Introduction to Small Cell Lung Cancer: Prevalence, Initial Symptoms, Work-Up, and Staging


General Introduction to Small Cell Lung Cancer

Lung cancer consists of two major types: small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC). Approximately 85% percent of all lung cancer patients have NSCLC,  and the remaining 15% have SCLC.

histology-breakdown-of-lung-cancer (click on image to enlarge)

In 2010, the American Cancer Society has estimated that approximately 222,000 new cases of lung cancer will be diagnosed, of which 35,000 will have SCLC. Even though both subtypes are lung cancers, they are considered as separate diseases in most ways, and the management of these two cancers is different. It is important to recognize that the treatments applicable for NSCLC, including many newer agents that have been approved and are the subject of increasing research and media attention, are not clearly relevant for patients with SCLC.

Symptoms and Work up

Nearly all the patients with SCLC have symptoms at the time of diagnosis. The common symptoms that many patients have at that time are chest pain, cough, and shortness of breath. Some patients may note fatigue and weight loss at the time of initial presentation.

sclc-table-of-symptoms

Patients may also have symptoms related to the sites to which the cancer has spread. For example, patients may develop headache or blurring of vision due to spread to the brain, abdominal pain from spread to the liver, or focal bone pain from spread to the bones. However, we often find that patients have tumor spread to areas of the body for which they do not have any specific symptoms.

Importantly, patients generally have symptoms for only a short period of time before diagnosis. This is related to the relatively rapid growth of SCLC.

Symptoms related to Paraneoplastic Syndromes-

Paraneoplastic syndromes are changes in different body parts that can occur in cancer patients, not related to direct spread of the cancer. Almost 50% of SCLC patients could have one or more paraneoplastic syndromes, with symptoms that often precede the diagnosis of SCLC. Some of the common paraneoplastic syndromes are listed in the table below.

paraneoplastic-syndrome-table

Many symptoms from the paraneoplastic syndromes improve with treatment, but this does not always occur. Worsening of the symptoms from paraneoplastic syndromes typically indicates progression of cancer.

Staging of Patients with SCLC

The purpose of staging is to find out

1. What is the extent of SCLC? In other words, where the cancer has spread to, since the extent of the cancer determines the treatment

2. What is the general condition of the patient?

The following tests are done in patients who are diagnosed with SCLC or suspected to have SCLC:

  • Blood work, including a complete blood count, blood chemistries such as sodium level, liver and kidney tests
  • CT scan of the chest (should include the liver and adrenal glands)
  • MRI or CT scan of the brain
  • Bone Scan

Note that PET scans are not an approved test for SCLC, even though it is approved for NSCLC (due to it being better studied in that setting).  However, if a PET scan is done, then a bone scan is not needed, but a brain scan is still required, since the brain is not well examined on a routine PET scan.

These studies are routinely performed because the areas in the body to which SCLC most typically spreads include the lymph nodes within the chest (hilar: lymph nodes within the lungs, and mediastinal lymph nodes: lymph nodes in the middle of the chest), the brain, other portions of the lung or the opposite lung, pleura (lining of the lungs), adrenal glands, liver, and bones (see figure below).

sclc-staging

It is important to recognize, however, that SCLC can spread to any other part of the body, such as the kidneys. It is also important to recognize that many patients have SCLC that has not spread widely throughout the body.

Unfortunately, even if the scans of the different body parts reveal no evidence of cancer, we cannot rule out that there is cancer involvement of these areas; rather, we can only safely conclude that if the cancer has spread to the other parts in the body, it has not grown sufficiently big enough for it to be seen on the scans.

Small Cell Lung Cancer Stages

Generally, every cancer patient’s cancer is assigned a stage. The stage of the cancer represents the extent of the spread of the cancer as can be detected with physical exam, blood tests, and scans.

In lung cancer, both NSCLC and SCLC, there are four stages. In stage I and II, the lung cancer is detected only in the lung or in the lung and in the hilar lymph nodes. In stage III, the lung cancer is detected not only in the lung, but also there is evidence that the cancer has spread to the mediastinal lymph nodes. In stage IV, spread of lung cancer can be detected in other parts of the body.  Spread to the opposite lung also represents stage IV lung cancer.

The most important features of SCLC are its proclivity to spread to other parts of the body early in the course of the cancer and its ability to grow relatively rapidly. Due to its ability to spread to other parts of the body early, we recommend chemotherapy even for earlier stage SCLC based on recognized risk that the cancer has at least microscopic spread (micrometastases), even if it is not detected in the other parts of the body on any of the scans.

Traditionally small cell lung cancer has been grouped into one of 2 stages: limited or extensive stage.

Limited Stage: SCLC is considered to be limited if the cancer is detected only in the lung itself, or the lung and in the hilar or mediastinal lymph nodes. In terms of the stages mentioned earlier, limited stages consists of stage I, II and III.

chest-anatomy-figure

About 25-30% of all patients with SCLC have limited disease at the time of diagnosis.

Extensive Stage; SCLC is considered extensive disease (ED) if the spread of the cancer can be detected in other parts of the body.  In terms of the stages mentioned earlier, extensive stage consists of stage IV.  The areas of the body that SCLC commonly spreads to are the brain, bones, liver, adrenal glands, or other parts of the lungs.

Another important area of spread is the pleura. The pleural lining is a thin wrap (like a saran wrap) that surrounds each of the two lungs and is normally too thin to be seen on scans.  The wrap doubles on itself and forms a pleural cavity between the two folds of the wrap.   The inner fold of the wrap is called the visceral pleura, while the outer fold is called the parietal pleura, as shown in the figure below.

chest-anatomy-pleura1

Normally, this cavity has a tiny amount of fluid. Please note that the image shown above shows a pleural cavity that is far larger than normal for easier illustration.

Spread of the cancer to the pleura usually leads to formation of excess fluid in the pleural cavity. Accumulation of fluid in the pleural cavity, as shown in the illustration below, compresses the lung and leads to shortness of breath and sometimes a cough.

pleural-effusion1

Even if the spread in a patient is only observed in the pleura, or cancer cells are seen within the pleural fluid, the patient is generall considered to have ED-SCLC.  Spread to the pleura is not a result of direct extension of the cancer to the pleura, but spread through the blood stream. Thus if it has spread to the pleura, it demonstrates the presence of micrometastatic SCLC cells in the blood stream.  This also means that SCLC cells have also reached some other parts of the body, though this is presumably not seen only because evidence of cancer in these other parts of the body has not grown big enough to be seen on the scans.

Data show that survival of patients is better for patients who have disease limited only to the pleura or pleural effusion compared with more widespread metastatic disease.

About 70-75% of all patients with SCLC have extensive disease at the time of diagnosis.

Treatment of SCLC will be covered in a separate summary chapter.

The GRACE Lung Cancer Reference Library is made possible by an unrestricted educational grant from Pfizer Oncology.

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Posted in: A Reference Library on Lung Cancer, Evaluation and Work-Up, Extensive Disease Small Cell Lung Cancer (ED-SCLC), Limited Disease Small Cell Lung Cancer (LD-SCLC), Lung Cancer, SCLC, Extensive Disease and Recurrent, SCLC, Limited Disease, Small Cell Lung Cancer (SCLC)

3 Comments  

Catharine
Posted on August 3, 2010 at 2:58 pm

Dr. Gadgeel -

Thank you for an informative summary on SCLC.

- Catharine


Simon54
Posted on August 4, 2010 at 6:01 am

Dr Gadgeel,

My thanks also for your summary. I know from experience how aggressive the spread and manifestation of ED-SCLC can be, so I always find myself surprised by the quite high percentage of cases that are diagnosed at the limited stage. Is it perhaps the case that limited SCLC can exist for quite a long while before ‘exploding’ into extensive disease? The answer is of no practical use to me at this stage, but I do idly wonder how long ago I might have been able to spot the symptoms of my disease when it was still limited (in retrospect I think I may have been going downhill for up to a couple of years before my ED-SCLC diagnosis in January of this year, though I guess that is far too long a period to imagine it may have been a limited SCLC stage….?).

Incidentally, one of the clearest symptoms at the time of my dx was palpable enlarged supraclavicular lymph nodes (enlarged mediastinum nodes also - obviously not palpable but evidenced in loss of voice from pressure on the vocal nerve). I’m just wondering whether or not lymph node symptoms have their place on the ‘common’ list for ED-SCLC.


Dr West
Posted on August 7, 2010 at 9:01 pm

Dr. Gadgeel sent me this summary via e-mail, actually as he was on the road, so I’m sorry that I don’t think he’ll be checking in to respond.

To answer on his behalf, I’d say that we’re not that impressed that a 25-30% incidence of limited disease is that high, though perhaps for such potentially rapidly growing disease, it’s not bad. We actually suspect that for most people, there’s a very short window for detecting small cell lung cancer before it’s extensive stage. We rarely see SCLC in staging studies, likely because the interval between initial detectability and obvious declaration with symptoms is typically short, such as just weeks to a few months. In contrast, NSCLC nodules are more likely to grow over a period of many months out to a few years.

There’s actually reason to question whether the people who have SCLC detected while it’s limited stage may have a different and more favorable tumor biology than the people with SCLC detected as extensive disease. In essence, the question is whether people do well because you detected it early enough to be limited disease, or because they have a disease that is more indolent than most SCLC that allows it to be detected as limited disease (with a longer interval between initial symptoms and distant spread, which is also likely to correlate with a longer interval until other measures of progression, and longer survival). In my discussion of surgery for SCLC, I discuss the question of whether the biology of the small minority of SCLC cases that are small enough to be candidates for surgery is really the main driver of this group having such favorable results, rather than the surgery itself. It’s the same idea.

The biology markedly influences our ability to detect a cancer at earlier vs. later stage, and this may be as important a driver in prognosis as the treatment we deliver.

And yes, palpably enlarged lymph nodes are pretty common, and lymphadenopathy (abnormally enlarged lymph nodes) contributes to cough and hoarseness in many patients. Lymph node symptoms may not merit a special call-out just because they contribute to many of the symptoms on the list, along with the effects of the primary lung tumor.