Chemotherapy versus personalized therapy for EGFR mutant lung adenocarcinoma resistance to EGFR-tyrosine kinase inhibitors: a retrospective dual-center study

Lung cancer is notorious for its high morbidity and mortality rate worldwide [1], in which non‐small cell lung cancer (NSCLC) accounts for 80%‐85% of the incidences [2]. In the NSCLC population, epidermal growth factor receptor (EGFR) gene is found in 10–20% of Caucasians and at least 50% of Asian NSCLC patients [3]. EGFR tyrosine kinase inhibitors (EGFR-TKIs) have dramatically improved survival outcomes and are the first-line treatment for patients with EGFR-mutants [4].

Unfortunately, patients undergoing tyrosine kinase inhibitor (TKI) treatment eventually develop acquired resistance (AR). The common ARs include: (i) secondary mutations to EGFR, such as T790M mutation, C797S mutation [5]; (ii) activation of alternative pathways, such as MET amplification [6], ERBB2 amplification [7]; (iii) activation of downstream targets, for instance, RAS-MAPK pathway signaling [8], PIK3CA mutations [9]; (iv) histologic transformation, for example, small-cell lung cancer (SCLC) transformation [10]; (v) others: fibroblast growth factor receptor (FGFR) amplification, cell cycle gene alterations [8]. Certain EGFR-mutant NSCLCs may harbor multiple mechanisms of EGFR-TKI resistance [9]. However, the potential mechanisms underlying the AR remains obscured in up to 50% of cases [11].

After the progression with EGFR-TKIs, different options are available, including chemotherapy and personalized therapy that is based on individual ARs. For example, the combined treatment with EGFR and MET-TKIs can inhibit the growth of EGFR-mutated NSCLC coupled with MET amplification [12]. The combination with 3rd and 1st or 2nd EGFR-TKIs is also a reasonable strategy against the AR of T790M-trans-C797S [13]. Except for the 3rd EGFR-TKIs, which is approved for the treatment of NSCLC patients with positive T790M mutation after developing AR to the first-line EGFR-TKIs [14], the efficacy of other personalized therapeutic strategies is largely compromised by small samples and absence of comparison with chemotherapy.

Here we conducted a retrospective multi-center study to explore the efficacy of chemotherapy and personalized therapy. We found that the efficacy of chemotherapy approximated to that of personalized therapy, which indicates that chemotherapy may still serve as a promising option for patients who develop resistance to EGFR-TKIs.

For patients with disease progression after EGFR-TKI failure, the optimal treatment strategy remains controversial and no consensus has been reached. Our retrospective study found that the therapeutic efficacy of chemotherapy was comparable to that of personalized therapy. Interestingly, we found that when chemotherapy was supplemented with immune checkpoint inhibitors (ICIs) and anti-angiogenic drugs, there was a trend towards providing additional clinical benefits compared to personalized therapy. This highlights the enduring clinical significance of chemotherapy for patients experiencing relapse after prior EGFR-TKI therapy. Moreover, in some cases, combination therapy based on chemotherapy may provide incremental benefits. This emphasizes that chemotherapy is a promising option for treating patients with EGFR-TKI resistance.

PFS with traditional chemotherapy offers a length of 4.4–5.4 months for previously EGFR-TKI treated patients [16]. The data from clinical trials have not shown substantial survival benefits of single-agent ICI [17]. The combination therapy of chemotherapy and ICI or chemotherapy with anti-angiogenesis reported an efficacy with an ORR of 30–60% and a PFS of 5.0–7.0 m [18‐20]. ICIs combined with chemotherapy and anti‐angiogenic drugs showed excellent benefits for patients receiving prior EGFR-TKI treatment, with an ORR of 73.5% and a PFS of 10.2 m in the IMpower150 subgroup, and an ORR of 43.9% and a PFS of 6.9 m in the ORIENT-31 trail [21‐23]. In our study, the efficacy of the combined modality was superior to the chemotherapy alone, particularly in the “quad” model. The patients with EGFR mutations reported a high Treg infiltration, reduced CD8 + T-cell number and decreased tumor mutation burden (TMB) [24‐26], which induced a poor clinical efficacy of ICI. EGFR-TKIs can remodel the tumor microenvironment (TME) by increasing CD8⁺ T cell infiltration and the presentation of MHC class I and II molecules, reducing the infiltration and function of Tregs [27]. So immunotherapy is applied after EGFR-TKIs failure. However, the efficacy and responsiveness of ICI monotherapy are far from satisfactory. Anti‐angiogenic drugs can reduce hypoxia, increase the delivery and efficacy of cytotoxic agents, and reduce immunosuppression through preventing angiogenesis and normalizing the tumor vasculature [28]. Consistent with the previous study, the current study revealed a satisfactory outcome when anti-angiogenics was combined with chemotherapy and immunotherapy. It would be beneficial to conduct further large-scale and prospective studies to confirm these results.

To date, many efforts have been invested in the search for effective treatment strategies to overcome EGFR-TKI resistance according genetic testing and histologic transformation. In case of EGFR C797S mutation, the follow-up treatment depends on the allelic relationship with T790M: T790M-trans-C797S is sensitive to the combination of first and third-generation of EGFR-TKIs [29], and a combination of brigatinb with cetuximab can achieve a favorable outcome with a PFS of 14 months and an ORR of 60%, in patients with T790M-cis-C797S [30]. The concomitant treatment with Trastuzumab and EGFR-TKIs has been demonstrated to possibly overcome the resistance to EGFR-TKIs as result of ERBB2 amplification [31]. SCLC transformation is responsive to platinum etoposide regimens with a PFS of 3.0–4.0 m [10, 32]. A retrospective trial found it is invalid to ICIs [10]. But another retrospective trial discovered that immunochemotherapy significantly prolonged the OS than chemotherapy. Positive PD-L1 status was associated with PFS benefit. And the expression of SFTPA1 in RNA sequencing predicted the durable clinical benefit. Large sample and prospective studies were needed to explore the efficacy of ICIs in SCLC transformation patients [33]. In our study, the patients reported a PFS of 4.2 m and an ORR of 34% in the PG, which is no better than the data in the CG and the data of previous studies, demonstrating that chemotherapy is an acceptable choice after the EGFR-TKIs failure. The above-mentioned findings also suggest that the evidence from personalized treatment is insufficient, for most of the above data are derived from retrospective research, preclinical studies, or small sample trials.

MET amplification has been implicated as one of the bypass resistance mechanisms to EGFR-TKI therapy. Numerous case reports and a growing number of clinical studies have documented the efficacy of the combinatorial regimen of EGFR-TKI and MET-TKI in simultaneously inhibiting both EGFR and MET signaling pathways to overcome EGFR-TKI resistance [34]. The combination of Tepotinib and Gefitinib has reported an amazing efficacy, with an ORR of 66.7% and a PFS of 16.6 m in the INSIGHT study [12]. Osimertinib plus savolitinib demonstrates a strong anti-tumor activity, with an ORR of 52% and a median duration of response (DOR) of 7.1 months in the TATTON Phase Ib expansion cohort [35]. In some trials and the real-world study, however, other MET inhibitors combined with EGFR-TKIs report a PFS of only 5-6 m [34, 36‐38]. Amivantamab (EGFR-MET bispecific antibody) with lazertinib has shown anti-tumor activity with ORR 36% and PFS 4.9 m in patients of disease progression upon EGFR-TKI [39]. But emibetuzumab (monoclonal bivalent MET antibody) plus erlotinib could not reverse the AR to EGFR-TKI [40]. In our research, the PFS was 4.2 m and ORR was 40.7% in patients with MET amplification in the PG. Therefore, the “quad” model chemotherapy may be a favorable choice to these patients and further studies are awaited to explore the beneficiary group of a personalized therapy.

The analysis of circulating tumor DNA from NSCLC patients reveals that 46% of patients treated with EGFR-TKIs may have multiple resistance mechanisms [41]. Alterations to cell cycle gene and the PI3K pathway were the most common co-occurring resistance mechanism [42]. The multiple resistance mechanisms pose a challenge to personalized therapy. Our study found that 13 patients had the multiple resistance mechanisms; cell cycle gene alterations and EGFR amplification were the most common co-occurring resistance mechanisms; 10 PG patients displayed multiple resistance mechanisms, with an ORR of 20% and a PFS of 4.0 m, which indicated no impact on the efficacy of the therapy.

Some limitations remain in this retrospective study. First, the data of overall survival and adverse events were not available, which may affect the benefit elucidation between the CG and PG. Second, only a small number of patients received ICI plus chemotherapy with or without anti‐angiogenic drugs, which might limit the interpretation to determine the optimal therapeutic strategy. Third, the data regarding PD-L1 expression were insufficient to determine whether PD-L1 expression was balanced across groups or to analyze the correlation between PD-L1 expression and ICI efficacy. There is not ongoing study to compare OS between two therapy modes, a prospective study in these patients can be conducted.

This retrospective study demonstrates that chemotherapy, especially combined with antiangiogenic therapy and immunotherapy, may serve as the standard treatment strategy for patients who experience disease progression after EGFR-TKIs failure.