The impact of disease progression on perceived health status and quality of life of long-term cancer survivors.

INTRODUCTION: The number of cancer survivors experiencing disease progression (DP) is increasing with the number of cancer survivors. However, little is known whether DP affects health-related quality of life (HRQL) of long-term cancer survivors. We aimed therefore to compare the health status (HS) and HRQL of DP and disease-free (DF) survivors up to 15 years after initial diagnosis.
METHODS: 232 cancer survivors with DP identified through the Eindhoven Cancer Registry were matched with 232 DF survivors of similar demographic and clinical characteristics. Patients completed generic HS (SF-36) and cancer-specific HRQL (QOL-CS) questionnaires 5-15 years after diagnosis.
RESULTS: Compared with DF survivors, DP survivors exhibited significantly lower scores on all SF-36 and QOL-CS (except spiritual well-being) dimensions. DF survivors had better scores than the normative population on all SF-36 dimensions. Among survivors with DP, those with short survival (<5 years) had significantly poorer HS scores on all dimensions except bodily pain compared with the normative population. Comparatively, the long survival (>or=5 years) DP group had better HRQL than the short DP group but poorer HRQL than the normative population. In multivariate analyses, DP and DF survival time were independently associated with aspects of HS and HRQL in cancer survivors. DISCUSSIONS/
CONCLUSIONS: DP cancer survivors have poorer long-term HS and HRQL compared with DF survivors. However, there is suggestion that HS and HRQL does improve over time following DP. IMPLICATION FOR CANCER SURVIVORS: Although DP survivors report poorer long-term HRQL compared with DF cancer survivors, results suggest that time can attenuate the distress of DP on HRQL. Psycho-educational programs could help to increase patients' sense of empowerment and personal control should DP occur.

Introduction

Due to earlier diagnosis and improvement in cancer treatments, cancer survivors are living longer after an initial diagnosis of cancer [1]. Cancer is now often considered a chronic illness rather than a life-threatening disease [2]. However with longer survival after initial diagnosis, the number of cancer survivors experiencing disease progression (DP) such as a recurrence, a metastasis or a new tumor could also increase [3-5]. Survivors of a first primary cancer have an increased risk of up to 50% of developing subsequent primary cancers [6, 7], while recurrence rates range from 5% to >30% for endometrial cancer, prostate cancer, and non-Hodgkin lymphoma [8-10].

Previous studies suggest that DP can cause greater distress than the initial cancer diagnosis [11], and is associated with reduced psychological well-being [12-16], poorer physical functioning [12, 17], high symptom burden [15, 18], and poorer health-related quality of life (HRQL) [19, 20]. However, most of these studies focused on breast cancer, had small sample sizes, had no comparison with a disease-free control group or had short follow-up since DP. To our knowledge, no study has explored the association between DP, survival time since progression, and HRQL of long-term cancer survivors (i.e. patients who are alive >5 years since initial diagnosis).

In this secondary analysis of a cancer survivorship study whose details are reported elsewhere [21], we aim to investigate the effects of DP on health status (HS) and HRQL of long-term survivors of cancer of the endometrium or prostate, or Hodgkin’s or non-Hodgkin’s lymphoma. In specific, we hypothesized that DP survivors will have poorer HS and HRQL compared with patients who remain disease-free (DF) after initial diagnosis.

Methods

Setting and participants

From the Eindhoven Cancer Registry (ECR), all patients diagnosed with either Hodgkin’s lymphoma or non-Hodgkin’s lymphoma between 1989 and 1998, or endometrial or prostate cancer between 1994 and 1998 were eligible for participation in a population-based cross-sectional survey. Hodgkin’s and non-Hodgkin’s lymphoma have a longer inclusion period to increase the sample size. The ECR records data on all patients newly diagnosed with cancer in the southern part of the Netherlands, an area with 2.3 million inhabitants, 10 hospitals with 18 locations and two large radiotherapy institutes [22]. After excluding all persons who had died prior to 1 November 2004 (as according to the Central Bureau for Genealogy which collects information on all deceased Dutch citizens via the civil municipal registries), data collection started in November 2004. A local certified Medical Ethics Committee approved of this study. Additional details of the study methodology have been described elsewhere [21].

Clinical characteristics

Patients’ sociodemographic and clinical information were available from the ECR. The ECR routinely collects data on tumor characteristics, including date of diagnosis, tumor grade according to the Tumor-Node-Metastasis clinical classification [23], clinical stage [23], treatment, and patient background characteristics including date of birth and comorbidity at the time of diagnosis. Comorbidity was categorized according to an adapted Charlson comorbidity index [24]. In this study, cancer was not included as a comorbid condition. Socioeconomic status was determined by an indicator developed by Statistics Netherlands based on individual fiscal data from the year 2000 on the economic value of the home and household income, and provided as aggregate level for each postal code (average 17 households) [25], which were then categorized into tertiles.

DP was defined as at least the first recurrence, metastasis or new primary tumor experienced since initial diagnosis. DP was indicated by patients in the self-report questionnaire. Patients were asked to report on any DP and the month/year that this was diagnosed. Affirmative answers were then confirmed by registry staff against ECR records, together with information on the date of this new diagnosis and subsequent treatment received. For DP patients, survival time was calculated from the date of last DP diagnosis to time of survey. If the date of last diagnosis was not available from ECR records, we used the date as reported by the patient. The survival time for DF patients was calculated from date of initial diagnosis to time of survey. We used the term ‘survival time’ rather than ‘DF time’ to indicate time since last diagnosis to time of study although mortality is not an outcome in this study as we cannot ascertain that patients are DF following DP. Patients with DP were matched with patients who remained DF since initial diagnosis till time of survey on: a) type of cancer, b) cancer stage at initial diagnosis, c) tumor grade at initial diagnosis, d) age at initial diagnosis (±2 years), e) age at time of survey (±5 years) and f) number of years since initial diagnosis (±3 years).

Data collection

Cancer survivors were informed of the study via a letter from their (ex)-attending physician. The letter explained that the completion and return of the enclosed questionnaire indicate patient’s consent to participation in the study and to agree to the linkage of the questionnaire data with their disease history in the ECR. Patients were reassured that non-participation had no consequences on their follow-up care or treatment. Non-respondents were sent a reminder letter within 2 months.

Measures

Generic health status was assessed with the Dutch version of the SF-36 questionnaire [26]. The SF-36 has 36 items measuring eight dimensions of health status: physical functioning, role limitations due to physical problems, role limitations due to emotional problems, social functioning, mental health, vitality, bodily pain, and general health perceptions. Items in each dimension are added together to form subscale scores, which are transformed to a 0–100 scale, with higher scores indicating better perceived health. The eight subscale scores can be further combined into the physical (PCS) and mental (MCS) component summary score. For the SF-36, differences of ≥5 points in the general health domain [27], 6.5 points in the physical domain and 7.9 points in the mental health domain were considered clinically meaningful [28]. We determined clinically meaningful differences for other subscales with Norman’s ‘rule of thumb’, whereby an ≈0.5 SD difference indicates a threshold of discriminant change in HRQL scores of a chronic illness [29]. The internal consistency and reliability of all scales had Cronbach alpha values above 0.70 as recommended for group comparisons.

The validated Dutch version of the Quality of Life–Cancer Survivors (QOL-CS) questionnaire assessed HRQL issues specific to cancer survivors [30]. The QOL-CS includes 45 visual analogue scales, with each ranging from 0 (worst outcome) to 10 (best outcome). These 45 visual analogue scales are grouped into four multi-item subscales on well-being: physical, psychological, social, and spiritual. Similarly, Norman’s rule was used to indicate clinically significant differences [29].

Statistical analyses

All statistical analyses were performed using SAS (version 9.1 for Windows, SAS institute Inc., Cary NC). Differences between demographic and clinical characteristics, and HS and HRQL scores between the two groups were compared with chi-square test or t-test where appropriate. Non-parametric equivalents were applied when normality and homogeneity assumptions were violated. The association between disease progression and long-term HRQL was investigated with linear regression analyses, with adjustments for DF survival time, marital status, SES, and comorbidity. Statistical differences were indicated if p < 0.05 and reported p-values were two-sided.

Results

Of the eligible survivors, 1511 (80%) returned a completed questionnaire (Fig. 1). Details of the data collection process for the whole sample, and the baseline characteristics of respondents and non-respondents have been discussed elsewhere [21]. From the respondents, 232 DP survivors (13 Hodgkin’s lymphoma, 53 non-Hodgkin’s lymphoma, 19 endometrial cancer, and 147 prostate cancer) were matched with 232 DF survivors of similar clinical and demographic characteristics (Table 1). No differences on the relevant clinical and demographic characteristics indicated a successful match of the two groups. Comparison on other demographic and clinical variables suggested that DP survivors had more comorbid conditions and were less likely to be working than DF survivors. Among the DP survivors, 30 had a second DP. The time since last progression to the date of completion of questionnaire was, on average, 3.4 ± 3.3 years.

FIGURE 1

Flow-chart of the data collection process.

Table 1

Demographic and clinical characteristics of patients by disease status

	No progression (n = 232)	Disease progression (n = 232)	p-value
Types of cancer (%)
Hodgkin’s lymphoma	13 (6)	13 (6)
Non-Hodgkin’s lymphoma	53 (23)	53 (23)
Endometrial cancer	19 (8)	19 (8)
Prostate cancer	147 (63)	147 (63)
Mean age at time of survey	69.0 ± 10.4	68.8 ± 10.3	0.40
Age at time of survey (%)
<55	23 (10)	21 (9)
55–64	39 (17)	41 (18)
65–74	94 (40)	97 (42)	0.87
75–84	73 (31)	72 (31)
>85	3 (1)	1 (0.4)
Mean years since diagnosis of initial cancer	8.2 ± 1.7	8.2 ± 1.8	0.72
Marital status (%)
Married	169 (76)	178 (77)
Single/Divorced	26 (12)	26 (11)	0.97
Widowed	26 (12)	26 (11)
Educational levela (%)
Low	108 (49)	98 (44)
Medium	66 (30)	87 (39)	0.14
High	46 (21)	36 (17)
Employment status (%)
Not working/ retired	185 (84)	201 (88)	0.03
Working	35 (16)	28 (12)
Socioeconomic status (%)
Low	49 (21)	51 (22)
Medium	97 (42)	92 (40)	0.97
High	77 (33)	79 (34)
Stage (%)
1	74 (32)	75 (32)
2	107 (46)	106 (46)	0.99
3	16 (7)	15 (6)
4	35 (15)	36 (16)
Tumor Gradeb (%)
Good	55 (24)	53 (22)
Moderate	76 (33)	76 (33)
Poor	35 (15)	36 (16)	0.97
Undifferentiated	0	1 (0.4)
T-cell (lymphoma)	2 (1)	3 (1)
B-cell (lymphoma)	51 (22)	50 (21)
Comorbidity (%)
None	91 (39)	75 (32)
1	90 (39)	82 (35)	0.04
>1	51 (22)	75 (32)
Most common comorbid conditions (%)
Hypertension	60 (26)	62 (27)	0.83
Arthritis	51 (22)	61 (26)	0.28
Diabetes mellitus	23 (10)	32 (14)	0.19
Asthma	27 (12)	29 (13)	0.77
Mean years since disease progression		3.4 ± 3.3
Years since disease progressionc (%)
< 2 years		94 (40)
2–5 years		58 (24)
>5 years		51 (21)

aEducation: Low (no or primary school); Medium (lower general secondary education or vocational training); High (pre-university education, high vocational training, university)

b13 patients with Hodgkin’s lymphoma were matched excluding the criterion tumor grade as these were not available

c29 patients have unknown date of progression

Table 2 outlines the HS and HRQL scores of DP and DF survivors. Although statistical significant differences in all dimensions of generic HS between both groups were noted, clinically significant differences were observed in the dimensions of general health, physical function, role function physical, role function emotional, and the physical component score. On the cancer-specific QOL-CS, DP survivors had statistically poorer scores on physical, psychological, social, and total well-being, but not spiritual well-being. However, only the differences in physical, social, and total well-being scores showed clinical significance. Similar HS and HRQL results were found between both the DP and DF groups when analysis was limited to either prostate cancer survivors or survivors of endometrial cancer and the lymphomas (excluding prostate cancer) (data not shown).

Table 2

Mean scores (± SD) of SF-36 and QOL-CS by disease status

	Disease progression (n = 232 )	No progression (n = 232 )	p-value
SF-36
General health	48.9 ± 23.5	62.9 ± 22.1	<0.0001a
Physical function	60.5 ± 29.7	73.2 ± 25.0	<0.0001a
Role function–physical	48.0 ± 45.7	70.1 ± 40.1	<0.0001a
Bodily pain	69.8 ± 27.0	78.2 ± 22.9	<0.001
Vitality	57.0 ± 24.3	67.5 ± 20.8	<0.0001
Social functioning	72.6 ± 26.9	83.5 ± 21.4	<0.0001
Role function–emotional	64.6 ± 44.1	86.5 ± 28.7	<0.0001a
Mental health	70.8 ± 20.7	77.5 ± 16.8	<0.001
PCS	40.0 ± 11.7	46.0 ± 9.8	<0.0001a
MCS	49.0 ± 11.2	51.0 ± 8.7	<0.0001
QOL-CS
Physical well-being	7.2 ± 1.9	8.0 ± 1.8	<0.0001a
Psychological well-being	5.9 ± 1.8	6.9 ± 1.6	<0.0001
Social well-being	6.6 ± 1.7	7.2 ± 1.7	<0.0001a
Spiritual well-being	4.6 ± 1.7	4.8 ± 1.4	n.s.
Total well-being	6.1 ± 1.4	6.8 ± 1.3	<0.0001a

PCS Physical Component Summary score, MCS Mental Component Summary score, QOL-CS Quality of Life–Cancer Survivors

aindicates that the difference in the HRQL score is also clinically significant

The generic HS of DF and DP survivors was compared with that of a normative population, standardized for age. DF survivors had better HS than the normative population on all dimensions of the SF-36, with physical functioning, bodily pain, social functioning, role functioning emotional, and physical component summary score statistically significantly better than that of the normative population (Fig. 2). Among the DP group with known time of progression, survival time was dichotomized into short (<5 years) and long (≥5 years) survival since progression. Compared with the normative population, the short DP group had statistically significantly poorer HS scores on all dimensions except on bodily pain. Clinically significant differences between the two groups were noted in general health and mental component summary scores. Similarly, the long DP group had poorer HS than the normative population, although only general health and the mental component summary scores showed statistically but not clinically significant differences. However long DP survivors report having better HS than short DP survivors (Table 3). Long DP survivors exhibited significantly better mental component summary score and the difference in general health scores approached significance. For those DP patients (n = 29) whose date of DP were not known, their HS scores were generally compatible with those of the long DP survivors (data not shown).

FIGURE 2

Comparison of SF-36 scores according to disease status to the normative population standardized for age. An asterisk above a subgroup indicates a difference in the mean score between that subgroup and the normative population. PCS=Physical Component Summary score. MCS=Mental Component Summary score. **p < 0.001; *p < 0.05. ξ Indicates clinically significant difference in mean score between the subgroup and the norm population.

Table 3

Mean scores (± SD) of SF-36 and QOL-CS of patients with disease progression by survival time since progressiona

	<5 years (n = 143)	≥5 years (n = 50)	p-value
SF-36
General health	47.1 ± 23.8	54.2 ± 23.8	0.05
Physical function	59.2 ± 30.6	63.2 ± 28.9	0.51
Role function–physical	45.1 ± 45.7	53.8 ± 45.3	0.27
Bodily pain	69.9 ± 26.2	70.7 ± 29.5	0.66
Vitality	56.2 ± 23.5	60.8 ± 26.6	0.20
Social functioning	72.0 ± 26.2	74.3 ± 32.1	0.20
Role function–emotional	61.1 ± 44.9	72.6 ± 40.4	0.16
Mental health	69.4 ± 21.3	74.5 ± 20.0	0.10
PCS	39.6 ± 11.5	41.1 ± 12.7	0.48
MCS	47.7 ± 11.2	51.5 ± 11.1	0.03
QOL-CS
Physical well-being	7.1 ± 2.0	7.5 ± 1.8	0.17
Psychological well-being	5.8 ± 1.9	6.1 ± 1.6	0.45
Social well-being	6.5 ± 1.7	6.8 ± 1.5	0.35
Spiritual well-being	4.5 ± 1.5	4.9 ± 1.7	0.13
Total well-being	6.0 ± 1.4	6.3 ± 1.3	0.19

PCS Physical Component Summary Score, MCS Mental Component Summary Score, QOL-CS Quality of Life–Cancer Survivors

atime since progression is missing for 29 patients

In univariate analyses, DP independently predicted HS and HRQL except for spiritual well-being (data not shown). Similarly, DF time was associated with most dimensions of the SF-36 and QOL-CS except for bodily pain and spiritual well-being (data not shown). In multivariate analyses, DP remained a significant predictor on most dimensions of the SF-36 and QOL-CS (Table 4). However, the association of DF time with HS and HRQL was reduced in the multivariate model, remaining significant only in the dimensions of role functioning emotional, mental health, mental component summary score, and total well-being. Poorer scores on all domains of the SF-36 and QOL-CS (except for spiritual well-being) were independently predicted by comorbidity in both univariate and multivariate analyses.

Table 4

Standardized betas of multivariate linear regression analyses indicating the association of disease progression with HRQL

	SF-36										QOL-CS
	GH	PF	RP	RE	BP	SF	VT	MH	PCS	MCS	Phy	Psy	Soc	Spi	Tot
Progression	−9.9*	−10.4*	−14.1*	−12.2*	−7.1*	n.s.	−7.1*	n.s.	−5.0*	n.s.	n.s.	−0.6*	−0.5*	n.s.	−0.5*
Disease-free survival time	n.s.	n.s.	n.s.	2.2*	n.s.	n.s.	n.s.	0.9*	n.s.	0.7*	n.s.	n.s.	n.s.	n.s.	0.1*
Married	n.s.	n.s.	n.s.	n.s.	n.s.	n.s.	n.s.	n.s.	n.s.	n.s.	n.s.	n.s.	0.4*	n.s.	n.s.
SES	n.s.	−9.0*	n.s.	−9.2*	−6.7*	n.s.	n.s.	n.s.	n.s.	n.s.	n.s.	−0.4*	n.s.	n.s.	−0.3*
Comorbidity	−8.9*	12.0**	18.6**	−9.1*	−11.9**	−11.0**	−6.8*	−5.3*	−5.5**	−2.4*	−0.8*	−0.5*	−0.4*	n.s.	−0.5*

SF-36: GH general health, PF physical functioning, RP role functioning physical, RE role functioning emotional, BP bodily pain, SF social functioning, VT vitality, MH mental health, PCS physical component summary score, MCS mental component summary score, QOL-CS Quality of Life–Cancer Survivors, Phy physical well-being, Psy psychological well-being, Soc social well-being, Spi spiritual well-being, Tot total well-being, SES socioeconomic status

*p < 0.05; **p < 0.001

Discussion

As hypothesized, our study showed that DP cancer survivors had poorer HS and HRQL than DF cancer survivors of similar clinical manifestation and age. Patients with DP within 5 years of our study reported the lowest HS and HRQL. Cancer survivors who remain DF up to 10 years since initial diagnosis have HS and HRQL better or comparable to an age-matched normative population. Moreover, DP and comorbid conditions predicted that aspects of long-term HS and HRQL would be lower.

Compared with DF survivors, DP survivors had clinically significant poorer scores on several aspects of HS and HRQL, namely that of physical, social, and psychological functioning. Similarly in a matched study, Oh, et al reported that survivors with recurrent breast cancer had poorer HRQL on multiple domains compared with DF survivors [19]. Survivors of multiple cancers had also poorer global HRQL, lower vitality, more cancer-specific stress and lower existential well-being compared with survivors of single primary cancer [31]. In another study, breast cancer survivors with and without recurrence had similar HRQL scores at baseline. At 8-years follow-up, although the HRQL of disease-free survivors had improved significantly, the HRQL scores of those with a recurrence remained similar to their baseline assessment [13].

Higher prevalence of comorbid conditions among DP survivors could partly explain their perceived poorer physical and social aspects of HS and HRQL. Moreover, comorbidity was a significant predictor of HS and HRQL in our multivariate analysis. Similarly in a study using CaPSURE data, prostate cancer survivors with moderate to severe cardiovascular comorbidity had significantly poorer physical component scale scores over 24 months follow-up compared with patients with no comorbidity [32]. A study of cervical cancer survivors also reported significant association between comorbidity and HRQL [33].

Although we performed a cross-sectional study, our results suggest that long-term DP survivors do report better HS and HRQL scores over time. DP patients with shorter survival time since last diagnosis had significantly poorer HS and HRQL compared with an age-standardized normative population. However, we noted that DP survivors with a progression ≥5 years ago had higher HS and HRQL scores than those with shorter survival time since last diagnosis. That we only found a significant difference in the mental component summary score between these two groups could be due to lack of power from the small sample of long DP survivors. A longitudinal study showed that patients with recurrent cancer had poorer HRQL compared with single diagnosis patients at 12 months follow-up, although the HRQL among the group with recurrence showed improvement over time [17]. Moreover, in that study while patients in both groups reported improved psychological well-being over time, patients with a recurrence had better psychological well-being at baseline and follow-up than patients with a single diagnosis. Similarly, a Swedish longitudinal study with recurrent breast cancer survivors reported a significant decrease in distress at 6 months follow-up [34]. This suggests that cancer survivors might initially be distressed with the diagnosis of DP [11, 13] but do have the resilience to adapt and cope with the new diagnosis and subsequent treatment over time. Gotay, et al found that survivors of multiple primary cancers coped better with the second diagnosis than the first [31]. Together with our current results, these studies suggest that previous experiences with cancer and its treatment could buffer a patient from the psychological distress of coping with DP and subsequent treatment. This reconceptualization of HRQL over the course of the disease trajectory has been termed ‘response shift’, and refers to the changes in self-evaluation of HRQL as cancer survivors adapt to their disease and treatment [35]. We further postulate that DP survivors with ≥5 years since progression could potentially believe that they are DF similar to the commonly held assumption cancer survivors in general have that they are ‘cured’ if they remain DF >5 years since initial diagnosis.

Response shift could also explain the significantly better physical health reported by DF survivors when compared to a normative population. Having survived cancer and remaining DF for up to 15 years since initial diagnosis could improve survivors’ self-evaluation of HRQL. DF survivors finding benefit following their cancer diagnosis and its subsequent cure could also impact on their HRQL. In a study of 96 breast cancer survivors of whom the majority remained DF, baseline benefit finding predicted better self-reported HRQL and positive emotion at follow-up 4 to 7 years after initial assessment [36].

Although studies suggest that patients with DP do adapt well to the new diagnosis over time, one study found that patients’ beliefs could impact on the adaptation process. In that study, breast cancer survivors with high baseline beliefs of personal control over their disease symptoms and who subsequently experienced a recurrence had poorer physical and mental functioning at 5-year follow-up compared with survivors with similar baseline beliefs who remained disease-free [37]. Higher symptom burden was associated with higher level of distress and decreased HRQL of women with recurrent breast cancer at 6 months follow-up [34].

These results have implications for clinical practice. As the numbers of cancer survivors is increasing, the number of cancer survivors experiencing DP will also increase. Although current results support our hypothesis that patients with DP have poorer HS and HRQL compared with DF survivors, our results also suggest that time can attenuate the distress of experiencing progression of their disease. Therefore, besides interventions to prevent DP, psycho-educational programs designed with an understanding of cancer survivors’ attributions of recurrence could help to increase empowerment and personal control in patients’ self-management of illness- and treatment-related symptoms should DP occur.

We acknowledge several limitations in our study. The inclusion of long-term survivors raises the possibility of survival bias in our sample selection. Moreover, the cross-sectional design of our study limits the determination of causal association between DP and HRQL as baseline HRQL of patients at diagnosis is not known. Therefore, future studies of incident cancer patients with baseline data before DP occur and followed longitudinally would be useful in exploring this association between DP and long-term HRQL, and the subsequent adaptation process to DP. Third, DP was established by patients’ self-report and thereafter confirmed via the ECR. Therefore, it is possible that there is an under-reporting of DP from patients who had progression but did not report on the questionnaire. Although our results suggest that DP survivors with longer survival time since last diagnosis had better HS and HRQL than those with shorter survival time, these results should be interpreted with caution due to the relatively small number of DP survivors with ≥5 years survival time (n = 50). Nevertheless, this result is intriguing and warrants further research. Future prospective studies with a larger group of DP survivors followed over a longer period could investigate if our current results are reflective of “survival of the fittest” or that HRQL does improve with time following DP. Also of interest will be the identification of predictors of better HRQL among DP survivors.

Strong points of our study include the HS and HRQL assessments of patients with DP up to 15 years since initial cancer diagnosis. Moreover, inclusion of the length of time since DP for consideration when assessing long-term HS and HRQL in cancer survivors has, to our knowledge, not been reported previously.

Conclusions

Cancer survivors who experience DP report poorer long-term HS and HRQL compared with disease-free survivors. However, results suggest that DP survivors do report better HS and HRQL over time.