CC BY-NC-ND 4.0 · South Asian J Cancer 2020; 09(04): 261
DOI: 10.1055/s-0040-1721178
Letter to the Editor

Gemcitabine in Recurrent Meningioma

Satvik Khaddar
1   Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Arti Bhelekar
1   Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Ochin Dale
1   Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Litty Varghese
1   Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Vijay Maruti Patil
1   Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India
› Author Affiliations
FundingNone.
 
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Dr Vijay M. Patil

Meningiomas are the most common primary intracranial neoplasms.[1] Grade I meningiomas are benign and managed by surgical resection alone.[1] However, Grade II and III require adjuvant radiation and are characterized by their aggressive nature and high rates of recurrence.[1] Unresectable recurrent high-grade meningiomas, refractory to radiotherapy, have a dismal prognosis with 26% progression-free survival of 6 months.[2] Systemic chemotherapy with interferon-α and somatostatin analogs, sunitinib, and bevacizumab has been tried with limited efficacy.[3] Recently, Takeda et al demonstrated in vitro and in vivo activity of gemcitabine in high-grade meningiomas.[4]

Inspired by these results, at our institute, we have given gemcitabine to three patients of recurrent meningioma on compassionate grounds. All these three patients had earlier underwent surgery, radiation, followed by reradiation at first progression and were not a candidate for local therapy anymore. The time to progression over immediate previous treatment was 1 month in the first patient and 5 months in the second and third patients. The schedule of gemcitabine used was weekly 1,000 mg/m2 on day 1, day 8, and day 15 for a 28-day cycle. The best response was stable disease in all three patients. The number of cycles of gemcitabine received was 12, 5, and 10 in the first, second, and third patient, respectively. No major adverse events were observed except Grade II thrombocytopenia in one patient. Time to progression was 12 months in the first patient, 6 months in second patient, and 11 months in the third patient. The results are exciting and warrant further evaluation of this drug in this setting. Currently, a single-arm phase 2 trial is undergoing at our institute (CTRI/2019/02/017499) evaluating the efficacy of gemcitabine in recurrent Grade II/III meningiomas.


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Conflicts of Interest

There are no conflicts of interest.

  • References

  • 1 Euskirchen P, Peyre M. Management of meningioma. Presse Med 2018; 47 (11-12 Pt 2) e245-e252
  • 2 Kaley T, Barani I, Chamberlain M. et al. Historical benchmarks for medical therapy trials in surgery- and radiation-refractory meningioma: a RANO review. Neuro-oncol 2014; 16 (06) 829-840
  • 3 Sioka C, Kyritsis AP. Chemotherapy, hormonal therapy, and immunotherapy for recurrent meningiomas. J Neurooncol 2009; 92 (01) 1-6
  • 4 Takeda H, Okada M, Kuramoto K. et al. Antitumor activity of gemcitabine against high-grade meningioma in vitro and in vivo. Oncotarget 2017; 8 (53) 90996-91008

Address for correspondence

Vijay Maruti Patil, MBBS, MD, DM
Department of Medical Oncology
Tata Memorial Hospital, Mumbai, Maharashtra
India   

Publication History

Article published online:
15 June 2021

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  • References

  • 1 Euskirchen P, Peyre M. Management of meningioma. Presse Med 2018; 47 (11-12 Pt 2) e245-e252
  • 2 Kaley T, Barani I, Chamberlain M. et al. Historical benchmarks for medical therapy trials in surgery- and radiation-refractory meningioma: a RANO review. Neuro-oncol 2014; 16 (06) 829-840
  • 3 Sioka C, Kyritsis AP. Chemotherapy, hormonal therapy, and immunotherapy for recurrent meningiomas. J Neurooncol 2009; 92 (01) 1-6
  • 4 Takeda H, Okada M, Kuramoto K. et al. Antitumor activity of gemcitabine against high-grade meningioma in vitro and in vivo. Oncotarget 2017; 8 (53) 90996-91008

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Dr Vijay M. Patil