Prognostic Impact of TP53 Mutations in Metastatic Nonsquamous Non–small-cell Lung Cancer

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Laurent Mathiot , Benoit Nigen , Thomas Goronflot , Sandrine Hiret , Ludovic Doucet , Elvire Pons-Tostivint , Jaafar Bennouna , Marc G. Denis , Guillaume Herbreteau , Judith Raimbourg
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Abstract

Background

The prognostic impact of TP53 mutations in advanced or metastatic nonsquamous non–small-cell lung cancer (nsNSCLC) patients treated with chemotherapy and/or immune checkpoint inhibitors (ICI) remains unclear.

Materials and Methods

We retrospectively collected data from patients with nsNSCLC treated in the first line from January 2018 to May 2021. The patient was separated into 2 groups according to their TP53 mutation status (wt vs. mut). Survival was estimated through the Kaplan-Meier method and compared by log-rank test.

Results

Of 220 patients included, 126 were in the mutTP53 group, and 94 were in the wtTP53wt group. Median OS (mOS) was not significantly different between the mutTP53 and wtTP53 groups [17.5 months (95% confidence interval (CI), 11.3-21.5) vs. 9.5 months (95% CI, 7.4-14.2), (P = .051)]. In subgroup analyses, the mutTP53 group treated with ICI had a significantly improved mOS compared to the wtTP53 group [(24.7 months (95% CI, 20.8–not reach) vs. 12.0 months (95% CI, 4.7–not reach), (P = .017)] and mPFS [(9.6 months (95% CI, 5.8–not reach) vs. 3.2 months (95% CI, 1.3-13.8) (P = .048)]. There was no difference in terms of mOS and mPFS between the mutTP53 and the wtTP53 group treated by chemotherapy alone or combined with ICI.

Conclusion

TP53 mutation had no survival impact in the overall population, but is associated with better outcomes with ICI alone. These results suggest that patients with TP53 mutations could be treated with ICI alone, and wild-type patients could benefit from the addition of chemotherapy.

TP53突变对转移性非鳞状非小细胞肺癌预后的影响
背景TP53突变对接受化疗和/或免疫检查点抑制剂(ICI)治疗的晚期或转移性非鳞状非小细胞肺癌(nsNSCLC)患者的预后影响仍不明确。根据TP53突变状态(wt vs mut)将患者分为两组。结果 在纳入的220例患者中,突变TP53组126例,wtTP53wt组94例。突变TP53组和wtTP53组的中位OS(mOS)无明显差异[17.5个月(95%置信区间(CI),11.3-21.5) vs. 9.5个月(95% CI,7.4-14.2),(p = 0.051)]。在亚组分析中,与 wtTP53 组相比,接受 ICI 治疗的 mutTP53 组的 mOS[(24.7 个月(95% CI,20.8 个月未达标)vs 12.0 个月(95% CI,4.7 个月未达标),(p = 0.017)]和 mPFS[(9.6 个月(95% CI,5.8 个月未达标)vs 3.2 个月(95% CI,1.3-13.8 个月)(p = 0.048)]显著改善。突变TP53组和wtTP53组在单独化疗或联合ICI治疗的mOS和mPFS方面没有差异。这些结果表明,TP53突变患者可单独接受ICI治疗,而野生型患者则可从化疗中获益。我们分析了TP53突变对220例nsNSCLC患者总生存期和无进展生存期的影响。单用免疫检查点抑制剂(ICI)对TP53突变患者有效,但对其他患者可能不利。对于没有TP53基因突变的患者,加用化疗可改善其预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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