How to choose first salvage therapy in Hodgkin lymphoma : traditional chemotherapy vs novel agents
Copyright © 2021 by The American Society of Hematology..
Approximately 10% to 30% of patients with classical Hodgkin lymphoma (cHL) develop relapsed or refractory (R/R) disease. Of those patients, 50% to 60% show long-term progression-free survival after standard salvage chemotherapy followed by high-dose chemotherapy (HDCT) and autologous stem cell transplant (ASCT). In the past decade, novel therapies have been developed, such as the CD30-directed antibody-drug conjugate brentuximab vedotin and immune checkpoint inhibitors, which have greatly extended the treatment possibilities for patients with R/R cHL. Several phase 1/2 clinical trials have shown promising results of these new drugs as monotherapy or in combination with chemotherapy, but unfortunately, very few randomized phase 3 trials have been performed in this setting, making it difficult to give evidence-based recommendations for optimal treatment sequencing. Two important goals for the improvement in the treatment of R/R cHL can be identified: (1) increasing long-term progression-free and overall survival by optimizing risk-adapted treatment and (2) decreasing toxicity in patients with a low risk of relapse of disease by evaluating the need for HDCT/ASCT in these patients. In this review, we discuss treatment options for patients with R/R cHL in different settings: patients with a first relapse, primary refractory disease, and in patients who are ineligible or unfit for ASCT. Results of clinical trials investigating novel therapies or strategies published over the past 5 years are summarized.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2021 |
---|---|
Erschienen: |
2021 |
Enthalten in: |
Zur Gesamtaufnahme - volume:2021 |
---|---|
Enthalten in: |
Hematology. American Society of Hematology. Education Program - 2021(2021), 1 vom: 10. Dez., Seite 240-246 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Driessen, Julia [VerfasserIn] |
---|
Links: |
---|
Themen: |
---|
Anmerkungen: |
Date Completed 16.02.2022 Date Revised 24.03.2022 published: Print Citation Status MEDLINE |
---|
doi: |
10.1182/hematology.2021000311 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM334259428 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM334259428 | ||
003 | DE-627 | ||
005 | 20231225223331.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2021 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1182/hematology.2021000311 |2 doi | |
028 | 5 | 2 | |a pubmed24n1114.xml |
035 | |a (DE-627)NLM334259428 | ||
035 | |a (NLM)34889399 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Driessen, Julia |e verfasserin |4 aut | |
245 | 1 | 0 | |a How to choose first salvage therapy in Hodgkin lymphoma |b traditional chemotherapy vs novel agents |
264 | 1 | |c 2021 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 16.02.2022 | ||
500 | |a Date Revised 24.03.2022 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2021 by The American Society of Hematology. | ||
520 | |a Approximately 10% to 30% of patients with classical Hodgkin lymphoma (cHL) develop relapsed or refractory (R/R) disease. Of those patients, 50% to 60% show long-term progression-free survival after standard salvage chemotherapy followed by high-dose chemotherapy (HDCT) and autologous stem cell transplant (ASCT). In the past decade, novel therapies have been developed, such as the CD30-directed antibody-drug conjugate brentuximab vedotin and immune checkpoint inhibitors, which have greatly extended the treatment possibilities for patients with R/R cHL. Several phase 1/2 clinical trials have shown promising results of these new drugs as monotherapy or in combination with chemotherapy, but unfortunately, very few randomized phase 3 trials have been performed in this setting, making it difficult to give evidence-based recommendations for optimal treatment sequencing. Two important goals for the improvement in the treatment of R/R cHL can be identified: (1) increasing long-term progression-free and overall survival by optimizing risk-adapted treatment and (2) decreasing toxicity in patients with a low risk of relapse of disease by evaluating the need for HDCT/ASCT in these patients. In this review, we discuss treatment options for patients with R/R cHL in different settings: patients with a first relapse, primary refractory disease, and in patients who are ineligible or unfit for ASCT. Results of clinical trials investigating novel therapies or strategies published over the past 5 years are summarized | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Review | |
700 | 1 | |a Tonino, Sanne H |e verfasserin |4 aut | |
700 | 1 | |a Moskowitz, Alison J |e verfasserin |4 aut | |
700 | 1 | |a Kersten, Marie José |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Hematology. American Society of Hematology. Education Program |d 2000 |g 2021(2021), 1 vom: 10. Dez., Seite 240-246 |w (DE-627)NLM115942556 |x 1520-4383 |7 nnns |
773 | 1 | 8 | |g volume:2021 |g year:2021 |g number:1 |g day:10 |g month:12 |g pages:240-246 |
856 | 4 | 0 | |u http://dx.doi.org/10.1182/hematology.2021000311 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 2021 |j 2021 |e 1 |b 10 |c 12 |h 240-246 |