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Interim PET-guided ABVD or ABVD/escalated BEACOPP for newly diagnosed advanced-stage classic Hodgkin lymphoma (JCOG1305).
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- Additional Information
- Source:
Publisher: Wiley Publishing on behalf of the Japanese Cancer Association Country of Publication: England NLM ID: 101168776 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1349-7006 (Electronic) Linking ISSN: 13479032 NLM ISO Abbreviation: Cancer Sci Subsets: MEDLINE
- Publication Information:
Publication: 2005- : Oxford : Wiley Publishing on behalf of the Japanese Cancer Association
Original Publication: Tokyo : Japanese Cancer Association, c2003-
- Subject Terms:
- Abstract:
This single-arm confirmatory study (JCOG1305) aimed to evaluate the utility of interim positron emission tomography (iPET)-guided therapy for newly diagnosed advanced-stage classic Hodgkin lymphoma (cHL). Patients aged 16-60 years with cHL received two cycles of doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) and then underwent an iPET scan (PET2), which was centrally reviewed using a five-point Deauville scale. PET2-negative patients continued an additional four cycles of ABVD, whereas PET2-positive patients switched to six cycles of escalated bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (eBEACOPP). The co-primary endpoints were 2-year progression-free survival (PFS) among all eligible and PET2-positive patients. Ninety-three patients were enrolled between January 2016 and December 2019. One patient was ineligible because of a diagnostic error. The median age of the 92 eligible patients was 35 (interquartile range, 28-48) years. Forty (43%) patients had stage III disease, and 43 (47%) had stage IV disease. The remaining nine (10%) patients had stage IIB disease with risk factors. Nineteen PET2-positive (21%) patients received eBEACOPP, 18 completed six cycles of eBEACOPP, 73 PET2-negative (79%) patients continued ABVD, and 70 completed an additional four cycles of ABVD. With a median follow-up period of 41.1 months, the 2-year PFS of 92 eligible patients and 19 PET2-positive patients were 84.8% (80% confidence interval [CI], 79.2-88.9) and 84.2% (80% CI, 69.7-92.1), respectively. Both primary endpoints were met at the prespecified threshold. This study demonstrates that iPET-guided therapy is a useful treatment option for younger patients with newly diagnosed advanced-stage cHL. Registration number: jRCTs031180218.
(© 2024 The Author(s). Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.)
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- Grant Information:
JP16ck0106220 Japan Agency for Medical Research and Development; 19ck0106509 Japan Agency for Medical Research and Development; 25-A-13 National Cancer Center Research and Development Funds; 26-A-4 National Cancer Center Research and Development Funds; 29-A-3 National Cancer Center Research and Development Funds; 2020-J-3 National Cancer Center Research and Development Funds; 2023-J-03 National Cancer Center Research and Development Funds
- Contributed Indexing:
Keywords: ABVD; advanced‐stage; cHL; escalated BEACOPP; interim PET‐guided
- Accession Number:
11056-06-7 (Bleomycin)
7GR28W0FJI (Dacarbazine)
80168379AG (Doxorubicin)
35S93Y190K (Procarbazine)
5J49Q6B70F (Vincristine)
5V9KLZ54CY (Vinblastine)
6PLQ3CP4P3 (Etoposide)
VB0R961HZT (Prednisone)
8N3DW7272P (Cyclophosphamide)
- Subject Terms:
ABVD protocol; BEACOPP protocol
- Publication Date:
Date Created: 20240722 Date Completed: 20241003 Latest Revision: 20241005
- Publication Date:
20241005
- Accession Number:
PMC11447878
- Accession Number:
10.1111/cas.16281
- Accession Number:
39034771
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