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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1134513 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
' K# m) \/ g4 x! {6 \NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ) \2 P: `9 U3 ?1 m0 {
+ Author Affiliations+ ?2 C1 [8 f+ P9 M" v

) b# q" U1 Q: u( {1 r3 h1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ' K. b* ]9 C( e0 a( ~
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
# X( K. E$ h; M: z3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 2 b- }3 F$ {6 P
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 1 ~9 b- }/ \3 Q, l$ E7 Z, t5 F
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan . P' w4 A% T$ I. u
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
  x0 c$ Y; B3 A0 I1 U! h7Kinki University School of Medicine, Osaka 589-8511, Japan
0 U9 N7 b3 ], V# p8Izumi Municipal Hospital, Osaka 594-0071, Japan
; ^" M& s8 ]# S  P8 f9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
0 i7 l! j! s& ~Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
" M  a& h( g7 v7 a' r$ IAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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1 }9 k9 `) d8 R; TAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ( q, ^$ a, ]3 |8 i) i. Z3 p7 S
5 j9 X) }7 z- y6 |' U. i. g
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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; \; C9 s; E) e7 e  M  O+ ^Published online on: Thursday, December 1, 2011
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/ q4 L3 ~$ |' D  G' QDoi: 10.3892/ol.2011.507
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7 e. |3 l3 t6 UPages: 405-410 2 C% ?. X- p5 g* i, n2 k7 j

; m: l/ W7 i8 j5 y% Z; ?- w$ ~Abstract:! W% b6 v  k1 Y0 K  Z" K; z
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population+ H9 C+ M5 {% p! k; S+ b+ @; r
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 - V  ~: l* Q3 e$ }
+ Author Affiliations( @: |: y9 F* R2 e" B
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
. a+ ~3 \$ c1 O2 B2 B# q2Department of Thoracic Surgery, Kyoto University, Kyoto ! A  t) A3 }$ H! r2 b& ~# v# E
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
! L* A+ H' K2 x8 W3 Y+ q, e  }&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp / P% p( z! K) \  o) W
Received September 3, 2010. 7 p! D" r1 H, O
Revision received November 11, 2010. & Q$ D8 v) H& @" ~: l" E8 ~
Accepted November 17, 2010. 4 T8 S/ x/ ~& M/ f+ N3 x& i8 C: t
Abstract
( z; g3 _0 C2 |3 I7 r0 |Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
7 c7 S: F/ u6 v: l6 D, ^+ N4 v* MPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. 2 z/ e' C( s0 I( F+ l! ]. m0 i7 _
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
9 _) B2 e' y! M# iConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
  [" |! B5 u; \' i今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?# [* t! h* K3 X8 S! B; f
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy: J  L5 l' H! z! r" I$ D2 u7 \  f+ x
http://clinicaltrials.gov/ct2/show/NCT01523587
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. ?* t* _! Q* n3 P5 U6 {( h" IBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
, R0 C. R$ W) X8 [! Q! Phttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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9 t- [0 V$ V' m* U* F# o3 {% o从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。( l3 j# J  O# k5 o7 x) a) u! o
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53 & P  K& u4 q5 g. B/ C
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
; V# _9 S# O. q. B& H& h& x& I) N- d至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。
# P5 h2 p, p9 @- L0 t+ \. V$ l不错。

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