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Second-line treatment of pediatric patients with relapsed rhabdomyosarcoma adapted to initial risk stratification : Data of the European Soft Tissue Sarcoma Registry (SoTiSaR)

Heinz, Amadeus (författare)
Univ Childrens Hosp Tuebingen, Dept Pediat Hematol & Oncol, Tubingen, Germany.
Ebinger, Martin (författare)
Univ Childrens Hosp Tuebingen, Dept Pediat Hematol & Oncol, Tubingen, Germany.
Schoenstein, Anton (författare)
Heidelberg Univ, Network Aging Res, Heidelberg, Germany.
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Fuchs, Joerg (författare)
Univ Childrens Hosp Tuebingen, Dept Pediat Surg & Urol, Tubingen, Germany.
Timmermann, Beate (författare)
Univ Med Ctr Essen, German Canc Consortium DKTK, West German Canc Ctr WTZ, Dept Particle Therapy,West German Proton Therapy, Essen, Germany.
Seitz, Guido (författare)
Univ Hosp Giessen Marburg, Dept Pediat Surg, Marburg, Germany.
Vokuhl, Christian W. (författare)
Univ Hosp Bonn, Sect Pediat Pathol, Bonn, Germany.
Muenter, Marc W. (författare)
Klinikum Landeshauptstadt Stuttgart, Stuttgart Canc Ctr, Dept Radiat Oncol, Stuttgart, Germany.
Pajtler, Kristian (författare)
Heidelberg Univ, Hopp Childrens Canc Ctr Heidelberg KiTZ, Heidelberg, Germany.;Heidelberg Univ, German Canc Res Ctr DKFZ, Div Pediat Neurooncol, Heidelberg, Germany.;Heidelberg Univ, German Canc Consortium DKTK, Heidelberg, Germany.;Heidelberg Univ Hosp, Dept Pediat Oncol Hematol & Immunol, Heidelberg, Germany.
Stegmaier, Sabine (författare)
Klinikum Landeshauptstadt Stuttgart, Zentrum Kinder Jugend & Frauenmed Olgahosp, Stuttgart Canc Ctr, Padiatr Padiatr Onkol Hamatol Immunol 5, Stuttgart, Germany.
von Kalle, Thekla P. (författare)
Klinikum Landeshauptstadt Stuttgart, Zentrum Kinder Jugend & Frauenmed Olgahosp, Stuttgart Canc Ctr, Dept Radiol, Stuttgart, Germany.
Kratz, Christian (författare)
Hannover Med Sch, Pediat Hematol & Oncol, Hannover, Germany.
Roessler, Jochen (författare)
Inselspital Bern, Dept Pediat, Div Pediat Hematol & Oncol, Univ Hosp Bern, Bern, Switzerland.
Ljungman, Gustaf, 1958- (författare)
Uppsala universitet,Barnonkologisk forskning - särskilt fokus på komplikationer
Klingebiel, Thomas (författare)
Univ Hosp Frankfurt, Dept Children & Adolescents, Frankfurt, Germany.
Koscielniak, Ewa (författare)
Klinikum Landeshauptstadt Stuttgart, Zentrum Kinder Jugend & Frauenmed Olgahosp, Stuttgart Canc Ctr, Padiatr Padiatr Onkol Hamatol Immunol 5, Stuttgart, Germany.;Univ Tubingen, Med Fac, Tubingen, Germany.
Sparber-Sauer, Monika (författare)
Klinikum Landeshauptstadt Stuttgart, Zentrum Kinder Jugend & Frauenmed Olgahosp, Stuttgart Canc Ctr, Padiatr Padiatr Onkol Hamatol Immunol 5, Stuttgart, Germany.;Univ Tubingen, Med Fac, Tubingen, Germany.
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Univ Childrens Hosp Tuebingen, Dept Pediat Hematol & Oncol, Tubingen, Germany Heidelberg Univ, Network Aging Res, Heidelberg, Germany. (creator_code:org_t)
John Wiley & Sons, 2023
2023
Engelska.
Ingår i: Pediatric Blood & Cancer. - : John Wiley & Sons. - 1545-5009 .- 1545-5017. ; 70:7
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Outcome of relapsed disease of localized rhabdomyosarcoma remains poor. An individual treatment approach considering the initial systemic treatment and risk group was included in the Cooperative Weichteilsarkom Studiengruppe (CWS) Guidance. Methods: Second-line chemotherapy (sCHT) ACCTTIVE based on anthracyclines (adriamycin, carboplatin, cyclophosphamide, topotecan, vincristine, etoposide) was recommended for patients with initial low- (LR), standard- (SR), and high-risk (HR) group after initial treatment without anthracyclines. TECC (topotecan, etoposide, carboplatin, cyclophosphamide) was recommended after initial anthracycline-based regimen in the very high-risk (VHR) group. Data of patients with relapse (n = 68) registered in the European Soft Tissue Sarcoma Registry SoTiSaR (2009-2018) were retrospectively analyzed. Results: Patients of initial LR (n = 2), SR (n = 16), HR (n = 41), and VHR (n = 9) group relapsed. sCHT consisted of ACCTTIVE (n = 36), TECC (n = 12), or other (n = 15). Resection was performed in 40/68 (59%) patients and/or radiotherapy in 47/68 (69%). Initial risk stratification, pattern/time to relapse, and achievement of second complete remission were significant prognostic factors. Microscopically incomplete resection with additional radiotherapy was not inferior to microscopically complete resection (p =.17). The 5-year event-free survival (EFS) and overall survival (OS) were 26% (+/- 12%) and 31% (+/- 14%). The 5-year OS of patients with relapse of SR, HR, and VHR groups was 80% (+/- 21%), 20% (+/- 16%), and 13% (+/- 23%, p =.008), respectively. Conclusion: Adapted systemic treatment of relapsed disease considering the initial risk group and initial treatment is reasonable. New treatment options are needed for patients of initial HR and VHR groups.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Hematologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Hematology (hsv//eng)

Nyckelord

localized disease
relapsed disease
rhabdomyosarcoma
second-line chemotherapy
Soft Tissue Sarcoma Registry (SoTiSaR)

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