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Thymalin

Thymulin, Thymic Factor, Serum Thymic Factor, Facteur Thymique Serique

Quick Stats
Studies 202
Trials 37
Score 2
1997 pubmed

[Effect of various chemotherapy regimens on survival and cause of death in patients with multiple myeloma (retrospective study)].

Abdulkadyrov. K M KM; Bessmel'tsev. S S SS; Stel'mashenko. L V LV; Shmidt. A V AV; Rukavitsyn. O A OA

Key Findings

  • Poly‑chemotherapy increased median survival from 27 to 43 months
  • Adding thymalin and similar immune‑correction drugs cut infection‑related complications from 22% to 8.3%
  • Supportive measures such as heavy hydration, diuretics, rheologic agents and plasmapheresis were highlighted as crucial

Practical Outcomes

  • For biohackers, thymalin might help lower infection risk when the immune system is heavily stressed, but the evidence comes from an old, uncontrolled cancer study. It’s not a proven anti‑aging or performance aid for healthy people, and any use should be cautious and under medical supervision.

Summary

In a look‑back study of 109 multiple‑myeloma patients, those who got a mix of chemo drugs lived longer (average 43 vs 27 months) and, when they also received immune‑boosting drugs like thymalin, infections dropped from about 22% to 8%. The authors say good hydration, detox steps and immune support are important alongside chemo.

Abstract

A retrospective analysis of survival time and causes of death has been undertaken in 109 patients treated for multiple myeloma (MM) at the Hematologic Clinic of the Russian Research Institute of Hematology and Transfusiology in 1979-1995. Group I included cases of mono- and group II-polychemotherapy (PCT). Survival in patients with MM increased significantly (from 27 to 43 months) after PCT. The main causes of death in MM patients of group I were chronic renal failure and infectious complications, while in group II-intoxication syndrome including blood toxicity, toxic hepatitis, etc. In cases of this grave disease, the effectiveness of therapy appeared to depend on both main and supporting treatment. Of great importance was profuse hydration using diuretics, active rheologic preparations, plasmapheresis and other counter-complication means. Following the administration of immunity correction drugs (thymaline, tactivin, immunoglobulin), infectious complication incidence in group II dropped from 22 to 8.3%. It is suggested that the effectiveness of MM therapy is determined by stage-by-stage approach, course cycling of PCT and adequate evaluation of its criteria. PCT courses should be supplemented with infusion detoxication measures, particularly, in cases of highly aggressive PCT schemes, and procedures of immunity correction, hemo-component therapy and plasmapheresis.

Study Information

Provider

pubmed

Year

1997