Abstract
Primary tumors have common sites of metastasis such as lymph nodes, bones, liver, lungs, and brain; however, they can also metastasize to other uncommon sites such as adrenals, bone marrow, and skin among others. Our study aimed to investigate the relationship between uncommon sites of metastasis at the time of diagnosis and median survival in a number of primary tumors using the Surveillance, Epidemiology, and End Results (SEER) database.
This retrospective cohort study conducted between September–October 2021 included patient-level SEER data for 2016–2018 using SEER Research Data, 9 Registries, Nov 2020 Sub (1975–2018). Descriptive analysis for complete cohort and median survival for each primary within the cohort was performed using R software.
A total of 25,345 patients (females, 51.4%) were diagnosed with primary tumors with metastasis to uncommon sites at the time of diagnosis; the mean age at diagnosis was 68 years. Lung and bronchus primaries constituted the largest proportion of cohort (41.9%) that metastasized to uncommon sites, followed by nonHodgkin lymphoma-nodal (7.4%), pancreas (6.6%), stomach (3.7%), and ovarian (3.4%). The incidence of metastasis to uncommon sites was most common in respiratory cancers in ages 61–80 years (25%) and least in breast primaries in ages 18–40 years (0.1%), and was higher in Whites compared to other races. Regarding median survival, liver cancer with metastasis to uncommon sites had the worst prognosis (1 month), whereas small intestine tumors were associated with a better prognosis, median survival of 13 months.
In this cohort study, the lung and bronchus cancers were the most common primaries metastasized to uncommon sites at diagnosis. The liver tumor had the worst survival compared to other tumors. These findings will help redirect the available screening tools to improve survival in patients with primary tumors with metastasis at diagnosis and may also play an essential role in future research and achieve a better prognosis for cancer patients.
Keywords: cohort, SEER database, survival, prognosis, metastasis
1. Introduction
Cancers are among the leading causes of death worldwide. International Agency for Research on Cancer by the World Health Organization (WHO) reported the global incidence of cancers in 2020 being approximately 19.2 million, resulting in a mortality of 9.9 million annually.[1] By 2040, the number of new cancer cases is expected to rise to 30.2 million and the mortality to 16.3 million.[2] In the United States (US), the overall incidence of cancers was 442.4 per 100,000, and mortality was reported to be 158.3 per 100,000.[3]
The leading cause of death in most cancer patients is metastasis.[4] Morbidity and mortality associated with metastasis are often due to direct organ damage or compression secondary to growing lesions, paraneoplastic syndromes, or treatment complications.[4] Most metastatic lesions are surgically untreatable and may need chemotherapy, hormone therapy, and radiation therapy for palliative purposes to prolong survival.
Although various sites of tumor metastasis have been defined, some sites have a higher prevalence of metastasis than others. Liver is a common site of metastasis, especially for gastrointestinal tumors.[5,6] Erichsen et al reported an increased prevalence of liver metastasis through the decades with no improvement in prognosis.[7] Bone metastases have a high prevalence, especially in prostate, breast, and renal cancers.[8] Brain metastases are common in lung cancers, melanomas, and renal cancers.[9] Lung metastasis is common in cancers of head and neck, breast, stomach, pancreas, kidney, bladder, genitourinary tract, and sarcomas.[10] Lymph nodes (LNs) are also common sites of metastasis and may be a predictor of survival.[11]
Cancer preventive measures have been negatively affected during the COVID-19 pandemic with decreased numbers of screening tests and the subsequently reported number of new cases.[12] American Cancer Society recommended postponing all routine screening programs and elective procedures.[12,13] This led to a delay in the diagnosis of new cancer cases affecting the clinical management and prognosis due to late presentation. Therefore understanding the different sites of metastasis at the time of diagnosis and the associated survival may help to redirect the available resources to improve cancer care and improve the survival and the quality of life of cancer patients.
In our study, we used the Surveillance, Epidemiology, and End Results (SEER) database to identify the patients with uncommon sites (other than liver, bone, brain, lung, and distal lymph nodes) and calculated their associated survival in each primary to provide a comparative prognosis.
2. Methodology
2.1. Data source and cohort population
The SEER database (SEER Research Data, 9 Registries, Nov 2020 Sub (1975–2018)) included around 28% of the US population and was used to access all the patients presented with metastasis at diagnosis in uncommon sites between 2016 and 2018.[14] Uncommon sites of metastasis coded as other sites in SEER database are those that do not involve the liver, bone, brain, lung, and distal LNs. Some examples include but are not limited to the adrenal gland, bone marrow, pleura, malignant pleural effusion, peritoneum, and skin.
Patients with metastasis at diagnosis in uncommon sites were included in our study, without restrictions on age, race, year of diagnosis, or histological type. All included patients were with malignant behavior and known age and otherwise excluded. For survival analysis, patients with unknown survival months were excluded from the analysis.
Informed consent from patients was not obtained as the data is publicly available. No human or animal objects were directly involved thus ethical review was also not required.
2.2. Statistical analysis
National Cancer Institute SEER*Stat software (www.seer.cancer.gov/seerstat), version 8.3.9 was used to extract the data. Data were exported to R software to conduct the analysis.[15] Analysis was conducted showing the number of patients in different primaries, their proportions in the whole cohort, concomitant common sites of metastasis, and median survival in months. Primary tumors were subsequently sorted and combined into 6 main categories; respiratory, gastrointestinal (GI), genitourinary (GU), miscellaneous, lymph-blood-nervous, and breast to compare the different age groups, races, and gender. Primary tumors that fall under each category are summarized in Table S1, Supplementary Material http://links.lww.com/MD/G794. Patients in each broader category were divided into 4 groups according to age: 18-–40 years, 41–60 years, 61–80 years, and older than 80 years. Gender was divided into males and females. Race was divided into White, Black, and Other (American Indian/Alaska Native, Asian/Pacific Islander).
3. Results
3.1. Baseline characteristics
Our analysis showed 25,345 patients diagnosed with metastasis to uncommon sites with a mean age of 68 ± 17 years. There was a female predominance in our cohort of 13,033 (51.4 %). About 33.4%, 34.9%, and 32.5% of the patients were diagnosed in 2016, 2017, and 2018, respectively. There were 6144 (24.2%) patients who had concomitant bone metastasis, 6045 (23.8%) had liver metastasis, and 5232 (20.6 %) had lung metastasis. Incidence of concomitant distant LNs and brain metastasis was the lowest, 4903 (19.3%) and 2731(10.8%), respectively. Table 1 summarizes the baseline characteristics of our cohort.
Table 1.
Baseline characteristics of the included cohort with metastasis to uncommon sites
| Characteristic | Number | Percentage |
|---|---|---|
| Number of pts with Mets at DX-Other | 25,345 | 100 |
| Age | 68 (17) * | |
| Sex | ||
| Male | 12,312 | 48.6 |
| Female | 13,033 | 51.4 |
| Race | ||
| White | 19,372 | 76.4 |
| Other (American Indian/Alaska Native, Asian/Pacific Islander) | 2743 | 10.8 |
| Black | 3164 | 12.5 |
| Unknown | 66 | 0.3 |
| Year of diagnosis | ||
| 2016 | 8463 | 33.4 |
| 2017 | 8640 | 34.9 |
| 2018 | 8242 | 32.5 |
| Cause of death | ||
| Dead (attributable to cancer dx) | 14,628 | 57.7 |
| Alive or dead of other cause | 10,585 | 41.8 |
| Dead (missing/unknown COD) | 130 | 0.5 |
| Co-existent Mets at DX† | ||
| Mets at DX-Distant LN | 4903 | 19.3 |
| Mets at DX-lung | 5232 | 20.6 |
| Mets at DX-liver | 6045 | 23.8 |
| Mets at DX-bone | 6144 | 24.2 |
| Mets at DX-brain | 2731 | 10.9 |
Mets at DX: metastasis at diagnosis; COD: cause of death; dx: diagnosis.
Mean (SD).
NB: the numbers are not summable because categories are not mutually exclusive.
3.2. The common sites and other sites of metastasis.
Lung and bronchus cancers were the most common tumors metastasized to uncommon sites with 10,612 (41.9%) patients. The most common type of systematic metastasis was bone with 3754 (35.4%), followed by the lung 2307 (21.7%). NHL (nonHodgkin lymphoma)-nodal metastasized to uncommon sites in 1871 (7.9%) patients with a systemic metastasis to lung in 177 (9.5%) patients followed by liver in 167 (8.9%) patients. Pancreas metastasized to other sites in 1690 (6.7%) patients with concomitant systematic metastasis to liver (49.5%) and lung (20.3%). Stomach metastasized to uncommon sites in 940 (3.7%) patients with concomitant systematic metastasis to LNs (23.1%) and liver (22.4%). Finally, ovary metastasized to uncommon sites in 885 (3.4%) patients with concomitant systematic metastasis to liver (18.9%) and LNs (18.4%). Detailed numbers and analysis of the primary tumors with their median survival is represented in Table 2 and Figure 1A.
Table 2.
Incidence proportion and median survival of patients identified with uncommon or other sites of metastases by primary cancer site
| Site | Number of patients with uncommon metastases at diagnosis | Incidence proportion of uncommon metastases among entire cohort (%) | Median survival among patients with uncommon metastases (mo, IQR) | Type of systemic metastasis | Number of patients* | (%) | Median survival (mo, IQR) |
|---|---|---|---|---|---|---|---|
| Lung and bronchus | 10,612 | 41.9 | 3(7) | Distal LNs | 1991 | 18.8 | 3(7) |
| Lung | 2307 | 21.7 | 2(6) | ||||
| Brain | 2191 | 20.7 | 3(6) | ||||
| Bone | 3754 | 35.4 | 3(6) | ||||
| Liver | 2236 | 21.1 | 2(5) | ||||
| NHL – nodal | 1871 | 7.4 | 11(18) | Distal LNs | 109 | 5.8 | 11(13) |
| Lung | 177 | 9.5 | 7.5(14) | ||||
| Brain | 37 | 2 | 5(9) | ||||
| Bone | 303 | 16.2 | 10(16) | ||||
| Liver | 167 | 8.9 | 7(16.25) | ||||
| Pancreas | 1690 | 6.7 | 2(6) | Distal LNs | 263 | 15.6 | 2(4) |
| Lung | 343 | 20.3 | 1(4) | ||||
| Brain | 25 | 1.5 | 1.5(4.5) | ||||
| Bone | 129 | 7.6 | 1(4) | ||||
| Liver | 836 | 49.5 | 1(4) | ||||
| Stomach | 940 | 3.7 | 3(8) | Distal LNs | 217 | 23.1 | 3(7) |
| Lung | 95 | 10.1 | 2(4) | ||||
| Brain | 16 | 1.7 | 1(1.25) | ||||
| Bone | 82 | 8.7 | 2.5(5) | ||||
| Liver | 211 | 22.5 | 2(4) | ||||
| Ovary | 885 | 3.5 | 8(17) | Distal LNs | 163 | 18.4 | 8(16) |
| Lung | 111 | 12.5 | 5(15) | ||||
| Brain | 4 | 0.5 | 14(10) | ||||
| Bone | 17 | 1.9 | 7(15) | ||||
| Liver | 168 | 19 | 2(4) | ||||
| Breast | 770 | 0.3 | 7(15) | Distal LNs | 295 | 38.3 | 7(14.5) |
| Lung | 276 | 35.8 | 6(11.75) | ||||
| Brain | 81 | 10.5 | 4(10) | ||||
| Bone | 449 | 58.3 | 7(14) | ||||
| Liver | 183 | 23.8 | 4(10.5) | ||||
| Corpus uteri | 715 | 2.8 | 8(14) | Distal LNs | 121 | 16.9 | 5(11) |
| Lung | 92 | 12.9 | 5.5(9) | ||||
| Brain | 7 | 1 | 5(3) | ||||
| Bone | 35 | 5 | 4(6.5) | ||||
| Liver | 71 | 9.9 | 6(10.5) | ||||
| Kidney and renal pelvis | 618 | 2.4 | 5(11) | Distal LNs | 199 | 32.2 | 4(8) |
| Lung | 329 | 53.2 | 4(9.25) | ||||
| Brain | 69 | 11.2 | 2(6) | ||||
| Bone | 212 | 34.3 | 4(7) | ||||
| Liver | 131 | 21.2 | 4(10.5) | ||||
| NHL - extranodal | 433 | 1.7 | 12(19) | Distal LNs | 31 | 7.2 | 9(15) |
| Lung | 31 | 7.2 | 10(18.5) | ||||
| Brain | 4 | 0.9 | 5.5(14) | ||||
| Bone | 37 | 8.6 | 5(10) | ||||
| Liver | 23 | 5.3 | 4(12.5) | ||||
| Cecum | 404 | 1.6 | 7(13) | Distal LNs | 64 | 15.8 | 5(12) |
| Lung | 60 | 14.9 | 3.5(9.25) | ||||
| Brain | 1 | 0.2 | 3(0) | ||||
| Bone | 15 | 3.7 | 3(8) | ||||
| Liver | 160 | 39.6 | 4(12) | ||||
| Melanoma of the skin | 379 | 1.5 | 6(13) | Distal LNs | 114 | 30.1 | 4(9) |
| Lung | 162 | 42.7 | 4(8) | ||||
| Brain | 120 | 31.7 | 4(8) | ||||
| Bone | 93 | 24.5 | 3(6) | ||||
| Liver | 92 | 24.3 | 3.5(9.25) | ||||
| Sigmoid colon | 344 | 1.4 | 7(12) | Distal LNs | 63 | 18.3 | 8(12) |
| Lung | 60 | 17.4 | 4(10.5) | ||||
| Brain | 6 | 1.7 | 2.5(6.25) | ||||
| Bone | 20 | 5.8 | 3.5(9.75) | ||||
| Liver | 157 | 45.6 | 5(12) | ||||
| Esophagus | 327 | 1.3 | 3(7) | Distal LNs | 131 | 40.1 | 3(5.5) |
| Lung | 88 | 26.9 | 2.5(4.25) | ||||
| Brain | 21 | 6.4 | 2(4) | ||||
| Bone | 110 | 33.6 | 3(6) | ||||
| Liver | 127 | 38.8 | 2(4.5) | ||||
| Prostate | 290 | 1.1 | 10(16) | Distal LNs | 117 | 10.3 | 9(17) |
| Lung | 41 | 14.1 | 7(14) | ||||
| Brain | 8 | 2.8 | 2(5.75) | ||||
| Bone | 184 | 63.5 | 9(14) | ||||
| Liver | 32 | 11 | 5.5(14.5) | ||||
| Liver | 286 | 1.1 | 1(5) | Distal LNs | 54 | 18.9 | 2(4.75) |
| Lung | 71 | 24.8 | 1(3) | ||||
| Brain | 2 | 0.7 | 2(0) | ||||
| Bone | 42 | 14.7 | 2(4) | ||||
| Liver | 17 | 5.9 | 3(7) | ||||
| Small intestine | 271 | 1.1 | 13(19) | Distal LNs | 30 | 11.1 | 8.5(23.5) |
| Lung | 21 | 7.8 | 3(10) | ||||
| Brain | 3 | 11.1 | 5(13.5) | ||||
| Bone | 10 | 3.8 | 10(12) | ||||
| Liver | 104 | 38.4 | 11(18) | ||||
| Appendix | 258 | 1 | 11(15) | Distal LNs | 15 | 5.8 | 5(12.5) |
| Lung | 9 | 3.5 | 6(7) | ||||
| Brain | 0 | 0 | NA | ||||
| Bone | 2 | 0.8 | 1.5(.5) | ||||
| Liver | 19 | 7.4 | 11(16) | ||||
| Ascending colon | 227 | 0.9 | 6(11) | Distal LNs | 67 | 29.5 | 6(9.5) |
| Lung | 33 | 14.5 | 4(5) | ||||
| Brain | 3 | 1.3 | 4(4.5) | ||||
| Bone | 13 | 5.7 | 3(7) | ||||
| Liver | 101 | 44.5 | 5(9) | ||||
| Large intestine, NOS | 227 | 0.9 | 2(9) | Distal LNs | 38 | 16.7 | 3(5.5) |
| Lung | 47 | 20.7 | 2(5.5) | ||||
| Brain | 3 | 1.3 | 1(2) | ||||
| Bone | 17 | 7.5 | 1(6) | ||||
| Liver | 98 | 43.2 | 2(7.75) | ||||
| Rectum | 222 | 0.9 | 6(12) | Distal LNs | 66 | 29.7 | 3.5(7.75) |
| Lung | 54 | 37.8 | 4.5(13) | ||||
| Brain | 9 | 4.1 | 2(6) | ||||
| Bone | 34 | 14.3 | 4.5(7.75) | ||||
| Liver | 105 | 47.3 | 5(12) | ||||
| Intrahepatic bile duct | 191 | 0.8 | 3(6) | Distal LNs | 64 | 33.5 | 3.5(6) |
| Lung | 43 | 22.5 | 2(5.5) | ||||
| Brain | 0 | 0 | NA | ||||
| Bone | 21 | 11 | 2(5) | ||||
| Liver | 46 | 24.1 | 3(6) | ||||
| Gallbladder | 179 | 0.7 | 3(7) | Distal LNs | 28 | 15.6 | 5.5(6.25) |
| Lung | 20 | 11.2 | 3(7) | ||||
| Brain | 1 | 0.6 | 7(0) | ||||
| Bone | 10 | 5.6 | 6.5(7.5) | ||||
| Liver | 78 | 43.6 | 2(7) | ||||
| Urinary bladder | 179 | 0.7 | 2(6) | Distal LNs | 49 | 27.8 | 2(4) |
| Lung | 47 | 26.3 | 1(2) | ||||
| Brain | 8 | 4.5 | 5.5(10.75) | ||||
| Bone | 36 | 20.1 | 1(5) | ||||
| Liver | 42 | 23.5 | 1(2) | ||||
| Cervix uteri | 121 | 0.5 | 7(12) | Distal LNs | 49 | 40.5 | 6(12) |
| Lung | 23 | 19 | 3(10) | ||||
| Brain | 1 | 0.8 | 1(0) | ||||
| Bone | 15 | 12.4 | 9(13) | ||||
| Liver | 19 | 15.7 | 3(7) | ||||
| Anus, anal canal and anorectum | 28 | 0.1 | 5(12.25) | Distal LNs | 8 | 28.6 | 9(16.5) |
| Lung | 2 | 7.1 | 3.5(1.5) | ||||
| Brain | 0 | 0 | NA | ||||
| Bone | 4 | 14.3 | 3.5(2.25) | ||||
| Liver | 7 | 0.3 | 4(2) |
IQR: Interquartile range.
The numbers are not summable because categories are not mutually exclusive.
Figure 1.
A: The number of patients with identified metastases to uncommon sites at diagnosis by primary cancer site. NHL = nonHodgkin lymphoma. B: The number of patients with identified metastases to uncommon sites at diagnosis by the subtypes of the primary cancer site. NOS = not otherwise specified.
The most common subsites to metastasize to other sites are the upper lobe of the lung 4825 (19%), lower lobe of the lung 2610 (10.3%), lung, not otherwise specified 2020 (8%), and lymph nodes of multiple regions 906 (3.6%) (Fig. 1B).
3.3. Incidence proportion of patients with identified metastases to other sites at diagnosis by primary cancer site as stratified by age, race, and gender.
Incidence of metastasis to uncommon sites was most common in respiratory cancers in ages of 61-80 years and least in breast cancer primaries in young ages 18–40 years. GI and GU primaries still show a higher number in all ages with more predilection in 61–80 years (Table S2, Supplementary Material http://links.lww.com/MD/G794).
There was a noticeable higher number for metastasis to other sites with White race with the same order of incidence in primaries; respiratory primaries were the most common. Despite Black and other races (American Indian/Alaska Native, Asian/Pacific Islander) did not show a remarkable difference; there were higher incidences with Black race except for GI primaries and lymph, blood, and nervous primaries, which were higher in other races (Table S3, Supplementary Material http://links.lww.com/MD/G794).
The differences in incidence are somewhat minor between both sexes, with more prediction to higher incidence to males. Respiratory primaries are still the most common between both genders. (Table S4, Supplementary Material http://links.lww.com/MD/G794).
3.4. Survival
Liver cancer was associated with the worst prognosis, with a median survival of 1 month among patients with uncommon metastases. In the case of systemic metastasis, the median survival ranged between 1 month in LNs metastasis and 3 months in liver metastasis. The pancreas, large intestine, and urinary bladder followed by liver have a median survival of two months. Lung and bronchus, stomach, esophagus, intrahepatic bile duct gallbladder have a median survival of 3 months. Small intestine tumors were associated with a better prognosis than the aforementioned tumors, with a median survival of 13 months.
Survival was affected with concomitant systematic affection. For example, lung and bronchus primaries were associated with earlier death if metastasis to the liver. NHL-nodal showed worse survival if metastasized to the brain; 5 months while 11 months if metastasized to LNs. The detailed survival rates are represented in Table 2 and Figure 2.
Figure 2.
The median survival (in months) of the primary cancer site with identified metastases to uncommon sites at diagnosis. NHL = nonHodgkin lymphoma.
4. Discussion
Our study showed that the most common primaries metastasized to uncommon sites were the lung and bronchus cancers, followed by NHL-nodal, pancreas, stomach, and ovary. Demographically, metastasis to uncommon sites was more common among 61–80 years age group (55.6%), followed by the age group of 41–60 years (23.3%), which implicates the elderly to be a subset of the population, not only being at risk of developing cancer, but also developing metastasis to uncommon sites. In the USA, 80% of all cancers are diagnosed at the age of 55 years or older.[11] Respiratory, GI, GU, and lymph-blood-nervous categories showed a male predilection except for breast, which is more common in females. The incidence proportion of uncommon metastasis was highest for the White race, 76.6% of all incidence followed by African Americans (12.5%) and other races (10.9%). Such a high incidence proportion of uncommon metastasis correlates with the 76.3% of the cohort being White.
Lung and bronchus cancers accounted for the most common primary with uncommon metastasis at diagnosis, with a median survival of 3 months. Lung cancer, when are detected, is often in a metastatic stage IV.[16] Bone, brain, and liver are common sites of metastasis for respiratory cancers, which is consistent with our findings.[17–19] Heart and skin may be uncommon sites of metastasis.[20,21]
NHL is the second most common cancer with uncommon metastasis at diagnosis. Our findings suggest that the nodal form of NHL is more common than the extranodal form. Survival rates vary from 4 to 11 months. Our results showed the worse prognosis with liver and brain metastasis in nodal NHL meanwhile worse prognosis in liver and bones in extranodal NHL.
GI tumors had a high tendency to metastasize with the pancreas, followed by the stomach cancers found to commonly have metastasized at diagnosis. The liver was seen to be a common site of systemic metastasis for GI cancers which is supported by previous literature which is also consistent with our findings.[5,6] Lymph node metastasis is common, especially in stomach and esophageal cancers, which has prognostic value and is an important factor for surgical resection in high-grade stomach cancers.[22] Our findings suggested that the esophagus followed by stomach and large intestine tumors had the worse survival rates of 2 and 3 months, respectively. In most GI cancers, brain metastasis was found to have a lower survival rate.
Pancreatic cancer is often detected at an advanced stage due to the lack of highly sensitive screening techniques. Yachida et al reported that distant metastasis occurs late during the genetic evolution of pancreatic cancer, at least 5 years after the initial mutation. Still, the median survival is only 2 years once the metastasis occurs, which is diagnosed at an even later stage.[23] On the other hand, anorectal cancers have the least number of metastatic to other sites at diagnosis.
Ovarian cancers are commonly metastasized to the liver, lymph nodes, and lungs. Deng et al also reported the common sites of ovarian cancer metastasis are the liver, distant LNs, lung, bone, and brain.[24] Deng et al reported the site of distant metastases to be an independent prognostic factor with lung metastases having the worst overall survival and distant lymph node metastases had the best survival[24]; however, our study found liver metastasis to have the worse prognosis with a median survival of only 2 months and brain metastasis with a comparatively better prognosis with a median survival of 14 months. Breast cancer commonly metastasized to bone, followed by liver and lymph nodes. Tahara also reported bones as the most common sites of breast cancer metastasis.[25]
We also found that almost all the GU cancers metastasized to the liver, followed by LNs and bone. GU cancer mainly spreads to the LN basins before dispersing to the lungs and liver. Bone tends to be a common site of metastasis among lung, NHL, and breast cancers. The possible reason for this may be 2-fold- one being the small caliber of blood vessels in the bone, filtering the cancer cells, and another being the constant cell turnover rate in the bones providing a fertile home for cancer cells to proliferate. Central nervous system (CNS) essentially remains the site of least common metastasis among all the cancers except malignant melanoma, where significant patients present with brain metastasis is only second to the lung by a narrow margin. Supportive evidence came from Yashin et al, who reported that the blood-brain barrier’s integrity must be compromised for melanoma cells to metastasize to the brain.[26] Another theory is that melanoma cells had the same embryonic origin as CNS cells and share common antigens such as MAG-1 and MAG-2, hence the CNS metastasis.[27]
Niu Fy et al studied uncommon metastasis in nonsmall cell lung cancer in 2872 patients. They postulated that metastasis to uncommon sites is rare because the microenvironment of these organs is not suitable for tumor survival.[28] For example, skin is a rare site for metastatic growth as it shares only 5% of cardiac output and is immunologically active against tumor cells.[29] Skeletal muscles also have a special microenvironment characterized by its changes in PH, blood flow, and pressures.[30] Spleen’s high concentration of immune cells and its role as “immune surveillance” also makes it an unfavorable site of metastatic seeding. Anti-angiogenesis factors in the spleen further discourage metastatic growth.
Our study is limited by the national registries contributing to the SEER database. Over the years, some states have been excluded, like Mississippi, Nevada, North Dakota, due to unsatisfied criteria, contributing to missing numbers of advanced cancer. As the SEER includes only US patients only, biases were reported due to the lack of external validity of the results and the retrospective nature of the analysis. Also, Seeking expert care at an early stage of symptoms often is affected by the availability of premium cancer institutes and the affordability of the patients. These significantly impact the stage of diagnosis and course of treatment, thus affecting survival. Hence, the regional variations of cancer care and financial capacity lend to the disparity in the numbers over the years. Finally, summation of patients with different systematic affection will not equal the total population because patients may have concomitant multiple site affection.
5. Conclusions
The results of this study provide population-based estimates of the incidence and survival rate of the different tumors with metastasis to other sites at the time of diagnosis. We have shown that lung and bronchus cancers were the most common tumors metastasized to other sites at diagnosis, followed by NHL-nodal, pancreas, stomach, and ovary. We also found that the survival rate and prognosis were worse in the liver, pancreas, large intestine cancers. On the other hand, small intestine, NHL-extra nodal, anorectum, and appendix cancers had better survival and prognosis. These data can help clinicians justify the use of different screening tools, which may also play an essential role in future research and achieve a better prognosis for cancer patients.
The author(s) of this work have nothing to disclose.
Author contributions
Conceptualization: Kirellos Said Abbas, Basel Abdelazeem.
Data curation: Kirellos Said Abbas, Basel Abdelazeem, Ahsan Wahab.
Formal analysis: Kirellos Said Abbas, Basel Abdelazeem, Ahsan Wahab.
Investigation: Basel Abdelazeem, Ahsan Wahab.
Methodology: Kirellos Said Abbas, Basel Abdelazeem, Ahsan Wahab.
Project administration: Basel Abdelazeem.
Software: Kirellos Said Abbas.
Supervision: Basel Abdelazeem, Ahsan Wahab.
Validation: Basel Abdelazeem, Ahsan Wahab.
Writing – original draft: Deepti Nagaraja Rao, Rabeet Tariq, Kirellos Said Abbas.
Writing – review & editing: All authors.
Supplementary Material
Abbreviations:
- CNS =
- Central nervous system
- GI =
- Gastrointestinal
- GU=
- Genitourinary
- LNs=
- Lymph nodes
- NHL=
- Non-Hodgkin lymphoma
- NOS =
- Not otherwise specified
- SEER =
- Surveillance, Epidemiology, and End Results.
BA and KSA are equal contributors.
Supplemental Digital Content is available for this article.
The datasets generated during and/or analyzed during the current study are publicly available.
How to cite this article: Abdelazeem B, Abbas KS, Rao DN, Tariq R, Wahab A. Incidence and comparative prognosis of cancers with metastasis to noncommon sites: A population-based study. Medicine 2022;101:29(e29743).
The authors declare no funding and no conflicts of interest.
Contributor Information
Kirellos Said Abbas, Email: kirellossaid98@gmail.com.
Deepti Nagaraja Rao, Email: deepti8688@gmail.com.
Rabeet Tariq, Email: rabeet_tariq@hotmail.com.
Ahsan Wahab, Email: drahsan.wahab@gmail.com.
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