While brain metastases are common, some patients seem to be at higher risk than others. As previously noted, SCLC has a very high risk of spread to the brain. For NSCLC subtypes, several studies have shown that patients with non-squamous lung cancers have a greater tendency to develop brain metastases than those with squamous cancers, which tend toward more local spread. Here is the figure for development of brain metastases in patients treated for stage IIIA NSCLC out of the Harvard/Dana Farber system (abstract here).
Another trial just published from UCSF evaluating the stage IIIA NSCLC population also found a high risk (55%) of recurrence in the brain after aggressive treatment, and that the risk of brain metastases was higher for patients with adenocarcinoma vs. squamous cell carcinoma (57% vs 34%, a statistically significant difference (abstract here)). The Boston study also demonstrated that patients who had a good response to pre-operative treatment (chemo, radiation, or a combination of both for all but 3 patient who had unsuspected N2 nodal disease at surgery) and cleared their mediastinal nodes at the time of subsequent surgery had significantly lower risk of developing brain metastases than patients who had N2 nodes positive at the time of surgery:
Finally, another trial out of Columbia in NYC was just published in the journal Radiology (abstract here), looking at the clinical variables that predicted for development of brain metastases among 264 patients with full imaging and clinical information available. Like the other studies, they reported that the patients with adenocarcinomas had a higher risk of developing brain metastases than those with squamous cell cancers, and the folks with undifferentiated cancers fall between them (likely actualy a mix of adenocarcinomas and squamous cell cancers). This study also reported that higher nodal stage predicts higher risk of developing brain metastases, and that the risk of brain metastases increased steadily as the size of the primary tumor increased, as shown here:
This study also reported that there was not an association of increased risk with being male or female, with patient age, or with location of the tumor being central or peripheral, toward the outer edge of the lung.
Practically speaking, this doesn’t change our management. At this point, prophylatic cranial irradiation (PCI) is not a standard recommendation after potentially curative treatment for locally advanced NSCLC (topic reviewed in prior post), but with so many trials showing a high risk of “brain first” or “brain only” recurrence in this setting, it’s a very important question. I routinely recommend that my patients who have undergone treatment for stage III NSCLC consider a clinical trial in this setting of PCI vs. observation here, because we don’t know if it will be helpful or harmful or have no effect. I might be particularly inclined to recommend the trial in a patient with an adenocarcinoma, given the consistently higher risk of brain metastases seen in this population, but I recommend this trial for pretty much everyone. We need to see if there is a way to reduce the risk of brain metastases in both NSCLC and SCLC. There will be an important trial presented about PCI in extensive disease SCLC at our big international oncology meeting, ASCO, in early June, so I’ll provide an update when the data are available. In the meantime, I’ll continue the discussion with more on prognosis and management options in the coming posts.
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Good Morning Dr. West,
I want to thank you with all my heart for this website. I marvel that you find the time, and am vey thankful that you do and make the efforts to reach out to all of us. This is my primary website to educate myself on cancer.
My question: Having LungCancer 3 Adenocarcinoma, T1N2,
I understand brain metastases is pretty high. What is the usual window of time that it moves from lung to brain?
I have 3 children so I must be prepared with as much info and preparation.
Thanks so much.
The overall risk is about one in three of developing brain mets as the first or only site of recurrence, and the risk is lower with squamous cancers and those who had a good response to their initial treatment (chemo or chemo with RT).
The time line is often early. Many cases that develop brain mets are discovered within 6 months of starting, and the vast majority become evident within a year or two. After two years, recurrences do occasionally occur, but the risk is greater earlier than later.
-Dr. West
Hello Dr West:
I am a stage 3 T4, recently completed chemo/radiation for large, non-operable RUL tumour. When I ask the med oncologist about diagnostics for brain mets, she states that will be done only if i become symptomatic for brain tumour. Isn’t that leaving things a bit late? And what should the symptoms be? Wait for blinding headaches and seizures? I don’t quite understand. Please advise. Thank you so much.
Toosje
Toosje,
After screening with a head MRI or CT to clarify staging, we don’t routinely do surveillance scans on the brain to see if anything has changed. It is most typical to do a scan of the brain to check for potential brain metastases if a person develops such symptoms as vision changes, new headaches (including just persistent or progressing but not necessarily the most staggeringly severe ones), balance problems, focal weakness, numbness, or, yes, seizures. The risk of brain recurrence is real, but it’s often heralded by symptoms that don’t need to be very severe, especially if the patient and oncologist know what to look for.
-Dr. West
Thank you, Dr West.
I too so much appreciate the clarity you provide to our issues. What a wonderful website.
Thanks again.
Toosje
Thank you so much for the insightful write up on brain mets. This is the scariest thing for a Lung Cancer patient. What about stage IV Lung Cancer? What are the chances of developing brain mets.
My husband had brain MRI at the time of staging, i.e. eight months ago and nothing was found, thank God. Now he has had three Pet scans where the scans say there is nothing in the brain but suggest MRI if clinica symptoms are there. Should we still go ahead and have a brain MRI even though no symptoms exist? Everyone wants to catch the beast early.
Thank you once again
Apra