Richter’s Syndrome or Transformation

Richter’s syndrome (RS), also known as Richter’s transformation, refers to the transformation of one specific blood cancer type into a different, more aggressive type.

RS refers to the development of high-grade non-Hodgkin lymphoma in a person who has chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL). Other variants of RS are also known to occur, such as transformation to Hodgkin lymphoma.

This article explores what Richter's syndrome/transformation is along with symptoms and risk factors. It also covers treatment and life expectancy.

What Is Richter's Syndrome?

RS develops in someone who already has a cancer of the white blood cells.

This initial cancer a person is diagnosed with has two different names, depending on where in the body the cancer is found. Chronic lymphocytic leukemia (CLL) is mostly found in the blood and bone marrow, and small lymphocytic lymphoma (SLL) is found mostly in the lymph nodes.

People with RS develop aggressive disease with rapidly enlarging lymph nodes, enlargement of the spleen and liver, and elevated levels of a marker in the blood known as serum lactate dehydrogenase.

Who Develops Richter's Syndrome?

The development of RS in people with CLL or SLL is relatively uncommon. Estimates are that Richter’s transformation occurs in only about 5% of patients with CLL or SLL. Other sources cite a range between 2% and 10%.

If RS does develop, it is very unusual that it would occur at the same time the CLL or SLL is diagnosed. People who develop RS from CLL commonly do so several years after the CLL or SLL diagnosis.

The New Cancer Typically Behaves Aggressively

New cancer occurs when a person with CLL or SLL goes on to develop what’s known as a transformation, most often to a high-grade non-Hodgkin lymphoma (NHL).

“High grade” means cancer tends to grow more rapidly and be more aggressive. Lymphoma is a cancer of the lymphocyte white blood cells.

According to one study, about 90% of transformations from CLL or SLL are to a type of NHL called diffuse large B-cell lymphoma, while about 10% transform to Hodgkin lymphoma.

It is actually termed “Hodgkin variant of Richter syndrome (HvRS)” in the latter case, and it is not clear whether the prognosis is any different from Hodgkin lymphoma. Other transformations from CLL or SLL are also possible.

Symptoms of Richter's Syndrome 

If your CLL or SLL has transformed to diffuse large B-cell lymphoma, you will notice a distinct worsening of your symptoms.

The characteristics of RS include rapid tumor growth with or without extranodal involvement—that is, new growths may be confined to the lymph nodes, or cancer may involve organs other than the lymph nodes, such as the spleen and liver.

You may experience:

• Rapidly enlarging lymph nodes
• Abdominal discomfort related to an enlarged spleen and liver called hepatosplenomegaly
• Symptoms of low red blood cell count (anemia), such as fatigue, pale skin, and shortness of breath
• Symptoms of low platelet count (thrombocytopenia), such as easy bruising and unexplained bleeding
• Signs of extranodal involvement, including in unusual sites, such as the brain, skin, gastrointestinal system, and lungs

Risk Factors for Richter's Syndrome

The risk of developing RS from CLL or SLL is not related to the stage of your cancer, how long you have had it, or the type of response to therapy you have received. In fact, scientists do not fully understand what actually causes the transformation.

Older studies have described that some patients whose CLL cells show a specific marker called ZAP-70 may have an increased risk of transformation.

TP53 disruption and c-MYC abnormalities are the most common genetic lesions associated with Richter’s transformation. Less commonly, NOTCH1 mutations have also been described in patients with Richter’s transformation.

One study shows the median age at Richter’s transformation diagnosis was 69 years, while the majority of patients (72.5%) were male. Additionally, patients with Richter’s transformation who received no prior CLL treatment had a significantly better overall survival rate, with a median overall rate of approximately four years.

Another theory is that it is the prolonged length of time with a depressed immune system from CLL that causes the transformation. In patients who have had decreased immune function for a long time, such as those with HIV or those who have had organ transplants, there is also an increased risk of developing NHL.

Whatever the case may be, it does not appear there is anything you can do to cause or prevent your CLL from transforming.

How Do You Treat Richter's Syndrome? 

Treatment of RS usually involves chemotherapy protocols that are commonly used for NHL. These regimens have typically produced overall response rates of about 30%.

Currently, the treatment of Richter’s transformation with diffuse large B-cell lymphoma consists of combination chemotherapy plus rituximab. Adding ofatumumab—a monoclonal antibody that targets a unique tag on B lymphocytes—to CHOP chemotherapy led to an overall response rate of 46% in one study.

However, a significant number of serious adverse events were noted; as a result, this agent is not currently routinely recommended. In most patients who are transplant candidates, non-myeloablative allogeneic hematopoietic cell transplantation is recommended after the first remission has been achieved.

Some smaller studies have looked at the use of stem cell transplants to treat this population. Most of the patients in these studies had received prior chemotherapy.

Of the types of stem cell transplants tested, non-myeloablative transplants had less toxicity, better engraftment, and a possibility of remission. Further studies will be needed to determine whether this is a viable option for RS patients.

What Is the Life Expectancy for Richter's Syndrome?

Unfortunately, the average survival with regular chemotherapy is less than six months after RS transformation. However, new therapies and combinations are continually being tried in clinical trials.

As with all lymphomas, survival statistics can be hard to interpret. Individual patients differ in their general health and strength prior to their diagnosis. Additionally, even two cancers with the same name can behave very differently in different individuals. With RS, however, the new cancer is more aggressive.

In some people with RS, survival has been reported with a statistical average of fewer than 10 months from diagnosis. However, some studies have shown a 17-month average survival, and other people with RS may live longer. Stem-cell transplantation may offer a chance for prolonged survival.

Future Research

To improve survival in patients with RS, scientists need to gain a better understanding of what causes the transformation from CLL to occur. With more information about RS at a cellular level, better-targeted therapies could be developed against those specific abnormalities.

Experts caution, however, that since there are a number of complicated molecular changes associated with RS, there may not ever be a single “all-purpose” targeted treatment and that any of these medications would likely need to be combined with regular chemotherapy to get their best effect. As scientists unfold the causes of RS, they are seeing that RS is not a single uniform or consistent process.

In the meantime, patients who have had their CLL transform to RS are encouraged to enroll in clinical studies in an effort to improve treatment options and outcomes from the current standards.

Summary

Richter's syndrome is a relatively uncommon transformation of CLL and SLL that occurs in 2-10% of patients with CLL or SLL. Symptoms can include swollen lymph nodes, abdominal pain, low red blood cell count, and low platelet count. Treatment can be difficult, but more research is being done to find effective treatments.