Objective To systematically evaluate and analyze the qualitative research on the experience of volunteers in palliative care practice，thereby providing health professionals with evidence in training and support to palliative care volunteers. Methods Chinese and English databases including PubMed，Web of Science，Cochrane Library，ProQuest，Scopus，CINAHL，CNKI，Wanfang，VIP and CBM were searched for qualitative studies exploring the true feelings of volunteers in palliative care practice from inception to November 2023. The JBI Critical Appraisal Tool for Qualitative Studies from Australia was used to evaluate the quality of the studies. The results were synthesized using the meta-integration method. Results 14 studies were included in the final review. Totally 49 findings were extracted，leading to the creation of 10 new categories. 4 integrated results were synthesized as follows：① The motivations for palliative care volunteers to participate in volunteering are intricate and varied；②Palliative care volunteers encounter a range of challenges；③ Palliative care volunteers exhibit a positive attitude and utilize diverse approaches to overcome challenges；④Palliative care volunteers recognize dual benefits from their volunteering. Conclusion The experience of volunteering in palliative care is multifaceted and intricate. During the recruitment process，it is advisable for health professionals to evaluate the motivations and mental states of potential volunteers for their participation. Throughout the service tenure，volunteers should be guided to cultivate and sustain positive psychological experiences，mitigate any negative emotions，and concurrently，efforts should be made to bolster the training and support system to enhance their volunteering capabilities.

Objective To systematically evaluate the role transition experience of cancer caregivers，thereby identifying their support needs to develop targeted interventions. Methods The databases of PubMed，the Cochrane Library，Embase，EBSCO，Web of Science，CNKI，VIP，Wanfang，and CBM were retrieved for qualitative research about the role transition experience of caregivers of cancer patients. The retrieval period is from the establishment of the databases to March 2022. The quality of the literature was evaluated by JBI Critical Appraisal Tool for qualitative studies. Results A total of 14 studies were included，and 65 research results were extracted，which were grouped into 9 new categories. 3 integrated themes were finally synthesized：the process of cancer diagnosis was lengthy and complicated，and caregivers experienced difficulties in coping and especially had challenges in diagnosis disclosure；caregivers adopted different coping strategies to help patients to better cope with disease-related challenges，and to adapt to the role of caregivers；the newly derived meaning in the caregiving experience and role growth was gained. Conclusion Healthcare workers should be aware of the transitioning experience of cancer caregivers in taking this new role，and develop targeted ability training and psychological intervention programs，so as to promote the successful transition of the caregiver’s role and provide a family-centered transitional care plan in the future.

Objective To systematically review the qualitative research on the disease experience of patients with prostate cancer,and to provide references for improving the mental health of this population and establishing a support system. Methods The databases of PubMed,Web of Science,Cochrane,Embase,Cochrane Library,CNKI,VIP,Wanfang,CBM were retrieved on qualitative research about the disease experience of prostate cancer patients. The retrieval period is from the establishment of the database to April 2021. The quality of the literature was evaluated by JBI Critical Appraisal Tool for qualitative studies. Results A total of 13 studies were included,and 50 clear study results were extracted. Similar study results were summarized into 8 new categories,and 3 integrated results were synthesized：self-perception changes in symptomatic prostate cancer patients accompanied by regression,leading to impaired male self-esteem and alienation in the intimate relationship of couples;differences in coping strategies among patients with different emotional experiences,which are manifested as avoidance of surrender and post-traumatic growth;patients have unmet needs in multiple dimensions,such as poor doctor-patient communication,lack of peer support,and low social attention,and they strive to seek relevant support. Conclusion Prostate cancer patients have many aspects of disease experience in the whole disease process. Healthcare professionals tend to ignore patients’ feelings and experiences,and should pay attention to and evaluate patients’ psychological feelings from multiple perspectives in the future. They should also provide comprehensive physical and mental care from the perspective of positive psychology to improve social support and improve their quality of life.