Melatonin and Metformin Failed to Modify the Effect of Dacarbazine in Melanoma.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
05 2021
Historique:
received: 01 11 2020
accepted: 09 03 2021
pubmed: 23 3 2021
medline: 6 7 2021
entrez: 22 3 2021
Statut: ppublish

Résumé

Melatonin did not increase the efficacy of systemic chemotherapy in melanoma. Metformin did not increase the efficacy of systemic chemotherapy in melanoma. Current data support the possibility of antitumor activity of melatonin and metformin. From March 2014 to December 2016, 57 patients with disseminated melanoma received dacarbazine (DTIC) 1,000 mg/m ORR was 7% and did not differ among the treatment groups. Median TTP was 57, 57, and 47 days, respectively, in the first, second, and third groups (р = .362). Median OS was 236, 422, and 419 days, respectively (p = .712). Two patients from the combinations groups showed delayed response to therapy. The increase of CD3 No benefit was found in either combination over DTIC monotherapy. Delayed responses in melatonin and metformin combination groups were registered. The increase of lymphocyte subpopulations responsible for antitumor immune response demonstrates the immune system's potential involvement in clinical activity.

Sections du résumé

LESSONS LEARNED
Melatonin did not increase the efficacy of systemic chemotherapy in melanoma. Metformin did not increase the efficacy of systemic chemotherapy in melanoma.
BACKGROUND
Current data support the possibility of antitumor activity of melatonin and metformin.
METHODS
From March 2014 to December 2016, 57 patients with disseminated melanoma received dacarbazine (DTIC) 1,000 mg/m
RESULTS
ORR was 7% and did not differ among the treatment groups. Median TTP was 57, 57, and 47 days, respectively, in the first, second, and third groups (р = .362). Median OS was 236, 422, and 419 days, respectively (p = .712). Two patients from the combinations groups showed delayed response to therapy. The increase of CD3
CONCLUSION
No benefit was found in either combination over DTIC monotherapy. Delayed responses in melatonin and metformin combination groups were registered. The increase of lymphocyte subpopulations responsible for antitumor immune response demonstrates the immune system's potential involvement in clinical activity.

Identifiants

pubmed: 33749049
doi: 10.1002/onco.13761
pmc: PMC8100566
doi:

Substances chimiques

Dacarbazine 7GR28W0FJI
Metformin 9100L32L2N
Melatonin JL5DK93RCL

Banques de données

ClinicalTrials.gov
['NCT02190838']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

364-e734

Informations de copyright

© AlphaMed Press; the data published online to support this summary is the property of the authors.

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Auteurs

Aleksei Viktorovich Novik (AV)

Department of Oncoimmunology, N.N. Petrov National Medical Research Center of Oncology, St. Petersburg, Russia.
Department of Oncology, Child Oncology and Ray Therapy, St. Petersburg State Pediatric Medical University, St. Petersburg, Russia.

Svetlana Anatolievna Protsenko (SA)

Department of Chemotherapy and Innovative Technologies, N.N. Petrov National Medical Research Center of Oncology, St. Petersburg, Russia.

Irina Alexandrovna Baldueva (IA)

Department of Oncoimmunology, N.N. Petrov National Medical Research Center of Oncology, St. Petersburg, Russia.

Lev Michailovich Berstein (LM)

Department of Endocrinology, N.N. Petrov National Medical Research Center of Oncology, St. Petersburg, Russia.

Vladimir Nikolaevich Anisimov (VN)

Carcinogenesis and Oncogerontology, N.N. Petrov National Medical Research Center of Oncology, St. Petersburg, Russia.

Irina Nikolaevna Zhuk (IN)

Department of Chemotherapy, N.N. Petrov National Medical Research Center of Oncology, St. Petersburg, Russia.

Anna Igorevna Semenova (AI)

Department of Chemotherapy and Innovative Technologies, N.N. Petrov National Medical Research Center of Oncology, St. Petersburg, Russia.

Dilorom Khamidovna Latipova (DK)

Department of Chemotherapy and Innovative Technologies, N.N. Petrov National Medical Research Center of Oncology, St. Petersburg, Russia.

Elena Viktorovna Tkachenko (EV)

Department of Chemotherapy, N.N. Petrov National Medical Research Center of Oncology, St. Petersburg, Russia.

Tatiana Yurievna Semiglazova (TY)

Department of Chemotherapy and Innovative Technologies, N.N. Petrov National Medical Research Center of Oncology, St. Petersburg, Russia.

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Classifications MeSH