Background
Primary intracardiac neoplasms are rare tumors, with an estimated prevalence of between 0.02 and 0.25% of the population [
1‐
3]. Atrial myxomas originating in the left atrium make up most of these tumors [
4,
5]. Greater than 90% of atrial myxomas are sporadic and the rest are the result of a hereditary condition known as the Carney complex. Carney complex is inherited in an autosomal dominant fashion due in most cases to inactivating mutations of the
PRKAR1A gene and is characterized by pigmented lesions of the skin, myxomas (cardiac and cutaneous), and multiple endocrine tumors [
6]. Mutations in
PRKAR1A were previously not thought to be responsible for the development of isolated, sporadic cardiac myxomas, but genetic alterations in this gene have recently been identified in a minority of such tumor samples [
7,
8]. Cardiac myxomas are considered to be benign and cured by complete surgical resection of the cardiac lesion. Recurrences have been observed, but are much more likely to be seen in cases of familial myxoma (12–22% recurrence rate) than sporadic myxoma (1–3%) [
4,
9].
Despite their generally benign nature, cardiac myxomas may have devastating consequences due to their location and ability to spread through the blood. Embolic events occur in 30 to 40% of patients with cardiac myxomas and the central nervous system (CNS) is the most frequent site of embolism [
4,
10,
11]. This generally manifests as ischemic events, but aneurysmal dilation due to tumor invasion into cerebral vessel walls and resultant intracerebral hemorrhages are also seen [
12]. In very rare cases, metastatic disease with clear-cut invasion into the CNS parenchyma is observed. The mechanism behind viable, invasive tumor cell dissemination to the CNS from tumors with benign histopathology is not well understood. There is currently no evidence to the best of our knowledge that patients with tumors due to Carney complex are more likely to experience metastatic consequences. Due to the very small number of patients experiencing CNS metastases, there is no standardized management when they do occur.
Here we describe a rare case of a patient who developed progressive brain metastases as a delayed consequence of tumor embolism a year after removal of an atrial myxoma. Whole exome sequencing of tumor tissue from her heart and brain revealed multiple somatic mutations in PRKAR1A. Additional tissue from an earlier benign cystadenoma and buccal swab showed no similar mutation. Our patient had no known family history of myxomas or Carney complex.
Whole exome sequencing
Methods
Deoxyribonucleic acid (DNA) was extracted from tumor tissue microdissected from sections after deparaffinization. The concentration of tumor cells in the regions dissected was estimated from adjacent sections cut from the paraffin blocks. DNA from buccal swabs (Isohelix) was prepared by methods similar to those used for tissue, except for skipping deparaffinization and reversal of formalin crosslinking. The DNA was resuspended in a buffer solution (10 mM Tris, 0.1 mM EDTA) and DNA concentration determined using the Qubit® 2.0 Fluorometer (Thermo Fisher Scientific).
Libraries of DNA fragments for sequencing were prepared by multiplex polymerase chain reaction (PCR) of the genomic DNA. The Ion AmpliSeq™ Exome RDY 4×2 panel (Thermo Fisher Scientific) was used for whole exome sequencing of the heart valve, left ovary, right ovary, and brain samples. The amounts of input genomic DNA for whole exome sequencing were 80 ng for the heart valve, 100 ng for the brain, and 60 ng for the ovarian sample. The Ion AmpliSeq Comprehensive Cancer Panel (Thermo Fisher Scientific) (primer pools 2 and 3 only) was used to prepare libraries for targeted DNA sequencing of the heart valve and right ovary (10 ng input DNA for each pool).
The PCR, amplicon digestion, and barcode adapter ligation were performed using Eppendorf® Mastercycler® Pro S Thermal Cyclers (Eppendorf). Libraries were quantitated by quantitative PCR (qPCR) using the Ion Library TaqMan® Quantitation Kit (Thermo Fisher Scientific) and the ViiA 7 real-time PCR system (Thermo Fisher Scientific). DNA libraries from tumor and buccal swab germline DNA were separately barcoded, mixed in a 3:1 tumor to germline ratio, and sequenced together.
Sequences obtained for fragments were aligned to the hg19 reference sequence using the Ion Torrent Suite™ software version 5.2 (Thermo Fisher Scientific). Variant calling and annotation were performed by the Ion Reporter™ software version 5.0 (Thermo Fisher Scientific) using the AmpliSeq™ Exome tumor-normal pair workflow and the AmpliSeq™ CCP single sample workflow for whole exome and targeted sequencing, respectively. Called variants were individually inspected and evaluated using the Integrative Genomics Viewer (IGV).
Results
The microdissected tissue from the heart was estimated to contain approximately 90% tumor cells. The whole exome sequencing of DNA from this lesion had a mean read depth of 223.3 nucleotides, along with a mean read depth of 171.8 for the accompanying germline DNA. The assembled sequence showed 46 somatic mutations – variants not found in the germline DNA collected by buccal swab – within or closely bordering the coding sequences of 39 different genes. Attention was focused on 12 mutations that were non-synonymous, and had a variant allelic fraction (VAF) of ≥ 10 with a read depth of > 50×. Four of these mutations involved the
PRKAR1A gene (one missense mutation, one insertion, one deletion, and a 5× amplification; Table
1). In addition, a synonymous mutation was found within
PRKAR1A. None of the other mutations were in genes that have been generally implicated in tumor cell proliferation or survival.
Table 1PRKAR1A mutations detected within the tissues
Three of the mutations in PRKAR1A (the missense and synonymous mutations, and a five-base pair deletion) were tightly clustered within the gene and were present at comparable VAFs (44–55%). The phase of a 20-base pair insertion present at 12% could not be directly determined with respect to these three mutations based on next generation sequence analysis, in which DNA is sequenced in small fragments (average read length 175 nucleotides).
To confirm the presence of the PRKAR1A mutations and better assess the VAFs for these alterations, targeted sequencing was carried out on the same lesional DNA using pools of multiplex primers from the Ion AmpliSeq™ Comprehensive Cancer Panel that separately covered the regions of the mutations within the gene. The mutations detected by whole exome sequencing were again found by targeted sequence with roughly the same VAF score for the five-base pair deletion and at a slightly reduced level for the missense mutation (VAF 41%, 250/617 reads and 29%, 249/863 reads, respectively). The 20-base pair insertion was found at an identical VAF (12%, 1027/8409 reads). Resequencing of DNA from normal tissue using the Comprehensive Cancer Panel failed to detect any of the PRKAR1A mutations, with an average read depth of 1852 covering the regions containing those mutations.
The lesional tissue examined from the brain had a much lower concentration of tumor cells, estimated to be approximately 20%. All of the PRKAR1A mutations identified in the heart tissue were present in the brain tissue, albeit at much lower VAFs (the 5-base pair deletion at 7%, the missense and synonymous mutations at 6% each, and the 20-base pair insertion at 1.9%).
Mutations within the PRKAR1A gene were not detected in DNA from the cystadenoma of the right ovary using the Comprehensive Cancer Panel. Attempts to sequence DNA extracted from the much less abundant tissue available from the cystadenoma of the left ovary yielded results that did not meet quality metrics.
Discussion and conclusions
In general, atrial myxomas are pathologically benign lesions; however, their malignant potential has been described in small case series and individual case reports in the literature [
4,
9,
15‐
25]. The CNS is the most common location for remote growth of myxomatous material. Autopsy series and retrospective reviews of patient cohorts have estimated the incidence of cerebral parenchymal metastases to be between 1.8 and 4.5% of patients with myxomas [
12,
15]. Risk factors leading to metastasis are poorly understood and the clinical and pathological features of patients with cerebral parenchymal metastases are varied. In several case reports of myxoma metastases, metastatic lesions appeared more cellular and pleomorphic than the original tumor, suggesting there had been malignant transformation [
26]. In another report of a patient with sarcomatous-appearing metastases and a history of benign cardiac myxoma, a retrospective review of the initial cardiac tissue revealed an area at the periphery of the tumor that had more malignant features, suggesting a possible “malignant myxoma” at the outset [
15]. Other patients had metastatic disease at distant sites from typical benign-appearing myxomas without any aggressive features on histopathology [
16,
21].
As demonstrated in our case, myxoma cells from tumor emboli to the CNS vasculature can attach to the endothelial wall, weaken the endothelium, and invade the elastic lamina leading to vascular wall dilatation and so called “oncotic-aneurysm” formation [
27]. The natural history of these aneurysms is not certain given their rarity and varied outcomes. Lesions have been reported to behave anywhere on the spectrum from self-resolving to enlarging and may cause both ischemic and hemorrhagic events [
28,
29]. In rare circumstances, as evidenced by our patient’s pathology, myxoma cells may penetrate through the vessel wall of these aneurysms and into the surrounding brain tissue, leading to the formation of parenchymal lesions. This mechanism has been demonstrated previously and other case reports of brain metastases describe cerebral aneurysms on imaging in association with parenchymal lesions [
12,
30]. However, not all reported cases of brain metastases describe these imaging findings. Factors affecting the ability of tumor cells to disseminate to the brain, penetrate blood vessel walls, and proliferate within the brain remain to be identified. Prior work has suggested that production of IL-10 by the tumor may play a role, but further studies are needed [
25,
31].
Genetic analysis of our patient’s tissue showed multiple mutations within the
PRKAR1A gene in both the brain metastasis and cardiac tumor sample, but not within tissue derived from a benign ovarian cystadenoma or a buccal DNA swab. While ovarian cystadenomas may be a feature of Carney complex, the absence of
PRKAR1A mutations in the cystadenoma suggests that her heart tumor was a sporadic myxoma. The failure to find the
PRKAR1A mutations in the material collected by buccal swab is consistent with this conclusion, although there is a very small possibility that our patient is mosaic for a mutation at a very low level of mutant cells and that the buccal mucosa and ovarian tissues were spared the mutation present in other somatic tissues. The
PRKAR1A gene encodes the type 1A regulatory subunit of the cyclic adenosine monophosphate (cAMP)-dependent enzyme protein kinase A (PKA) and functions as a tumor suppressor [
32]. The PRKAR1A protein exerts a repressive effect on the kinase activities of the PKA complex. Mutations inactivating this subunit lead to increased cell proliferation in cAMP-responsive tissues and are believed to play a role in tumorigenesis. All of the intragenic mutations detected within the
PRKAR1A gene in this case (with the exception of the synonymous mutation) should inactivate the protein encoded by the allele containing the mutation. Both indel mutations result in frameshifts and the missense mutation is predicted to have a deleterious effect on the structure and function of the protein, according to the SIFT and PolyPhen prediction programs. Whether both alleles are affected by these mutations is not possible to determine by next generation sequencing, so the extent to which
PRKAR1A activity is lost within the tumor cells is not known. However, the 5× amplification (five copies of the
PRKAR1A gene) suggests that the allele carrying the deletion, missense, and synonymous mutations is the allele that underwent amplification, resulting in four copies of that allele within the tumor cells of the heart. This ratio was somewhat lower (3×) in the metastatic tumor analyzed from the brain. If this interpretation is true, both
PRKAR1A alleles had suffered deleterious mutations. (The amplification of the tumor suppressor is unexpected and unexplained. Amplification is usually associated with oncogenes, not tumor suppressors like
PRKAR1A, and may coexist with activating mutations within the amplified genes).
The VAFs for the mutations in genes other than PRKAR1A found in the tumor cells (not shown) – all approximately 25% – are consistent with a tumor cell concentration of approximately 50% in the tissue analyzed (despite a higher estimate by histopathology), assuming that these mutations are heterozygous. That the insertion mutation in PRKAR1A is lower (12%) probably reflects the likely amplification in the opposite allele. The absence of detectable PRKAR1A mutations in the germline DNA from the buccal swab and right cystadenoma of the ovary argues against mosaicism for Carney complex, although ovarian cystadenomas have been noted to be more prevalent in patients with Carney complex compared to the general population. In this case, the ovarian cystadenomas resected many years earlier were probably sporadic and coincidental with the later development of a cardiac myxoma.
There has been debate as to whether mutations in
PRKAR1A play a role in the development of isolated cardiac myxoma. Initially, genetic analyses conducted on small patient cohorts with isolated cardiac myxomas showed that mutations were not found in these cases. In two recent studies,
PRKAR1A mutations were found in sporadic cardiac myxomas. In one of these studies, 33 out of 103 tumors lacked expression of the PRKAR1A protein and nine patients had mutations in
PRKAR1A identified [
7]. A subsequent study found that seven out of eight sporadic tumors had mutations in
PRKAR1A on whole exome sequencing analysis [
8]. Whether this mutation alters the clinical course of sporadic myxomas is not clear. On histopathologic examination, myxomatous tissues from hereditary and isolated myxomas appear very similar. Although a cardiac myxoma associated with Carney complex is more likely to recur, there are no data to the best of our knowledge that these tumors are more likely to metastasize. In addition, prior case reports on brain metastases have not included whole exome sequencing data from the tumor tissues.Unfortunately, our patient’s lesions grew quickly and caused significant neurological deficits, prompting the rapid initiation of treatment. As brain metastases are an infrequent complication of a rare tumor, there is no standard accepted treatment and therapeutic strategies derive from experience with small numbers of patients. There are as yet no available agents to target the
PRKAR1A mutation. Therapy with doxorubicin has been attempted in a patient with an oncotic aneurysm but the aneurysm continued to enlarge despite treatment [
28]. Altundag
et al. treated a patient similar to ours with whole brain radiotherapy and achieved stability for at least 4 years (the patient was still alive and stable at time of publication) [
16]. Another report described decrease in size of multiple parenchymal lesions with whole brain radiotherapy [
33]. A third patient was treated with whole brain radiotherapy followed by chemotherapy with ifosfamide and doxorubicin and achieved long-term control [
34]. Our patient’s lesions showed partial response to whole brain radiotherapy and she has now been stable by imaging and clinical criteria for 1 year.
Our case illustrates a rare occurrence of atrial myxoma with brain parenchymal metastases and highlights the ability of myxoma cells to migrate though cerebral vessel walls, form an oncotic aneurysm, and then invade the brain parenchyma. It also provides further evidence that PRKAR1A mutation can occur in sporadic myxomas. The precise molecular features and risk factors that allow myxoma cells to invade surrounding tissue have yet to be elucidated. Among genes recognized as having functions related to tissue invasion and metastasis, none were found to be mutated within the tissue of the heart or brain lesions. Whether the PRKAR1A mutation in sporadic myxomas alters the clinical course of disease or increases the likelihood of metastasis is not clear. Further information on the genotype–phenotype correlation of PRKAR1A mutations is needed to help predict the clinical behavior of tumors with this abnormality. In addition, the PKA pathway regulated by PRKAR1A offers a possible target for systemic therapy for tumors harboring PRKAR1A mutations, in particular those tumors associated with the most serious complication of cardiac myxomas: cerebral metastases.
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