Caroline Stenman1*
Andreas Wallinder1,2Erik Holmberg3,4Kristjan Karason1,5,6
Jesper Magnusson1,7,6Göran Dellgren1,2,6- 1Transplant Institute, Sahlgrenska University Hospital, Gothenburg, Sweden
- 2Department of Cardiothoracic Surgery, Sahlgrenska University Hospital, Gothenburg, Sweden
- 3Regional Cancer Center West, Region Västra Götaland, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
- 4Department of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
- 5Department of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden
- 6Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
- 7Department of Internal Medicine/Respiratory Medicine and Allergology, Sahlgrenska University Hospital, Gothenburg, Sweden
Heart transplant patients have an increased risk of developing cancer. Patients who underwent HTx between 1985 and 2017 were included. Detection of cancer was obtained by cross-checking the study population with the Swedish Cancer-Registry and the Cause-of-Death-Registry. A total of 664 patients were followed for a median of 7.7 years. In all, 231 malignancies were diagnosed in 138 patients. Compared to the general population the excess risk of cancer following HTx was 6.2-fold calculated as the standardized incidence ratio (SIR) and 2.9-fold after exclusion of non-melanoma skin cancer (NMSC). The most common malignancies were NMSC, non-Hodgins lymphoma, and lung cancer. There was no significant difference in overall survival between those with and without a history of cancer before HTx (p = 0.53). During a median follow-up of 7.7 years, 19% of HTx recipients developed cancer, 6.2-fold higher relative to the general population, and 2.9-fold higher when excluding NMSC. Risk factors for malignancies (excluding NMSC) included previous smoking, hypertension and prolonged ischemic time; and for NMSC, increasing age, seronegative CMV-donors, and azathioprine. A previous cancer in selected recipients results in similar survival compared to those without cancer prior to HTx.
Introduction
Heart transplantation (HTx) is a life-saving treatment for end-stage heart failure. Long-term survival after HTx is limited by several risk factors.; one of them being malignancies. As compared with the general population, solid organ recipients have a 2-4-fold higher risk of developing cancer [1–3], a major cause of morbidity and mortality [4].
Compared with recipients of abdominal organs, thoracic transplant recipients have a higher risk of developing cancer. The leading cause is the higher doses of immunosuppressive agents needed to prevent organ rejection [5–7]. The most frequent cancers after HTx have been reported to be non-melanoma skin cancer (NMSC), lung cancer and lymphomas [8].
The present study examines the incidence of post-transplant cancer and the survival rate among HTx recipients diagnosed with cancer at the Sahlgrenska University Hospital (SUH). Survival rates are compared with the general population in Sweden. It was also studied if a history of treated cancer before HTx affected post-transplant cancer incidence and survival.
Patients and Methods
Between June 1985 and December 2017, 708 HTx were performed at the SUH. After exclusion of patients treated with re-transplantation (n = 21) and patients followed abroad (n = 23), a total of 664 patients were included in the study. Baseline characteristics are shown in Table 1. The mean age was 48 years and 74% of the cohort were men. The median follow-up time was 7.7 years generating a total of 5,668 patient-years. Figure 1 depicts the etiology of heart failure in the study population. The study was conducted in accordance with the Declaration of Helsinki and was approved by the Regional Ethical Review Board at University of Gothenburg (EPN no. 019-09, approval date 22nd October 2009, amendments approved 29th November 2010, 10th December 2012, 17th December 2013, 10th May 2017). The main outcome was the detection of cancer among participants, by cross-checking the study cohort with the Swedish Cancer Register (SCR) [9] and the Swedish Cause of Death Register (SCDR), which both are operated by the Swedish National Board of Health and Welfare. The following cancer diagnosis codes were used: 140-239 (International Classification of Diseases-9 until 1996) and codes C00-D48 (International Classification of Diseases-10 from 1997). Data on basal cell carcinoma (BCC) were not available from these registers, and are, therefore, not included in our NMSC population.
Table 1. Patient characteristics*.
Figure 1. Etiology of heart failure as proportions of patients by diagnosis prior to heart transplantation. DCM = dilated cardiomyopathy, IHD = ischemic heart disease, CHD = congenital heart disease, HCM = hypertrophic cardiomyopathy.
All Swedish citizens have a specific personal identity number that is registered at all healthcare contacts. This allows tracking of how the Swedish population interacts with the healthcare system [10]. The SCR, that originates from 1958 holds information on all citizens registered in Sweden with a cancer diagnosis. The SCDR, which stems from 1961, registers the cause of death, including cancer, for all deceased citizens registered in Sweden. All cancer diagnoses in this report were verified by a histopathological examination. The International Rules for Multiple Primary Cancers (IARC, ICD-0 Third Edition) were applied to ensure correct numbers of cancer tumors reported [11]. These rules enable comparison of cancer risk and outcome between different populations.
Listing criteria for HTx were coherent with established international guidelines [12]. Recipients and donors were matched for ABO blood group compatibility. Complement-dependent cytotoxicity assays were performed to assess the recipient serum’s ability to lyse a panel of T or B cells and, if positive above a certain level, a prospective donor-specific cross-match was performed. At the beginning of our HTx program, bi-atrial technique was initially used but this was slowly changed to bi-caval technique during the period as formerly described [13]. Over time, the complexity of surgery has increased, and the number of patients bridged with mechanical circulatory support has risen. Survival has improved over time, which has previously been reported [14].
Induction therapy has been applied throughout our HTx program (n = 573), mainly anti-thymocyte globulin. All patients received a regime with three different immunosuppressive agents, including a calcineurin inhibitor (cyclosporine or tacrolimus), an antimetabolite (azathioprine or mycophenolate mofetil (MMF) and a corticosteroid, tapered during the first year. Previously, cyclosporine and azathioprine constituted the primary immunosuppressive treatment but were replaced with tacrolimus and MMF during the 2000s. According to a routine protocol, percutaneous transvenous myocardial biopsies were used for rejection monitoring. All patients received acetylsalicylic acid and a statin as a preventive measure for graft vasculopathy.
Data are presented as means and standard deviations, medians and interquartile ranges, or numbers and percentages. Overall survival curves were generated using Kaplan-Meier estimates and comparisons between groups were performed with the log rank test. Relative survival was calculated using the Ederer II method [15]. Mortality data for the general population in Sweden were used to estimate expected survival rates. The mortality data comprised the probability of death for single-year age groups in 1-year calendar period. Cumulative incidence of cancer was analyzed using competing risk methods with death as a competing event [16]. When analyzing cancer incidence for different cancer types, person-years were calculated from date of the transplantation to the first of the following events: diagnosis of the cancer site; death; or end of surveillance period, i.e., 31 December 2018 The standardized incidence ratio (SIR) was defined as the observed number of cancers during the observation time divided by the expected number of cases, using incidence rates from the Swedish population stratified for 5-year age groups (0–4, 5–9, … 80–84, 85-), gender and calendar year. Incidence rates for different cancer sites were used from the NORDCAN project. Furthermore, the coding of cancer followed definitions according to International rules for multiple primary cancers [11]. Univariable and multivariable risk factor analyses by Cox proportional hazards regression model for the development of posttransplant malignancy were performed. The following parameters were tested by univariable analyses: age (per 10 years), sex, BMI (<20; 20–30; >30), smoking (never; cessation >6 months before HTx listing; cessation <6 months before HTx listing), hypertension, diabetes mellitus, TIA/stroke, previous cardiac surgery, donor age (per 10 years), CMV+/− donor, CMV+/− recipients, CMV mismatch, ventricular assist device (VAD), ischemic time (<3; 3–4; >4 h), total induction dose with ATG (<200; 200–800; >800 mg) and proliferation inhibitors (azathioprine vs. MMF). Significant risk factors in the univariate models for all cancers and NMSC, respectively (Supplementary Tables S1, S2) were tested also in a multivariable model. All statistical tests were two-sided, and a p-value of <0.05 was considered statistically significant. Statistical analyses were carried out with Stata/IC 16.1.
Results
Mortality for the whole patient cohort within 30 days and 1-year was 51/664 (8%) and 78/664 (12%), respectively. Overall survival was for the whole cohort at 1, 5, 10, 15 and 20 years was: 88% (95% CI 86%–90%); 80% (95% CI 76%–83%); 67% (95% CI 63%–71%); 53% (95% CI 48%–58%) and 37% (95% CI 32%–43%), respectively. Overall survival for HTx patients increased significantly over time (p < 0.001). Five-year overall survival for those who underwent HTx between 1985 and 2000 was: 70% (95% CI: 64%–75%); between 2001 and 2010 81% (95% CI: 75%–86%); and between 2011 and 2017 92% (95% CI: 85%–96%) (Supplementary Figure S1).
A total of 231 de novo cancers were diagnosed in 138 HTx patients during follow-up, which corresponds to 19.6% of the total study population (Table 2). In contrast 37.5 detected cancers would have been in a cohort from the general population matched by age, sex and time period. This resulted in a SIR of 6.2 (95% CI 5.4–7.0) for all cancers and a SIR of 2.9 (95% CI: 2.4–3.5) after exclusion of NMSC.
Table 2. Number of cancers after HTx according to ICD-10.
The cumulative incidence of a de novo malignancy between 1 and 5 years after transplant was 4.6%. The cumulative incidence of cancer for the total cohort at 1, 5, 10, 15 and 20 years was 2.4% (95% CI 1.5–3.9), 7.0% (95% CI 5.2–9.3), 19% (95% CI 15.8–23), 26% (95% CI 22–31) and 33% (95% CI 28–38), respectively.
Cumulative incidence of post-HTx cancers by three prespecified time periods showed no difference over time (Figure 2A). During these same eras there was a significant decrease in overall cumulative mortality (Figure 2B).
Figure 2. Cumulative incidence of competing risks cancer (A) and death (B), and related to time-era after heart transplantation. Both outcomes cancer and death need to be assessed together since they are competing outcomes. Estimates and 95% confidence intervals are shown under the number of patients at risk.
The type and frequency of solid tumors for the total group, and for men and women separately, are listed in Table 2. The most common type of cancer was NMSC (55% of all cancers), non-Hodgin’s lymphoma (11.7% of all cancers) and lung cancer (4.3% of all cancers).
Among the patients who developed lung cancer (eight men and two women), 80% had a smoking history. Among them, four patients had stopped smoking <6 months before HTx listing and four had stopped >6 months before HTx listing.
A total of 44 patients (32%) had multiple tumors; 18 patients had 2 tumors, 6 patients had 3 tumors, 3 patients had 4 tumors and 5 patients had 5 tumors. Two patients developed 7 tumors each. One had 5 NMSC, one lip tumor and one salivary gland tumor, and the other had 5 NMSC, 1 anal cancer and 1 salivary gland tumor.
The SIR for cancer types diagnosed in four persons or more, are shown in Table 3. The excess risk of all cancers for the total population was 6.2 and similar between men and women (SIR 6.39 and SIR 5.18, respectively).
Table 3. Observed and expected cancer risks following HTx.*
The overall incidences of cancers in the cohort were higher than expected for: NMSC (SIR 82.6, 95% CI 69.4–98.3); non-Hodgkin lymphoma (SIR 24.8, 95% CI 17–36.1); malignant melanoma (SIR 9.42, 95% CI 4.24–21.0); multiple myeloma (SIR 9.08, 95% CI 3.41–24.2); gastric (SIR 7.86, 95% CI 3.27–18.9); lung (SIR 3.68, 95% CI 1.98–6.84); and kidney (SIR 3.20, 95% CI 1.03–9.92).
Among the 138 HTx patients who developed post-HTx cancer, 29 died from their malignancy: non-Hodgkin lymphoma (n = 13), lung cancer (n = 8), NMSC (n = 5), and gastric (n = 3).
Univariable and multivariable associations between baseline factors and cancer (omitting NMSC) are shown in Table 4. Independent predictors of cancer development included: smoking cession <6 months before HTx listing [HR 3.46 (95% CI 1.69–7.07), p < 0.001]; hypertension [HR 2.16 (95% CI 1.10–4.26), p < 0.026]; ischemic time (reference: <3 h) 3–4 h [HR 1.93 (95% CI 1.09–3.40), p = 0.024]; and treatment with azathioprine (vs. MMF) [HR 1.69 (95% CI 0.99–2.90), p < 0.055]. Interestingly, CMV mismatch was not significantly associated with cancer [HR 0.79 (95% CI 0.39–1.62), p = 0.53].
Table 4. Uni- and multivariable Cox proportional hazard regression for developing cancer.*
Significant risk factors in the multivariable model predicting NMSC only (Table 4) were: age per 10 years [HR 2.90 (95% CI 1.85–4.55), p < 0.001]; hypertension [HR 1.87 (95% CI 0.91–3.84), p < 0.091], seronegative CMV-donor [HR 2.14 (95% CI 1.11–4.14), p = 0.024], and treatment with Azathioprine [HR 2.53 (95% CI 1.20–5.36), p < 0.015].
A total of 26 patients (4%) had a malignancy history >5 years before HTx. The median age at their first tumor was 34 years (IQR; 11.3–52.2 years). The most common cancers were: acute lymphoblastic leukemia, lymphosarcoma, and Hodgkin lymphoma, shown in Table 1. There were no significant differences in overall survival between those with and without cancer before HTx (Figure 3). Furthermore, there was no significant difference in post-HTx relative survival between patients who were cancer-free before and after HTx (Figure 4).
Figure 3. Pretransplant malignancy overall survival compared to those without. Estimates and 95% confidence intervals are shown under the number of patients at risk.
Figure 4. Pretransplant malignancy relative survival compared to those without. Estimates and 95% confidence intervals are shown under the number of patients at risk.
Discussion
In the current study, we observed a 6.2-fold excess risk of cancer following HTx relative to the general population. When excluding NMSC, the excess risk was 2.9-fold. The cumulative incidence of a de novo malignancy between 1 and 5 years after HTx was 4.6%, which is lower compared to previous studies. In a study by Yoan et al., including over 17,000 patients [17] the corresponding incidence rate of de novo malignancy was 10.7%, which is considerably higher than the 4.6% rate observed in the present study. Yoan et al., derived data from the ISHLT registry, with a high rate of missing data supported by the fact that 24,000 HTx patients were excluded from the analyses. We therefore argue that they overestimated the risk of cancer due to positive selection. In contrast, we have derived data from national full coverage registries with a very low risk of missing any cancer. Data extraction from complete registries with detailed information on individual level makes this study unique. An improved post-HTx survival was observed during later eras, this could not be explained by a reduction in cancer incidence, which remained stable over the study period. This could indicate earlier detection and/or improved post-HTx cancer treatment.
It is well known that transplanted patients, as compared to the general population, have a higher incidence of NMSC, and the detected tumors are more aggressive [18]. It is also acknowledged that the incidence of NMSC increases with the intensity and duration of immunosuppression [19]. The SIR for NMSC of 82.6 in our cohort was more than four times higher as compared to the SIR of 18.5 reported by Collett et al. [3]. However, Collett et al. noted that their results might have been underestimated, since lesions might have been removed without a histological examination. A study from Finland, including 479 patients reported a SIR of 51.9 for squamous cell carcinoma (SCC) [20], which is also lower than we observed. Crespo Leiro et al. [21] and Vaan Keer et al. [22] studied the incidence of NCSC in a Spanish and Belgian population, but didn´t compare the cancer incidence to the general population, why SIR could not be calculated. In our study, almost 55% of the tumors (127 of 231) were NMSC. Corresponding numbers in the studies by Crespo-Leiro et al. and Vann Keer et al. were 51% (324 of 490) and 22% (58 of 263). The median duration of patient follow-up was 7.7 years in the present study compared to with 5.8 years in the study by Crespo-Leiro et al. and 10.7 years in the study by Vaan Keer et al.
While lung cancer in men has declined in Sweden since the 1980s, the opposite trend has been observed in women, to the point where more women than men now develop lung cancers [23]. The overall SIR for lung cancer (3.68) was higher than observed in other comparable studies (2.0–2.79) [3, 24–27]. There was no significant increased risk for lung cancer in transplanted women presented in a Spanish study by Crespo-Lieiro et al. [25], with over four thousand patients. Among patients with a history of smoking in our study, 284 patients (43%) had stopped smoking 6 months or more before being listed for transplantation. Crespo-Lieiro et al [25] showed an association between previous smoking and development of post-HTx lung cancer. In that study the median time between HTx and the lung cancer diagnosis was 6.4 years, compared to 7.8 years (IQR: 4.1–12.2) in our study. In addition to hypertension and longer ischemic time, previous smoking was also a risk factors for the development of NMSC in the present study.
The SIR for prostate cancer in our cohort was low (1.13), indicating that immunosuppression after HTx was not associated with a significantly increased prostate cancer risk. Similar findings have also been reported in a meta-analysis including six independent studies, with over 21,000 heart transplant patients [28]. Why immunosuppression does not increase the risk for prostate cancer remains largely unknown, but this may in part be explained by intensive screening before HTx, and the possibility that male HTX recipients don’t survive long enough to develop prostate cancer, which mostly occurs after the age of 70 years [23]. These findings support that patients with low-grade prostate cancer could be accepted for HTx without the often applied 5-year cancer free waiting period.
An excess risk of lip cancer was demonstrated (SIR 72.6) corroborating findings by Collet et al (SIR 60) and Jääma-Holmberg et al (SIR 47.4). The reason remains unclear, but may be related to the fact that this is a NMSC, and therefore can be classified as skin cancer. There is an association between smoking and lip cancer and the fact that two patients diagnosed with lip cancer (seven lip cancers among four persons) had a history of smoking may partially explain our findings. Sun exposure is also a well-established risk factor for the development of lip cancer [29]. Among the seven patients with a lip cancer, five (71%) also had a NMSC.
A history of malignancy within 5 years has been considered to be a contraindication for transplantation because of the increased risk of recurrence following initiation of immunosuppressive therapy. Sigurdardottir et al. [30] reported a cancer recurrence rate of 63%, if the disease-free interval between malignancy and HTx was less than 1 year, but only 6% if the HTx recipient had been cancer free for more than 5 years. However, prostate cancer was not presented as a separate entity, why the post-HTx relapse of prostate cancer remains unclear. In a review article by Mistiaen et al [31], patients with localized prostate cancer before transplantation had no increased risk of reduced survival post-HTx [31]. At present, there is no consensus regarding the optimal time interval between cancer treatment and HTx [32, 33], but a relapse free period of ≥5 years is a common criterion, which has also been applied at our center. However, when post HTx survival is constantly improving, at the same time as cancer incidence remains unchanged, it might be time to revise and consider individualization of these criteria.
Limitations
The current study did not investigate whether the patients had BCC before or after HTx, since this cancer form has been considered rather benign and, therefore, not reported in the SCR. The growth rate of BCC is slow and this cancer rarely metastasizes [34]. Post-transplant lymphoproliferative disease (PTLD), a well-known complication after HTx [35] is not recorded as a specific entity in the SCR, why the exact number of patients with PTLD is cannot be reported. Instead, such cases are presented as lymphomas.
There are multiple primary cancer coding rules to count incident cases. Cancer registries in the U.S. and Canada use, for example, SEER multiple primary rules. In this study, the International Rules for Multiple Primary Cancers (IARC/IACR, ICD-0 Third Edition) was applied. Compared to SEER rules, IARC/IACR recognizes fewer multiple primary cancers [36], which may explain the differences compared to other studies [26].
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
Ethics Statement
Regional Ethical Review Board at University of Gothenburg (EPN no. 019-09) approved the study and waived the need for individual consent.
Author Contributions
CS: Conceived and designed the analysis, collected the data, wrote the paper. AW: Conceived and designed the analysis. EH: Collected the data, performed the analysis, wrote the paper. KK: Conceived and designed the analysis, collected the data, wrote the paper JM: Collected the data, wrote the paper. GD: Conceived and designed the analysis, collected the data, performed the analysis, wrote the paper. All authors contributed to the article and approved the submitted version.
Funding
The authors declare that financial support was received for the research, authorship, and/or publication of this article. This work was supported by grants from the Swedish Heart and Lung Foundation, and from the Swedish state under the agreement between the Swedish government and the county councils, the ALF-agreement (ALFGBG-717811 to GD).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We would like to thank all participants of the heart transplant team for their dedicated clinical work.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontierspartnerships.org/articles/10.3389/ti.2024.12109/full#supplementary-material
References
1. Hall, EC, Pfeiffer, RM, Segev, DL, and Engels, EA. Cumulative Incidence of Cancer After Solid Organ Transplantation. Cancer (2013) 119(12):2300–8. doi:10.1002/cncr.28043
2. Adami, J, Gabel, H, Lindelof, B, Ekström, K, Rydh, B, Glimelius, B, et al. Cancer Risk Following Organ Transplantation: A Nationwide Cohort Study in Sweden. Br J Cancer (2003) 89(7):1221–7. doi:10.1038/sj.bjc.6601219
3. Collett, D, Mumford, L, Banner, NR, Neuberger, J, and Watson, C. Comparison of the Incidence of Malignancy in Recipients of Different Types of Organ: A UK Registry Audit. Am J Transplant (2010) 10(8):1889–96. doi:10.1111/j.1600-6143.2010.03181.x
4. Vajdic, CM, and van Leeuwen, MT. Cancer Incidence and Risk Factors After Solid Organ Transplantation. Int J Cancer (2009) 125(8):1747–54. doi:10.1002/ijc.24439
5. Krynitz, B, Edgren, G, Lindelof, B, Baecklund, E, Brattström, C, Wilczek, H, et al. Risk of Skin Cancer and Other Malignancies in Kidney, Liver, Heart and Lung Transplant Recipients 1970 to 2008--A Swedish Population-Based Study. Int J Cancer (2013) 132(6):1429–38. doi:10.1002/ijc.27765
6. Roithmaier, S, Haydon, AM, Loi, S, Esmore, D, Griffiths, A, Bergin, P, et al. Incidence of Malignancies in Heart and/or Lung Transplant Recipients: A Single-Institution Experience. J Heart Lung Transplant (2007) 26(8):845–9. doi:10.1016/j.healun.2007.05.019
7. Jensen, P, Hansen, S, Møller, B, Leivestad, T, Pfeffer, P, Geiran, O, et al. Skin Cancer in Kidney and Heart Transplant Recipients and Different Long-Term Immunosuppressive Therapy Regimens. J Am Acad Dermatol (1999) 42(2):307–186. doi:10.1016/S0190-9622(00)90154-3
8. Crespo-Leiro, MG, Alonso-Pulpón, L, Vázquez de Prada, JA, Almenar, L, Arizón, JM, Brossa, V, et al. Malignancy After Heart Transplantation: Incidence, Prognosis and Risk Factors. Am J Transplant (2008) 8(5):1031–9. doi:10.1111/j.1600-6143.2008.02196.x
9. Barlow, L, Westergren, K, Holmberg, L, and Talbäck, M. The Completeness of the Swedish Cancer Register: A Sample Survey for Year 1998. Acta Oncol (2009) 48(1):27–33. doi:10.1080/02841860802247664
10. Ludvigsson, JF, Otterblad-Olausson, P, Pettersson, BU, and Ekbom, A. The Swedish Personal Identity Number: Possibilities and Pitfalls in Healthcare and Medical Research. Research Support, Non-U.S. Gov’t. Eur J Epidemiol (2009) 24(11):659–67. doi:10.1007/s10654-009-9350-y
11. International Rules for Multiple Primary Cancers (ICD-0 Third Edition). International Rules for Multiple Primary Cancers (ICD-0 Third Edition). Eur J Cancer Prev (2005) 14(4):307–8. doi:10.1097/00008469-200508000-00002
12. Mehra, MR, Kobashigawa, J, Starling, R, Russell, S, Uber, PA, Parameshwar, J, et al. Listing Criteria for Heart Transplantation: International Society for Heart and Lung Transplantation Guidelines for the Care of Cardiac Transplant Candidates--2006. J Heart Lung Transpl (2006) 25(9):1024–42. doi:10.1016/j.healun.2006.06.008
13. Carlstrom, M, Dahlin, S, Gabel, J, Doanhu, R, Hörlinge, J, Jeppsson, A, et al. 265 Tricuspid Regurgitation and Surgical Technique Influences Outcome After Heart Transplantation. J Heart Lung Transplant (2012) 31(4):S96. doi:10.1016/j.healun.2012.01.272
14. Dellgren, G, Westerlind, A, Liden, H, Gäbel, J, Bartfay, SE, Bollano, E, et al. Continuous Improvement in Outcome After Heart Transplantation — Long-Term Follow-Up After Three Decades of Experience. Int J Cardiol (2017) 231:188–94. doi:10.1016/j.ijcard.2016.12.186
15. Ederer, F, Axtell, LM, and Cutler, SJ. The Relative Survival Rate: A Statistical Methodology. Natl Cancer Inst Monogr (1961) 6:101–21.
16. Fine, JP, and Gray, RJ. A Proportional Hazards Model for the Subdistribution of a Competing Risk. J Am Stat Assoc (1999) 94(446):496–509. doi:10.1080/01621459.1999.10474144
17. Youn, J-C, Stehlik, J, Wilk, AR, Cherikh, W, Kim, IC, Park, GH, et al. Temporal Trends of De Novo Malignancy Development After Heart Transplantation. J Am Coll Cardiol (2018) 71(1):40–9. doi:10.1016/j.jacc.2017.10.077
18. Euvrard, S, Kanitakis, J, Pouteil-Noble, C, Disant, F, Dureau, G, Finaz de Villaine, J, et al. Aggressive Squamous Cell Carcinomas in Organ Transplant Recipients. Transplant Proc (1995) 27(2):1767–8.
19. Fortina, AB, Piaserico, S, Caforio, AL, Abeni, D, Alaibac, M, Angelini, A, et al. Immunosuppressive Level and Other Risk Factors for Basal Cell Carcinoma and Squamous Cell Carcinoma in Heart Transplant Recipients. Arch Dermatol (2004) 140(9):1079–85. doi:10.1001/archderm.140.9.1079
20. Jäämaa-Holmberg, S, Salmela, B, Lemström, K, Pukkala, E, and Lommi, J. Cancer Incidence and Mortality After Heart Transplantation - A Population-Based National Cohort Study. Acta Oncologica (2019) 58(6):859–63. doi:10.1080/0284186X.2019.1580385
21. Crespo-Leiro, MG, Paniagua-Martin, MJ, Muniz, J, Marzoa-Rivas, R, Rodriguez, JA, Franco, R, et al. Malignancy After Heart Transplantation. Incidence and Survival From a Cohort of 378 Patients. Eur Heart J (2007) 28:352.
22. Van Keer, J, Droogne, W, Van Cleemput, J, Vörös, G, Rega, F, Meyns, B, et al. Cancer After Heart Transplantation: A 25-Year Single-Center Perspective. Transplant Proc (2016) 48(6):2172–7. doi:10.1016/j.transproceed.2016.03.037
23. Socialstyrelsen. Statistics on Cancer Incidence 2018 (2018-6-10). Stockholm: Socialstyrelsen (2018). p. 6. Available from: https://www.socialstyrelsen.se/publikationer2018/2018-6-10 (Accessed February 20, 2019).
24. Jiang, Y, Villeneuve, PJ, Wielgosz, A, Schaubel, DE, Fenton, SS, and Mao, Y. The Incidence of Cancer in a Population-Based Cohort of Canadian Heart Transplant Recipients. Am J Transpl (2010) 10(3):637–45. doi:10.1111/j.1600-6143.2009.02973.x
25. Crespo-Leiro, MG, Villa-Arranz, A, Manito-Lorite, N, Paniagua-Martin, MJ, Rábago, G, Almenar-Bonet, L, et al. Lung Cancer After Heart Transplantation: Results From a Large Multicenter Registry. Am J Transpl (2011) 11(5):1035–40. doi:10.1111/j.1600-6143.2011.03515.x
26. Kellerman, L, Neugut, A, Burke, B, and Mancini, D. Comparison of the Incidence of De Novo Solid Malignancies After Heart Transplantation to That in the General Population. Am J Cardiol (2009) 103(4):562–6. doi:10.1016/j.amjcard.2008.10.026
27. Secnikova, Z, Gopfertova, D, Hoskova, L, Hercogova, J, Dzambova, M, Jirakova, A, et al. Significantly Higher Incidence of Skin Cancer Than Other Malignancies in Patients After Heart Transplantation. A Retrospective Cohort Study in the Czech Republic. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub (2015) 159(4):648–51. doi:10.5507/bp.2015.011
28. Bao, J-M, Zhu, H-L, Yang, G-S, Chen, PL, Dang, Q, Chen, XX, et al. No Significant Association Between Immunosuppression in Solid Organ Transplantation and Prostate Cancer Risk: A Meta-Analysis of Cohort Studies. Translational Cancer Res (2019) 8(3):939–49. doi:10.21037/tcr.2019.06.03
29. Perea-Milla López, E, Miñarro-Del Moral, RM, Martínez-García, C, Zanetti, R, Rosso, S, Serrano, S, et al. Lifestyles, Environmental and Phenotypic Factors Associated With Lip Cancer: A Case-Control Study in Southern Spain. Br J Cancer (2003) 88(11):1702–7. doi:10.1038/sj.bjc.6600975
30. Sigurdardottir, V, Bjortuft, O, Eiskjær, H, Ekmehag, B, Gude, E, Gustafsson, F, et al. Long-Term Follow-Up of Lung and Heart Transplant Recipients With Pre-transplant Malignancies. J Heart Lung Transplant (2012) 31(12):1276–80. doi:10.1016/j.healun.2012.09.007
31. Peter Mistiaen, W. Heart Transplantation in Patients With Previous Malignancy. An Overview. Acta Cardiol (2015) 70(2):123–30. doi:10.1080/ac.70.2.3073502
32. Chapman, JR, Webster, AC, and Wong, G. Cancer in the Transplant Recipient. Cold Spring Harb Perspect Med (2013) 3(7):a015677. doi:10.1101/cshperspect.a015677
33. Mehra, MR, Canter, CE, Hannan, MM, Semigran, MJ, Uber, PA, Baran, DA, et al. The 2016 International Society for Heart Lung Transplantation Listing Criteria for Heart Transplantation: A 10-Year Update. J Heart Lung Transpl (2016) 35(1):1–23. doi:10.1016/j.healun.2015.10.023
34. Rubin, AI, Chen, EH, and Ratner, D. Basal-Cell Carcinoma. N Engl J Med (2005) 353(21):2262–9. doi:10.1056/NEJMra044151
35. Penn, I, Hammond, W, Brettschneider, L, and Starzl, TE. Malignant Lymphomas in Transplantation Patients. Transpl Proc (1969) 1(1):106–12.
Keywords: cancer, heart transplantation, epidemiology, cohort study, single center study
Citation: Stenman C, Wallinder A, Holmberg E, Karason K, Magnusson J and Dellgren G (2024) Malignancies After Heart Transplantation. Transpl Int 37:12109. doi: 10.3389/ti.2024.12109
Received: 24 September 2023; Accepted: 01 August 2024;
Published: 09 September 2024.
Copyright © 2024 Stenman, Wallinder, Holmberg, Karason, Magnusson and Dellgren. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Caroline Stenman, Y2Fyb2xpbmUuc3Rlbm1hbkB2Z3JlZ2lvbi5zZQ==