Evidence map›Paper›PMID 42105220›Full record

ArticleThe oncologist2026

Temozolomide reconsidered: Real-World evidence in resistant melanoma cases.

Jean Henri Maselli-Schoueri, Erika Martinez, Erick Lagos, Eduardo Felício de Campos, Erick F Saldanha, Thiago Pimentel Muniz, Marcus Otho Butler, Samuel David Saibil

Abstract readCase Reports
In one paragraph

Article in The oncologist, 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

8 authors.

Jean Henri Maselli-SchoueriPrincess Margaret Cancer Centre-Division of Medical Oncology & Hematology-Department of Medicine-Melanoma and Skin Cancer, University of Toronto, Toronto, ON M5G 2M9, Canada.ORCID 0000-0003-2509-3592
Erika MartinezPrincess Margaret Cancer Centre-Division of Medical Oncology & Hematology-Department of Medicine-Melanoma and Skin Cancer, University of Toronto, Toronto, ON M5G 2M9, Canada.
Erick LagosPrincess Margaret Cancer Centre-Division of Medical Oncology & Hematology-Department of Medicine-Melanoma and Skin Cancer, University of Toronto, Toronto, ON M5G 2M9, Canada.
Eduardo Felício de CamposPrincess Margaret Cancer Centre-Division of Medical Oncology & Hematology-Department of Medicine-Lung Cancer, University of Toronto, Toronto, ON M5G 2M9, Canada.
Erick F SaldanhaPrincess Margaret Cancer Centre-Division of Medical Oncology & Hematology-Department of Medicine-Phase I Study, University of Toronto, Toronto, ON M5G 2M9, Canada.
Thiago Pimentel MunizPrincess Margaret Cancer Centre-Division of Medical Oncology & Hematology-Department of Medicine-Melanoma and Skin Cancer, University of Toronto, Toronto, ON M5G 2M9, Canada.
Marcus Otho ButlerPrincess Margaret Cancer Centre-Division of Medical Oncology & Hematology-Department of Medicine-Melanoma and Skin Cancer, University of Toronto, Toronto, ON M5G 2M9, Canada.
Samuel David SaibilPrincess Margaret Cancer Centre-Division of Medical Oncology & Hematology-Department of Medicine-Melanoma and Skin Cancer, University of Toronto, Toronto, ON M5G 2M9, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors have transformed outcomes in melanoma and other aggressive malignancies. However, subsequent lines of therapy remain limited: modest efficacy, lack of publicly funded options, and declining performance status frequently restrict clinicians' choices. In this context, temozolomide has re-emerged as a feasible bridge therapy, with emerging evidence suggesting synergistic activity when used alongside anti-PD-1 agents. Here, we describe two cases of single-agent temozolomide administered after progression on prior systemic therapies, including anti-PD-1 and, in one case, targeted therapy, both demonstrating meaningful clinical responses and great patient tolerability. We also briefly discuss how these observations may support further exploration of temozolomide within modern treatment sequencing strategies.

Indexed as

Antineoplastic Agents, AlkylatingMelanomaTemozolomideDrug Resistance, NeoplasmFemaleHumansMaleMiddle AgedAntineoplastic Agents, AlkylatingTemozolomidemetastatic melanomasalvage therapytemozolomide

Identifiers

PMID42105220
PMCPMC13197114

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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 OpenQuestion graph.