Survival and pattern of failure after postoperative radiation therapy formedulloblastoma in adult patients

The disease stage was disregarded because of insufficient initial staging. Results . Actuarial 5- and 10- year OS rates were 55% and 44%, respectively. Actuarial 5- and 10- year DFS rates were 44% and 31% respectively. In univariate analysis age was the only significant prognostic factor for OS. For patients less than 30 years of age 5-year OS rate was 40%, for elders – 90%, p=0.004. A tendency to improve OS was observed with better performance and neurologic status, and location in the cerebellar hemisphere, whilst the presence of shunt and gross total resection worsened OS without statistical significance. Tumour recurred in 17 (63%) patients. Ten relapses (59%) occurred within the first 2 years of follow up. Seven recurrences were in the posterior fossa, either alone (3 patients) or both in the posterior fossa and other sites (4 patients). Other relapses occurred either alone or in 2 or more sites such as: the supratentorial region (3 patients), the spine (4 patients), outside the CNS (6 patients). The median SAR was 12 months (1-35 months). Mean SAR for patients receiving chemotherapy at relapse was 19 months, whilst for patients treated without chemotherapy the mean SAR was 5 months. A tendency for longer SAR was observed when recurrence occurred later after primary treatment. Mean SAR for patients relapsed after 3 years was 16 months, whilst for patients relapsed within 3 first years it was 9.5 months. Conclusions . Results are poor, but similar to those cited in literature. Results should be related to the presence of prognostic factors, especially the initial extent of disease. The frequency of recurrences in the posterior fossa and outside the CNS is similar. Accurate initial staging could differentiate patients for whom the use of chemotherapy or implementation of new radiotherapy techniques is meaningful. The majority of relapses were observed within the first 2 years. Older patients have better overall survival.

[1]  P. Black,et al.  Radiosurgery in the management of pediatric brain tumors. , 2001, International journal of radiation oncology, biology, physics.

[2]  J. Krischer,et al.  Low-stage medulloblastoma: final analysis of trial comparing standard-dose with reduced-dose neuraxis irradiation. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[3]  M. Mustafa,et al.  Prognostic factors for medulloblastoma. , 2000, International journal of radiation oncology, biology, physics.

[4]  A. Paulino,et al.  The cranial-spinal junction in medulloblastoma: does it matter? , 1999, International journal of radiation oncology, biology, physics.

[5]  M. Prados,et al.  Hyperfractionated craniospinal radiation therapy for primitive neuroectodermal tumors: results of a Phase II study. , 1999, International journal of radiation oncology, biology, physics.

[6]  J. Buatti,et al.  Medulloblastoma: time-dose relationship based on a 30-year review. , 1998, International journal of radiation oncology, biology, physics.

[7]  R. Sanford,et al.  Patterns of failure in children with medulloblastoma: effects of preirradiation chemotherapy. , 1997, International journal of radiation oncology, biology, physics.

[8]  M. Rosenblum,et al.  Medulloblastoma: long-term results for patients treated with definitive radiation therapy during the computed tomography era. , 1996, International journal of radiation oncology, biology, physics.

[9]  A. Jamshed,et al.  Treatment results for 149 medulloblastoma patients from one institution. , 1996, International journal of radiation oncology, biology, physics.

[10]  W. Simpson,et al.  Medulloblastoma in adults. , 1995, International journal of radiation oncology, biology, physics.

[11]  M. Prados,et al.  Medulloblastoma in adults. , 1995, International journal of radiation oncology, biology, physics.

[12]  M. Prados,et al.  Pattern of recurrence of medulloblastoma after low-dose craniospinal radiotherapy. , 1994, International journal of radiation oncology, biology, physics.

[13]  E. Bouffet,et al.  Metastatic medulloblastoma: the experience of the French Cooperative M7 Group. , 1994, European journal of cancer.

[14]  J. Blay,et al.  Medulloblastoma in adults: survival and prognostic factors. , 1993, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

[15]  J. Lagrange,et al.  Quality control of radiotherapeutic treatment of medulloblastoma in a multicentric study: the contribution of radiotherapy technique to tumour relapse. The French Medulloblastoma Group. , 1992, Radiotherapy and Oncology.

[16]  H. Bloom,et al.  Medulloblastoma in adults: a review of 47 patients treated between 1952 and 1981. , 1990, International journal of radiation oncology, biology, physics.

[17]  J. Skołyszewski,et al.  Results of postoperative irradiation of medulloblastoma in adults. , 1989, International journal of radiation oncology, biology, physics.

[18]  E. Halperin,et al.  Medulloblastoma: the Duke University Medical Center experience. , 1986, International journal of radiation oncology, biology, physics.

[19]  J. Simpson,et al.  Cerebellar medulloblastoma: the importance of posterior fossa dose to survival and patterns of failure. , 1982, International journal of radiation oncology, biology, physics.

[20]  W. Simpson,et al.  Radiation treatment for medulloblastoma. A 21-year review. , 1981, Journal of neurosurgery.

[21]  E. Housepian,et al.  An operative staging system and a megavoltage radiotherapeutic technic for cerebellar medulloblastomas. , 1969, Radiology.