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DOI 10.1038/s41416-026-03631-7

Медицинская библиотека · British journal of cancer · 2026

Paediatric therapeutic development workshop on desmoplastic small round cell tumours.

Baxter Joseph S, Molenaar Jan J, Agrawal Arushi, Amaral Ana Teresa, Blanc Patricia, Bowdidge Nikki, Bowdidge Richard, Brennan Bernadette, Casanova Michela, da Silva Moura David, Daems Sam, Danielson Laura, English Solomon, Grohar Patrick, Halliwell Emma, Huang Paul, Kearns Pamela, Klebanoff Christopher A, Klaourakis Konstantinos, Ladanyi Marc, Lass Geffen, Lawlor Katerina, Linardic Corinne M, Ludwig Joseph, Man Stella, Mascarenhas Leo, Metayer Lucy, Meister Michael Torsten, Minard-Colin Veronique, Oldham Siwan, Orbach Daniel, Patel Sheena, Pasquali Sandro, Schoot Reineke A, Sellar Rob, Shipley Janet, Sparber-Sauer Monika, Stacchiotti Silvia, Tap William, Torrezan Giovana Tardin, Truong Danh D, van de Wetering Marc, Wane Madina, Waterfall Joshua J, Weiss Aaron, Vasquez-Campbell Janet, Pearson Andrew Dj, Jenkinson David, Ferrari Andrea, Postel-Vinay Sophie, Slotkin Emily, LifeArc, Innovative Therapies for Children with Cancer (ITCC), Cancer Research UK, Cancer Grand Challenge Protect team

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Аннотация

The sixth Paediatric Therapeutic Development Workshop focused on desmoplastic small round cell tumours (DSRCT). Less than 20% of patients with DSRCT survive beyond 5 years and there is no targeted therapy for this disease, which represents an urgent unmet need for new therapeutics. High priority targets include the EWSR1::WT1 fusion protein, the oncogenic driver, and targeting a junction-derived neopeptide presented by HLA-A*03 and HLA-A*11 using a T-cell receptor (TCR) is a novel approach. Other targets (LRRC15, SSTR3 and SSTR5, NECTIN4, STEAP1 and mesothelin) require further validation. Targeting ERBB2/HER2 or claudin-6 by antibody-drug conjugates (ADCs) and NTRK3 by a small molecule inhibitor are promising approaches and are currently being evaluated. Existing clinical assets targeting (in order of importance) B7-H3, the DNA damage response, androgen signalling, FGFR4 and STEAP1 are also high priorities for evaluation in DSRCT, but obtaining therapeutics for clinical trials is a barrier. In view of the rarity of DSRCT, a global initiative in preclinical and clinical research to establish international trials and collect data from patients treated in a harmonised form would benefit patients. Progress can be made by a combined approach of developing new agents whilst evaluating existing therapeutics in well-designed trials.

Для цитирования: Baxter Joseph S, Molenaar Jan J, Agrawal Arushi, Amaral Ana Teresa, Blanc Patricia, Bowdidge Nikki, Bowdidge Richard, Brennan Bernadette, Casanova Michela, da Silva Moura David, Daems Sam, Danielson Laura, English Solomon, Grohar Patrick, Halliwell Emma, Huang Paul, Kearns Pamela, Klebanoff Christopher A, Klaourakis Konstantinos, Ladanyi Marc, Lass Geffen, Lawlor Katerina, Linardic Corinne M, Ludwig Joseph, Man Stella, Mascarenhas Leo, Metayer Lucy, Meister Michael Torsten, Minard-Colin Veronique, Oldham Siwan, Orbach Daniel, Patel Sheena, Pasquali Sandro, Schoot Reineke A, Sellar Rob, Shipley Janet, Sparber-Sauer Monika, Stacchiotti Silvia, Tap William, Torrezan Giovana Tardin, Truong Danh D, van de Wetering Marc, Wane Madina, Waterfall Joshua J, Weiss Aaron, Vasquez-Campbell Janet, Pearson Andrew Dj, Jenkinson David, Ferrari Andrea, Postel-Vinay Sophie, Slotkin Emily, LifeArc, Innovative Therapies for Children with Cancer (ITCC), Cancer Research UK, Cancer Grand Challenge Protect team. Paediatric therapeutic development workshop on desmoplastic small round cell tumours.. British journal of cancer. 2026. DOI: 10.1038/s41416-026-03631-7.
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