Literature DB >> 30864146

PET-adapted therapy after three cycles of ABVD for all stages of Hodgkin lymphoma: results of the GATLA LH-05 trial.

Astrid Pavlovsky1,2, Isolda Fernandez1,2, Nicolas Kurgansky3, Virginia Prates4, Lucia Zoppegno5, Pedro Negri6, Gustavo Milone1, Ider Cerutti7, Soledad Zabaljauregui8, Romina Mariano9, Horacio F Grecco10, Ana L Basquiera11, Silvia Saba12, Silvia Rudoy13, Federico Sackmann1,2, Vanesa Castano7, Guillermina Remaggi2,14, Maria Cabrejo15, Eriberto Roveri7, Maria F Casale16, Vanina Cabane17, Rossana Taus12, Claudia Venturini6, Francisco Sakamoto6, Ana I Varela18, Maximiliano Riddick19, Santiago Pavlovsky1,2.   

Abstract

The role of Ann Arbor staging in determining treatment intensity after achieving a negative positron emission tomography (PET) has not been established in classical Hodgkin lymphoma (cHL). Patients with stage I-IV cHL, received three cycles of ABVD (doxorubicin, bleomycin, vinblastine, dacarbazine) and an interim PET scan (PET3). PET3-negative patients received no further therapy. PET3-positive patients received three additional cycles of ABVD plus involved-field radiation therapy or salvage chemotherapy, if refractory to ABVD, and were re-evaluated by PET scan (PET6). Study endpoints were 3-year progression-free survival (PFS) and overall survival (OS) rates. Two hundred and thirty-nine patients with early-stage and 138 with advanced-stage were evaluable. Overall, 260 patients (70%) were PET3-negative and had higher 3-year PFS (90% vs. 65%; P < 0·0001) and OS (98% vs. 92%; P = 0·007) rates than PET3-positive patients. All PET3-negative patients, regardless of disease stage at diagnosis, achieved similarly good PFS (90-91%; P = 0·76) and OS (97-99%). The only independent prognostic factor for PFS was PET3-negativity (Hazard ratio 3·8; 95% confidence interval 2·4-6·3; P < 0·0001). This study suggests that cHL patients who achieve a negative PET3 following ABVD have an excellent outcome, regardless of stage at diagnosis. An appropriately powered, phase III trial will be necessary to confirm these findings.
© 2019 British Society for Haematology and John Wiley & Sons Ltd.

Entities:  

Keywords:  zzm321990ABVDzzm321990; Hodgkin lymphoma; PET adapted therapy; prognostic factors; stage at diagnosis

Mesh:

Substances:

Year:  2019        PMID: 30864146     DOI: 10.1111/bjh.15838

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  4 in total

1.  Interim PET-results for prognosis in adults with Hodgkin lymphoma: a systematic review and meta-analysis of prognostic factor studies.

Authors:  Angela Aldin; Lisa Umlauff; Lise J Estcourt; Gary Collins; Karel Gm Moons; Andreas Engert; Carsten Kobe; Bastian von Tresckow; Madhuri Haque; Farid Foroutan; Nina Kreuzberger; Marialena Trivella; Nicole Skoetz
Journal:  Cochrane Database Syst Rev       Date:  2019-09-16

2.  Interim PET-results for prognosis in adults with Hodgkin lymphoma: a systematic review and meta-analysis of prognostic factor studies.

Authors:  Angela Aldin; Lisa Umlauff; Lise J Estcourt; Gary Collins; Karel Gm Moons; Andreas Engert; Carsten Kobe; Bastian von Tresckow; Madhuri Haque; Farid Foroutan; Nina Kreuzberger; Marialena Trivella; Nicole Skoetz
Journal:  Cochrane Database Syst Rev       Date:  2020-01-13

3.  Prognostic significance of interim PET/CT response for the treatment of advanced-stage marginal zone lymphoma in the post-rituximab era.

Authors:  Ho-Young Yhim; Deok-Hwan Yang; Ga-Young Song; Sang Eun Yoon; Seok Jin Kim; Jin Seok Kim; Youngil Koh; Joon-Ho Moon; Sung Yong Oh; Ho Sup Lee; Ho-Jin Shin; Young Rok Do; Won Sik Lee; Dae Sik Kim; Yong Park
Journal:  Sci Rep       Date:  2020-07-15       Impact factor: 4.379

4.  Retrospective Multicenter Real-Life Study on the First-Line Treatment of Classical Hodgkin Lymphoma in Argentina.

Authors:  Carolina Mahuad; Otero Victoria; Korin Laura; Martinez Enriqueta; Warley Fernando; García Rivello Hernán; Cristaldo Nancy; Kohan Dana; Zerga Marta; Garate Gonzalo; Vicente Repáraz María de Los Ángeles; Aizpurua Florencia; Rojas Bilbao Erica; Cerana Susana; Funes Maria Eugenia; Plaza Iliana; Foncuberta Cecilia; Vijnovich Baron Anahí; Cranco Santiago; Vitriu Adriana; Gomez Mariela; Lavalle Justina; Casali Claudia; Clavijo Manuela; Melillo Luciana; Cabral Lorenzo Maria Cecilia; Miroli Augusto; Fischman Laura; Pavlove Maximiliano; Miodosky Marcela; Cugliari Silvana
Journal:  Clin Hematol Int       Date:  2022-06-22
  4 in total

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