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Anti-PD-1 therapy provides high response rates in Hodgkin lymphoma (HL) patients who have relapsed or are refractory (R/R) to autologous stem cell transplantation (ASCT) and brentuximab vedotin (BV), but median progression free survival (PFS) is only one year. The efficacy of treatment following anti-PD-1 is not well known.
In this context, the optimal treatment for patients who failed after anti-PD-1 therapy is an issue. To better assess their outcome, the investigators retrospectively analyzed the characteristics and outcome of patients from 14 LYSA (The Lymphoma Study Association) centers who lost response to anti-PD-1 therapy and received additional CT.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group 1 Sequential strategy | Patients for whom anti-PD-1 therapy was stopped with the introduction of a new treatment line (19 patients, 63%). |
| |
| Group 2 Concomitant strategy | Patients for whom a combination of CT with anti-PD-1 therapy was initiated (11 patients, 37 %). |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Evaluate the improvement in response from the end of anti-PD-1 monotherapy | Biological | Evaluate the improvement in response from the end of anti-PD-1 monotherapy to the first evaluation after introduction of CT alone (Group 1) or combined with anti-PD-1 (Group 2). |
| Measure | Description | Time Frame |
|---|---|---|
| Overall response rate after re-exposure to chemotherapy | Patient evaluation was timed by treating physicians according to the policy of each center, and all patients were evaluated after a median of 10 weeks (min 7 weeks, max 12 weeks) with PET/CT using Lugano criteria | 10 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Best response obtained (Group 1) | the best response obtained with CT after anti-PD-1 | 10 weeks |
| Best response obtained (Group 2) | the best response obtained with CT after the combination anti-PD-1 and CT |
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Inclusion Criteria:
Exclusion Criteria:
- radiotherapy in the treatment after anti-PD1
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The initial diagnosis of classical HL was established from biopsies in accordance with the 2008 World Health Organization classification14. We retrospectively analyzed 30 R/R classical HL patients from 14 LYSA centers who received anti-PD-1 therapy as part of a clinical trial (n=4), from an off-label program authorization for temporary use (ATU) from the French medical drug agency (Agence Nationale de Sécurité du Médicament, ANSM) (n=22), from the Belgian national system for the reimbursement of health care (Institut National d'Assurance Maladie Invalidité, INAMI) (n=4).
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| Name | Affiliation | Role |
|---|---|---|
| Hervé GHESQUIERES, MD | Hospices Civils de Lyon | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre Hospitalier Lyon Sud | Pierre-Bénite | France |
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| ID | Term |
|---|---|
| D006689 | Hodgkin Disease |
| ID | Term |
|---|---|
| D008223 | Lymphoma |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D008232 | Lymphoproliferative Disorders |
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| 10 weeks |
| The toxicities experienced during CT or anti-PD-1 plus CT combination | The toxicities were graded retrospectively according to the National Cancer Institute Common Toxicity Criteria for AEs (version 4.0). | 10 weeks |
| Outcomes including PFS | PFS was defined as the time from first relapse, or progression, to the next event (defined as either second relapse/progression, change of therapy, or death from any cause) | up to 12 months |
| Outcomes including overall survival (OS). | OS was defined as the time from first relapse, or progression, to death from any cause. | up to 24 months |
| D008206 |
| Lymphatic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |