CANCER NURSING肿瘤护理
CANCER NURSING(英文缩写 CANCER NURS),ISSN 0162-220X,eISSN 1538-9804,中文译名:肿瘤护理 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。
发文量统计区间：2025-10-01 至 2026-09-30，按本站收录文献的发表日期统计。
期刊介绍
历年影响因子趋势
| JCR 数据年份 | 影响因子 | JCR 分区 |
|---|---|---|
| 2021 | 2.760 | Q1 |
| 2022 | 2.600 | Q1 |
| 2023 | 2.400 | Q1 |
| 2024 | 2.500 | Q1 |
| 2025 | 2.600 | Q1 |
CANCER NURSING 最新收录文献
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1. Mapping an Overlooked Spiral of Trauma-Exposure to Sexual Abuse and Psycho-Spiritual Outcomes in Patients With Cancer: A Systematic Review and Meta-Analysis.
PMID:日期:2026-09-16Cancer and sexual abuse survivorship both involve trauma, yet little evidence synthesis has examined psycho-spiritual outcomes at the intersection of both. This may limit nurses' recognition of compounded distress in patients with cancer and sexual trauma, who often remain silent. To appraise psycho-spiritual outcomes associated with sexual abuse exposure in patients with cancer. A systematic search was conducted on 10 databases until April 21, 2026. Unadjusted and adjusted effect estimates were pooled separately. Of the identified sources, 11 studies involving 79,318 patients were included. Sexual abuse was associated with depression (unadjusted standardized mean difference [SMD] = 0.51, 95% confidence interval [CI] = 0.31-0.71; adjusted SMD = 0.32, 95% CI = 0.24-0.41), anxiety (unadjusted SMD = 0.42, 95% CI = 0.17-0.67), and spiritual concerns (unadjusted SMD = 0.32, 95% CI = 0.11-0.53; adjusted SMD = 0.27, 95% CI = 0.16-0.38). Findings on posttraumatic stress symptoms were inconclusive (unadjusted SMD = 0.34, 95% CI = 0.17-0.50; adjusted SMD = 0.02, 95% CI = -0.19 to 0.23). Childhood exposure demonstrated a stronger association with depression in adulthood (unadjusted SMD = 0.68, 95% CI = 0.65-0.70) than lifetime exposure (unadjusted SMD = 0.35, 95% CI = 0.07-0.63). This meta-analysis clarifies the extent to which past exposure to sexual abuse may aggravate psycho-spiritual symptoms in patients with cancer. Oncology nurses must practice trauma-informed care to prevent re-traumatization. Awareness of sexual abuse survivorship should be incorporated into continuing professional development in oncology nursing.
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2. Dyadic Coping in Patients With Hematologic Malignancies and Their Partners: A Scoping Review.
PMID:日期:2026-09-16Patients and their partners coping with hematologic malignancies (HMs) experience significant psychological and relational challenges. Dyadic coping (DC) plays a critical role in couples' adaptation under cancer treatments. To synthesize existing evidence on DC strategies, influencing factors, and outcomes among couples facing HMs. Guided by the JBI framework, this review systematically searched for and included original studies of any design that examined DC in adult couples where one partner had hematologic cancer. Data on study design, population characteristics, coping strategies, factors, and outcomes were extracted and summarized narratively. Nine articles across 8 studies were reviewed. Commonly used DC strategies included stress communication, protective buffering, and common coping. Some evidence suggested the potential usefulness of couple-based programs that incorporate communal coping training, but overall, no studies directly examined factors influencing DC. Studies using the Actor-Partner Interdependence Model revealed reciprocal associations between partners' coping and well-being. Negative strategies were consistently associated with higher distress, poorer relationship satisfaction, and greater unmet needs. Positive strategies showed mixed effects, generally associated with improved relationship satisfaction and quality of life, though sometimes related to increased distress or unmet needs. DC significantly affects relationship quality, psychological well-being, and quality of life in HM couples. Positive strategies can foster mutual support but may also increase strain, whereas negative strategies exacerbate distress. Findings highlight the clinical importance of supporting couples as relational units. Oncology nurses should integrate tailored, couple-based interventions that address both shared and individual coping needs.
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3. Utilizing Community Engagement Studios to Improve Participation of African American Cancer Survivors in Couples-Based Exercise Research.
PMID:日期:2026-09-10Evidence suggests exercise can improve health outcomes for individuals with cancer and their caregiving partners. Research to improve outcomes in African American (AA) couples coping with cancer is scarce, despite known disparities in AA survivors. Incorporating community-engaged, culturally relevant strategies to enhance intervention development may encourage AA couple engagement in exercise research. To consult AA cancer survivors and their caregiving partners using a community engagement studio approach and collect feedback about improving recruitment strategies and participation in an existing couples-based exercise trial. AA adults currently or previously diagnosed with any cancer and their partners were recruited. Three community engagement studio sessions were conducted virtually to collect participants' perceptions using semi-structured discussion guides. Verbatim transcripts were coded by two independent investigators using an open approach to identify themes. Twenty participants (mean age 60.6 ± 9.7 years; 90% AA; 85% survivors; 75% women) completed the study. Four themes emerged: Suggested Exercise Trial Improvements, Exercise Prescription Used in the Trial, Connections to the AA Cancer Community, and The Cancer Experience. Participants quickly developed camaraderie as AAs coping with cancer and expressed gratitude for the opportunity to connect. Caregiving partners were underrepresented, limiting dyadic findings. These qualitative data informed strategies to promote racial diversity in the exercise trial examined. Community input can benefit future exercise research to help reduce cancer-related disparities. Future exercise oncology research should include community-driven recruitment approaches, hiring diverse staff and study advocates, individual exercise tailoring, and facilitating the development of an AA cancer support community.
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4. The Meaning of a Cancer Diagnosis for the Rural Patient Through the Lenses of Merleau-Ponty and Heidegger: A Hermeneutic Phenomenological Study.
PMID:日期:2026-09-10In a rural setting, individuals who receive a cancer diagnosis experience an interconnected group of challenges that contribute to the lived experience of space and time. Philosophers offer a perspective of human experience that provides insight into how individuals manage life challenges. To understand the lived experiences by inserting the lenses of Merleau-Ponty (MP) and Heidegger as they relate to space and time, and work toward a holistic practice that is maximally effective. This qualitative secondary analysis applied hermeneutic phenomenology when reviewing interview transcripts from 15 participants. Participants discussed their experiences in ways that resonated with philosophical work from MP and Heidegger, highlighting their applicability to the nature of the participants' experiences. Two main themes and several subthemes were identified and interpreted using philosophical viewpoints. Theme 1, Experiencing limitations in one's space, and subthemes Sacrificing independence and personal space and Leaving the rural environment, are well explicated by MP's notion of "being-in-the-world.' Theme 2, Being thrown into life with a cancer diagnosis, and subthemes Prioritizing health, Striving for normalcy, and Living authentically, are well explained by Heidegger's impressions of temporality and thrownness. Incorporation of philosophers' viewpoints is valuable in providing a holistic understanding of the lived experience of participants. Nurses are on the frontline of healthcare and can ensure that individual needs are met while providing best-practice care for rural patients. Providing authentic care, recognizing the strengths of the rural community, and practicing advocacy for the rural patient are important.
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5. Menopausal Symptoms, Depression, and Sleep Quality Among Postmenopausal Women With and Without Breast Cancer.
PMID:日期:2026-08-18It remains unclear whether sleep quality in breast cancer (BC) survivors is primarily driven by BC-specific or menopausal factors, due to limited comparisons with cancer-free women. To compare sleep quality between postmenopausal BC survivors and healthy comparisons and to identify independent correlates of sleep quality across both groups. A cross-sectional secondary analysis was performed using baseline data from 102 postmenopausal women (BC, n = 64; health comparison, n = 38). Sleep quality, menopausal symptoms, and depressive symptoms were measured using the Pittsburgh Sleep Quality Index (PSQI), Breast Cancer Prevention Trial Symptom Checklist, and Center for Epidemiologic Studies Depression Scale, respectively. Hierarchical multiple linear regression identified correlates of sleep quality. Global PSQI scores were similar between groups. More than one-third (34.3%) were classified as poor sleepers (PSQI > 5). While most demonstrated adequate sleep latency (66.7%) and efficiency (74.5%), and subjective sleep quality (90.2%), only 25.5% achieved more than 7 hours per night. Employment (β = -0.21, P = .006), smoking (β = 0.18, P = .023), vasomotor symptoms (β = 0.22, P = .004), and depressive symptoms (β = 0.45, P < .001) together explained 54% of the variance in global PSQI. Musculoskeletal pain became nonsignificant after accounting for depressive symptoms. BC survivorship was not associated with sleep quality. Vasomotor and depressive symptoms emerged as the primary correlates, regardless of cancer history. Targeted interdisciplinary management of vasomotor and depressive symptoms, alongside routine sleep assessment, may enhance sleep outcomes in postmenopausal women.
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6. Longitudinal Use of the Pediatric PRO-CTCAE in Heterogeneous Oncology Population is Feasible and Highlights Individuality of the Adverse Event Experience.
PMID:日期:2026-08-18Documentation of the adverse events (AEs) experienced by pediatric oncology patients relies on input from patients, caregivers, and providers. Accurate AE reporting allows comparison of treatment options, preparation of supportive care guidance, as well as appropriate support of current patients. In this study, we aimed to assess the feasibility of collecting symptomatic AE information longitudinally from a diverse group of pediatric and adolescent oncology patients, to describe the most and least symptomatic parts of treatment, and to identify impactful AEs. Pediatric Patient-Reported Outcome version of the Common Terminology Criteria for Adverse Event (PRO-CTCAE) items were administered to a heterogeneous sample of pediatric and adolescent oncology patients and their caregivers over 6 time points: the start of 3 cycles of chemotherapy, 1 to 2 weeks following the start of 2 cycles, and at the end of treatment. Sixty-seven percent of participants completed all required surveys. The frequency of AEs peaked at the expected count nadir, after the first cycle of treatment, and decreased by the end of treatment/maintenance but did not reach zero. The most frequent AE reported was anorexia; the highest severity and interference ratings were for fatigue. The least common AEs were oral mucositis, constipation, diarrhea, and numbness. Age and diagnosis did not predict AE burden. Some AEs, for example, oral mucositis, had low frequency but high severity and interference reported. It is feasible and clinically important to ask families to complete the Pediatric PRO-CTCAE items regularly throughout treatment. Families will complete the Pediatric PRO-CTCAE. Identifying common AEs aids resource planning and design of supportive care guidelines; identifying unique AEs allows personalized care.
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7. The Impact of Social Determinants on Posttraumatic Growth Among Young Adult Childhood Cancer Survivors.
PMID:日期:2026-08-11Young adult childhood cancer survivors (YA CCSs) may experience posttraumatic growth (PTG), yet little is known about how neighborhood-level social determinants influence PTG. Posttraumatic stress may also shape PTG, but its mediating role in the relationship between neighborhood deprivation and PTG remains unclear. To examine associations between neighborhood deprivation and PTG among YA CCSs and determine whether posttraumatic stress mediates these associations. This cross-sectional study included 121 YA CCSs. Neighborhood deprivation was measured using the Area Deprivation Index (ADI) and the Environmental Justice Index (EJI). PTG and posttraumatic stress were assessed using the Posttraumatic Growth Inventory and the Impact of Event Scale-Revised. Linear regression examined associations between neighborhood deprivation and PTG. The MEDCURVE macro tested curvilinear mediation. Participants were mostly non-Hispanic White (71%) with a mean age of 19.4 years. Higher ADI scores were associated with greater PTG (B = 0.36, 95% confidence interval [CI], 0.17-0.55). Total EJI and its Social and Health Vulnerability subscale were positively associated with PTG. Posttraumatic stress curvilinearly mediated the ADI-PTG association, with stronger mediation in less deprived neighborhoods (B = 0.11, 95% CI, 0.02-0.30) and weaker mediation in more deprived neighborhoods (B = 0.07, 95% CI, 0.02-0.17). Similar mediation was observed for the EJI Social Vulnerability subscale. Greater neighborhood deprivation was associated with higher PTG in YA CCSs. Posttraumatic stress mediated this association, with its influence varying across neighborhood conditions. Findings support personalized interventions addressing socioecological environments and psychological determinants.
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8. Ringing the Bell in Cancer Care: A Scoping Review of Patients', Caregivers', and Healthcare Professionals' Experiences and Implications for Oncology Nursing.
PMID:日期:2026-08-11Bell-ringing rituals mark the end of active cancer treatment in oncology settings worldwide. Despite their growing prevalence, their emotional and clinical implications across patients, caregivers, and healthcare professionals remain underexplored. To map and synthesize the available evidence on bell-ringing rituals in cancer care, examining their meanings and implications from the perspectives of patients, informal caregivers, and healthcare professionals. A scoping review was conducted following Joanna Briggs Institute methodology and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews guidelines (Open Science Framework protocol: https://doi.org/10.17605/OSF.IO/UCPFV). Five databases (PubMed, Scopus, Embase, CINAHL, and Cochrane Library) were searched from January 1996 to July 2025. Qualitative, quantitative, and mixed-methods studies were eligible. Two independent reviewers performed selection, extraction, and thematic synthesis. Five studies met the inclusion criteria. Four themes emerged: (1) symbolic closure and transition, (2) emotional ambivalence encompassing joy, guilt, and anxiety, (3) visibility, recognition, and disparities, and (4) absence of institutional guidance. While many patients experienced achievement and community, those with ongoing treatments or advanced disease frequently reported exclusion and distress, including posttraumatic stress disorder triggers. Bell-ringing rituals support meaning-making for some patients but may unintentionally marginalize vulnerable individuals when implemented without adequate assessment. No evidence-based protocols currently exist for patient readiness or cultural appropriateness. Oncology nurses should conduct preritual readiness assessments and offer individualized symbolic options to protect nonparticipating patients. Findings support inclusive institutional protocols and the integration of ritual literacy into nursing education.
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9. Ethnic Differences in Psychosocial Factors for Cancer Survivorship Among Asian American Breast Cancer Survivors: Secondary Outcomes of a Randomized Controlled Trial.
PMID:日期:2026-08-11Asian American breast cancer survivors face substantial disparities in recurrence rates; however, ethnic differences in breast cancer survivorship remain understudied. To examine the associations between psychosocial factors and breast cancer survivorship, with a focus on ethnic differences among Chinese, Korean, and Japanese Americans. This secondary analysis used data from 167 participants in a randomized clinical trial of Asian American breast cancer survivors. Cancer survivorship was measured with the Supportive Care Needs Survey, the Memorial Symptom Assessment Scale, and the Functional Assessment of Cancer Therapy-Breast Cancer. Psychosocial factors included attitudes, self-efficacy, perceived barriers, and social influences. All assessments were administered at baseline, 4-week posttest, and 12-week posttest. Baseline differences across ethnic groups were examined with analysis of variance (ANOVA), post hoc, and chi-square tests. Panel data were analyzed with mixed-effects linear regression models. ANOVA tests indicated that Chinese Americans reported more negative attitudes toward cancer survivorship, whereas Japanese Americans reported lower levels of social influence. Mixed-effects linear regression models showed significant ethnic differences in associations: Compared with Japanese Americans, Chinese Americans exhibited stronger negative associations of cancer survivorship outcomes with a lack of social support and perceived barriers. Among Korean Americans, higher loneliness and lower social influence were associated with greater unmet needs (Supportive Care Needs Survey). To address survivorship experiences among Asian American breast cancer survivors, ethnic differences must be considered. Survivorship care for Asian American breast cancer survivors should incorporate ethnic differences and modifiable psychosocial factors to guide culturally tailored interventions.
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10. Benefit Finding in Patients With Lymphoma: A Phenomenological Investigation.
PMID:日期:2026-08-04Patients with lymphoma face profound psychological challenges that extend beyond physical symptomatology. While benefit finding has demonstrated positive effects on cancer adaptation, the temporal progression and underlying mechanisms of this process in lymphoma populations remain inadequately understood. Understanding these processes is essential for developing targeted psychosocial interventions. This study aimed to explore the lived experiences and developmental trajectory of benefit finding among patients with lymphoma and to identify factors facilitating this psychological transformation. A phenomenological qualitative design was employed using Colaizzi's seven-step analytical framework. Eighteen patients with lymphoma, aged 24 to 63 years (mean age 38.72 ± 10.97 years), participated in semi-structured in-depth interviews until data saturation was achieved. Thematic analysis revealed four sequential phases characterizing benefit-finding progression: benefit resistance and initial cognitive adaptation disruption, benefit emergence and initial cognitive adaptation formation, benefit construction and positive cognitive adaptation development, and benefit transcendence and cognitive adaptation maturation. Role models emerged as pivotal catalysts for cognitive transformation, while personal breakthroughs and social reintegration facilitated psychological transcendence. Benefit finding in lymphoma represents a dynamic, phase-specific developmental process grounded in cognitive adaptation mechanisms involving meaning reconstruction, perceived control restoration, and self-enhancement. Oncology nurses should assess patients' current benefit-finding phase to deliver stage-tailored psychological interventions. Facilitating connections with peer role models and supporting meaning-making activities can accelerate patients' progression toward benefit transcendence and enhanced psychological well-being.