Meaning-Making, Illness Acceptance, and Quality of Life Among Patients Living With Advanced Cancer: A Qualitative Inquiry

Authors

    Kamdin Parsakia Department of Psychology and Counseling, KMAN Research Institute, Richmond Hill, Ontario, Canada
    Seyed Hadi Seyed Ali Tabar * Department of Psychology and Counseling, KMAN Research Institute, Richmond Hill, Ontario, Canada h.alitabar@kmanresce.ca
https://doi.org/10.61838/c2zg5c58

Keywords:

Advanced cancer, Meaning-making, Illness acceptance, Quality of life, Palliative care, Qualitative inquiry, Patient experience

Abstract

Objective: This study aimed to explore the experiences of meaning-making, illness acceptance, and quality of life among patients living with advanced cancer in Canada.

Methods and Materials: This qualitative inquiry was conducted among 26 adult patients diagnosed with advanced or metastatic cancer who were receiving oncology or palliative care services in Canada. Participants were selected through purposive sampling to ensure variation in age, gender, cancer type, treatment status, and care setting. Data were collected through semi-structured interviews, a demographic and clinical information form, and researcher field notes. The interviews explored patients’ understanding of illness, experiences of acceptance, sources of meaning, perceived changes in identity and relationships, and definitions of quality of life during advanced disease. Interviews were audio-recorded, transcribed verbatim, and analyzed using thematic analysis. Coding was performed through repeated reading, identification of meaning units, development of initial codes, formation of categories, and extraction of overarching themes. Credibility, dependability, confirmability, and transferability were supported through peer discussion, reflexive memo writing, an audit trail, and detailed description of the research context.

Findings: The analysis identified three major themes. The first theme, reconstructing meaning in the face of advanced illness, showed that participants attempted to preserve identity, reinterpret life priorities, confront mortality, and find coherence through relationships, spirituality, contribution, and reflection. The second theme, negotiating acceptance without surrender, indicated that illness acceptance was not experienced as giving up, but as a fluctuating process of living with uncertainty, maintaining agency, balancing hope and realism, and preparing emotionally and practically for the future. The third theme, redefining quality of life in advanced cancer, revealed that participants associated quality of life with relief from physical suffering, dignity, relational closeness, normalcy in daily life, freedom from being a burden, and peace in the present.

Conclusion: The findings suggest that meaning-making, illness acceptance, and quality of life are reciprocal and dynamic processes among patients with advanced cancer. Patient-centered palliative oncology should therefore address existential meaning, emotional adjustment, dignity, family concerns, symptom relief, and personal definitions of quality of life.

Downloads

Download data is not yet available.

References

Agodirin, S. O., Rahman, G. A., Olatoke, S., & Durojaiye, A. O. (2022). Pattern of Breast Cancer Referral to Palliative Care and the Complimentary Role of a Palliative Care Unit in a Resource-Limited Country. Postgraduate Medical Journal of Ghana, 6(1), 42-46. https://doi.org/10.60014/pmjg.v6i1.110

Astuti, N. P., Sriyono, S., Yunitasari, E., Kurniawati, N. D., & Baidhowy, A. S. (2024). Dilemma of Identification Patients Palliative Care Needs in Critical Care Unit. Indonesian Journal of Global Health Research, 6(1), 223-230. https://doi.org/10.37287/ijghr.v6i1.2664

Boutib, A., Azizi, A., Youlyouz‐Marfak, I., Kouiti, M., Taiebine, M., Benfatah, M., Nejjari, C., Bounou, S., & Marfak, A. (2024). Electronic Patient-Reported Outcome Measures (ePROs) as Tools for Assessing Health-Related Quality of Life (HRQoL) in Women With Gynecologic and Breast Cancers: A Systematic Review. Digital Health, 10. https://doi.org/10.1177/20552076241297041

Devi, S., Kumar, A., & Rana, R. (2023). Profile of Palliative Patients Undergoing Radiotherapy. Acta Scientific Cancer Biology, 28-34. https://doi.org/10.31080/ascb.2023.07.0440

Dumnui, N., Nagaviroj, K., & Anothaisintawee, T. (2022). A Study of the Factors Associated With Emergency Department Visits in Advanced Cancer Patients Receiving Palliative Care. BMC Palliative Care, 21(1). https://doi.org/10.1186/s12904-022-01098-w

Fu, Y., Shi, W., Zhao, J., Cao, X., Cao, Y., Lei, M., Su, X., Cui, Q., & Liu, Y. (2023). Prediction of Postoperative Health-Related Quality of Life Among Patients With Metastatic Spinal Cord Compression Secondary to Lung Cancer. Frontiers in Endocrinology, 14. https://doi.org/10.3389/fendo.2023.1206840

García, W. G., Rivas, S., Paz, G., Bustamante, M., Castro, G., Gutiérrez, H., Chu, M., Gassant, P. Y., Lovo, R. L., Gamboa, Y., Nunez, M. R. T., García, X., & Okhuysen‐Cawley, R. (2021). Pediatric Oncology Palliative Care Programs in Central America: Pathways to Success. Children, 8(11), 1031. https://doi.org/10.3390/children8111031

Harrison, R. A., Tang, M., Shih, K. K., Khan, M. R., Pham, L., Moraes, A. R. d., O’Brien, B., Bassett, R. L., & Bruera, É. (2024). Characterization of Patients With Brain Metastases Referred to Palliative Care. BMC Palliative Care, 23(1). https://doi.org/10.1186/s12904-023-01320-3

Heuser, N., Heers, H., Gschnell, M., Urhahn, F., Schrade, S., & Volberg, C. (2025). Do We Have a Knowledge Gap With Our Patients?—On the Problems of Knowledge Transfer and the Implications at the End of Life. International journal of environmental research and public health, 22(2), 247. https://doi.org/10.3390/ijerph22020247

Higashibata, T., Hamano, J., Hisanaga, T., Hagiwara, S., Shimokawa, M., Yabuki, R., Yokomichi, N., Shimoinaba, J., Kamura, R., Baba, M., Funaki, H., Mori, M., Morita, T., Tsuneto, S., Kizawa, Y., Inoue, S., Imai, K., Tsukuura, H., Yamauchi, T., . . . Matsuda, Y. (2022). Does Urinary Catheterization Affect the Quality of Death in Patients With Advanced Cancer? A Secondary Analysis of a Multicenter Prospective Cohort Study. Journal of Palliative Medicine, 25(2), 205-212. https://doi.org/10.1089/jpm.2021.0178

Kardosod, A., Needham, J., & Coyne, E. (2023). The Experiences and Needs of Metastatic Spinal Cancer Family Caregivers at Home: A Systematic Review. Supportive Care in Cancer, 31(5). https://doi.org/10.1007/s00520-023-07777-5

Kim, W., Kim, B., Kim, M., & Choi, J. Y. (2025). The Impact of Advanced Care Planning on Hospice Utilization in Patients With Cancer: A Nationwide Analysis in Korea. Cancers, 17(9), 1471. https://doi.org/10.3390/cancers17091471

Koyama, N., Matsumura, C., Tahara, Y., Sako, M., Kurosawa, H., Nomura, T., Eguchi, Y., Ohba, K., & Yano, Y. (2021). Symptom Clusters and Their Influence on Prognosis Using EORTC QLQ-C15-PAL Scores in Terminally Ill Patients With Cancer. Supportive Care in Cancer, 30(1), 135-143. https://doi.org/10.1007/s00520-021-06380-w

Lee, C. Y., Laffoon, K., Mama, S. K., Liao, Y., Whisenant, M., Brewster, A. M., Mendoza, T. R., Mitchell, S., Tracy, P. V., Garza, G. M., & Basen‐Engquist, K. (2024). Outcomes for Breast Cancer Survivors With Metastatic Disease in a Physical Activity Program for Medically Underserved Cancer Survivors. Journal of Cancer Survivorship, 19(6), 1861-1870. https://doi.org/10.1007/s11764-024-01600-8

Liu, X., Liu, H., Ying, W., Zhang, Y., Gong, X., & Huang, J. (2025). Identifying Palliative Home Care Needs of Patients With Advanced Cancer: A Cross-Sectional Study. Frontiers in Psychiatry, 16. https://doi.org/10.3389/fpsyt.2025.1448973

Manjunath, G. N., Bilagi, A., Sunitha, L., Shriya, S. R., & Kamarthy, P. (2025). The Role of Yoga in Palliative Care: Insights From a Single Case Study. Cureus. https://doi.org/10.7759/cureus.83993

Matsumura, C., Koyama, N., Sako, M., Kurosawa, H., Nomura, T., Eguchi, Y., Ohba, K., & Yano, Y. (2020). Comparison of Patient Self-Reported Quality of Life and Health Care Professional-Assessed Symptoms in Terminally Ill Patients With Cancer. American Journal of Hospice and Palliative Medicine®, 38(3), 283-290. https://doi.org/10.1177/1049909120944157

Maurya, B. P., Gupta, R., Rathore, P., Mishra, S., Bharati, S. J., Kumar, V., Gupta, N., Garg, R., & Bhatnagar, S. (2024). End of Life Care Practices at a Tertiary Cancer Centre in India: An Observational Study. American Journal of Hospice and Palliative Medicine®, 42(5), 477-482. https://doi.org/10.1177/10499091241268585

Meneguetti, R. T., Felipe José Silva Melo, C., Giglio, A. d., Ana Claudia de Oliveira, L., Cheler, D., Alayne Magalhães Trindade Domingues, Y., & Eugênio, C. (2022). Palliative Care in Intensive Care Unit: Analysis of Oncological Patients Profile. International Journal of Health Science, 2(7), 2-9. https://doi.org/10.22533/at.ed.159272213023

Min, K. J., Ouh, Y. T., Kang, H. T., Fadhel, E., Yoo, J. W., Mojtahedi, Z., Lou, D. H., & Shen, J. J. (2021). Trends in Palliative Care and Life-Sustaining Procedure Provision for Patients With Cervical Cancer in the United States. European Journal of Gynaecological Oncology, 42(6), 1105. https://doi.org/10.31083/j.ejgo4206161

Ooko, F., Mothiba, T. M., Bogaert, P. V., & Wens, J. (2023). Access to Palliative Care in Patients With Advanced Cancer of the Uterine Cervix in the Low- And Middle-Income Countries: A Systematic Review. BMC Palliative Care, 22(1). https://doi.org/10.1186/s12904-023-01263-9

Rodriguez, R. R., Babar, L., Lo, H. H. M., Ashraf, O., Monga, D., Finley, G. G., Doverspike, L., Blackledge, A., Sethi, A., & Raj, M. S. (2021). A Retrospective Analysis of Factors Affecting Palliative Care Consults in Patients Undergoing Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy. Cureus. https://doi.org/10.7759/cureus.12589

Roij, J. v., Zeeuw, B. d., Zijlstra, M., Claessens, N., Raijmakers, N., Lonneke, V. v. d. P. F., & Brom, L. (2021). Shared Perspectives of Patients With Advanced Cancer and Their Informal Caregivers on Essential Aspects of Health Care: A Qualitative Study. Journal of Palliative Care, 37(3), 372-380. https://doi.org/10.1177/0825859721989524

Sánchez-Cárdenas, M. A., Iriarte‐Aristizábal, M. F., León, M., Rodríguez-Campos, L. F., Correa‐Morales, J. E., Cañón-Piñeros, A., & Parra, S. L. (2022). Rural Palliative Care Telemedicine for Advanced Cancer Patients: A Systematic Review. American Journal of Hospice and Palliative Medicine®, 40(8), 936-944. https://doi.org/10.1177/10499091221130329

Spine, K. (2022). Clinical Oncology Nurse Best Practices: Palliative Care and End-of-Life Conversations. Cjon. https://doi.org/10.1188/22.cjon.612-620

Stout, M., Thaper, A., Xu, V., Singer, E. A., & Saraiya, B. (2023). Early Integration of Palliative Care for Patients Receiving Systemic Immunotherapy for Renal Cell Carcinoma. J Cancer Immunol, 5(1), 5-12. https://doi.org/10.33696/cancerimmunol.5.072

Strang, P. (2022). Palliative Oncology and Palliative Care. Molecular Oncology, 16(19), 3399-3409. https://doi.org/10.1002/1878-0261.13278

Syarifudin, M., & Soares, D. (2022). Palliative Care to Improve Quality of Life Patient With Hepatocellular Carcinoma. Proceeding of International Conference on Science Health and Technology, 378-385. https://doi.org/10.47701/icohetech.v3i1.2215

Vaiphei, S. D. (2021). Assessment and Coping Strategies for Stress and Depression Among the Terminally Ill Patients: Focus on Cancer. Journal of Clinical Medicine of Kazakhstan, 18(6), 15-19. https://doi.org/10.23950/jcmk/11348

Vlčková, K., Poláková, K., Tučková, A., Houska, A., & Loučka, M. (2021). Association Between Quality of Life and Prognostic Awareness in Patients With Advanced Cancer. https://doi.org/10.21203/rs.3.rs-300257/v1

Wong, A., Wang, D., Alexander, M., Siew, B., Yap, N., Le, B., & Philip, J. (2024). Opioid Initiation Timing and Palliative Care Referrals in Advanced Cancer: Retrospective Study. BMJ Supportive & Palliative Care, 14(e2), e2128-e2134. https://doi.org/10.1136/spcare-2024-005028

Yıldırım, Ö. A., Poyraz, K., Erdur, E., Can, C., Gündoğan, C., Yerlikaya, H., Yıldırım, S., Güzel, Y., & Kömek, H. (2021a). Evaluation of Caregiver Burden and Quality of Life in Metastatic Prostate Cancer Patients; Effects of Clinical and Socioeconomic Factors. Dicle Medical Journal / Dicle Tip Dergisi, 48(4), 770-781. https://doi.org/10.5798/dicletip.1037634

Yıldırım, Ö. A., Poyraz, K., Erdur, E., Can, C., Gündoğan, C., Yerlikaya, H., Yıldırım, S., Güzel, Y., & Kömek, H. (2021b). Evaluation of Caregiver Burden, and Quality of Life in Metastatic Prostate Cancer Patients and Caregivers; Effects of Clinical and Socioeconomic Factors. https://doi.org/10.21203/rs.3.rs-359207/v1

Zeidman, A., Benedict, C., Zion, S. R., Fisher, S., Tolby, L., Kurian, A. W., Berek, J. S., Woldeamanuel, Y. W., Schapira, L., & Palesh, O. (2022). Association of Illness Mindsets With Health-Related Quality of Life in Cancer Survivors. Health Psychology, 41(6), 389-395. https://doi.org/10.1037/hea0001186

Downloads

Published

2025-07-01

Submitted

2025-04-10

Revised

2025-06-20

Accepted

2025-06-27

How to Cite

Parsakia, K. ., & Seyed Ali Tabar, S. H. . (2025). Meaning-Making, Illness Acceptance, and Quality of Life Among Patients Living With Advanced Cancer: A Qualitative Inquiry. Quality of Life and Health Sciences, 1(1), 1-16. https://doi.org/10.61838/c2zg5c58