Background

Non-small cell lung cancer (NSCLC) is the leading cause of cancer-related deaths worldwide. In Ireland alone, there are over 2500 new cases of lung cancer diagnosed each year. It ranks fourth among the most common cancers and causes 21% of all cancer-related deaths [1].

Lung cancers usually metastasize to the liver, brain, bone, and adrenal glands—rarely affecting the abdomen. To our knowledge, there are 8 previous studies in the literature to date which involve omental metastasis from NSCLC [2,3,4,5,6,7,8,9].

Case presentation

A 73-year-old lady presented with a history of worsening productive cough for 18 months. She did not initially seek any medical attention as she did not like going to her family doctor (GP). However, when the cough started interfering with her activities of daily living, she went to her GP. Physical exam by the GP revealed decreased air entry in the right base but no other significant findings. A chest X-ray showed a suspicious 6-cm mass in the right lower zone (Fig. 1).

Fig. 1
figure 1

Initial chest X-ray on presentation

She was immediately referred to the rapid lung access clinic and went on to have an endobronchial biopsy which confirmed a moderately differentiated adenocarcinoma of the lung which was ALK-positive. She went on to have staging PET and CT scans and was staged as cT3N2M0. She was not a suitable candidate for surgery so she had radical chemo-radiotherapy with 4 cycles of cisplatin pemetrexed followed by radical dose sequential radiotherapy (55 Gy/20 F). Post treatment CT showed the primary tumor to be more spiculated in appearance. She was deemed ineligible for durvalumab maintenance therapy due to the extensive pneumonitis following her radiotherapy which required a long course of steroids. Interval scans every 3 months did not show any progression of disease.

She presented to the hospital 13 months post her diagnosis with progressive abdominal swelling. A restaging CT scan showed restaging CT scans showed extensive omental infiltration, the presence of multiple peritoneal nodules and progression of her pulmonary disease with new brain metastasis (Figs. 2, 3 and 4). Cytological analysis of the ascitic fluid and omental biopsy confirmed metastatic ALK-positive NSCLC.

Fig. 2
figure 2

Extensive ascities

Fig. 3
figure 3

Omental nodularity

Fig. 4.
figure 4

CT Thorax prior to initiation of alectinib

Targeted therapy in the form of the tablet alectinib was commenced at a dose of 600 mg twice a day with a view to continue indefinitely until progression of disease or unacceptable toxicity. The reason for choosing alectinib over the more widely available crizotinib was that two studies have shown that alectinib has better CNS penetrance compared to crizotnib [10]. She tolerated the treatment well. Restaging scans done 3 months later showed good partial response to therapy (Fig. 5).

Fig. 5
figure 5

CT Thorax 3 months post treatment with alectinib

There was a decrease of the primary lung leision from 5 to 4 cm with no new lung leisions. The previous left paratracheal lymph node had also significantly decreased in size. There was a new left pleural effussion, but the patient was asymptomatic. The omental and disease was stable with no further progression in the brain metastasis.

Discussion

NSCLCs commonly metastasize to the brain, bone, and liver. They usually metastasize via the lymphatic system; however, they can spread hematologically. They very rarely involve the abdomen, and to the best of our knowledge, only 8 studies have reported cases of omental metastases from primary lung cancers in the literature [2,3,4,5,6,7,8,9].

ALK is a tyrosine kinase receptor that is rearranged in about 5% of NSCLCs [11]. Rearrangement results in dysregulation and inappropriate signaling through the ALK domain. It has been reported to be more common in light or never smokers and among people with adenocarcinoma histology without other genetic mutations for example EGFR which accurately describes the patient in this case. Gene mutations involving ALK are associated with responsiveness to ALK tyrosine kinase inhibitors such as crizotinib and alectinib. In this case, our patient showed good response to alectinib therapy.

ALK inhibitors like crizotinib and alectinib are not without their side effects. In a recent meta-analysis, it was found that visual disturbances were the most common side effects in patients on crizotinib while mild GI disturbances (nausea and diarrhea) were frequently encountered by patients on second generation ALK inhibitors.

Prior to the discovery of targetable mutations like ALK, EGFR, and ROS 1 patients with NSCLC were treated with standard platinum-based chemotherapy. Now with potential targetable mutations and availability of drugs like alectinib, we can have a more durable and well-tolerated response than standard chemotherapy in patients who carry these mutations.

Conclusion

In conclusion, ALK-positive NSCLC with metastasis to the omentum is very rare. However, in patients with atypical symptoms like ascites, the possibility of a metastasis must be considered and repeat biopsy is always recommended. Targeted therapy in selected patients has shown a more durable response than chemotherapy.