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Efficacy of combined immunosuppression with or without eltrombopag in children with newly diagnosed aplastic anemia.
Goronkova, Olga; Novichkova, Galina; Salimova, Tatiana; Kalinina, Irina; Baidildina, Dina; Petrova, Ulyana; Antonova, Kristina; Sadovskaya, Maria; Suntsova, Elena; Evseev, Dmitry; Matveev, Victor; Venyov, Dmitry; Khachatryan, Lili; Litvinov, Dmitry; Pshonkin, Alexey; Ovsyannikova, Galina; Kotskaya, Natalia; Gobadze, Darina; Olshanskaya, Yulia; Popov, Alexander; Raykina, Elena; Mironenko, Olga; Voronin, Kirill; Purbueva, Bazarma; Boichenko, Elmira; Dinikina, Yulia; Guseynova, Evgeniya; Sherstnev, Dmitry; Kalinina, Elena; Mezentsev, Sergey; Streneva, Olga; Yudina, Natalia; Plaksina, Olga; Erega, Elena; Maschan, Michael; Maschan, Alexey.
Afiliação
  • Goronkova O; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Novichkova G; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Salimova T; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Kalinina I; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Baidildina D; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Petrova U; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Antonova K; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Sadovskaya M; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Suntsova E; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Evseev D; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Matveev V; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Venyov D; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Khachatryan L; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Litvinov D; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Pshonkin A; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Ovsyannikova G; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Kotskaya N; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Gobadze D; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Olshanskaya Y; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Popov A; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Raykina E; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Mironenko O; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Voronin K; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Purbueva B; Pirogov Russian Clinical Children's Hospital, Moscow, Russia.
  • Boichenko E; St. Petersburg Children's City Hospital No 1, St. Petersburg, Russia.
  • Dinikina Y; Almazov National Medical Research Center, St. Petersburg, Russia.
  • Guseynova E; Krasnoyarsk Regional Clinical Hospital, Krasnoyarsk, Russia.
  • Sherstnev D; Shustov University Clinical Hospital No 3 of Razumovsky Saratov State Medical University, Saratov, Russia.
  • Kalinina E; Samara Regional Clinical Children's Hospital, Samara, Russia.
  • Mezentsev S; Perm Regional Clinical Hospital, Perm, Russia.
  • Streneva O; Ekaterinburg Regional Clinical Children's Hospital, Ekaterinburg, Russia.
  • Yudina N; Voronezh Regional Clinical Children's Hospital No 1, Voronezh, Russia.
  • Plaksina O; Regional Clinical Children's Hospital, Nizhniy Novgorod, Russia.
  • Erega E; Piotrovich Regional Clinical Children's Hospital, Khabarovsk, Russia.
  • Maschan M; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
  • Maschan A; Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, and Immunology, Moscow, Russia.
Blood Adv ; 7(6): 953-962, 2023 03 28.
Article em En | MEDLINE | ID: mdl-35446936
ABSTRACT
We compared the efficacy and safety of eltrombopag (ELTR) combined with immunosuppressive therapy (IST) and IST alone in treatment-naïve children with severe (SAA) and very severe (vSAA) aplastic anemia. Ninety-eight pediatric patients were randomized to receive horse antithymocyte globulin (hATG) and cyclosporin A (CsA) with (n = 49) or without (n = 49) ELTR. The primary endpoint was the overall response rate (ORR) at 4 months. After 4 months, nonresponders were crossed over to the alternative group. In all patients, the ORR in ELTR + IST and IST groups was similar (65% vs 53%; P = .218); however, the complete response (CR) rate was significantly higher in the ELTR + IST group (31% vs 12%; P = .027). In severity subgroups, the ORR was 89% vs 57% (P = .028) in favor of IST + ELTR in SAA, but it did not differ in patients with vSAA (52% vs 50%; P = .902). At 6 months after the crossover, 61% of initial ELTR(-) patients achieved a response compared with 17% of initial ELTR(+) patients (P = .016). No significant difference in ELTR + IST and IST groups was observed in the 3-year overall survival (OS) (89% vs 91%; P = .673) or the 3-year event-free survival (EFS) (53% vs 41%; P = .326). There was no unexpected toxicity related to ELTR. Adding ELTR to standard IST was well tolerated and increased the CR rate. The greatest benefit from ELTR combined with IST was observed in patients with SAA but not in those with vSAA. The second course of IST resulted in a high ORR in initial ELTR(-) patients who added ELTR and had limited efficacy among patients who received ELTR upfront. This trial was registered at Clinicaltrials.gov as #NCT03413306.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunossupressores / Anemia Aplástica Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Humans Idioma: En Revista: Blood Adv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Federação Russa

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunossupressores / Anemia Aplástica Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Humans Idioma: En Revista: Blood Adv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Federação Russa