Evidence map›Paper›PMID 42239618›Full record

ReviewTherapeutic advances in medical oncology2026

Treatment options in platinum-refractory male germ cell cancers: current standards and future directions.

Marco Oltrecolli, Domiziana Alaimo, Fabrizio Di Costanzo, Giovanni Rosti, Pasquale Rescigno, Massimo Dominici, Winfried Alsdorf, Carsten Bokemeyer, Christoph Oing, Christoph Seidel

Abstract readReview
In one paragraph

Review in Therapeutic advances in medical oncology, 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.

Marco OltrecolliNorthern Centre for Cancer Care, Freeman Hospital, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Domiziana AlaimoNorthern Centre for Cancer Care, Freeman Hospital, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Fabrizio Di CostanzoNorthern Centre for Cancer Care, Freeman Hospital, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Giovanni RostiDepartment of Oncology, Comprehensive Cancer Centre, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Pasquale RescignoNorthern Centre for Cancer Care, Freeman Hospital, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Massimo DominiciDepartment of Oncology and Hematology, Azienda Ospedaliero-Universitaria of Modena, Modena, Italy.
Winfried AlsdorfDepartment of Oncology, Hematology and Stem Cell Transplantation with Division of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Carsten BokemeyerDepartment of Oncology, Hematology and Stem Cell Transplantation with Division of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Christoph OingNorthern Centre for Cancer Care, Freeman Hospital, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Christoph SeidelDepartment of Oncology, Hematology and Stem Cell Transplantation with Division of Pneumology, University Medical Centre Hamburg-Eppendorf, Hamburg 20246, Germany.ORCID https://orcid.org/0000-0002-6023-6336

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Germ cell cancers (GCCs) represent the most common malignant tumours among men up to the age of 40 years. GCCs are characterised by high cure rates of >99% for localised stage I disease, but even at advanced metastatic stages, 67%-96% of patients can be cured with multimodal treatment approaches. The high curability owes to an exceptional responsiveness to cisplatin-based chemotherapy. However, about 30% of patients with metastatic disease eventually relapse after first-line multimodality treatment. At first relapse, salvage treatment still cures approximately 50% of patients. Platinum-based chemotherapy remains the standard of care in this setting, administered either as conventional-dose cisplatin-based regimens or as high-dose carboplatin-based combination chemotherapy. Across multiple large retrospective cohorts, high-dose chemotherapy has repeatedly been associated with superior progression-free and overall survival compared with conventional-dose approaches, although definitive prospective evidence is awaited. Patients suffering second or multiple relapses are considered platinum-resistant and face a very dismal prognosis with a life expectancy generally limited to less than 12 months. The mainstay of treatment in this setting is still conventional cytotoxic chemotherapy since no molecularly targeted treatments have shown clinically meaningful activity, to date. However, Claudin-6 (CLDN6)-directed approaches appear the most promising avenue of new treatment options in this situation. In this narrative review, we outline established and emerging treatment opportunities for this rare but challenging clinical scenario of platinum-resistant GCCs. This review provides a focused and up-to-date synthesis of therapeutic options for multiply relapsed, platinum-refractory GCCs, with a particular emphasis on late-line treatment sequencing and emerging biomarker-driven strategies, including CLDN6-directed therapies.

Indexed as

antibody–drug conjugatescellular therapychemotherapycisplatin resistancegerm cell cancertesticular cancer

Identifiers

PMID42239618
PMCPMC13226988

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Registered trials

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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.