Frontiers | ALK-rearranged and EGFR wild-type lung adenocarcinoma transformed to small cell lung cancer: a case report (2024)

Introduction

Chromosomal rearrangements within the Anaplastic lymphoma kinase (ALK) gene play a pivotal role in determining the heightened sensitivity of a subset of non-small cell lung cancers (NSCLC) to small molecule ALK tyrosine kinase inhibitors (ALK-TKIs) (1). As per guideline recommendations, targeted therapy has now become the primary standard of care for patients with locally advanced and metastatic ALK-positive NSCLC (2). The advent of ALK-TKIs, including first-generation crizotinib, second-generation alectinib, brigatinib, and ensartinib, as well as third-generation Lorlatinib, has significantly revolutionized treatment choices and prognosis for individuals with ALK-positive NSCLC. Nevertheless, it is essential to acknowledge the inevitability of drug resistance alongside challenges like distant metastasis, the potential for severe adverse effects, and a diminished quality of life encountered during therapy (3). Common drug resistance mechanisms include secondary mutations in ALK, amplification of ALK fusion gene copies, and activation of bypass and downstream pathways (4). While ALK-TKIs are still being updated and iterated to address issues such as drug resistance, the silent phenomenon of SCLC transformation does not appear to have received much attention.

Indeed, this transformation from NSCLC to SCLC occurs mostly in patients resistant to EGFR-TKIs (5–7). This transformation has been described as a mechanism of acquired resistance occurring in approximately 5% of patients who develop resistance to EGFR-TKIs (8). Despite case reports, transformation from NSCLC to SCLC due to resistance to ALK-TKIs remains a rare phenomenon.

We present a case of a patient with NSCLC who developed recurrence and metastasis after surgery, progressed and transformed to SCLC after being resistant to treatment with ALK-TKIs. Subsequent application of therapy targeting SCLC led to transient control of the disease. The current treatment regimen is albumin-bound pacl*taxel in combination with anlotinib, and the patient’s condition is still stable.

Case report

A 47-year-old male patient with a smoking history was admitted for evaluation of mild discomfort in the right chest and back on 30th November 2016. Physical examination revealed that the patient haddiminished breath sounds and audible rales in the right middlelung. Chest CT revealed a nodular shadow near the hilum of the right middlelobe, suggesting a high possibility of lung cancer with enlargedmediastinal lymph nodes. The patient had mild hypertension, no other diseases and no family history of tumors. After excluding contraindications for surgery, the patient underwent video-assisted thoracoscopic surgery for right middle lobe resection and mediastinallymph node dissection on 23rd December 2016. Postoperative pathology revealed poorly differentiated adenocarcinoma of the right middle lung (pT2N2M0, stage IIIA), with positive immunohistochemical markers for CK, CK7, TTF-1, CgA, and Ki67 (40% positive staining) (Supplementary Figure1). Starting from 17th January 2017, the patient received four cycles of post-operative adjuvant chemotherapy using the PP regimen (Pemetrexed 500mg/m² and cisplatin 75mg/m² once every three weeks) (specific treatment process illustrated in Figure1), followed by regular outpatient follow-ups. The patient achieved a PFS of 46 months postoperatively.

Figure1

In early September 2020, the patient experienced occasional hemoptysis. On October 19, 2020, a follow-up chest CT revealed slightly increased multiple nodules in the mediastinum compared to previous findings (Supplementary Figures2A, B). An upper abdominal MRI indicated hepatic metastases and enhanced lesions in the lumbar vertebrae, suggesting bone metastasis (Supplementary Figure2C). These findings suggested tumor recurrence and metastasis in the patient, prompting us to conduct genetic testing on the patient (Jinyu Medical Laboratory Center, Guangzhou, China). Due to the time required for waiting for genetic testing results, considering the progression of the patient’s condition and the patient’s desire for treatment, systemic chemotherapy was administered as the first step. Starting from November 1, 2020, the patient received two cycles of chemotherapy, including pemetrexed 500mg/m² and Nedaplatin 80-100mg/m² once every three weeks. After chemotherapy, patients exhibited poor tolerance, characterized by Grade II gastrointestinal adverse reactions and significant hematological adverse events. After aggressive symptomatic treatment, the patient’s symptoms were partially relieved. However, this led to a slight delay in subsequent treatment. Concurrently, genetic testing revealed the patient’s epidermal growth factor receptor (EGFR) mutation to be negative, while harboring an ALK rearrangement. At the beginning of 2021, the patient presented with lower back pain. Physical examination revealed tenderness in the lumbar region, without evidence of spinal deformities or signs of neural involvement. Considering the patient’s symptoms and lumbar spine MRI findings (Supplementary Figure2D), we considered that the lumbar pain is induced by bone metastasis. From March to April of the same year, palliative radiotherapy was administered to the L4 metastatic lesion in the lumbar spine at a dose of 39Gy in 13 fractions, whole-brain radiotherapy at a dose of 30Gy in 15 fractions, and a local boost of 12Gy in 6 fractions. The patient’s symptoms improved (additional brain metastasis images from the patient can be seen in Supplementary Figure3). Since genetic testing revealed the presence of an ALK rearrangement, the patient received oral crizotinib at a dose of 250 mg twice daily after radiotherapy and achieved a PFS of 15 months. In June 2022, a follow-up upper abdominal MRI showed progression of hepatic lesions compared to previous findings. Patients opted into the clinical trial after giving full informed consent. The patient’s treatment was switched to TGRX-326 (a third-generation ALK/ROS1 tyrosine kinase inhibitor) at a dose of 60 mg once daily to continued targeted therapy, with disease stability (SD) as the assessed treatment response, until April 24, 2023. The patient achieved a PFS of 11 months. Subsequently, progressive disease (PD) was observed (Figures2A, B), leading to the patient’s withdrawal from the clinical trial. Treatment was then switched to oral administration of the third-generation targeted therapy drug loratinib, at a dosage of 100mg once daily.

Figure2

Patient revisited on 2023-05-22 and was found to have a high level of neural-specific enolase (NSE), a tumor marker, reaching 287.6 ng/mL (Figure3). Percutaneous liver biopsy was performed, and pathological examination revealed metastatic small cell carcinoma, most likely from the lungs. Immunohistochemistry results showed: CD56 (+), CgA (+), broad-spectrum CK (+), P40 (-), TTF-1 (+), Ki-67 (+, 40%), CK7 (+), Napsin A(-), CK19 (+), CD10 (+), AFP (-), GPC-3 (+), HSP70 (+), GS (+), HepPar-1 (-), Syn (+) (Figure4). Therefore, we transitioned the treatment protocol to target SCLC. Starting from 2023-05-29, as palliative first-line treatment following transformation of the pathological type, the patient received treatment with 100mg/m² of etoposide on days 1-3, carboplatin injection (AUC of 5 mg/ml/min) on day 1, and 200mg of sintilimab on day 1, once every three weeks, for a total of 4 cycles. After treatment, NSE was significantly reduced compared to before and the patient achieved a PFS of 3 months. On 2023-09-06, follow-up chest and abdominal CT scans indicated increased lymph node metastasis in the mediastinum and multiple liver lesions compared to previous scans (Figure2C). In light of the deterioration in the patient’s condition, we opted to switch to pacl*taxel-based medication as palliative second-line treatment for SCLC. Starting on 8 September 2023, patients received a single course of systemic chemotherapy with intravenous albumin-bound pacl*taxel. Nevertheless, the patient’s tumor marker NSE continued to rise. Considering the patient’s satisfactory physical condition (with a PS score of 2) and tolerance, a combined approach with anlotinib targeted therapy was initiated. On October 7, 2023, the patient was readmitted for treatment and received intravenous administration of albumin-bound pacl*taxel at a dose of 260mg/m² every 3 weeks, along with concurrent oral administration of anlotinib at a daily dosage of 8 milligrams, administered for two weeks followed by a one-week break. After treatment, the patient’s mental state and appetite were satisfactory and his condition was stable (see Supplementary Table1 for detailed patient information).

Figure3

Figure4

Discussion

Lung cancer is the leading cause of cancer-related deaths globally, with NSCLC accounting for approximately 80-85% of lung cancer cases (9). Up to 8% of NSCLC patients have an ALK rearrangement, most commonly a fusion between ALK and the echinoderm microtubule-associated protein-like 4 (EML4), resulting in an EML4-ALK fusion that drives continuous cell proliferation and ultimately tumor formation (10). Crizotinib is currently the standard first-line therapy for ALK-positive NSCLC patients. However, due to various resistance mechanisms, most patients experience relapse within one year of treatment. The Phase III CROWN Study demonstrated that compared to the first-generation crizotinib, the third-generation ALK-TKI lorlatinib can improve progression-free survival (PFS) and reduce central nervous system progression in patients with advanced ALK-positive NSCLC (11). Nonetheless, drug resistance remains inevitable, with the most common mechanism being drug-resistant mutations in ALK. Case report have demonstrated that the NSCLC patient with ALK fusion mutations developed ALK fusion V1180L mutation and transformed into SCLC after acquiring resistance to alectinib (12). And, there was also a LUAD patient who developed ALK G1202R mutation and SCLC transformation after treatment resistance to second-generation ALK-TKIs (13). Although these are rare case reports, they carry significant implications. The poor response of patients to ALK-TKIs not only suggests the potential emergence of drug-resistant mutations but also necessitates consideration of the possibility of SCLC transformation.

In fact, cases of transformation from NSCLC to SCLC occurred mainly in patients with EGFR-mutated LUAD who were resistant to EGFR-TKIs (5–7, 14). To explore the molecular mutational mechanisms underlying this transformation, researchers have conducted next-generation sequencing (NGS) or whole-exome sequencing (WES) on samples from LUAD patients who transformed into SCLC after developing resistance to EGFR-TKIs. Multiple studies have consistently shown that this histological transformation is closely associated with inactivation mutations in the Retinoblastoma1 (Rb1) and TP53 genes, indicating that the inactivation of Rb1 and TP53 is an effective predictive factor for the transformation of LUAD into SCLC (7, 8, 15–18). Additionally, researchers reported a case of RET-rearranged LUAD transforming into SCLC, with acquired resistance to pralsetinib. Molecular analysis revealed the presence of the same RET fusion and TP53 mutation in the primary LUAD and recurrent SCLC (19). Previously, a patient with ALK-rearranged NSCLC experienced disease progression after treatment with ALK-TKIs, followed by SCLC transformation. Genomic profiling revealed the retention of ALK rearrangement, accompanied by inactivating Rb1 mutation (C706Y) and p53 exon deletion, which were not detected in the original tumor tissue at diagnosis (13). This also provides evidence supporting the significant roles of p53 and Rb1 loss in SCLC transformation. Additionally, other mutations possibly associated with transformation include PIK3CA mutation, WNK1 mutation, etc. (20, 21). Furthermore, research suggests that the presence of neuroendocrine differentiation in NSCLC may be one of the factors leading to SCLC transformation (22). The origin of this transformation from NSCLC to SCLC is a controversial topic, as it is not entirely clear whether the original lung cancer tissue harbored mixed components (23).

Transformed SCLC typically manifests rapid disease progression and poses therapeutic challenges. Currently, there is no standardized treatment strategy for patients who develop SCLC transformation after resistance to ALK-TKIs. Chemotherapy combined with immunotherapy is the most common treatment option. In the entirety of this patient’s therapeutic journey, the regimen devised was personalized, integrating the patient’s actual condition while adhering to treatment norms. For instances, following the pathological transformation to SCLC, commonly used treatment options carboplatin, etoposide, and atezolizumab or durvalumab (24, 25), were not selected; rather, carboplatin, etoposide, and sintilimab were chosen. The choice of immunotherapeutic agents primarily stemmed from the patient’s limited financial capacity, unable to afford imported PD-L1 inhibitors, thus opting for domestically produced sintilimab in combination with chemotherapy, yielding a 3-month PFS. Indeed, studies have demonstrated that sintilimab can serve as maintenance therapy post-chemotherapy for SCLC (26). The combination of sintilimab and anlotinib as second-line or beyond therapy for extensive disease (ED)-SCLC exhibits favorable antitumor activity with manageable toxicity (27). Additionally, prior reports have shown the efficacy of sintilimab in ED-SCLC refractory to multi-line treatments (28). Therefore, we opted for this regimen. This case underscores the necessity, in clinical practice, to tailor treatment approaches to individual patients by considering treatment guidelines alongside factors such as the patient’s actual physical condition and economic status.

According to the literature, it has been pointed out that a rapid elevation of serum NSE and poor response to targeted drugs usually indicate a transformation from LUAD to SCLC (29). This trend was also observed in the present case, where a follow-up liver imaging examination after approximately 26 months of taking ALK-TKIs indicated disease progression and an elevated NSE level of 287.6ng/ML (normal range: 0-12.5ng/ML). This also suggests that during treatment, clinicians should monitor serum tumor markers or perform genomic sequencing, especially in patients with disease progression, as this may aid in the early detection of SCLC transformation. Repeat biopsies may be performed if necessary, and treatment plans can be adjusted promptly based on molecular pathological examination results to achieve personalized and comprehensive management of patients. Additionally, in this case, despite developing drug resistance and multiple metastases during the course of treatment, the patient’s survival time since the initial diagnosis has over seven years. In a certain sense, regular follow-up visits, improved doctor-patient communication, and enhanced patient compliance hold great practical significance in improving patient prognosis.

Conclusion

This study reports a case of LUAD patient with postoperative recurrence and metastasis who developed acquired resistance andunderwent SCLC transformation following treatment with ALK-TKIs. This finding has influenced clinical practice, highlighting the importance of dynamic assessment of tumor markers and repeat biopsies when necessary. The results suggest the necessity of early development of personalized treatment plans for patients experiencing SCLC transformation after ALK-TKIs resistance, with regular follow-up appointments and timely adjustment of treatment strategies advised. This subset of patients appears to exhibit faster disease progression compared to typical SCLC patients.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.

Ethics statement

Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author contributions

RC: Investigation, Conceptualization, Data curation, Formal analysis, Visualization, Writing – original draft. YJ: Supervision, Writing – review & editing. YL: Supervision, Writing – review & editing. JX: Supervision, Writing – review & editing, Investigation.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The present study was funded by the National Natural Science Foundation of China (grant nos. 81960425 and 81160294).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2024.1395654/full#supplementary-material

Supplementary Figure1 | H&E staining and IHC staining of surgical resection specimens. (A) H&E staining of surgically excised specimens. (B-D) IHC staining of the surgically resected specimen showed positivity for TTF-1, CK, and Ki67.

Supplementary Figure2 | CT images of the patient’s chest and MRI images of the abdomen. (A, B) Mediastinal window of chest CT demonstrating the patient’s mediastinal lymph nodes. (C, D) Abdominal MRI images showed tumor invasion of the patient’s lumbar spine at L4.

Supplementary Figure3 | MRI image of the patient’s cranium. (A). Cranial MRI images of the patient before whole brain radiotherapy. (B, C) are cranial MRI images of the patient after whole brain radiotherapy.

Abbreviations

NSCLC, non-small cell lung cancer; ALK-TKIs, ALK tyrosine kinase inhibitors; SCLC, small cell lung cancer; LUAD, lung adenocarcinoma; NSE, neural-specific enolase; SD, disease stability; PD, disease progression; EML4, echinoderm microtubule-associated protein-like 4; PFS, progression-free survival; CNVs, copy number variations; NGS, next-generation sequencing; WES, Whole-exome sequencing.

References