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475 PET-Guided Strategy Improves the Safety of Beacopp-Based Treatment in Advanced Hodgkin Lymphoma: Prolonged Follow-up of the Lysa Ahl 2011 Phase 3 StudyClinically Relevant Abstract

Program: Oral and Poster Abstracts
Type: Oral
Session: 624. Hodgkin Lymphoma and T/NK Cell Lymphoma—Clinical Studies: Clinical Studies in Hodgkin Lymphoma
Hematology Disease Topics & Pathways:
Adult, Diseases, Non-Biological, Hodgkin Lymphoma, Therapies, chemotherapy, Adverse Events, Lymphoid Malignancies, Study Population, Clinically relevant
Sunday, December 6, 2020: 3:15 PM

Olivier Casasnovas, MD1*, Judith Racape, MD2*, Julie Dechene3*, Reda Bouabdallah, MD4*, Pauline Brice, MD5*, Julien Lazarovici, MD6*, Hervé Ghesquieres, MD, PhD7*, Aspasia Stamatoulas Bastard, MD8*, Jehan Dupuis, MD9*, Anne-Claire Gac, MD10*, Thomas Gastinne, MD11*, Bertrand Joly, MD12*, Krimo Bouabdallah, MD13*, Emmanuelle Nicolas-Virelizier, MD14*, Pierre Feugier, MD15*, Franck Morschhauser, MD, PhD16,17*, Marc André, MD18*, Alina Berriolo-Riedinger, MD19*, Veronique Edeline, MD20*, Clémentine Joubert, PhD21*, Michel Meignan, MD22* and Isabelle Demeestere, MD23*

1Hematology Department, University Hospital F. Mitterrand and Inserm UMR 1231, Dijon, France
2Research Center in Epidemiology, School of public Health, and Biomedical Research Department, CUB-Erasme Université Libre de Bruxelles, Brussels, Belgium
3Research Laboratory on Human Reproduction, Université Libre de Bruxelles, Brussels, Belgium
4Institut Paoli-Calmettes, Marseille, France
5Department of Hematology, APHP, Hopital Saint Louis, Paris, France
6Department of hematology, Gustave Roussy Cancer Campus Grand Paris, Villejuif CEDEX, France
7Department of Hematology, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Pierre Benite, France
8Department of Hematology, Centre Henri Becquerel, Rouen, France
9Lymphoid Malignancies, Henri Mondor Hospital, Creteil, France
10Institut d'Hématologie de Basse-Normandie, CHU de Caen Normandie, Caen, France
11Clinical Hematology, Nantes University Hospital, Nantes, France
12Department of hematology, CH Sud Francilien, Corbeil Essonnes, FRA
13Department of Hematology, University Hospital of Bordeaux, Pessac, France
14Hematology, Centre Leon Berard, Lyon, France
15Department of Hematology, Henri Poincaré University, CHU NANCY BRABOIS, Vandoeuvre Les Nancy, France
16Department of Hematology, University Lille, CHU Lille, EA 7365 - GRITA - Groupe de Recherche sur les forms Injectables et les Technologies Associées, Lille, France
17Clinical Hematology Department, Centre Hospitalier Régional Universitaire de Lille, Lille, France
18Department of Hematology, CHU UCL Namur - Site Godinne, Yvoir, Belgium
19Department of Nuclear Medicine, Centre Georges Francois Leclerc, University of Dijon, Dijon, France
20Service de Médecine Nucléaire, Hopital Rene Huguenin-Institut Curie, Saint Cloud, France
21Lymphoma Academic Research Organization, Lyon, France
22LYSA, Paris, France
23Fertility Clinic, CUB-Erasme Hospital, and Research Laboratory on Human Reproduction, Université Libre de Bruxelles, Brussels, Belgium

Background

AHL2011 study (NCT01358747) demonstrated that PET negativity after 2 cycles of upfront BEACOPPescalated (BEA) allows to switch to 4 cycles of ABVD 84% of patients (pts) with advanced Hodgkin lymphoma (HL) leading to reduce immediate treatment toxicity without loss of tumor control (Casasnovas RO, Lancet Oncol 2019). We report an updated follow-up of the study with a focus on the late treatment-related adverse events including secondary primary malignancies (SPM) and unfertility.

Methods

In AHL2011 823 patients aged 18-60 with a newly diagnosed advanced HL defined by an Ann Arbor stage III, IV or IIB with M/T>0.33 or extranodal involvement were prospectively randomized between a standard arm (n=413) delivering 6 x BEA and a PET-driven arm (n=410) after 2 x BEA delivering 4 x ABVD in PET2- pts and 4 x BEA in PET2+ pts. In both arms PET performed after 4 cycles of chemotherapy had to be negative to complete the planned treatment. We aimed at excluding inferiority of the PET-driven arm of at least 10% compared to the standard arm which was achieved with the analysis on 10/2017. The data cutoff for the present analysis was 29 April 2019.

A prospective fertility substudy for patients <45y at time of randomization was performed analyzing: - In females, ovarian function using serum levels of FSH, estradiol and centralized anti-mullerian hormone (AMH) measurements. Acute premature ovarian insufficiency (POI) was defined as FSH > 24 IU/L twice during 5y follow-up when available, with estradiol < 50pg/ml, and low ovarian reserve (OR) by AMH < 0.16ng/ml. – In males, FSH serum levels and sperm analysis.

Results

With a 5.6 year median follow-up, 5y PFS and OS were similar in both randomization arms (PFS: 87.5% vs 86.7% ; HR 1.07, 95%CI 0.74-1.57; p=0.67; OS: 97.7% in both arms; HR=1.012, 95%CI 0.50-2.10; p=0.53). In the whole cohort full interim PET assessment predicted patients PFS (5y PFS = 92.3% in PET2-/PET4-, 75.4% [HR= 3.26 ; 95%CI 18.3-5.77] in PET2+/PET4- and 46.5% [HR= 12.4 ; 95%CI : 7.31-19.51] in PET4+ pts respectively; p <0.0001; figure 1) independently of IPS. OS was also impacted by interim PET results and PET2+/PET4- patients (5y OS : 93.5% ; HR=3.3, 95%CI : 1.07-10.1; p=0.036) and PET4+ patients (5y OS 91.9%; HR=3.756, 95%CI 1.07-13.18, p=0.038) had a significant lower OS than PET2-/PET4- patients (98.2%).
22 patients (2.7%) developped a secondary primary (SPM), 13 (3.2%) and 9 (2.2%) in the standard and experimental arms respectively.
424 males and 145 females with a median age 27y (16 – 45) entered the fertility sub-study. Baseline ovarian functions based on FSH and AMH levels were similar in the 70 and 75 female of the standard and PET-driven arms. During follow-up, 32 pts experienced POI (46.1% versus 14.5% in the standard and PET-driven arms, respectively). The risk of POI was significantly associated with both age, total dose of alkylating agents, and was reduced in the PET-driven arm (HR=0.20, 95%CI 0.08-0.5; p<0.001). The risk of low OR was related to cumulative dose of etoposide >5g (HR=0.36, 95%CI 0.14-0.96; p=0.04) but not to arms. In males, median baseline FSH levels were similar in both arms but 19 and 23% experienced severe oligospermia at baseline in standard (n=214) and PET-driven arms (n=210), respectively. Chemotherapy dramatically reduced sperm numeration in both arms but recovery occured more frequently in the PET-driven arm (severe oligospermia at 4-5 year: 50% vs 93%). A total of 84 patients (14.7%) reported pregnancies including 49 (17.2%) in the PET driven arm vs 35 (12.3%) in the standard arm (p=0.12) and required assisted reproductive technology treatment more frequently in the standard arm (23% vs 14%).

Conclusions

The prolonged follow-up confirms that the PET-driven strategy delivering 4 cycles of ABVD in PET negative patients after 2 cycles of BEA is non inferior compared to standard 6 cycles of BEA. PET4 provides additionnal prognostic information to PET2 and identifies patients with particularly poor prognosis. The PET-driven treatment allows to reduce significantly the risk of infertility in both men (recovery of oligospermia) and women (decreasing by 5 the risk of POI) and improves the chances of spontaneous pregnancy after completion of HL treatment. With the current follow-up the risk of SPM was low (2.7%) and similar in both arms.

Disclosures: Casasnovas: Roche: Consultancy, Honoraria, Research Funding; Takeda: Consultancy, Honoraria, Research Funding; Gilead: Consultancy, Honoraria, Research Funding; MSD: Consultancy, Honoraria; BMS: Consultancy, Honoraria; AMGEN: Consultancy, Honoraria; abbvie: Consultancy, Honoraria. Brice: Takeda: Honoraria, Other: TRAVEL, ACCOMMODATIONS, EXPENSES; BMS: Honoraria; MSD: Honoraria; Roche: Other: TRAVEL, ACCOMMODATIONS, EXPENSES. Ghesquieres: Gilead: Consultancy, Honoraria, Other: TRAVEL, ACCOMMODATIONS, EXPENSES; CELGENE: Consultancy, Other: TRAVEL, ACCOMMODATIONS, EXPENSES; Roche: Consultancy, Other: TRAVEL, ACCOMMODATIONS, EXPENSES; Janssen: Honoraria. Stamatoulas Bastard: Takeda: Consultancy; Celgene: Honoraria; Pfizer: Other: TRAVEL, ACCOMMODATIONS, EXPENSES. Dupuis: Henri Mondor University Hospital Creteil France: Current Employment. Gac: Roche: Consultancy; Takeda: Consultancy. Bouabdallah: Takeda: Consultancy, Honoraria; Roche: Consultancy, Honoraria; Gilead Sciences: Consultancy, Honoraria. Morschhauser: Genentech, Inc.: Consultancy; Abbvie: Membership on an entity's Board of Directors or advisory committees; Janssen: Honoraria; Gilead: Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; Servier: Consultancy; Celgene: Membership on an entity's Board of Directors or advisory committees; Epizyme: Membership on an entity's Board of Directors or advisory committees; F. Hoffmann-La Roche: Consultancy, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau. André: Johnson & Johnson: Research Funding; Celgene: Other, Research Funding; Takeda: Consultancy; Bristol-Myers-Squibb: Consultancy, Other: TRAVEL, ACCOMMODATIONS, EXPENSES (paid by any for-profit health care company); CHU UCL Namur, site Godinne, Yvoir, Belgium: Current Employment; Seattle Genetics: Consultancy; Novartis: Consultancy, Research Funding; Gilead: Consultancy, Other: TRAVEL, ACCOMMODATIONS, EXPENSES (paid by any for-profit health care company); Karyopharm: Consultancy; Abbvie: Consultancy; Amgen: Other: TRAVEL, ACCOMMODATIONS, EXPENSES (paid by any for-profit health care company), Research Funding; Roche: Other: TRAVEL, ACCOMMODATIONS, EXPENSES (paid by any for-profit health care company), Research Funding. Meignan: ROCHE: Consultancy, Honoraria, Other: TRAVEL, ACCOMMODATIONS, EXPENSES (paid by any for-profit health care company). Demeestere: Roche: Consultancy, Membership on an entity's Board of Directors or advisory committees; Novartis: Honoraria; THERAMEX FERRING: Other: TRAVEL, ACCOMMODATIONS, EXPENSES.

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