21.8)	—
I	152 (60.3)	—
II	40 (15.9)	—
III	5 (2.0)	—
Treatment group			—
Chemotherapy	51 (19.5)	—
Hormonal therapy	211 (80.5)	—
County COVID‐19 death rate: Mean ± SD	0.8 ± 0.9	0.9 ± 0.8	.714
Time from the last pre–COVID‐19 assessment to the COVID‐19 survey: Mean ± SD, mo	10.6 ± 5.6	10.4 ± 3.8	.630

Abbreviation: COVID‐19, coronavirus disease 2019.

P values were derived from t tests or χ2 tests.

TABLE 2

Psychosocial Characteristics Among Older Breast Cancer Survivors and Frequency‐Matched Noncancer Controls

Psychosocial Variables [Score Range]	Study Enrollment		Last Pre–COVID‐19 Assessment		COVID‐19 Survey
	Survivors, n = 192	Controls, n = 122	Survivors, n = 262	Controls, n = 165	Survivors, n = 262	Controls, n = 165	P a
Loneliness item [0‐3]: Mean ± SD	0.3 ± 0.7	0.3 ± 0.7	0.3 ± 0.6	0.4 ± 0.7	0.5 ± 0.7	0.6 ± 0.8	<.001
Loneliness difference scoreb [−3 to +3]: Mean ± SD	—	—	—	—	0.3 ± 0.8	0.2 ± 0.8	.360
Depression symptoms [0‐57]: Mean ± SD	—	—	6.3 ± 7.0	4.5 ± 5.4	8.1 ±7.6	7.6 ± 8.0	<.001
Anxiety symptoms [20‐80]: Mean ± SD	—	—	27.9 ± 6.5	27.5 ± 7.1	30.1 ± 9.1	30.6 ± 9.6	<.001
Perceived stress [0‐16]: Mean ± SD	—	—	—	—	4.0 ± 3.0	3.9 ± 3.1	.704
Emotional support [0‐100]: Mean ± SD	—	—	—	—	75.2 ± 22.0	72.2 ± 24.1	.188
Tangible support [0‐100]: Mean ± SD	—	—	—	—	78.0 ± 24.2	73.5± 26.8	.076
Living circumstances; No. (%)							.003
Living alone	—	—	—	—	68 (26.0)	65 (39.4)
Living with others	—	—	—	—	194 (74.0)	100 (60.6)

Abbreviation: COVID‐19, coronavirus disease 2019.

P values were derived from analyses of variance, t tests, or χ2 tests that tested differences between survivors and controls across the available timepoints. Some variables do not have data at study enrollment and the last pre–COVID‐19 assessment because analyses focused on the COVID‐19 survey.

The loneliness difference score was calculated by subtracting the Center for Epidemiologic Studies‐Depression (CES‐D) loneliness item at the last pre–COVID‐19 assessment from the CES‐D loneliness at the COVID‐19 survey.

Longitudinal Changes in Loneliness

Loneliness did not change from study enrollment to the last pre–COVID‐19 assessment (−0.056; P = .421) but significantly increased from the last pre–COVID‐19 assessment to the COVID‐19 survey (0.211; P < .001), even after considering living circumstances (living alone vs with others) and availability of social support at the time of the COVID‐19 survey (Fig. 2) (see Supporting Table 1). However, contrary to our hypothesis, survivors and controls showed similar increases in loneliness from the last pre–COVID‐19 assessment to the COVID‐19 survey (0.064; P = .425), adjusting for covariates.

Figure 2

Longitudinal changes in loneliness are illustrated among older breast cancer survivors and noncancer controls. Piecewise mixed‐effects models illustrate adjusted loneliness scores at study enrollment, at the last pre–coronavirus disease 2019 (COVID‐19) assessment, and at the COVID‐19 survey, adjusting for age, race, county COVID‐19 death rate, and months from the last pre–COVID‐19 assessment to the COVID‐19 survey. Loneliness increased from the last pre–COVID‐19 assessment to the COVID‐19 survey (P < .001), with no difference between survivors and controls (P = .425).

Associations Between Loneliness and Mental Health

There were no differences between survivors and controls in associations between changes in loneliness and depression, anxiety, or perceived stress. Changes in loneliness from the last pre–COVID‐19 assessment to the COVID‐19 survey were associated with changes in depression and anxiety symptoms, adjusting for covariates (Table 3). Follow‐up analyses revealed that a 1‐point increase in loneliness (simple slope ± SE, 5.395 ± 0.439; P < .001) and, to a lesser degree, no change in loneliness (simple slope ± SE, 1.437 ± 0.334; P < .001) were associated with worsening depression symptoms, whereas a 1‐point decrease in loneliness was associated with improving depression symptoms (simple slope ± SE, −2.522 ± 0.599; P < .001) (Fig. 3A). Similarly, a 1‐point increase in loneliness (simple slope ± SE, 5.080 ± 0.553; P < .001) and, to a lesser degree, no change in loneliness (simple slope ± SE, 1.838 ± 0.420; P < .001) were associated with worsening anxiety symptoms, whereas a 1‐point decrease in loneliness was marginally associated with improving anxiety symptoms (simple slope ± SE, −1.403 ± 0.755; P = .064) (Fig. 3B). Increases in loneliness from the last pre–COVID‐19 assessment to the COVID‐19 survey were also associated with higher perceived stress (1.172; P < .001) (see Supporting Table 2) during the pandemic, adjusting for covariates.

TABLE 3

Mixed‐Effects Models With Interactions Between Timepoint and Change in Loneliness (Difference Score) Predicting Change In Depression And Anxiety Symptoms From the Last Pre–Coronavirus Disease 2019 (COVID‐19) Assessment to the COVID‐19 Survey

Variable	Change in Depression Symptoms		Change in Anxiety Symptoms
	coefficient ± SE	P	coefficient ± SE	P
Timepoint	1.437 ± 0.334	<.001	1.838 ± 0.420	<.001
Loneliness difference scorea	−0.720 ± 0.452	.002	−0.308 ± 0.519	.004
Timepoint*loneliness difference score	3.958 ± 0.405	<.001	3.242 ± 0.511	<.001
Age	−0.011 ± 0.060	.856	0.029 ± 0.065	.661
Race: Non‐White vs White	−1.513 ± 0.921	.101	−2.098 ± 1.030	.042
County COVID‐19 death rate	0.814 ± 0.406	.046	1.638 ± 0.449	<.001
Time from last pre–COVID‐19 assessment to COVID‐19 survey, mo	0.026 ± 0.066	.696	−0.091 ± 0.074	.219
Group: Survivors vs controls	1.022 ± 0.647	.115	−0.001 ± 0.722	.999

The loneliness difference score was calculated by subtracting the Center for Epidemiologic Studies‐Depression (CES‐D) loneliness item at the last pre–COVID‐19 assessment from the CES‐D loneliness item at the COVID‐19 survey.

Figure 3

Associations between changes in loneliness and changes in depression and anxiety symptoms during the pandemic are illustrated. Mixed‐effects models show adjusted (A) depression and (B) anxiety symptoms as a function of timepoint and change in loneliness (continuous difference score) from the last pre–coronavirus disease 2019 (COVID‐19) assessment to the COVID‐19 survey, adjusting for age, race, county COVID‐19 death rate, months from the last pre–COVID‐19 assessment to the COVID‐19 survey, and group. Point estimates for simple slopes representing changes in depression and anxiety symptoms from the last pre–COVID‐19 assessment to the COVID‐19 survey suggest that a 1‐point increase (red lines) and no change (blue lines) in loneliness were associated with worsening depression (P < .001) and anxiety (P < .001) symptoms, whereas a 1‐point decrease in loneliness (green lines) was associated with improving depression (P < .001) and anxiety (P = .064) symptoms.

Discussion

This is one of the first US studies to examine changes in loneliness and mental health during the COVID‐19 pandemic in older breast cancer survivors compared with matched controls without cancer. This study is unique because we were able to query women who were part of a well defined longitudinal cohort study of older breast cancer survivors. We found that older women experienced a significant increase in loneliness from before to during the pandemic that was not accounted for by their living circumstances (living alone vs with others) or availability of social support at the time of the COVID‐19 survey. However, contrary to expectation, there was no difference between breast cancer survivors and matched noncancer controls. Also of note, older women in this sample reported significant increases in depression and anxiety symptoms from before to during the pandemic. As hypothesized, women who experienced increases in loneliness also reported worsening depression and anxiety symptoms and higher perceived stress during the pandemic, but, again, there were no differences between survivors and controls.

The proportion of older women in this study who reported feeling lonely during the pandemic (39.0%) is higher than population‐based estimates of loneliness in older adults before the pandemic (19.3%). These findings are consistent with the emerging literature on the impact of the COVID‐19 pandemic on loneliness and mental health among cancer survivors. For instance, studies in the Netherlands and China found that patients with cancer and survivors reported increased loneliness and worsening depression and anxiety symptoms during the pandemic., Longitudinal research with older adults has also found increases in loneliness, depression, and anxiety symptoms from before to during the pandemic, , as well as over, the first few months of the pandemic.

In our cohort, older cancer survivors and controls showed similar increases in loneliness and associations with depression, anxiety, and stress. Although one previous study found that patients with cancer and survivors in China had higher psychological symptoms than their family members and the Chinese general population in the early months of the pandemic, another study conducted in Hong Kong found that female breast cancer and colorectal cancer survivors reported fewer depression and anxiety symptoms during the pandemic than noncancer controls. One possible explanation for the overall lack of differences between the 2 groups in this study is that cancer survivors may have experienced losses, adapted, and developed adaptive coping responses through their experience of cancer. This could have helped them to cope with future stressors such as the COVID‐19 pandemic, although this remains to be specifically tested. Alternatively, it is also possible that, as older women, COVID‐19–related concerns and isolation affected cancer survivors and noncancer controls equally. Researchers have also proposed that wisdom, which includes compassion, emotion regulation, and self‐reflection, is a resilience factor for older adults during times of stress that is inversely associated with loneliness and may be beneficial for cancer survivors as well. The investigation of protective factors that may buffer against increased vulnerability to the adverse effects of the COVID‐19 pandemic on mental health in cancer survivors is an important direction for future research.

Findings from this study should be considered in light of several limitations, which suggest directions for future research. First, our sample was well educated, and nearly all had Medicare, so they may have been buffered from some of the effects of the pandemic. Second, although we identified statistically significant worsening of depression and anxiety symptoms during the pandemic, the average increases in depression and anxiety scores were smaller than minimal clinically important differences published in the literature (ie, >10‐point increase on the CES‐D and STAI), and below established cutoffs for clinically meaningful symptoms (ie, CES‐D scores ≥16, STAI scores >44)., Third, the longitudinal analyses for this study relied on a single‐item measure of loneliness. Although it correlated highly with a longer measure of loneliness on the COVID‐19 survey, the findings should be replicated. Finally, it will be important to assess whether these initial increases in loneliness, depression, and anxiety persist, increase, or decrease over subsequent study visits and whether changes during the COVID‐19 pandemic impact subsequent physical and cognitive health. For instance, loneliness and social isolation have been associated with increased inflammation and decreased antiviral immunity,, , , as well as prometastatic molecular profiles in primary tumors (eg, gene expression patterns consistent with epithelial‐mesenchymal transition),, poorer cognitive function, and increased risk for recurrence and mortality, among cancer survivors. Although older breast cancer survivors and noncancer controls experienced similar increases in loneliness in this study, it remains unclear whether the biologic effects of loneliness may be more detrimental for survivors than controls. Future research might also consider whether individuals undergoing active cancer treatment or those with advanced or metastatic disease experience greater loneliness than noncancer controls given the severity of disease and elevated risk of COVID‐19 complications.

Overall, this is the first study to examine longitudinal changes in loneliness and mental health during the COVID‐19 pandemic in older breast cancer survivors and noncancer controls. We found a high rate of loneliness in both cancer survivors and noncancer controls as well as increases in loneliness, depression, and anxiety symptoms from before to during the pandemic. However, findings from this study demonstrate that older breast cancer survivors do not appear to be at greater risk for loneliness or declines in mental health relative to their peers. Given the associations between loneliness and morbidity and mortality,, it will be important to screen for loneliness during medical care interactions to identify all women who are at risk for adverse mental health effects of the pandemic.

Funding Support

This research was supported by the National Cancer Institute of the National Institutes of Health through grants R01CA129769, R35CA197289, and R01AG068193 (Jeanne S. Mandelblatt). This study was also supported in part by the National Institutes of Health through grants K01AG065485 (Kelly E. Rentscher), P30AG028716 (Harvey J. Cohen), K01CA212056 (Traci N. Bethea), K08CA241337 (Kathleen M. Van Dyk), K12HD001441 (Zev M. Nakamura), R01CA172119 (Tim A. Ahles), U54CA137788 (Tim A. Ahles), P30CA008748 (Tim A. Ahles), R01CA244673 (Brenna C. McDonald and Andrew J. Saykin), and P30AG010133 (Brenna C. McDonald and Andrew J. Saykin); by the American Cancer Society through grants 17‐023‐01‐CPPB (Sunita K. Patel) and 128660‐RSG‐15‐187‐01‐PCS (Judith E. Carroll); and by the University of California‐Los Angeles Cousins Center for Psychoneuroimmunology at the University of California, Los Angeles (Kelly E. Rentscher and Judith E. Carroll).

Conflict of Interest Disclosures

Brent J. Small reports institutional grant support from the National Institutes of Health outside the submitted work and service as a member of the National Institutes of Health Data Safety Monitoring Board. Asma A. Dilawari attended the Cardinal Health 2020 Advisor Board Oncology Committee. Kathleen M. Van Dyk reports a postdoctoral fellowship award from the American Cancer Society outside the submitted work. Heather S. L. Jim reports grants from the National Institutes of Health, the Department of Defense, the State of Florida, Kite Pharma, and Pfizer Inc; personal fees from Red Hill Biopharma and Janssen Scientific Affairs; personal fees and travel support from Merck all outside the submitted work; has a patent “Methods of Treating Cognitive Impairment” (no. 10806772), issued October 20, 2020; is a member of a data safety monitoring board or advisory board at Northwestern University; and is a member of the Society of Behavioral Medicine. Andrew J. Saykin reports grants from the National Institutes of Health (R01 AG068193, R01 CA129769, and P30 AG010133); service on a Bayer Oncology Advisory Committee; and other support from Avid Radiopharmaceuticals/Eli Lilly all outside the submitted work. Judith E. Carroll reports grants from the STOP Cancer Foundation and the National Institute of Aging outside the submitted work and is a member of the Psychoneuroimmunology Research Society. The other authors made no disclosures.

Author Contributions

Kelly E. Rentscher: Conceptualization, writing–original draft, and writing–review and editing. Xingtao Zhou: Data curation, formal analysis, and writing–review and editing. Brent J. Small: Conceptualization, data curation, formal analysis, and writing–review and editing. Harvey J. Cohen: Funding acquisition, conceptualization, and writing–review and editing. Asma A. Dilawari: Funding acquisition, conceptualization, investigation, and writing–review and editing. Sunita K. Patel: Conceptualization, investigation, and writing–review and editing. Traci N. Bethea: Conceptualization and writing–review and editing. Kathleen M. Van Dyk: Conceptualization and writing–review and editing. Zev M. Nakamura: Conceptualization and writing–review and editing. Jaeil Ahn: Conceptualization, data curation, formal analysis, and writing–review and editing. Wanting Zhai: Data curation and writing–review and editing. Tim A. Ahles: Funding acquisition, investigation, and writing–review and editing. Heather S. L. Jim: Funding acquisition, investigation, and writing–review and editing. Brenna C. McDonald: Funding acquisition, investigation, and writing–review and editing. Andrew J. Saykin: Funding acquisition, investigation, and writing–review and editing. James C. Root: Funding acquisition, investigation, and writing–review and editing. Deena M. A. Graham: Funding acquisition, investigation, and writing–review and editing. Judith E. Carroll: Conceptualization and writing–review and editing. Jeanne S. Mandelblatt: Funding acquisition, conceptualization, investigation, and writing–review and editing.

Tables1‐2

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