Quality of life of breast and cervical cancer survivors
BMC Women's Health volume 17, Article number: 30 (2017)
Breast and cervical cancer are the most common cancers affecting women. The symptom distresses experienced by cancer survivors are critical factors influencing their quality of life (QOL). This study investigated the QOL of breast and cervical cancer survivors, their physical, psychological and social conditions.
The participants were older than 20 years, had been diagnosed with breast or cervical cancer for more than 2 years, and had completed their cancer treatment. The survey incorporated the QOL questionnaires developed by the European Organization of Research and Treatment for Cancer and a self-designed questionnaire.
The mean age at diagnosis was 48.89 ± 8.53 years for the breast cancer survivors and 49.00 ± 10.30 years for the cervical cancer survivors. The corresponding QOL scores were 75.33 ± 20.25 and 75.56 ± 17.93. The factors influencing QOL of breast cancer survivors were household income, number of comorbidities, stage of cancer, type of cancer treatment and duration of illness, whereas the factor related to QOL of cervical cancer survivors was only household income.
The QOL of the two groups was similar. Healthcare providers should demonstrate greater concern toward breast and cervical cancer survivors.
The International Agency for Research on Cancer reported that the number of new cancer cases worldwide was 14.1 million in 2012 . Breast and cervical cancer are common cancers among women, affecting approximately 1.67 million and 530,000 people each year worldwide, respectively. In 2012, 522,000 and 270,000 women died of breast and cervical cancer, respectively, accounting for the highest and fourth-highest mortality rates among women .
According to the Ministry of Health and Welfare, Taiwan, cancer has been the leading cause of death in Taiwan for 32 consecutive years, accounting for 29% of all deaths in 2013, and the standardized mortality rate was 130.4 per 100,000 persons . As indicated by the Health Promotion Administration of Taiwan, breast and cervical cancer are the most hazardous illnesses affecting women’s health; if detected early, the 5-year survival rates for women with breast and cervical cancer are 88.7–97.5% and 88.8–96.8%, respectively .
The World Health Organization defined quality of life (QOL) as involving a person’s physical health, psychological state, degree of independence, social relationships, personal beliefs and environment . Female cancer survivors are faced with physical, psychological and social distress in addition to fatigue, irritability, memory loss, decreased energy level, recurring pain and decreased QOL [6–9]. The symptom distress experienced by cancer survivors is a critical factor influencing their QOL [10, 11]. Following a cancer diagnosis, patients with breast and cervical cancer must undergo a series of long-term treatments and follow-up examinations to prevent recurrence and improve survival . In addition to symptom distress resulting from cancer treatment and physical discomfort caused by the illness, other factors, such as body image impairment, psychological fear, anxiety and low self-esteem, can affect the QOL of patients [8, 11, 13]. After undergoing surgery and other forms of treatment, patients with breast cancer frequently experience various types of discomfort, including stomach upset, a lack of appetite, nausea, vomiting, fatigue, arm pain and difficulty breathing, all of which introduce many inconveniences into their lives and greatly influence their QOL [10, 14, 15]. In the early treatment of cervical cancer, the most common types of discomfort and the primary factors influencing the long-term QOL of patients are constipation, lower extremity edema, urinary incontinence, hot flashes, diarrhea and increased vaginal discharge .
Although numerous studies have separately measured the QOL of cancer patients, few studies have explored the QOL of breast and cervical cancer survivors. Because breast and cervical cancer are among the top ten cancers in terms of incidence in Taiwan and are both cancers affecting women, we simultaneously addressed these two types of cancer in the present study. We investigated the QOL of breast and cervical cancer survivors, as well as their physical, psychological and social conditions. In addition, we explored whether patients characteristics, health status, household income, health behaviors, disease severity, medical care provider characteristics, treatment methods and illness duration were associated with the patients’ QOL.
This adopted a cross-sectional design. In accordance with Klug et al., we defined cancer survivors as patients who survived for more than 2 years following a cancer diagnosis . Breast and cervical cancer survivors were recruited according to the following inclusion and exclusion criteria. Inclusion criteria: patients who were older than 20 years, had been diagnosed with breast or cervical cancer for >2 years, and had completed their cancer treatment (i.e., were currently receiving only regular follow-ups). Exclusion criteria: patients who were currently receiving cancer treatment (excluding those with breast cancer who were currently undergoing hormone therapy [HT]), who had terminal cancer, whose cancer stage was unknown, who had multiple types of cancer, who had carcinoma in situ, and who were men with breast cancer.
Sampling and data collection
Patient consent for this study was received from the cooperating hospitals and approved by the institutional review boards (IRB No. CMU-REC-101-013). According to the proportion of patients at the cooperating hospitals, as indicated by the Taiwan Ministry of Health and Welfare, we calculated the number of cases that should be collected from five medical centers and three regional hospitals in Northern, Central and Southern Taiwan. Subsequently, interviewer training was conducted and doctors, nurses, and case managers at the collaborating hospitals were entrusted with selecting and recruiting respondents who met the inclusion criteria. After patient consent was obtained, the questionnaire surveys were distributed.
Questionnaire design and content
The questionnaire used in this study incorporated QOL questionnaires (QLQs) developed by the European Organization of Research and Treatment for Cancer (EORTC) as well as a self-designed questionnaire. The questionnaire was designed to elucidate the QOL of cancer survivors.
To assess the QOL of the participants, we acquired permission to use the Chinese version of the EORTC questionnaires, including the core QLQ-C30 and QLQ supplementary modules [16, 18–21] for breast cancer QLQ (QLQ-BR23) and cervical cancer QLQ (QLQ-CX24). The QLQ-C30 contains 30 questions, comprising five groups of questions on functioning, namely physical functioning (five questions), role functioning (two questions), emotional functioning (four questions), cognitive functioning (two questions) and social functioning (two questions); two questions on global health status and QOL; and 12 questions on the symptoms or problems frequently experienced by patients with cancer, namely fatigue (three questions), pain (two questions), nausea and vomiting (two questions), difficulty breathing (one question), insomnia (one question), lack of appetite (one question), constipation (one question) and financial difficulty (one question).
The QLQ-BR23 contains eight questions, comprising four groups of questions on functioning, namely body image (four questions), sexual functioning (two questions), sexual enjoyment (one question) and future perspective (one question); and 15 questions on the symptoms or problems frequently experienced by patients with breast cancer, namely side effects from treatment (seven questions), symptoms related to the breasts (four questions), symptoms related to the arms and shoulders (three questions), and hair loss (one question).
The QLQ-CX24 contains nine questions, comprising four groups of questions on functioning, namely body image (three questions), sexual activity (one question), sexual enjoyment (one question) and sexual/vaginal functioning (four questions); and 15 questions on the symptoms or problems frequently experienced by patients with cervical cancer, namely general symptoms (11 questions), lymphatic symptoms (one question), peripheral neuropathy (one question), menopausal symptoms (one question) and sexual anxiety (one question).
The EORTC questionnaire has been employed in previous studies to clarify the QOL of the cancer survivors [21–24]. A high score on the global health status (i.e., overall QOL score) and functioning dimension (0–100) represents a high level of QOL and functioning, whereas a high score on a symptom dimension (0–100) indicates a high level of (or severe) symptoms. The EORTC questionnaire is widely known to demonstrate acceptable validity [16, 19, 24, 25]. In the present study, the reliability Cronbach’α coefficients of the EORTC QLQ-30 and QLQ-BR23 for breast cancer survivors (n = 252) were 0.93 and 0.88, respectively and those of the EORTC QLQ-30 and QLQ-CX24 for cervical cancer survivors (n = 75) were 0.91 and 0.81, respectively.
Self-designed questionnaire and its validity
On the basis of related literature and data, the content of the self-designed questionnaire was divided into two major parts: one part was completed by the respondents and the other part was completed by the healthcare professionals after reviewing the patients’ medical records. The part completed by the respondents incorporated items from four major categories: health condition (e.g., disease history and medical history), lifestyle (e.g., cigarette smoking, alcohol consumption and exercise), (4) demographic information (e.g., sex, educational attainment, marital status, living conditions and household income). The part completed by the healthcare professionals comprised items on the therapeutic situation of the patients (e.g., date of diagnosis, stage of cancer, methods of treatment and whether the cancer recurred or metastasized). The content validity of the self-designed questionnaire was assessed by seven experts, including specialists, case managers, cancer registrars and scholars, who were invited to assess the content of the questionnaire for survivors of the two types of cancer. The questionnaire was revised according to feedback from the experts, with ambiguous questions reworded for clarity to ensure the integrity of the instrument. Subsequently, the content validity index (CVI) was employed to evaluate the revised questionnaire according to the mean CVI; in general, a mean CVI of >0.8 indicates adequate validity [26, 27]. The mean CVIs derived from the self-designed questionnaire for breast cancer and cervical cancer survivors were 0.98 and 0.97, respectively, indicating a high level of validity. The self-designed questionnaire used in our study contained items on personal information and disease information; these items were unrelated to the conception of any specific dimension and were thus unsuitable for any reliability analysis.
The frequencies, percentages and means of the following demographic characteristics were statistically analyzed: personal characteristics (sex, age and educational attainment), socioeconomic status (household income), social support (marital status and living conditions), health conditions (comorbidities), specifics pertaining to cancer treatment (cancer stage, recurrence or metastasis, treatment method, illness duration and medical institution level), lifestyle (e.g., cigarette smoking, alcohol consumption and exercise), participants’ apprehension regarding the recurrence or metastasis of cancer, and the various dimensions of QOL.
A t test and one-way analysis of variance (ANOVA) were conducted on the following characteristics: personal characteristics (sex, age and educational attainment), household income, social support (marital status), health conditions (comorbidities), specifics pertaining to cancer treatment (cancer stage, recurrence or metastasis, treatment method, illness duration and medical institution level), and global health status. In addition, the participants who received treatment at the same hospitals may exhibit homogeneity, and cancer treatments offered in a single hospital are similar in nature; therefore, the cluster effect of participants from the same hospital was considered. Medical institution was employed as a repeated measure variable in the multiple regression model analysis using generalized estimating equations, in which the global health status was taken as the dependent variable, and the patients’ personal characteristics, socioeconomic status, social support, health condition and specifics pertaining to cancer treatment were taken as independent variables. Among the independent variables, in addition to the variables that achieved p < 0.25 in the bivariate analysis, the two variables “cancer stage” and “cancer recurrence or metastasis” were used as control variables in analyzing and exploring the relevant factors influencing the QOL of the cancer survivors.
A total of 327 valid questionnaires were returned by the breast cancer survivors (n = 252) and cervical cancer survivors (n = 75). In Table 1, the mean age at diagnosis was 54.48 ± 8.33 years for the breast cancer survivors and 55.26 ± 10.50 years for the cervical cancer survivors, showing that these two groups were of similar age. Participants who had graduated from high school or vocational school accounted for the highest percentage of all participants (breast cancer, 42.06%; cervical cancer, 26.67%), and most participants were married (breast cancer, 75%; cervical cancer, 70.7%). The monthly household income among the breast cancer patients was relatively even, with the largest group (50.80%) earning > US$2,001. Among the cervical cancer patients, the largest group (36.00%) earned < US$1,000.
Health condition, health behavior and cancer treatment condition
Regarding the health condition of the breast cancer and cervical cancer survivors (Table 1), 56.35 and 57.33% did not have any comorbidities and 96.43 and 85.33% were nonsmokers, respectively. Regarding the severity of the patients’ cancer, 43.25 and 37.70% of the breast cancer survivors had stage I and II cancer, respectively, whereas most of the cervical cancer patients (73.33%) had stage I cancer. Most of the breast cancer survivors received a combination of surgical treatment, radiation therapy (RT), chemotherapy (CH) and HT (30.56%); followed by a combination of surgical treatment, CH and HT (21.43%); whereas most of the cervical cancer patients received surgical treatment alone (49.33%), followed by a combination of RT and CH (13.33%). The average illness duration among the breast and cervical cancer survivors at the time of recruitment was 5.58 ± 2.58 and 6.26 ± 4.19 years, respectively and 49.21% of the breast cancer survivors and 45.33% of the cervical cancer survivors had cancer for >5 years. The proportion of cancer recurrence and metastasis was 4.76 and 2.67%, respectively.
Quality of life of the participants
First, the results of the QLQ-C30 (Table 2) indicated that the global health status of the two groups was similar. The mean score was 75.33 ± 20.25 (range, 8.33 ~ 100) for the breast cancer survivors and 75.56 ± 17.93 (range, 33.33 ~ 100) for the cervical cancer survivors. Regarding the functioning dimension, breast cancer survivors scored the lowest in the cognitive dimension (77.12 ± 19.42), whereas the cervical cancer survivors had the lowest scores in the emotional dimension (85.22 ± 18.00). In the symptom dimension, the three leading symptoms experienced by the breast cancer survivors were insomnia (26.06 ± 23.71), fatigue (19.27 ± 17.76), and constipation (15.08 ± 22.51), whereas those experienced by the cervical cancer survivors were insomnia (16.89 ± 24.73), constipation (16.89 ± 22.84), and fatigue (14.81 ± 16.87). The results of the EORTC QLQ revealed that the highest scores in the functioning dimension were for body image (breast cancer, 83.04 ± 22.38; cervical cancer, 89.93 ± 15.41), whereas the lowest scores were for sexual/vaginal functioning (breast cancer, 13.49 ± 16.66) and sexual activity (cervical cancer, 16.00 ± 22.83). In the symptom dimension, the most severe symptoms were hair loss (breast cancer, 23.56 ± 25.22) and peripheral neuropathy (cervical cancer, 16.89 ± 20.04).
Relevant factors influencing quality of life
Bivariate ANOVA was employed to explore the relevant factors influencing the global health status of the cancer survivors. Table 3 indicates that the primary factors influencing the global health status of the breast cancer survivors were their monthly household income, number of comorbidities, stage of cancer, method of cancer treatment and duration of illness. Relative to those earning monthly household incomes of < US$1,000, patients with a monthly household income of > US$2,000 or US$1,000–US$2,000 had a significantly higher global health status (10.99 ± 3.83 and 8.75 ± 3.37, respectively; both p < 0.05). Compared with the participants without comorbidities, the global health status of those with three comorbidities was significantly lower (−15.27 ± 4.94; p < 0.05). Furthermore, compared with the participants who had stage I cancer, the global health status of those who had stage II cancer was significantly lower (−5.08 ± 2.53; p < 0.05). Compared with the participants who received CH alone, those who received a combination of CH and surgical treatment exhibited a lower global health status. The breast cancer survivors who were ill for 3–5 years had a significantly higher global health status (9.54 ± 3.73; p < 0.05) than that of the participants who had been ill for 2–3 years.
Table 3 suggests that monthly household income was the only relevant factor influencing the global health status of the cervical cancer survivors, and those with monthly incomes of US$1,000–US$2,000 or > US$2,000 had a significantly higher global health status (11.72 ± 4.91 and 15.45 ± 3.55, respectively; both p < 0.05) compared with those with a monthly income of < US$1,000. Among the cervical cancer survivors, the stage of cancer and cancer recurrence or metastasis did not lead to significant differences (p > 0.05) in the global health status.
Global health status of the patients with cancer
Scott et al.  revealed that the global health status for breast cancer was 61.8 ± 24.6. Because of the difference in cancer stage, the global health status for the breast cancer survivors in our study was higher (75.33 ± 20.25). Our results are similar to those reported by Fehlauer et al. , who performed a 12-year follow-up of breast cancer survivors and reported that their global health status was high. Compared with a study by Huang et al. , in which breast cancer patients who had received their diagnosis at least 9 months prior and received surgical treatment had a global health status of 56.3, the breast cancer survivors in the present study with an illness duration of >2 years had a higher global health status. In the symptom dimension, fatigue and insomnia were the more serious symptoms experienced by the breast cancer survivors in the present study. In addition, this group had low emotional functioning and cognitive functioning, which is similar to the finding of Mols et al. , who indicated that anxiety influenced the global health status of the breast cancer survivors in that study. Such an influence is due to HT causing menopausal symptoms, namely insomnia, depression, hot flashes, nausea, vomiting and cognitive dysfunction .
A study conducted by Dahiya et al.  in India reported that after treatment, the global health status of advanced cervical cancer patients (excluding critically ill patients) was 59.5 ± 10.9. Another study by Kumar et al.  excluded cervical cancer patients with stage IV and reported a global health status of 77.9 ± 7.17 for cervical cancer patients at 6 months after they had completed cancer treatment. In our study, the global health status for the cervical cancer survivors was 75.6 ± 17.9. The differences in the global health status scores between these studies is related to the differences in cancer stage, treatment methods and level of comorbidity .
Regarding the functioning dimension, the cervical cancer survivors in the present study had poor emotional functioning and typically experienced fatigue, insomnia, constipation and financial difficulty. Such findings are similar to those of Park et al. . In contrast to the results of Hsu et al. , our results present more favorable scores in the patients’ global health status and the functioning and symptom dimensions. This difference might be because Hsu et al. focused on stage IB and IIA cervical cancer patients with an mean age was 61.5 ± 11.4 years, whereas the participants recruited in the present study were breast and cervical cancer survivors with mean ages of 54.48 ± 8.33 and 55.26 ± 10.50 years, respectively and who had stage IA cancer (22.7%). Compared with other related studies [16, 34, 35], the global health status of the breast cancer survivors (75.33 ± 20.25) and cervical cancer survivors (75.56 ± 17.93) in the present study indicate that they had a higher global health status, more favorable functional performance and experienced less severe symptoms. The higher scores might be because most of the participants recruited in the present study had early-stage cancer. For example, >60% of the breast cancer patients had stage I or stage IIA cancer, and a high proportion of cervical cancer survivors had stage I or II cancer.
Relevant factors influencing the quality of life of cancer survivors
The factors influencing the QOL of breast cancer survivors were household income, number of comorbidities, stage of cancer, method of treatment and duration of illness. After the other factors were controlled for, the patients who received multitherapy (including surgical treatment) had a significantly lower global health status than those who received CH alone. Because patients with breast cancer typically receive a mastectomy or complete axillary lymph node dissection, they are likely to experience such symptoms as shoulder pain, swelling of the arms and inability to stretch the arms; moreover, such symptoms are generally persistent. Patients who receive a complete axillary lymph node dissection or RT are likely to experience allergy symptoms following surgery, and such conditions cause inconveniences in their daily life, thereby affecting their QOL. Previous studies have indicated that the physiological discomfort experienced by breast cancer survivors after treatment differs according to the type of treatment they received .
In order to reduce cancer survivors’ discomfort or recover their health, for the cancer survivors who have received multitherapy, they not only need to receive a long term plan of rehabilitation but also need to have psychological consultations.
High QOL was observed among patients with a high household income or who had been ill for a long period. These findings are similar to previous findings [37–39]. In the present study, the breast cancer survivors who had an illness duration of ≥3 years had higher QOL compared with those who had been ill for 2–3 years; among these patients, the breast cancer survivors with an illness duration of 3–5 years attained the highest QOL scores. Based on a short illness duration, we considered that the treatment method may influence the speed of physical recovery; patients who received multitherapy recovered more slowly. Although most of the participants in this study were long-term cancer survivors (>80% had an illness duration of ≥3 years), the influence of the cancer treatment methods on their current QOL was persistent. Therefore, this might explain why the cancer survivors’ current global health status was lower among those who underwent a combination of surgery and other treatment methods than among those who underwent CH alone. The other factors influencing the QOL of cancer survivors require further exploration.
Household income was the only relevant factor influencing the global health status of the cervical cancer survivors, with higher household incomes indicating a significantly higher global health status. Because only 75 cervical cancer survivors were recruited in this study, future studies should consider investigating other relevant factors influencing the global health status of cervical cancer survivors and increasing the sample size.
Strengths and limitations
This study collected data on the global health status of cancer survivors with two of the most common cancers affecting women. The main strength of this study is that it not only simultaneously explored the associated factors of global health status for cancer survivors but also compared the differences in QOL and global health status between breast cancer and cervical cancer survivors. The limitations of this study are the lack of information on nonresponse cases. In addition, because we could not interview cancer survivors through random selection methods, the generalizability of the study results to all Taiwanese breast and cervical cancer survivors is limited. However, our study results may provide a reference for other countries.
Regarding the QOL dimensions, the participants exhibited lower cognitive and emotional functioning and experienced more severe fatigue and insomnia. Compared with the cervical cancer survivors, the breast cancer survivors had lower QOL in all functioning dimensions. In addition, compared with the cervical cancer survivors, a higher proportion of breast cancer survivors were concerned about cancer recurrence and metastasis.
Household income, comorbidities, cancer stage, method of treatment and illness duration were relevant factors influencing the global health status of the breast cancer survivors; however, household income was the only factor influencing that of the cervical cancer survivors.
Analysis of variance
Content validity index
European Organization of Research and Treatment for Cancer
Institutional review board
Quality of Life Questionnaire-Breast Cancer Module 23
Quality of Life Questionnaire-Core 30
Quality of Life Questionnaire-Cervical Cancer Module 24
Quality of life
Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, Parkin DM, Forman D, Bray F. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136(5):E359–386.
World Health Organization. GLOBOCAN 2012: Estimated Cancer Incidence, Mortality and Prevalence Worldwide in 2012. http://globocan.iarc.fr/Pages/fact_sheets_cancer.aspx.
Ministry of Health and Welfare. 2013 statistical results on causes of death in Taiwan. http://www.mohw.gov.tw/EN/Ministry/DM1_P.aspx?f_list_no=378&fod_list_no=4999&doc_no=46611.
Health Promotion Administration of Taiwan. Cancer Prevention. 2013. http://health99.hpa.gov.tw/Box2/Cancer/toknow.aspx.
Harrington S, Gilchrist L, Sander A. Breast cancer EDGE task force outcomes: clinical measures of pain. Rehabil Oncol. 2014;32(1):13–21.
Ashing-Giwa KT, Padilla G, Tejero J, Kraemer J, Wright K, Coscarelli A, Clayton S, Williams I, Hills D. Understanding the breast cancer experience of women: a qualitative study of African American. Asian American, Latina and Caucasian cancer survivors. Psychooncology. 2004;13(6):408–28.
Chopra I, Kamal KM. A systematic review of quality of life instruments in long-term breast cancer survivors. Health Qual Life Outcomes. 2012;10:14.
Kim KR, Chung HC, Lee E, Kim SJ, Namkoong K. Body image, sexual function and depression in Korean patients with breast cancer: modification by 5-HTT polymorphism. Support Care Cancer. 2012;20(9):2177–82.
Ness S, Kokal J, Fee-Schroeder K, Novotny P, Satele D, Barton D. Concerns across the survivorship trajectory: results from a survey of cancer survivors. Oncol Nurs Forum. 2013;40(1):35–42.
Schmidt ME, Chang-Claude J, Vrieling A, Heinz J, Flesch-Janys D, Steindorf K. Fatigue and quality of life in breast cancer survivors: temporal courses and long-term pattern. J Cancer Surviv. 2012;6(1):11–9.
Torkzahrani S, Rastegari L, Khodakarami N, Akbarzadeh-Baghian A, Alizadeh K. Quality of life and its related factors among Iranian cervical cancer survivors. Iran Red Crescent Med J. 2013;15(4):320–3.
Bodai BI, Tuso P. Breast cancer survivorship: a comprehensive review of long-term medical issues and lifestyle recommendations. Perm J. 2015;19(2):48–79.
Sanders SL, Bantum EO, Owen JE, Thornton AA, Stanton AL. Supportive care needs in patients with lung cancer. Psychooncology. 2010;19(5):480–9.
Janz NK, Mujahid M, Chung LK, Lantz PM, Hawley ST, Morrow M, Schwartz K, Katz SJ. Symptom experience and quality of life of women following breast cancer treatment. J Womens Health (Larchmt). 2007;16(9):1348–61.
Knobf MT. Clinical update: psychosocial responses in breast cancer survivors. Semin Oncol Nurs. 2011;27(3):e1–e14.
Park SY, Bae DS, Nam JH, Park CT, Cho CH, Lee JM, Lee MK, Kim SH, Park SM, Yun YH. Quality of life and sexual problems in disease-free survivors of cervical cancer compared with the general population. Cancer. 2007;110(12):2716–25.
Klug C, Neuburg J, Glaser C, Schwarz B, Kermer C, Millesi W. Quality of life 2–10 years after combined treatment for advanced oral and oropharyngeal cancer. Int J Oral Maxillofac Surg. 2002;31(6):664–9.
Greimel ER, Kuljanic Vlasic K, Waldenstrom AC, Duric VM, Jensen PT, Singer S, Chie W, Nordin A, Bjelic Radisic V, Wydra D, et al. The European Organization for Research and Treatment of Cancer (EORTC) Quality-of-Life questionnaire cervical cancer module: EORTC QLQ-CX24. Cancer. 2006;107(8):1812–22.
Shin DW, Ahn E, Kim YM, Kang S, Kim BG, Seong SJ, Cha SD, Park CY, Yun YH. Cross-cultural application of the Korean version of the European Organization for Research and Treatment of Cancer quality of life questionnaire cervical cancer module. Oncology. 2009;76(3):190–8.
Sprangers MA, Groenvold M, Arraras JI, Franklin J, te Velde A, Muller M, Franzini L, Williams A, de Haes HC, Hopwood P, et al. The European Organization for Research and Treatment of Cancer breast cancer-specific quality-of-life questionnaire module: first results from a three-country field study. J Clin Oncol. 1996;14(10):2756–68.
Scott NW, Fayers PM, Aaronson NK, Bottomley A, de Graeff A, Groenvold M, Gundy C, Koller M, Petersen MA, Sprangers MAG. EORTC QLQ-C30. Reference Values. EORTC; 2008. p.1-427.
Hoopman R, Muller MJ, Terwee CB, Aaronson NK. Translation and validation of the EORTC QLQ-C30 for use among Turkish and Moroccan ethnic minority cancer patients in the Netherlands. Eur J Cancer. 2006;42(12):1839–47.
Levine MN, Guyatt GH, Gent M, De Pauw S, Goodyear MD, Hryniuk WM, Arnold A, Findlay B, Skillings JR, Bramwell VH, et al. Quality of life in stage II breast cancer: an instrument for clinical trials. J Clin Oncol. 1988;6(12):1798–810.
Safaee A, Moghim DB. Validation study of a quality of life (QOL) questionnaire for use in Iran. Asian Pac J Cancer Prev. 2007;8(4):543–6.
Kobayashi K, Takeda F, Teramukai S, Gotoh I, Sakai H, Yoneda S, Noguchi Y, Ogasawara H, Yoshida K. A cross-validation of the European Organization for Research and Treatment of Cancer QLQ-C30 (EORTC QLQ-C30) for Japanese with lung cancer. Eur J Cancer. 1998;34(6):810–5.
Ayana BA, Negash S, Yusuf L, Tigeneh W, Haile D. Reliability and Validity of Amharic Version of EORTC QLQ-C 30 Questionnaire among Gynecological Cancer Patients in Ethiopia. PLoS One. 2016;11(6):e0157359.
Nikan F, Asghari Jafarabadi M, Mohammad-Alizadeh-Charandabi S, Mirghafourvand M, Montazeri A, Asadi S. Psychometric properties of the Iranian version of a postpartum women’s quality of life questionnaire (PQOL): a methodological study. Iran Red Crescent Med J. 2016;18(7):e35460.
Fehlauer F, Tribius S, Mehnert A, Rades D. Health-related quality of life in long term breast cancer survivors treated with breast conserving therapy: impact of age at therapy. Breast Cancer Res Treat. 2005;92(3):217–22.
Huang CC, Lien HH, Tu SH, Huang CS, Jeng JY, Chao HL, Sun HL, Chie WC. Quality of life in Taiwanese breast cancer survivors with breast-conserving therapy. J Formos Med Assoc. 2010;109(7):493–502.
Mols F, Vingerhoets AJ, Coebergh JW, van de Poll-Franse LV. Quality of life among long-term breast cancer survivors: a systematic review. Eur J Cancer. 2005;41(17):2613–9.
Paganini-Hill A, Clark LJ. Preliminary assessment of cognitive function in breast cancer patients treated with tamoxifen. Breast Cancer Res Treat. 2000;64(2):165–76.
Dahiya N, Acharya AS, Bachani D, Sharma D, Gupta S, Haresh K, Rath G. Quality of life of patients with advanced cervical cancer before and after chemoradiotherapy. Asian Pac J Cancer Prev. 2016;17(7):3095–9.
Kumar S, Rana ML, Verma K, Singh N, Sharma AK, Maria AK, Dhaliwal GS, Khaira HK, Saini S. PrediQt-Cx: post treatment health related quality of life prediction model for cervical cancer patients. PLoS One. 2014;9(2):e89851.
Hsu WC, Chung NN, Chen YC, Ting LL, Wang PM, Hsieh PC, Chan SC. Comparison of surgery or radiotherapy on complications and quality of life in patients with the stage IB and IIA uterine cervical cancer. Gynecol Oncol. 2009;115(1):41–5.
Becker ST, Menzebach M, Kuchler T, Hertrampf K, Wenz HJ, Wiltfang J. Quality of life in oral cancer patients--effects of mandible resection and socio-cultural aspects. J Craniomaxillofac Surg. 2012;40(1):24–7.
Schultz PN, Klein MJ, Beck ML, Stava C, Sellin RV. Breast cancer: relationship between menopausal symptoms, physiologic health effects of cancer treatment and physical constraints on quality of life in long-term survivors. J Clin Nurs. 2005;14(2):204–11.
Bloom JR, Stewart SL, Chang S, Banks PJ. Then and now: quality of life of young breast cancer survivors. Psychooncology. 2004;13(3):147–60.
Kobayashi K, Morita S, Shimonagayoshi M, Kobayashi M, Fujiki Y, Uchida Y, Yamaguchi K. Effects of socioeconomic factors and cancer survivors’ worries on their quality of life (QOL) in Japan. Psychooncology. 2008;17(6):606–11.
Short PF, Mallonee EL. Income disparities in the quality of life of cancer survivors. Med Care. 2006;44(1):16–23.
We appreciate the generous funding support from Asia University and China Medical University (CMU103-ASIA-23) and the Health Promotion Administration (DOH101-HP-1504), Taiwan.
This study was supported by China Medical University and Asia University (CMU103-ASIA-23) and the Health Promotion Administration (DOH101-HP-1504), Taiwan.
Availability of data and materials
This study conducted a survey to collect participants’ personal information, including their demographic information, health condition, lifestyle and QOL. These personal data cannot be shared with the public.
Conception and design were by HYH, PTK and WCT; data collection and assembly were by WYC, YCH, LCL, KFH, WCW, KWL and RKH; data analysis and interpretation were by HYH, PTK, WCT and WYC; manuscript writing was by HYH, PTK and WCT; and final approval of the manuscript was by all authors.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Patient consent for this study was received from the cooperating hospitals, and this study was approved by the institutional review boards (IRB No. CMU-REC-101-013).
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Huang, HY., Tsai, WC., Chou, WY. et al. Quality of life of breast and cervical cancer survivors. BMC Women's Health 17, 30 (2017). https://doi.org/10.1186/s12905-017-0387-x