Raadpleeg ook: 

https://kanker-actueel.nl/NL/studiepublicaties-van-niet-toxische-middelen-en-behandelingen-uit-literatuurlijst-van-arts-bioloog-drs-engelbert-valstar-gerelateerd-aan-vormen-van-darmkanker.html 


PRM1201 is samengesteld uit zeven kruiden: Ligustrum lucidum WTAiton fructus (Nv Zhen Zi), Cistanche deserticola YCMa herba (Rou Cong Rong), Iphigenia indica (L.) A. Gray ex Kunth pseudobulb (San Ci Gu), Vitis quinquangularis Rehder wijnstok ( Ye Pu Tao Teng), Panax ginseng CAMey. wortel (Ren Sen), Akebia trifoliata (Thunb.) Koidz. fruit (Yu Zhi Zi), en Salvia miltiorrhiza Bunge-wortel (Dan Shen).

Raadpleeg Natuurapotheek voor deze kruidencombinatie.

14 juli 2021: Bron:  2021; 11: 618793. Published online 2021 Mar 3

De Chinese kruidenmix PRM1201 (bevat 7 verschillende kruiden) naast chemotherapie geeft na drie jaar 8,5 procent betere ziektevrije overleving voor patiënten met operabele darmkanker stadium III. Ook minder recidieven en betere kwaliteit van leven. Dit blijkt uit de resultaten van een placebo gecontroleerde gerandomiseerde studie bij totaal 370 darmkankerpatiënten. 
Chemotherapie is de standaard behandeling van darmkanker. Uit eerdere studies is gebleken dat de Chinese kruidenmix PRM1201 (bevat 7 verschillende kruiden) de werkzaamheid van chemotherapie verbetert bij gebruik in combinatie met Cetuximab of Bevacizumab bij patiënten met uitgezaaide darmkanker.

In deze placebo gecontroleerde gerandomiseerde studie werden patiënten die een volledige operatie hadden ondergaan voor stadium III darmkanker willekeurig toegewezen aan adjuvante chemotherapie (FOLFOX q2w gedurende 6 maanden, of CapeOx q3w gedurende 6 maanden) plus PRM1201 (chemo + PRM1201-groep) of adjuvante chemotherapie plus placebo (chemo + placebogroep).

Het primaire einddoel was ziektevrije overleving (DFS) en de secundaire einddoelen waren kwaliteit van leven (QOL) en toxiciteit.

  • Totaal 370 patiënten werden willekeurig toegewezen aan chemotherapie plus PRM1201-groep (n = 184) en chemotherapie plus placebogroep (n = 186).
  • Tot 30 oktober 2019 waren 96 voorvallen van een recidief, metastase of overlijden gemeld, waarvan 38 voorvallen in de groep chemotherapie plus PRM1201 en 58 voorvallen in de chemo + placebogroep.
  • Het 3-jaars ziektevrije-percentage was respectievelijk 77,1 procent en 68,6 procent in de chemo + PRM1201 groep en chemo + placebogroep (hazard ratio 0,63; 95% BI 0,42 tot 0,94). Een verbetering dus van 8,5 procent in overleving zonder recidief of uitzaaiingen.
  • De kwaliteit van leven van patiënten in de chemo + PRM1201-groep was significant verbeterd in termen van globale kwaliteit van leven, fysiek functioneren, rolfunctioneren, emotioneel functioneren, vermoeidheid en verlies van eetlust. De incidentie van graad 3 of 4 behandelingsgerelateerde bijwerkingen (TRAE's) was vergelijkbaar tussen de twee groepen.

Conclusie:
Chemotherapie in combinatie met PRM1201 verbeterde de adjuvante behandeling van darmkanker. PRM1201 kan worden aanbevolen als een effectieve optie in de klinische praktijk.

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Het volledige studierapport is gratis in te zien met gedetailleerde grafieken n beschrijvingen. En gepubliceerd in Frontiers Oncology. Hier het abstract:

Abstract

Background

Chemotherapy is the standard adjuvant treatment for colon cancer. Chinese herbal formula PRM1201 improves the efficacy of chemotherapy when used in combination with Cetuximab or Bevacizumab in patients with metastatic colorectal cancer. This study aims to explore the benefits of treatment with chemotherapy plus PRM1201 in the postoperative adjuvant setting.

Methods

In this parallel-group study, patients who had undergone curative resection for stage III colon cancer were randomly assigned to receive adjuvant chemotherapy (FOLFOX q2w for 6 months, or CapeOx q3w for 6 months) plus PRM1201 (chemo+PRM1201 group) or adjuvant chemotherapy plus placebo (chemo+placebo group). The primary endpoint was disease-free survival (DFS), and the secondary endpoints were quality of life (QOL) and toxicity.

Results

A total of 370 patients were randomly assigned to chemotherapy plus PRM1201 group (n = 184) and chemotherapy plus placebo group (n = 186). Up to October 30, 2019, 96 events of recurrence, metastasis, or death had been reported, of which 38 events were in the group of chemotherapy plus PRM1201 and 58 events in the chemo+placebo group. The 3-year DFS rate was 77.1 and 68.6% in the chemo+PRM1201 and chemo+placebo group, respectively (hazard ratio , 0.63; 95% CI, 0.42 to 0.94). The QOL of patients in the chemo+PRM1201 group were significantly improved in terms of global quality of life, physical functioning, role functioning, emotional functioning, fatigue, and appetite loss. The incidence of grade 3 or 4 treatment-related adverse event (TRAEs) were similar between the two arms.

Conclusions

Chemotherapy in combination with PRM1201 improved the adjuvant treatment of colon cancer. PRM1201 can be recommended as an effective option in clinical practice.

Clinical Trial Registration Chinese Clinical Trials Registry, identifier ChiCTR-IOR-16007719.


Data Availability Statement

The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding authors.

Ethics Statement

The studies involving human participants were reviewed and approved by IRB of Shuguang Hospital affiliated with Shanghai University of TCM. The patients/participants provided their written informed consent to participate in this study.

Author Contributions

QL was involved in the conception and design of the study. RJ, NL, GC, HX, PZ, HML, JH, XY, HG, WY and QL were involved in provision of study materials or patients. RJ, YuZ, LHZ, YiZ, CW, XS, YF, HJL, HL, ZH, YL, YaZ and GH were involved in acquisition of data. RJ, QJ, ZL and WY were involved in data analysis and interpretation. RJ drafted the manuscript and QL, WY and NL were involved in the critical revision of the manuscript. All authors contributed to the article and approved the submitted version.

Funding

This research was supported by grants from the Key projects of the National Natural Science Foundation of China (No.82030118), Three-year Plan of Action for the Development of Traditional Chinese Medicine in Shanghai (ZY(2018-2020)-CCCX-2003-03), and key Projects of Shanghai Science and Technology Commission (16401970500).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2021.618793/full#supplementary-material

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Articles from Frontiers in Oncology are provided here courtesy of Frontiers Media SA





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