Lung cancer in recipients after lung transplant: single-centre experience and literature review.

INTRODUCTION: Lung cancer is a major challenge facing modern medicine. It is the leading cause of cancer-related death in the USA. Little is known of the incidence, prevalence and disease characteristics in lung transplant recipients, a population unique in its vulnerability and exposure to carcinogenic risk factors. We aimed to elaborate these characteristics of lung cancer in our population through a retrospective cohort study.
METHODS: We retrospectively reviewed our institution's 8-year experience with lung transplantation and searched for patients with a post-transplant diagnosis of lung cancer, neoplasia or mass. We focused on patient demographics, indication for transplant, smoking history, stage at diagnosis, location of the tumour, length of time between transplant and diagnosis, the treatment offered and length of time from diagnosis to death or last follow-up. Descriptive statistics and survival analysis standard Kaplan-Meier method was conducted from the date of cancer diagnosis to death from all-cause mortality or last follow-up as of August 2021.
RESULTS: We identified 24 patients with de novo lung cancer postlung transplant in 905 recipients. More patients with an underlying diagnosis of idiopathic pulmonary fibrosis developed lung cancer. Twenty-one patients were diagnosed with non-small cell lung cancer and three had small cell lung cancer. The remaining native lung was involved most in single lung recipients with 17 patients. Patients with a diagnosis of lung cancer had a mean survival of 17.6 months after diagnosis. DISCUSSION: The incidence rate of lung cancer in our cohort was higher than reported for smokers from the general population in previous studies. In this study, we compare our findings with available literature. We also explore screening strategies, treatment modalities, survival and postulated mechanisms for the development of lung cancer in lung transplant recipients. © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Lung cancer affects recipients of lung transplant at an increased frequency when compared with the general population.

This study adds to the current published literature and describes the incidence rates.

It also examines the utility of current screening guidelines, and mortality in our lung transplant population.

This study advocates for heightened suspicion for lung cancer in the transplant recipient.

Our findings may encourage transplant pulmonologists to screen patients routinely.

Introduction

Lung cancer (LC) is a major clinical and public health challenge facing modern medicine. It remains a leading cause of death in the USA and comprises 23% of cancer deaths.1 2 While many risk factors are known for LC development, there are cohorts where the description of occult risks may be complex. Lung transplant recipients (LTRs) are one such group of patients. Lung transplantation (LT) is the ultimate treatment for advanced lung diseases. This therapeutic option has matured into a life-altering intervention, with >60 000 patients have received LT since its inception in 1963.3 Survival has improved from 18 days in the first patient to a median 1-year survival of 88% in North America. As most LTRs have predisposing conditions or exposure to carcinogens such as tobacco smoke, in addition to immunosuppressive therapy, it is essential to be wary of LC in these patients. Herein, we aim to explore LC in the LTR population at our institution. We also review current literature and discuss postulated mechanisms underlying the development of LC in LTR.

Materials and methods

After obtaining IRB approval (IRB # 28862), we retrospectively reviewed our institution’s 8-year experience with LT. We then searched for patients with a post-transplant diagnosis of LC, neoplasia or mass. We undertook a retrospective chart review of Temple University Hospital’s electronic medical record. We focused on patient demographics, indication for transplant, smoking history, stage at diagnosis, location of the tumour, length of time between transplant and diagnosis, the treatment offered and length of time from diagnosis to death or last follow-up.

Transplant candidates at our institution undergo a thorough preoperative evaluation. This includes a comprehensive laboratory workup, CT of the chest, abdomen and pelvis as well as pulmonary function testing and immunotyping.

Post-transplant, all patients follow-up a minimum of weekly in the first month, every other week over the next 5 months, then monthly until the first 12 months post-transplant. Patients receive a spirometry the day of an outpatient visit, and a surveillance bronchoscopy with bronchoalveolar lavage and surveillance transbronchial biopsies at 1, 3, 6 and 12 months post-transplant. However, this is at the discretion of the transplant pulmonologist and any diagnostic procedure is usually ordered in response to symptoms or changes in spirometry. Annually, all transplant recipients receive an echocardiogram and non-contrast chest CT. In the event of a nodule or lung mass being identified, a tailored approach to diagnosis is usually employed. The use of navigational bronchoscopy, endobronchial ultrasound with transbronchial biopsy, transthoracic biopsy or excisional biopsy have been used depending on the clinical stage.

Following the transplant, all patients receive standard immunosuppression per protocol. Intraoperatively, induction therapy with either basiliximab or alemtuzumab is initiated along with methylprednisolone. Immunosuppressive treatment is maintained postoperatively with tacrolimus (TAC), mycophenolate mofetil (MFM) and prednisone. MFM is usually discontinued if cancer is diagnosed, and the TAC dose is lowered.

If a malignancy is diagnosed, a multidisciplinary approach to treatment is usually taken through discussion with the thoracic tumour board which comprises the patient’s pulmonologist, thoracic surgery, medical and radiation oncology and radiology.

Statistical analysis

Descriptive statistics were reported as mean or median, with SD and IQR. Survival was calculated from the date of cancer diagnosis to death from all-cause mortality or last follow-up as of August 2021. We performed a survival analysis with the standard Kaplan-Meier method. All statistical analyses were performed using IBM SPSS V.25.

Patient and public involvement

Patients or the public were not involved in the design, or conduct, or reporting, or dissemination plans of our research.

Results

Incidence of lung cancer post-transplant

From January 2013 to August 2021, our institution performed 905 lung transplants. Of these, 594 were single and 311 were double lung transplants (DLT). LTRs at our institution had a cumulative follow-up of 2298.67 patient-years to the analysis time (August 2021). Our search initially found 36 patients with a diagnosis of LC. We excluded two patients listed for transplant originally but were not transplanted because of a subsequent diagnosis of current LC on initial workup. After a thorough evaluation, we excluded three patients with lung lesions suspicious for LC but ultimately received alternate diagnoses. Of the 31 patients with LC, 7 had an in situ carcinoma on the explanted lung’s pathological evaluation, and thus were excluded from the analysis. Twenty-four patients were diagnosed with LC during follow-up after transplant and were the primary cohort of interest for this study (figure 1).

Figure 1

Patient selection.

The overall incidence of LC in our LTR population was 10.4 cases per 1000 patient-years. Of these, three (12.5%) patients received a DLT, with the incidence rate of LC in DLT 3.1 cases per 1000 patient-years. Twenty-one (87.5%) received a single lung transplant (SLT), with an incident rate of 15.76 per 1000 patient-years. The incidence of LC in patients with idiopathic pulmonary fibrosis (IPF) was 9.17 cases per 1000 patient-years, whereas in patients with chronic obstructive pulmonary disease (COPD), a rate of 21.1 per 1000 patient-years was observed.

Patient characteristics

Patient characteristics are described in table 1.

Table 1

Recipient characteristics

Gender
Male	20 (83.3 %)
Female	4 (16.7 %)
Age	69.5 (SD 6.6)
Diagnosis
IPF	11 (45.8 %)
COPD	8 (33.3 %)
CPFE	5 (20.8 %)
Smoking history
Yes	21 (87.5 %)
No	3 (12.5 %)
Mean pack-years	33.2 (SD 36.4)
Type of transplant
Double lung	3 (12.5 %)
Single lung	21 (87.5 %)

The mean age of patients was 69.5±6.6 years; there were 20 men and 4 women.

COPD, chronic obstructive pulmonary disease; CPFE, combined pulmonary fibrosis with emphysema; IPF, idiopathic pulmonary fibrosis.

IPF was the most common indication for transplant in this cohort at 45.8%. COPD was the second most common indication at 33.3%. Combined pulmonary fibrosis with emphysema indicated transplant in 20.8% of patients.

All patients had been on maintenance immunosuppression with at least tacrolimus and prednisone at the time of diagnosis, and none had received a mammalian target of rapamycin inhibitor. The use of mycophenolate was less uniform.

All but three patients had a history of smoking (87.5%). The mean pack-year history was 33.2 pack-years.

Screening, diagnosis and treatment

Tumour characteristics are described in table 2.

Table 2

Lung cancer characteristics

Pathology
Adenocarcinoma	8 (33.3%)
Squamous cell carcinoma	10 (41.6%)
Small cell carcinoma	3 (12.5%)
NSCLC NOS	2 (8.3%)
Smooth muscle tumour	1 (4.2%)
Involved lung
Allograft	7 (29.2%)
Native	17 (70.8%)
Treatment
Surgical	9 (37.5%)
Chemotherapy	7 (29.2%)
Radiation	3 (12.5%)
None	8 (33.3%)
Survival (in months)	17.6 (95% CI 9.2 to 25.4)

NOS, not otherwise specified; NSCLC, non-small cell lung cancer.

Patients were diagnosed with LC at variable times post-transplant. The mean time to diagnosis from transplant was 24.2 months (±20.3). The native lung was involved in 17 patients (70.8%), whereas the allograft was involved in 7 patients (29.2%). This included the DLT recipients (DLTRs). Squamous cell carcinoma (SCC) was the most common histopathological type, with 10 patients (41.6%), followed by adenocarcinoma in 8 patients (33.3%), small cell carcinoma (SCLC) in 3 patients. Two (8.3%) patients were diagnosed with non-small cell carcinoma not specified (NSCLC NOS), and one patient had an Epstein-Barr virus (EBV)-related smooth muscle tumour.

Fifteen patients had some symptoms suspicious of malignancy at diagnosis, with dyspnoea, cough and weight loss being the most common. Nine patients had no symptoms and were diagnosed on routine CT surveillance. Half (n=12) of the patients met the United States Preventive Services Task Force (USPSTF) criteria for lung cancer screening, whereas 67% met the more sensitive Pamplona International Early Lung Cancer Detection Program (P-IELCAP) criteria.

Eight patients had stage I disease at the time of diagnosis. Three patients had stage II and stage III each. At the same time, 10 patients had metastatic disease by the time of diagnosis.

The patients with metastatic disease chose no treatment and opted for hospice care. Three received either palliative chemotherapy or radiation.

Survival

A survival analysis using the standard Kaplan-Meier method showed a mean survival of 17.6 months after diagnosis, with a SEM of 3.9. The cumulative survival fell below 50% less than a year after receiving a diagnosis of LC. A cumulative survival curve from the time of diagnosis for patients with LC is shown in figure 2.

Figure 2

Survival curve for lung transplant recipients developing lung cancer post-transplant. Cumulative survival in months following the diagnosis is indicated by the blue line.

Nine patients had survived to follow-up at the analysis time (August 2021). Of these, all but two had a curative surgical resection. One patient received adjuvant chemotherapy, whereas one received chemotherapy alone for metastatic disease. The predominant histopathology remained SCC in six patients. The remaining three patients had been diagnosed with NSCLC NOS, adenocarcinoma and SCLC, respectively.

Six out of seven patients (85.7%) with an allograft-derived LC did not survive at the analysis time. These patients did not receive any cancer-directed therapy and opted for hospice care. Three patients had a diagnosis of adenocarcinoma. One had SCC with metastasis to the pericardium and survived less than a month after diagnosis. An EBV-associated smooth muscle tumour was diagnosed on excision from the right upper lobe of one patient; the patient survived recurrence-free for 24 months, ultimately expiring from respiratory complications 9 years post-transplant.

Patients with stage I disease had a median survival of 14 months postdiagnosis. Median survival for stage II and III disease was 21 and 5 months, respectively. Patients with stage IV disease at presentation were limited to a median survival of 3.5 months.

When surgical excision was performed, the median survival was 21 months. Patients who received chemotherapy alone had a median survival of 6 months, compared with 5 months in patients receiving chemoradiation and 1 month in patients receiving no treatment.

Survival post-transplant of patients with and without LC is shown in figure 3. Detailed characteristics of LTRs and LC are shown in tables 3 and 4. Relative frequencies of the malignancy are show in figure 4.

Figure 3

Survival curves for lung transplant recipients with and without lung cancer. Cumulative survival in months following transplant. The red curve indicates patients with a diagnosis of cancer, the blue curve indicates patients without lung cancer.

Figure 4

Relative frequencies by pathology. Adeno, adenocarcinoma; NOS, not otherwise specified; NSCLC, non-small cell lung cancer; SCC, squamous cell carcinoma; SCLC, small cell lung cancer.

Discussion

Our findings add to the available data,4–20 summarised in table 5.

Table 5

Summary of available literature

Study	Patients with lung cancer/Total patients	Patients with native lung cancer	Patients with donor lung cancer	Indication for transplant	Documentedpathology
Choi et al4	1/99	1	N/A	IPF	SCC
Spiekerkoetter et al5	1/219	1	N/A	N/A	SCC
de Perrot et al6	1/396	1	N/A	COPD	BAC
Stagner et al7	2/46	2	N/A	COPD	SCC ×1Adeno ×1
Schulman et al8	2/82	1	N/A	COPD ×2	SCC ×1Adeno ×1
Collins et al9	3/111	N/A	N/A	COPD ×2IPF ×1	SCC ×1NSCLC NOS ×2
Roithmaier et al10	5/200	4	N/A	COPD ×4	NOS*
Arcasoy et al11	6/251	6	N/A	COPD ×5IPF ×1	SCC ×2Adeno ×3Poorly diff ×1
Raviv et al12	7/290	6	1	COPD ×2IPF ×4SSc ×1	SCC ×3Adeno ×3Poorly diff ×1
Dickson et al13	9/131	9	N/A	COPD ×8IPF ×1	SCC ×6Adeno ×2Sarcoma ×1
Espinosa et al14	9/340	8	N/A	COPD ×5IPF ×3CF ×1	SCC ×3Adeno ×3LCC ×2SCLC ×1
Gonzalez et al15	11/258	11	N/A	COPD ×11	N/A
Minai et al16	12/286	11	1	COPD ×11IPF ×1	SCC ×3Adeno ×4LCC ×3SCLC ×1
Belli et al17	13/335	6	1	COPD ×7IPF ×6	SCC ×5Adeno ×4Poorly diff ×2SCLC ×1Carcinoid ×1
Yserbyt et al18	13/494	9	4	COPD ×8PF ×4GIP ×1	SCC ×3Adeno ×4LCC ×3SCLS ×1NOS ×2
Ekström et al19	18/331	11	7	COPD ×18	N/A
Pérez-Callejo et al20	23/633	12	6	COPD ×10IPF ×11Primary pulmonary Hemosiderosis ×1NSIP ×1	SCC ×7Adeno ×13LCC ×1SCLC ×1Poorly diff ×1
Collins et al9	24/2168	24	N/A	COPD ×18IPF ×3	SCC ×8Adeno ×4Poorly diff ×1Anaplastic ×1BAC ×10
This study	24/905	17	7	COPD ×8IPF ×11CPFE ×5	SCC ×10Adeno ×8Other NSCLC ×2SCLC ×3
Total	184/7575	140	27	COPD ×121IPF ×43Others ×20	SCC ×47Adeno ×50Other NSCLC ×36SCLC ×8

Adeno, adenocarcinoma; BAC, Bronchoalveolar Carcinoma; COPD, chronic obstructive pulmonary disease; CPFE, chronic pulmonary fibrosis with emphysema; diff, differentiated; GIP, giant cell interstitial pneumonia; IPF, idiopathic pulmonary fibrosis; N/A, not available; NOS, not otherwise specified; NSIP, Non-specific Intersitial Pneumonia; PF, Pulmonary Fibrosis; SCC, squamous cell cancer; SCLC, small cell lung cancer; SSc, systemic sclerosis.

Incidences

The development of LC in LTR is a complex clinical problem, and data are limited to case series owing to the small patient population.

Our study demonstrates an overall incidence of LC at 10.4 cases per 1000 patient-years in LTRs. In perspective, smokers recruited in the NELSON study (Dutch-Belgian Randomised Lung Cancer Screening Trial (Dutch acronym: NELSON study)) had an incidence rate of 5.58 per 1000 patient-years.1 The nearly double incidence indicates the magnitude of the problem, limited only by the number of LTRs.

Non-transplant patients with COPD have an incidence rate of 16.7 cases per 1000 patient-years21; this was higher at 21.1 per 1000 patient-years in LTRs with COPD in our study. Whereas in IPF incidence of LC ranges between 11.2 and 36 cases per 1000 patient-years.22 Patients with IPF who received a LT at our centre had a LC incidence of 9.17 cases per 1000 patient-years.

DLTs appear to be at a lower risk of developing LC, with 3.1 cases per 1000 patient-years identified in our cohort. Single Lung Recipients (SLRs) have a higher incidence; 15.76 per 1000 patient-years.

Single lung transplant versus double lung transplant

Although scant, there is literature describing LC development in the explanted, allograft and remaining native lung.17 A recent review spanning two decades found 24 cases of native LC after a SLT in 2168 patients.9 Smaller series have reported similar findings.11 Across the literature, it appears that single lung transplant recipients (SLTRs) have a higher incidence of LC than DLTRs. Notably, in a study comparing 131 consecutive SLTRs with 131 successive DLTRs matched by native disease, 9 SLTRs developed primary LC in the native lung, whereas none of the matched bilateral lung transplant patients developed LC.13 Our results, highlighted above, mirror this finding, indicating a prevalence of LC in Double Lung Recipients (DLRs) of 0.96%, compared with 3.5% in SLRs.

Screening and diagnosis

The diagnosis of LC in the early stages is important to offer curative treatment and has indeed informed the lung cancer screening guidelines. However, no such guidelines exist for LTRs. The use of USPSTF to offer low-dose CT (LDCT) screening may not be clinically appropriate in these patients. In our cohort, if the USPSTF criteria were to be applied at the time of diagnosis, half of all cases would not have qualified for an LDCT. This signifies the lack of sensitivity of these criteria when applied to LTR populations. The P-IELCAP criteria, noted to be more sensitive for patients with underlying COPD in detecting LC,23 performed better in our population. If these were used for screening purposes, 67% of our patients would have qualified for an LDCT.

While patients at our institution usually get a CT chest at least once a year, a remarkable finding was the number of patients that were diagnosed with advanced disease. Diagnosis of LC at advanced stage has also been reported in a previous study.16 While the precise cause is unknown, the presence of occult malignancy aided in metastasis by immunosuppression may be one potential explanation.24 There appears to be a need for developing highly sensitive screening criteria and protocol in this population, and specifically designed clinical studies are required.

Treatment and survival

The biased difference in median survival heavily in favour of surgical resection likely reflects survival of early stage disease and not treatment modality. However, it does augment the argument for early detection. Due to the limited number of cases of stage II and III disease, and overall poor survival of LC, it is difficult to comment on the efficacy of systemic chemotherapy or locoregional radiation therapy. It is also important to note that the longer median survival noted in stage II disease when compared with stage I is likely due to the small number of patients with stage II disease. It is also interesting to note that among all fatalities that we observed in patients with LC, only one was unrelated to the underlying malignancy.

Postulated mechanisms

The mechanisms behind LC in LTRs are not clearly defined; however, many potential explanations for this phenomenon exist. Intuitively, the underlying diagnosis of lung disease in LTRs may be contributing factor. Interstitial lung disease is the underlying diagnosis in 34% of all LTRs.3 Among fibrotic lung disease, IPF has been described to have a fivefold increased risk of LC when compared with the general population.25 26 There are varied reports of prevalence ranging between 13.5% and 31%.26 27 An interesting finding is the predilection of LC in the lower lobes and peripheral lung zones.28 29 This anatomic distribution mimics the fibro-inflammatory changes in IPF. This obvolute distribution may be related to persistent inflammation. Myofibroblast activation proliferation, cellular stress, alterations of growth factors expression, oxidative injury and genetic factors are implicated as common denominators in both conditions.30 Genetic associations are involved in the pathogenesis of both IPF and LC, and some may be shared. There is increasing evidence for the importance of functional mutations of SFTPA 1 and SFTPA2 surfactant protein genes that lead to endoplasmic reticulum stress in the development of adenocarcinoma as well as IPF. Telomere instability caused by impaired enzymatic activity from mutations of the telomerase reverse transcriptase mutation is similarly shared by both processes. In addition, mutations of p53, p21, p16 and KRAS genes are also implicated in both processes.31 It is important to note, however, the frequency of KRAS mutation is lower in IPF associated adenocarcinoma when compared with smokers, indicating perhaps more endogenous carcinogenesis in IPF related to lung inflammation.32 Ongoing research into specific synergism between anticancer and antifibrotic agents may lead to the evolution of therapies for IPF and a better understanding of LC development in IPF.

COPD is the second leading indication of LT and is the underlying diagnosis in 21.4% of all LTRs.3 Abundant epidemiological evidence links the presence of COPD to the development of LC and remains a risk for all SLRs with native lung COPD. The connection between COPD and LC appears to be a complex interaction of multiple factors. When considering COPD, differentiating airflow obstruction and emphysema may be helpful. Chronic airway inflammation and adaptation to chronic irritant exposure is the hallmark of airflow limitation. Repeated injury and repair with metaplastic changes are one explanation for the increased frequency of LC in these patients. However, emphysematous destruction of the lung parenchyma appears to confer an increased risk of LC when compared with airflow obstruction.33–37 These findings suggest that the relationship between COPD and LC may be more profound than smoking alone. Emphysema is characterised by an imbalance of proteinases and inhibitors, an abundance of oxidative stress and an excessive infiltration of inflammatory cells leading to permanent airspace destruction. Chronic inflammation is also a common occurrence in LC. CD4+, CD8+ and macrophage recruitment and infiltration are shared among both disorders.38 Oxidative stress from tobacco smoke is abundantly linked to the pathogenesis of both COPD and LC. The xenobiotic metabolic pathway is known to metabolise many tobacco smoke constituents. Carbon monoxide, N-nitroso derivatives and polycyclic aromatic hydrocarbons are converted into carcinogens, generating oxygen free radicals as a by-product, leading to damaged cellular organelles and genetic material.39

SLRs with emphysema may be at an increased risk of LC when compared with those without. This can be attributed to the persistence of inflammation and maladaptive response in the remaining native lung.

Beyond underlying pathophysiology, there are other recipient and donor risk factors that could be associated with the development of LC in LTRs. The risk of LC in the general population increases with advancing age. The rate of LC in individuals aged 60 years or older is 284 per 100 000 individuals when compared with 32 per 100 000 in those aged <60 years. Simply crossing the age of 60 years appears to increase the risk of LC drastically; the rate of LC between ages 55 and 59 years is 92 per 100 000, whereas this increases to 151 per 100 000 for individuals aged 60–64 years in the USA.40 Over the past two decades, the proportion of LTRs aged >60 years has continued to increase and now forms almost a quarter of all recipients.3 Similarly, the pool of donors has also increased over this period, and organs from older individuals are more frequently acceptable. According to the International Society for Heart and Lung Transplantation (ISHLT) registry, up to 5% of organs are derived from donors aged 60 years or above. Additionally, as post-transplant outcomes and survival improve, current data suggest that many middle-aged recipients will live into high-risk decades.41 The age of donors and recipients can thus increase the individual risk of LC in LTRs.

LTRs are uniquely exposed to long-term immunosuppression. Unlike other solid organ transplant patients, therapeutic targets for immunosuppression in lung transplants are usually higher, owing to the higher risk of rejection. Calcineurin inhibitors (CNI) form the backbone of immunosuppression therapy. In addition to inhibiting calcineurin, tacrolimus and ciclosporin enhance the production and secretion of transforming growth factor β1 (TGFβ1).42 43 TGFβ1 has been known to increase tumour invasiveness and spread through angiogenesis, extracellular matrix production and suppression of host antitumour immune response.44 Suppression of the antitumour immune system is augmented by the inherent effects of CNI.

Immunosuppression also exposes the patient to infections with oncogenic viruses, which have been linked to bronchogenic carcinomas in mammalian models. Examples include Jaagsiekte sheep retrovirus causing pulmonary adenocarcinoma in sheep and Simian virus 40-related DNA sequences isolates in NSCLC.45 An association between oncogenic viruses and LC in humans is much less clear, and further work is required in this field.

Conclusion

LTRs represent a particularly vulnerable population in terms of LC development. The combination of underlying risk factors, exposures, immunosuppression and age all factor into an increased risk of LC development. The lack of data on the underlying mechanisms of development, and consensus screening and treatment guidelines add to the complexity of this clinical problem. The development of consensus statements and further study on this subject are required to inform clinical decision-making.

Table 3

Patient and transplant characteristics

PATIENT characteristics			Transplant characteristics
					Immunosuppression
Patient #	Age	Ethnicity	Indication	Single versus double	Induction agent	Calcineurin inhibitor maintenance	Antimetabolite maintenance	Steroid maintenance	mTOR inhibitor maintenance
1	76	Caucasian	COPD	D	N/A	TAC	None	Pred	N/A
2	73	Caucasian	IPF	D	BXB	TAC	None	Pred	N/A
3	67	Caucasian	IPF	R	BXB	CYC	None	Pred	N/A
4	74	Caucasian	IPF	L	AMB	TAC	MFM	Pred	N/A
5	61	Caucasian	IPF	R	BXB	TAC	None	Pred	N/A
6	74	Caucasian	COPD	D	BXB	TAC	None	Pred	N/A
7	60	Caucasian	CPFE	R	AMB	TAC	MFM	Pred	N/A
8	63	Caucasian	COPD	L	BXB	TAC	MFM	Pred	N/A
9	75	Caucasian	IPF	L	AMB	TAC	MFM	Pred	N/A
10	75	Caucasian	CPFE	R	BXB	TAC	MFM	Pred	N/A
11	76	Caucasian	IPF	L	BXB	TAC	MFM	Pred	N/A
12	61	Caucasian	ILD	L	AMB	TAC	MFM	Pred	N/A
13	73	Caucasian	COPD	L	BXB	TAC	AZA	Pred	N/A
14	80	Caucasian	CPFE	R	AMB	TAC	AZA	Pred	N/A
15	73	Caucasian	CPFE*	L	BXB	TAC	MFM	Pred	N/A
16	82	Caucasian	IPF	L	BXB	TAC	None	Pred	N/A
17	61	Caucasian	COPD	L	BXB	TAC	None	Pred	N/A
18	76	Caucasian	IPF	R	BXB	TAC	MFM	Pred	N/A
19	70	Caucasian	CPFE	R	AMB	TAC	AZA	Pred	N/A
20	63	Caucasian	IPF	R	AMB	TAC	MFM	Pred	N/A
21	76	African-American	COPD	L	BXB	TAC	MFM	Pred	N/A
22	66	Caucasian	COPD	L	BXB	TAC	MFM	Pred	N/A
23	59	Caucasian	COPD	R	AMB	TAC	None	Pred	N/A
24	58	Caucasian	IPF	L	BXB	TAC	MFM	Pred	N/A

*Features of bronchiectasis present with underlying CPFE.

AMB, alemtuzumab; AZA, azathioprine; BXB, basiliximab; COPD, chronic obstructive pulmonary disease; CPFE, combined pulmonary fibrosis with emphysema; CYC, ciclosporin; ILD, interstitial lung disease; IPF, idiopathic pulmonary fibrosis; MFM, mycophenolate mofetil; mTOR, mammalian target of rapamycin; Pred, prednisone; TAC, tacrolimus.

Table 4

Lung cancer characteristics

Patient #	Months since transplant	Location of tumour native versus allograft	Location of tumour	Smoking history in pack-years	Nodule size (mm)	Histology	TNM staging	Treatment	Mortality	Length of follow-up in months
1	84	Allograft	RUL	18	14	EBV smooth muscle tumour	T1N0M0	Surgical	Yes	24
2	0	Allograft	RML, LUL	0	N/A	AdenoSCC	N/A	None	Yes	13
3	24	Native	LLL	90	10	SCC	T1aN2M0	Surgical, chemotherapy, radiation	Yes	8
4	46	Native	RUL	24	29	Adeno	T1cN0M1a	Chemotherapy	Yes	2
5	48	Allograft	RUL	0	N/A	Adeno	TxN2M1	None	Yes	1
6	13	Allograft	R hilum	180	N/A	Adeno	TxN3M0	None	Yes	1
7	22	Native	LLL	25	20	SCLC	T2N1M0	Surgical, chemotherapy	No	33
8	26	Native	RML	60	40	SCC	T2N0M0	Surgical	No	21
9	48	Native	RUL	41	43	SCC	T3N0M0	Surgical	No	9
10	44	Native	LUL	36	22	SCC	T1cN0M0	Surgical	No	7
11	14	Native	RUL	6.6	45	Adeno	T2aN3M1a	None	Yes	4
12	12	Native	R hilum	30	52	SCC	T4N2M1c	Chemotherapy, radiation	Yes	5
13	26	Allograft	L hilum and pericardium	35	62	SCC	T3N0M1c	None	Yes	<1
14	48	Native	LUL	57	23	Adeno	T1cN0M0	Radiation	Yes	9
15	14	Native	RUL	13	14	SCC	T1aN0M0	Surgical	No	30
16	24	Native	RUL	0	88	SCC	T4N0M1a	Radiation	Yes	2
17	6	Allograft	LUL	40	19	NSCLC	T1bN3M1a	None	Yes	3
18	37	Allograft	Right lung	25	N/A	Adeno	TxN3M1c	None	Yes	1
19	23	Native	LUL	40	79	SCC	T4N0M0	Chemotherapy, radiation	Yes	5
20	19	Native	LLL	7	30	SCC	T1cN0M0	SRS SBRT	No	8
21	30	Allograft	L hilum	80	N/A	NSCLC	N/A	None	No	19
22	0	Native	LUL	30	6	Adeno	T1cN0M0	Surgical resection	No	44
23	5	Native	LUL	80	25	SCLC	T3N1M1	Chemotherapy	Yes	6
24	40	Native	RLL	52	10	SCLC	T1cN1M1a	Chemotherapy	No	6

Adeno, adenocarcinoma; EBV, Epstein-Barr virus; N/A, not available; NSCLC, non-small cell lung cancer; SBRT, Stereotactic Body Radiotherapy; SCC, squamous cell carcinoma; SCLC, small cell lung cancer; SRS, Stereotactic Radiosurgery; TNM, tumour, node, metastases.