Evidence map›Paper›PMID 42649862›Full record

ReviewCancers2026

Small Cell Lung Cancer in Transition: Recent Advances in Biology, Treatment, and Precision Medicine.

Supriya Peshin, Ehab Takrori, Mohammad Sajid Mithani, Deepthi Devagudi, Joseph H Yazji, Ayse Gul Korkmaz, Adit Dharia, Waleed Maher Mohammad Tayyem, Shaas Ibrahim Qadoumi, Sakshi Singal

Abstract readReview
In one paragraph

Review in Cancers, 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

10 authors.

Supriya PeshinDivision of Geriatrics, Department of Internal Medicine, University of Arkansas for Medical Sciences, Little Rock, AR 72204, USA.ORCID 0000-0002-3895-9474
Ehab TakroriCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.ORCID 0009-0009-9062-9761
Mohammad Sajid MithaniCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
Deepthi DevagudiDepartment of Hospital Medicine, Adventist Health Hanford, Hanford, CA 93230, USA.
Joseph H YazjiDepartment of Internal Medicine, HCA Florida Oak Hill Hospital, Brooksville, FL 34613, USA.
Ayse Gul KorkmazDepartment of Internal Medicine, HCA Florida Oak Hill Hospital, Brooksville, FL 34613, USA.ORCID 0009-0009-3062-2680
Adit DhariaDepartment of Internal Medicine, HCA Florida Oak Hill Hospital, Brooksville, FL 34613, USA.
Waleed Maher Mohammad TayyemFaculty of Medicine, Jordan University of Science and Technology (JUST), Irbid 22110, Jordan.
Shaas Ibrahim QadoumiCollege of Medicine, Misr University for Science and Technology, Giza 12566, Egypt.
Sakshi SingalDivision of Hematology and Oncology, Department of Internal Medicine, East Tennessee State University, Johnson City, TN 37614, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small cell lung cancer (SCLC) is a highly aggressive neuroendocrine malignancy associated with rapid proliferation, early metastatic spread, and poor long-term survival. Despite high initial responsiveness to chemotherapy and radiotherapy, most patients experience relapse, and therapeutic progress historically remained limited. Recent years, however, have seen meaningful advances that are beginning to reshape the management of SCLC. In extensive-stage disease, the incorporation of PD-L1 inhibitors into platinum-etoposide chemotherapy has established chemoimmunotherapy as the first-line standard, while underscoring the continued need for more durable disease control. In limited-stage SCLC, consolidation durvalumab following concurrent chemoradiotherapy has emerged as a practice-changing strategy with significant survival benefit. In relapsed disease, DLL3-targeted therapy has opened a new therapeutic avenue, with tarlatamab demonstrating clinically relevant efficacy in previously treated extensive-stage SCLC and becoming the first approved bispecific T-cell engager in this setting. Alongside these milestones, ongoing investigation is focused on maintenance strategies, novel targeted agents, biomarker development, molecular subtyping, and more effective integration of systemic therapy with radiation-based approaches. Nevertheless, resistance, toxicity management, central nervous system involvement, and the absence of validated predictive biomarkers remain major barriers to sustained progress. This narrative review examines recent advances in the biology and clinical management of SCLC, with emphasis on practice-changing developments, emerging therapeutic platforms, and future strategies aimed at improving outcomes in this historically difficult-to-treat disease.

Indexed as

brain metastasischemoimmunotherapycirculating tumor DNADLL3durvalumabliquid biopsymolecular subtypesprecision medicinesmall cell lung cancertarlatamab

Identifiers

PMID42649862
PMCPMC13511499

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.