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CANCER:

Hodgkin Lymphoma

Related cancers:
24h
Feasibility of High Intensity Interval Training in Survivors of Childhood, Adolescent, and Young Adult Hodgkin Lymphoma (clinicaltrials.gov)
P=N/A, N=20, Recruiting, St. Jude Children's Research Hospital | Not yet recruiting --> Recruiting
Enrollment open
4d
A Study of AUR104 in Patients With Relapsed/Refractory Lymphoid Malignancies (VIJAY-1) (clinicaltrials.gov)
P1, N=9, Terminated, Aurigene Discovery Technologies Limited | N=42 --> 9 | Trial completion date: Jan 2027 --> Feb 2026 | Recruiting --> Terminated | Trial primary completion date: Nov 2026 --> Feb 2026; Patient recruitment problems
Enrollment change • Trial completion date • Trial termination • Trial primary completion date
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AU7R-104 • XL114
4d
SURYA-1: First in Human, Dose Escalation, Dose Expansion Study of AUR105 (clinicaltrials.gov)
P1, N=17, Terminated, Aurigene Discovery Technologies Limited | N=40 --> 17 | Recruiting --> Terminated; Patient recruitment problems.
Enrollment change • Trial termination • First-in-human
6d
Autologous Stem Cell Transplant Followed by Polatuzumab Vedotin in Patients With B-cell Non-Hodgkin and Hodgkin Lymphoma (clinicaltrials.gov)
P1/2, N=20, Recruiting, New York Medical College | Trial completion date: Aug 2025 --> Aug 2027 | Trial primary completion date: Aug 2024 --> Aug 2026
Trial completion date • Trial primary completion date
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CD20 (Membrane Spanning 4-Domains A1) • CD34 (CD34 molecule)
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Polivy (polatuzumab vedotin-piiq)
7d
Adriamycin, Vinblastine and Dacarbazine With Immunotherapy Achieves Complete Metabolic Response in a Patient With Classical Hodgkin Lymphoma and Dyskeratosis Congenita. (PubMed, J Hematol)
To mitigate pulmonary and myelotoxicity risks, he received a modified regimen of brentuximab vedotin (BV) combined with adriamycin, vinblastine, and dacarbazine (BV-AVD), with full omission of bleomycin. It underscores the critical need for individualized therapy in patients with DC and supports careful consideration of radiation omission to reduce secondary malignancy risk. These findings provide a potential therapeutic framework for managing Hodgkin lymphoma in patients with DC.
Journal • IO biomarker
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TNFRSF8 (TNF Receptor Superfamily Member 8)
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doxorubicin hydrochloride • Adcetris (brentuximab vedotin) • dacarbazine • bleomycin • vinblastine
7d
Trial initiation date
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TMB (Tumor Mutational Burden) • MSI (Microsatellite instability)
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TMB-H • MSI-H/dMMR
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Keytruda (pembrolizumab)
8d
The Prospective Collection, Storage and Reporting of Data on Patients Undergoing Hematopoietic Stem Cell Transplantation Utilizing a Standard Preparative Regimen (clinicaltrials.gov)
P=N/A, N=2000, Recruiting, Wake Forest University Health Sciences | Trial completion date: Jun 2026 --> Dec 2026 | Trial primary completion date: Jun 2026 --> Dec 2026
Trial completion date • Trial primary completion date
8d
Trial completion date
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Opdivo (nivolumab) • doxorubicin hydrochloride • Adcetris (brentuximab vedotin) • dacarbazine • vinblastine • Neulasta (pegfilgrastim) • ABP 206 (nivolumab biosimilar) • Neupogen (filgrastim)
11d
SSTR2 expression in EBV-positive and EBV-negative lymphomas. (PubMed, J Hematop)
Our study demonstrates that EBV infection is required, but not sufficient, to upregulate SSTR2 in classic Hodgkin lymphoma, but not in other EBV-associated lymphomas. We also provide data to suggest that SSTR2 is associated with "higher-grade" germinal center-derived B-cell lymphomas in EBV-negative non-Hodgkin lymphomas.
Retrospective data • Journal • IO biomarker
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BCL2 (B-cell CLL/lymphoma 2) • SSTR (Somatostatin Receptor) • SSTR2 (Somatostatin Receptor 2)
12d
Phase Ib of L-NMMA and Pembrolizumab (clinicaltrials.gov)
P1, N=12, Completed, The Methodist Hospital Research Institute | Active, not recruiting --> Completed
Trial completion • Mismatch repair • Tumor mutational burden • IO biomarker • MSI-H • dMMR
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PD-L1 (Programmed death ligand 1) • BRAF (B-raf proto-oncogene) • TMB (Tumor Mutational Burden) • MSI (Microsatellite instability)
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PD-L1 expression • TMB-H • MSI-H/dMMR • BRAF mutation
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Keytruda (pembrolizumab) • tilarginine (L-NMMA)
13d
Circulating miR-148a-3p Correlates with Inadequate Induction Response in Pediatric Hodgkin Lymphoma. (PubMed, Immunotargets Ther)
Subsequent quantitative reverse transcription-polymerase chain reaction (qRT-PCR) validation demonstrated significantly elevated miR‑148a‑3p levels at diagnosis in inadequate responders to induction therapy than in adequate responders (p=0.009). These results indicate that circulating miR‑148a‑3p may enhance current predictive approaches by identifying high‑risk patients less likely to achieve rapid metabolic remission.
Journal
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MIR148A (MicroRNA 148a)
13d
BRESELIBET: BREntuximab Vedotin in SEcond LIne Therapy BEfore Transplant (clinicaltrials.gov)
P2, N=150, Active, not recruiting, Grupo Español de Linfomas y Transplante Autólogo de Médula Ósea | Not yet recruiting --> Active, not recruiting
Enrollment closed
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TNFRSF8 (TNF Receptor Superfamily Member 8)
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cytarabine • Adcetris (brentuximab vedotin) • methylprednisolone sodium succinate