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DOI 10.1016/j.jpedsurg.2010.07.021

Медицинская библиотека · Journal of pediatric surgery · 2010

Impact of tumor viability at second-look procedures performed before completing treatment on the Intergroup Rhabdomyosarcoma Study Group protocol IRS-IV, 1991-1997: a report from the children's oncology group.

Raney Beverly, Stoner Julie, Anderson James, Andrassy Richard, Arndt Carola, Brown Ken, Crist William, Maurer Harold, Qualman Stephen, Wharam Moody, Wiener Eugene, Meyer William, Hayes-Jordan Andrea, Soft-Tissue Sarcoma Committee of the Children's Oncology Group

Клиническое исследование IV фазыСравнительное исследованиеСтатьяРандомизированное исследованиеПоддержка NIH: внешняя программаПеревод пока не подготовлен

Аннотация

PURPOSES: The aims of the study were to compare results of clinical/radiographic studies before second-look procedures (SLP) with SLP specimens from patients with gross residual sarcoma at diagnosis and to relate tumor viability to outcome.

PATIENTS: Seventy-three patients underwent SLP before completing chemotherapy, with (n = 59) or without (n = 14) radiotherapy. Tumor sites were bladder/prostate (n = 27), head/orbit/parameningeal (n = 22), extremity/trunk (n = 14), and retroperitoneum/pelvis (n = 10).

RESULTS

Of 14 patients, 1 (7%) with clinical/radiographic complete response (CR) had viable tumor. Of 59 patients, 35 (59%) without CR had viable tumor. Five-year failure-free survival (FFS) rates were 81% in 37 patients without viable tumor and 53% in 36 patients with viable tumor (Cox proportional hazards adjusted P = .05). Five-year FFS rates were 67% in 15 patients with clear margins and 43% in 21 patients with tumor-involved margins (n = 18) or viable gross tumor (n = 3) (Cox proportional hazards adjusted P = .04). Five-year survival was 78% to 79% among 73 patients with and 333 patients without SLP during treatment.

CONCLUSIONS

Second-look procedures can show whether viable tumor is present and may be beneficial in selected patients with rhabdomyosarcoma. Disappearance of tumor (CR) usually correlated with no viable tumor at SLP. However, 41% of patients without CR had no viable tumor. Those without viable tumor had increased FFS but not survival compared to those with viable tumor.

Для цитирования: Raney Beverly, Stoner Julie, Anderson James, Andrassy Richard, Arndt Carola, Brown Ken, Crist William, Maurer Harold, Qualman Stephen, Wharam Moody, Wiener Eugene, Meyer William, Hayes-Jordan Andrea, Soft-Tissue Sarcoma Committee of the Children's Oncology Group. Impact of tumor viability at second-look procedures performed before completing treatment on the Intergroup Rhabdomyosarcoma Study Group protocol IRS-IV, 1991-1997: a report from the children's oncology group.. Journal of pediatric surgery. 2010. DOI: 10.1016/j.jpedsurg.2010.07.021.

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