Miliary lung metastases from non‑small cell lung cancer with Exon 20 insertion: A dismal prognostic entity: A case report

Introduction

Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs), including gefitinib, erlotinib, and afatinib, have a dramatic effect on non-small cell lung cancer (NSCLC) with major EGFR mutations consisting of exon 19 deletion and exon 21 L858R point mutation (1,2). More recently, some clinical and radiological characteristics of NSCLC with major EGFR mutations were revealed: Miliary lung metastases are frequently observed in NSCLC with EGFR mutation (3,4). In addition, miliary brain metastases have been reported to be correlated with exon 19 deletion (5,6).

However, it remains undetermined whether NSCLC with minor EGFR mutations possesses characteristics similar to those with major EGFR mutations. Exon 20 insertion is reportedly rare and accounts for only 4% of EGFR mutations (7–9). Between January 2014 and September 2017, we observed four cases of NSCLC with exon 20 insertion. Among them, two patients presented with miliary lung metastases at the time of NSCLC diagnosis. In the present study, we describe notable clinical courses in these two patients.

Case report

Case 1

A 53-year old non-smoking woman developed cough and visited a hospital on July 12, 2016. A chest radiograph demonstrated multiple pulmonary nodules (Fig. 1A), which suggested miliary tuberculosis. The patient was referred to our hospital on July 13. Chest CT showed numerous miliary nodules throughout bilateral lungs (Fig. 1B and C); however, a sputum smear stain for mycobacteria was negative. Transbronchial lung biopsy on July 19 revealed papillary adenocarcinoma staged cT4N3M1b (PUL, BRA) and cobas version 2 method detected exon 20 insertion. Because the performance status (PS) score was zero, cisplatin plus pemetrexed were administered as first-line therapy on August 16. However, pleural effusion and multiple lung nodules deteriorated after two-courses of this regimen. On September 9, docetaxel plus ramucirumab were administered as second-line treatment. However, the patient developed lymphangitis with deterioration of her respiratory condition. After methylprednisolone was administered to treat the lymphangitis on September 17 (Fig. 1D), afatinib was administered as third-line chemotherapy on September 19th. Although the patient exhibited temporary improvement in her respiratory condition on 30th September from required oxygen of 15 to 1 l/min (Fig. 1E), the lesions in the right lower lung deteriorated and progression of disease was confirmed on October 24 (Fig. 1F). Subsequently, nivolumab was administered on October 25, but it failed to produce the desired outcome. Finally, she died of lung cancer on November 2.

Figure 1. (A) Chest radiograph showed multiple nodules bilaterally in the lungs. (B and C) Chest CT on admission demonstrated numerous tiny nodules bilaterally in the lungs. (D) Chest radiograph before steroid and afatinib treatment showed extensive consolidations bilaterally in the lungs. (E) On September 27, right lung consolidations slightly improved, although left lung lesions deteriorated. (F) On October 23, extensive consolidations progressed especially bilaterally in the lower lung fields.

Case 2

A 61-year-old non-smoking woman developed cough and dyspnea during exercise in December 2016. Consequently, she visited a hospital on January 14 2017. Because both chest radiograph and CT revealed miliary lung nodules (Fig. 2A-C) and miliary tuberculosis was suspected, she was transferred to our hospital on the same day. Because a sputum smear stain for mycobacteria was negative, transbronchial lung biopsy was performed on January 17 and micropapillary adenocarcinoma staged cT4N3M1b (PLE, PUL, OSS) was diagnosed. Furthermore, exon 20 insertion was detected by cobas version 2 method. Because the PS score was 1, carboplatin plus nab-paclitaxel were administered as first-line treatment on February 1. However, this therapeutic regimen did not produce a satisfactory outcome (Fig. 2D). Therefore, we administered docetaxel as second-line therapy on February 23 but the outcome was the same as that produced by first-line treatment, and the patient rapidly developed respiratory failure. Finally, she died of lung cancer on March 17.

Figure 2. (A) Chest radiograph showed multiple small nodules bilaterally in the lungs. (B and C) Chest CT demonstrated numerous tiny nodules throughout bilaterally in the lungs with some consolidations. (D) The consolidation in the right upper-lung field developed with bilateral pleural effusion.

Discussion

The results of our two cases would provide the following two important clinical issues.

First, NSCLC with exon 20 insertion can present miliary type of lung metastases. In fact, two in four NSCLC patients (with exon 20 insertion) (50%) had miliary lung metastases. To the best of our knowledge, there is no report regarding the radiological characteristics of patients with NSCLC with exon 20 insertion. Furthermore, it is widely accepted that NSCLC with major EGFR mutations, especially exon 19 deletion, occasionally presents a miliary metastatic pattern in lungs. Laack et al reported five cases of miliary lung metastases from NSCLC with exon 19 deletion, which dramatically responded to EGFR-TKIs (10). In addition, two recent studies by Togashi et al and Wu et al revealed that NSCLC patients with miliary lung metastases had a high EGFR mutation rate in the range of 70–87.5% (3,4). However, in these studies, exon 20 insertions were not observed (4), and the details of EGFR mutation status were not provided (3). Most of EGFR mutations were major EGFR mutation (4). More recently, miliary type of metastases in lung and/or brain was reported in NSCLC harboring non-EGFR oncogene driver mutation such as echinoderm microtubule associated protein like 4-anaplastic lymphoma kinase (EML4-ALK) gene translocation (11) and c-ros oncogene 1 (ROS-1) rearrangement (12). Taking together these reports and the two cases presented in this study, miliary type of metastases can be closely correlated not only with major EGFR mutation, but also other oncogene driver mutation including exon 20 insertion.

Second, miliary lung metastases from NSCLC with exon 20 insertion appear to be an extremely poor prognostic entity. As reported in this study, disease progression in the two patients was rapid, and both the patients died within 3 months from beginning first-line treatment. To date, the prognosis in NSCLC patients with exon 20 insertions has been reported to vary, with a median OS of 5–26 months (7,8,13–15). However, most studies included a high proportion of patients with post-operation recurrence, which suggests low-tumor burden. In contrast, a study by Noronha et al included more patients with PS≥3 (40%) and revealed a dismal poor prognosis, with a median OS of 5 months (8). The authors proposed that the reasons for poor prognosis were attributable to high tumor burden and poor response to EGFR-TKIs (8), which were observed in the prospective randomized trial (16). In the two cases presented in this study, despite high tumor burden, when the first-line treatment was commenced, the PS score was low (0 for the first and 1 for the second case). However, miliary lung metastases easily and rapidly caused respiratory failure resulting in PS reduction. Therefore, NSCLC patients with miliary lung metastases and exon 20 insertions seem to have a poor prognosis with low chances of receiving further chemotherapy.

In conclusion, we presented two cases of miliary lung metastases from NSCLC patients with exon 20 insertion. PS rapidly deteriorated and the efficacy of chemotherapies including cytotoxic agents and EGFR-TKIs was limited. Chest physician should be aware that NSCLC with exon 20 insertion could present as miliary type of lung metastases and rapid disease progression. The accumulation of additional case series is necessary to confirm our results.

Acknowledgements

Not applicable.

Funding

No funding was received.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

AS and HS participated in the conception and design of the case report, analyzed and interpreted the data and wrote the manuscript. AS, TaK, TsO, SI and TaO evaluated the patient and participated in the therapy. SI, HS and TaO revised the manuscript for intellectual content. TI, ToK, and KO evaluated radiological images or pathological specimens. All authors have read and approved the final draft.

Ethics approval and consent to participate

The patient provided written informed consent for participation in the present study.

Patient consent for publication

The patient provided written informed consent for the publication of any associated data and images in this case report.

Competing interests

The authors declare that they have no competing interests.

References