Benefit of delayed primary excision in rhabdomyosarcoma: A report from the Children's Oncology Group (COG)

被引:32
作者
Lautz, Timothy B. [1 ,2 ]
Chi, Yueh-Yun [3 ]
Li, Minjie [4 ]
Wolden, Suzanne L. [5 ]
Casey, Dana L. [6 ]
Routh, Jonathan C. [7 ]
Granberg, Candace F. [8 ]
Binite, Odion [9 ]
Rudzinski, Erin R. [10 ]
Hawkins, Douglas S. [11 ]
Venkatramani, Rajkumar [12 ]
Rodeberg, David A. [13 ]
机构
[1] Ann & Robert H Lurie Childrens Hosp Chicago, Dept Surg, Chicago, IL 60611 USA
[2] Northwestern Univ, Chicago, IL 60611 USA
[3] Univ Southern Calif, Dept Pediat & Prevent Med, Los Angeles, CA 90007 USA
[4] Univ Florida, Dept Biostat, Gainesville, FL USA
[5] Mem Sloan Kettering Canc Ctr, Div Radiat Oncol, 1275 York Ave, New York, NY 10021 USA
[6] Univ N Carolina, Div Radiat Oncol, Chapel Hill, NC 27515 USA
[7] Duke Univ, Sch Med, Div Urol Surg, Durham, NC USA
[8] Mayo Clin, Dept Urol, Rochester, MN USA
[9] H Lee Moffitt Canc Ctr & Res Inst, Dept Orthoped Surg, Tampa, FL USA
[10] Univ Washington, Seattle Childrens Hosp, Dept Pathol, Seattle, WA 98195 USA
[11] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle Childrens Hosp, Div Hematol Oncol, Seattle, WA 98195 USA
[12] Baylor Coll Med, Texas Childrens Canc Ctr, Div Hematol Oncol, Houston, TX 77030 USA
[13] East Carolina Univ, Dept Surg, Div Pediat Surg, Greenville, NC 27858 USA
关键词
delayed primary excision; pediatric; radiation; rhabdomyosarcoma; survival; SOFT-TISSUE SARCOMA; INTERMEDIATE-RISK RHABDOMYOSARCOMA; CHILDHOOD RHABDOMYOSARCOMA; RADIATION-THERAPY; RADIOTHERAPY; 2ND;
D O I
10.1002/cncr.33275
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Most children with intermediate-risk rhabdomyosarcoma (RMS) have gross disease (group III) at the initiation of chemotherapy. Delayed primary excision (DPE) after induction chemotherapy allows for a reduction in adjuvant radiation dose, but with the risk of potential surgical morbidity. The objectives of this study were to compare outcomes in children with group III RMS who did and did not undergo DPE and to assess surgical morbidity. Methods The study included 369 patients who had clinical group III RMS at sites amenable to DPE from intermediate-risk Children's Oncology Group studies D9803 (encouraged DPE) and ARST0531 (discouraged DPE). Results The primary tumor site was bladder/prostate (136 patients; 37%), extremity (97 patients; 26%), trunk (24 patients; 7%), retroperitoneum (91 patients; 25%), or intrathoracic/perineum/perianal (21 patients; 6%). In total, 112 patients (53.9%) underwent DPE in D9803, and 26 patients (16.2%) underwent DPE in ARST0531 (P< .001), with loss of vital organ or function in 30 of 138 patients (22%). DPE allowed for a reduced radiation dose in 110 of 135 patients (81%; 51% were reduced to 36 Gy, and 30% were reduced to 42 Gy). Patients who underwent DPE had improved unadjusted overall survival (P= .013). In adjusted regression analysis, the risk of death (hazard ratio, 0.71; 95% CI 0.43-1.16) was similar for patients who did and did not undergo DPE and was improved for the subset of patients who had tumors of the trunk and retroperitoneum (hazard ratio, 0.44; 95% CI, 0.20-0.97). Conclusions Children with group III RMS have equivalent or improved outcomes with DPE and can receive a decreased radiation dose for definitive local control. The choice of local control modality should weigh the potential morbidity of surgery versus that of higher dose irradiation.
引用
收藏
页码:275 / 283
页数:9
相关论文
共 26 条
[1]   What is the evidence for radical surgery in the management of localized embryonal bladder/prostate rhabdomyosarcoma? [J].
Alexander, Nicholas ;
Lane, Sheila ;
Hitchcock, Rowena .
PEDIATRIC BLOOD & CANCER, 2012, 58 (06) :833-835
[2]   Vincristine, Actinomycin, and Cyclophosphamide Compared With Vincristine, Actinomycin, and Cyclophosphamide Alternating With Vincristine, Topotecan, and Cyclophosphamide for Intermediate-Risk Rhabdomyosarcoma: Children's Oncology Group Study D9803 [J].
Arndt, Carola A. S. ;
Stoner, Julie A. ;
Hawkins, Douglas S. ;
Rodeberg, David A. ;
Hayes-Jordan, Andrea A. ;
Paidas, Charles N. ;
Parham, David M. ;
Teot, Lisa A. ;
Wharam, Moody D. ;
Breneman, John C. ;
Donaldson, Sarah S. ;
Anderson, James R. ;
Meyer, William H. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (31) :5182-5188
[3]   Treatment Approach and Outcomes in Infants With Localized Rhabdomyosarcoma: A Report From the Soft Tissue Sarcoma Committee of the Children's Oncology Group [J].
Bradley, Julie A. ;
Kayton, Mark L. ;
Chi, Yueh-Yun ;
Hawkins, Douglas S. ;
Tian, Jing ;
Breneman, John ;
Wolden, Suzanne L. ;
Walterhouse, David ;
Rodeberg, David A. ;
Donaldson, Sarah S. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2019, 103 (01) :19-27
[4]   Increased local failure for patients with intermediate-risk rhabdomyosarcoma on ARST0531: A report from the Children's Oncology Group [J].
Casey, Dana L. ;
Chi, Yueh-Yun ;
Donaldson, Sarah S. ;
Hawkins, Douglas S. ;
Tian, Jing ;
Arndt, Carole A. ;
Rodeberg, David A. ;
Routh, Jonathan C. ;
Lautz, Timothy B. ;
Gupta, Abha A. ;
Yock, Torunn, I ;
Wolden, Suzanne L. .
CANCER, 2019, 125 (18) :3242-3248
[5]   Oncologic Outcome and Urinary Function after Radical Cystectomy for Rhabdomyosarcoma in Children: Role of the Orthotopic Ileal Neobladder Based on 15-Year Experience at a Single Center [J].
Castagnetti, Marco ;
Angelini, Lorenzo ;
Alaggio, Rita ;
Scarzello, Giovanni ;
Bisogno, Gianni ;
Rigamonti, Waifro .
JOURNAL OF UROLOGY, 2014, 191 (06) :1850-1855
[6]   Complete second look operation and radiotherapy in locally advanced non-alveolar rhabdomyosarcoma in children: A report from the AIEOP soft tissue sarcoma committee [J].
Cecchetto, Giovanni ;
Carretto, Elena ;
Bisogno, Gianni ;
Dall'Igna, Patrizia ;
Ferrari, Andrea ;
Scarzello, Giovanni ;
Donfrancesco, Alberto ;
Alaggio, Rita ;
Indolfi, Paolo ;
Carli, Modesto .
PEDIATRIC BLOOD & CANCER, 2008, 51 (05) :593-597
[7]  
COX DR, 1972, J R STAT SOC B, V34, P187
[8]   Second Solid Cancers After Radiation Therapy: A Systematic Review of the Epidemiologic Studies of the Radiation Dose-Response Relationship [J].
de Gonzalez, Amy Berrington ;
Gilbert, Ethel ;
Curtis, Rochelle ;
Inskip, Peter ;
Kleinerman, Ruth ;
Morton, Lindsay ;
Rajaraman, Preetha ;
Little, Mark P. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2013, 86 (02) :224-233
[9]   Treatment and outcome of patients with localized intrathoracic and chest wall rhabdomyosarcoma: a report of the Cooperative Weichteilsarkom Studiengruppe (CWS) [J].
Fuchs, Joerg ;
Urla, Cristian ;
Sparber-Sauer, Monika ;
Schuck, Andreas ;
Leuschner, Ivo ;
Klingebiel, Thomas ;
Blumenstock, Gunnar ;
Seitz, Guido ;
Koscielniak, Ewa .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2018, 144 (05) :925-934
[10]   Addition of Vincristine and Irinotecan to Vincristine, Dactinomycin, and Cyclophosphamide Does Not Improve Outcome for Intermediate-Risk Rhabdomyosarcoma: A Report From the Children's Oncology Group [J].
Hawkins, Douglas S. ;
Chi, Yueh-Yun ;
Anderson, James R. ;
Tian, Jing ;
Arndt, Carola A. S. ;
Bomgaars, Lisa ;
Donaldson, Sarah S. ;
Hayes-Jordan, Andrea ;
Mascarenhas, Leo ;
McCarville, Mary Beth ;
McCune, Jeannine S. ;
McCowage, Geoff ;
Million, Lynn ;
Morris, Carol D. ;
Parham, David M. ;
Rodeberg, David A. ;
Rudzinski, Erin R. ;
Shnorhavorian, Margarett ;
Spunt, Sheri L. ;
Skapek, Stephen X. ;
Teot, Lisa A. ;
Wolden, Suzanne ;
Yock, Torunn I. ;
Meyer, William H. .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (27) :2770-+