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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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1395314 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 Type7 V8 }% V3 [; C2 |* h
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 * G' @7 b+ J0 O; e6 d- S  i: }2 @
+ Author Affiliations* h# z; q9 ~6 d0 f/ C# T1 [; T
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
5 s! y( ]- A! ?1 g  m$ w2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
0 @1 e( s5 n( M3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
8 E3 B2 A, L! K1 F* G0 p% [' B4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan , `6 d( ~+ P7 U, l' ^6 W
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 5 s' h$ }# S3 K. a8 ~- j- O$ m
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
. S4 c/ ]9 H9 @7Kinki University School of Medicine, Osaka 589-8511, Japan
! t5 T: Q7 n( C% i" }* G) D; D8Izumi Municipal Hospital, Osaka 594-0071, Japan
* e' I0 z+ J4 q/ j" D9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 0 f& k8 t9 m5 D6 c5 i4 N, |
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 6 q1 G5 M) X  ]& q
AbstractBackground: 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. 9 q* Y$ n9 S$ a1 L
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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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2 ^9 v/ b1 V% {( D0 kAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
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9 y$ d! u1 N+ n) }/ hAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  1 E& B9 E; e9 `" u' r8 o

: @% _# S* `) Z/ [3 _Published online on: Thursday, December 1, 2011
9 E# v( e! a4 d4 v( H( q6 @+ O& W4 v7 }5 L* H) ~1 A6 N1 E
Doi: 10.3892/ol.2011.507
( E9 j- u" @  o6 t: x! \5 C
3 w9 s4 I% s) dPages: 405-410
( ^7 A0 [" s: n4 R. [: G; Q
8 |" [& I  p' R4 `1 U0 P! i. N' iAbstract:* y& a  a& B0 D/ \
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
5 j& Q0 C2 u( Y( i& U' q3 @- BF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 1 u; j! N* P, _* ?1 c
+ Author Affiliations" X% N4 _: ]/ z3 d$ u) K
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
! I& E2 D3 r, H2Department of Thoracic Surgery, Kyoto University, Kyoto
' l1 y( U( s; o6 b. S; R3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
8 J; S# V8 x9 x4 q; o6 M&#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
2 ~; {  e7 Q- i2 l% O' _# GReceived September 3, 2010. . _9 `4 R/ F5 j8 C$ ^1 t
Revision received November 11, 2010. 6 f4 x. ^$ V5 \9 _. {5 a; F
Accepted November 17, 2010. 8 m4 `% P! f' n5 }, S
Abstract0 E) i! X$ F4 y4 B) W1 Z5 ]
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.
0 V% T" D* U8 k  P0 uPatients 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 e3 {/ m; P* ?: Q: C0 JResults: 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.
# o3 ]; S  R7 ^9 t- {; gConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 7 j; s& V; e5 t+ h
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。
: q% @( v0 J$ l+ ~$ u! }5 h( |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?
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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
  t2 E8 V: H" G, H1 Y2 vhttp://clinicaltrials.gov/ct2/show/NCT015235878 O) R7 P  D2 G: J5 b5 h1 K

  r/ L6 }( K3 T" R- `: m$ ^+ rBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC4 D% d0 s0 ?* S+ |  ~0 a8 i. u" y
http://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 a+ X$ I: `; U7 }" ?; ~7 q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。
  r- C8 l# @2 ?+ e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 ' M! h- w, r5 L# b6 R# ]
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。0 B# Q$ V2 ?% @' d& L' k, K' j
至今为止,未出 ...

  b# H6 B$ b- \, o" |4 ?没有副作用是第一追求,效果显著是第二追求。
. p! u- o8 @  x& D8 s) _不错。

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