Evidence map›Paper›PMID 42131879›Full record

ArticleEcancermedicalscience2026

Pattern of resistance on first-line EGFR-directed therapy in EGFR-positive metastatic NSCLC.

Sree Siva Kumar Raja Addagalla, Vanita Noronha, Nandini Menon, Minit Shah, Amit Joshi, Anokhi Shah, Kumar Prabhash

Abstract read
In one paragraph

Article in Ecancermedicalscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Sree Siva Kumar Raja AddagallaDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute (HBNI), Mumbai 400094, India.
Vanita NoronhaDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute (HBNI), Mumbai 400094, India.
Nandini MenonDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute (HBNI), Mumbai 400094, India.
Minit ShahDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute (HBNI), Mumbai 400094, India.
Amit JoshiDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute (HBNI), Mumbai 400094, India.
Anokhi ShahDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute (HBNI), Mumbai 400094, India.
Kumar PrabhashDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute (HBNI), Mumbai 400094, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and purpose: Resistance to epithelial growth factor receptor gene (EGFR)-tyrosine kinase inhibitors, both intrinsic and acquired, presents a major challenge in EGFR mutant non-small cell lung carcinoma (NSCLC), with the T790M mutation being the most common acquired resistance mechanism. Data on resistance patterns in the Indian population remains limited. Materials and methods: This Results: Of the 275 (78.6%) patients experiencing progressive disease (PD), a total of 206 patients were available for the final analysis after excluding patients without histological/molecular analysis.Histological transformation to small cell lung carcinoma (SCLC) occurred in 12 patients (6%), with various EGFR mutation statuses identified. T790M mutations were observed in 44 (37%) of 119 patients in the gefitinib arm and 17 (19%) of 87 patients in the gefitinib plus chemotherapy arm ( Interpretation: Emergence of T790M was lower than reported in previous studies, likely due to the addition of chemotherapy to gefitinib. T790M mutations were more prevalent in the gefitinib-alone arm. Histological transformation and loss of sensitising mutations highlight the importance of repeat biopsy and molecular testing to guide subsequent treatment decisions.

Indexed as

chemotherapyEGFR-TKIsNSCLCresistanceT790M

Identifiers

PMID42131879
PMCPMC13161586

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